Treatment and Diagnosis of Chemotherapy-Induced Peripheral Neuropathy (CIPN) PDF

Biomedicine & Pharmacotherapy 147 (2022) 112671 Contents lists available at ScienceDirect Biomedicine & Pharmacotherapy journal homepage: www.elsevier.com/locate/biopha Review Treatment and diagnosis of chemotherapy-induced peripheral neuropathy: An update Allison D. Desforges a, Chance M. Hebert a, Allyson L. Spence b, Bailey Reid c, Hemangini A. Dhaibar d, Diana Cruz-Topete d, Elyse M. Cornett e, *, Alan David Kaye f, Ivan Urits g, Omar Viswanath h a LSU Health Shreveport, Shreveport, LA, USA Department of Pharmaceutical Sciences, Regis University School of Pharmacy, Denver, CO 80221, USA Regis University School of Pharmacy, Denver, CO 80221, USA d Department of Molecular and Cellular Physiology, LSU Health Shreveport, 1501 Kings Highway, Shreveport, LA 71103, USA e Department of Anesthesiology, LSU Health Shreveport, 1501 Kings Highway, Shreveport, LA 71103, USA f Departments of Anesthesiology and Pharmacology, Toxicology, and Neurosciences, LSU Health Shreveport, 1501 Kings Highway, Shreveport, LA 71103, USA g Beth Israel Deaconess Medical Center, Department of Anesthesia, Critical Care, and Pain Medicine, 330 Brookline Ave, Boston, MA 02215, USA h Valley Anesthesiology and Pain Consultants – Envision Physician Services, Phoenix, AZ, University of Arizona College of Medicine - Phoenix, Department of Anesthesiology, Phoenix, AZ, Creighton University School of Medicine, Department of Anesthesiology, Omaha, NE, USA b c A R T I C L E I N F O A B S T R A C T Keywords: Chemotherapy-induced peripheral neuropathy Neuropathy Pain Pain management Ion channel-targeted therapies When peripheral neuropathy occurs due to chemotherapy treatment, it is referred to as chemotherapy-induced peripheral neuropathy (CIPN). Typically, symptoms are sensory rather than motor and include reduced feeling and heightened sensitivity to pressure, pain, temperature, and touch. The pathophysiology of CIPN is very complex, and it involves multiple mechanisms leading to its development which will be described specifically for each chemotherapeutic class. There are currently no approved or effective agents for CIPN prevention, and Duloxetine is the only medication that is an effective treatment against CIPN. There is an unavoidable necessity to develop preventative and treatment approaches for CIPN due to its detrimental impact on patients’ lives. The purpose of this review is to examine CIPN, innovative pharmacological and nonpharmacological therapy and preventive strategies for this illness, and future perspectives for this condition and its therapies. 1. Introduction Peripheral neuropathy is used to describe many disorders resulting from damage to peripheral nerves that can present in many different patterns [1,2]. The primary responsibility of peripheral nerves is to relay sensory and motor information of the extremities [2]. Therefore, dam age to these nerves can result in both sensory and motor deficits. [1,3]. Sensory manifestations include paresthesias felt as a burning, tingling, or pins-and-needles [1,4]. It also encompasses mixed perceptions of hyperpathia and hypoesthesia [1,4]. Hyperpathia is increased sensi tivity to stimuli in which normal touch can be painful (allodynia), whereas hypoesthesia is decreased sensitivity, feeling more like numb ness [1,4]. Motor symptoms, although less common, can present as weakness, atrophy, and even decreased reflexes [1,4]. When peripheral neuropathy occurs due to chemotherapy treatment, it is termed Chemotherapy-induced peripheral neuropathy (CIPN) [1,2,5]. CIPN is a frequent adverse effect of anticancer agents most commonly presenting with sensory symptoms more than motor symptoms in a symmetrical “glove and stocking” distribution [3–6]. Patients will typically experi ence various pain, tingling, and numbness beginning at the fingers and toes that progress proximally to involve the arms and legs [4]. Some may even describe it as feeling like they are wearing stockings and gloves when they are not [4]. CIPN develops shortly after onset and continues through chemotherapy treatment [2,4]. Symptoms are dose-dependent, meaning they progress and worsen with continued treatment [2,4,6]. This can ultimately lead to premature cessation or reductions in * Corresponding author. E-mail addresses: [email protected] (A.D. Desforges), [email protected] (C.M. Hebert), [email protected] (A.L. Spence), [email protected] (B. Reid), [email protected] (H.A. Dhaibar), [email protected] (D. Cruz-Topete), [email protected] (E.M. Cornett), [email protected] (A.D. Kaye), [email protected] (I. Urits), [email protected] (O. Viswanath). https://doi.org/10.1016/j.biopha.2022.112671 Received 26 October 2021; Received in revised form 21 January 2022; Accepted 25 January 2022 Available online 29 January 2022 0753-3322/Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). A.D. Desforges et al. Biomedicine & Pharmacotherapy 147 (2022) 112671 treatment doses, potentially altering overall survival [3,6]. CIPN symptoms often diminish with time but, in some cases, can pursue for months after treatment discontinuation [1,2]. Patients with a more se vere CIPN presentation experience a decreased quality of life physically, emotionally, and socially [7]. They also reported more pain, fatigue, and GI symptoms [7]. Furthermore, CIPN has been associated with inter fering with patients’ ability to work and a greater financial burden [7–9]. On average, healthcare costs of cases with CIPN were $17,344 higher when compared to a control group [9]. The pathophysiology of CIPN is rather complex, with multiple factors and processes leading to its development which varies with the different classes of chemotherapy drugs. What is well known is that larger doses and several courses of treatment correlate to patients being more likely to develop CIPN [2]. In addition, patients have an increased risk of CIPN if they have diabetes or already have peripheral neuropathy [2,10]. The treatments repeatedly shown to have an increased chance of causing peripheral neuropathy include taxanes, vinca alkaloids, platinum drugs, Bortezomib, and thalidomide [2,5,6,11]. The main mechanisms responsible for the development of CIPN are mitochondrial toxicity and oxidative stress, DNA damage, axonal transport disruption, and ion channel remodeling in peripheral nerves [12,13]. Taxanes and vinca alkaloids act on microtubules leading to their dysfunction [3,5,13]. While taxanes hyperstabilize the tubules, vinca alkaloids prevent poly merization [3,5,13]. The loss of normally functioning microtubules impairs axonal transport of cell products crucial to the function and structure of axons [13]. There is also evidence of taxane-induced CIPN sexual dimorphism in rodents, where Toll-like receptor 9 (TLR9) expression in macrophages infiltrating the dorsal root ganglion may play a role in the development of pathological, physiological, and behavioral changes in male mice but not females [14]. Platinum agents change the structure of DNA and appear to induce neural toxicity mainly through the dorsal root ganglion (DRG) [3,5]. They have been shown to reduce nucleolar size in the sensory DRG cells in which the degree of nucleolar size change correlated with the degree of neurotoxicity [15]. Oxaliplatin specifically induces acute neuropathy via alterations in axonal voltage-gated sodium channels [3,5]. Bortezomib is a proteasome in hibitor that seems to encourage apoptosis and prevent regular rates of cell division [13]. Pathogenesis of how Boretzomib promotes neuropa thy is not completely understood [3,5,13]. One possibility is through its alterations on sphingolipid metabolism in astrocytes, which is involved in pain modulation and perception [16]. Thalidomide is another chemotherapeutic whose mechanism of causing CIPN is poorly under stood [3,5]. It is thought to be related to immunomodulation, angio genesis inhibition, and cytokine alteration [5]. Schwann cell damage, which myelinates peripheral nerves, is involved in the pathogenesis of CIPN, and drugs that inhibit anticancer agent-induced Schwann cell damage are expected to be therapeutic agents for CIPN [17]. Prevention and treatment of CIPN are tremendously challenging because of the varying underlying pathophysiological causes with differing chemotherapy agents [18,19]. While multiple hypotheses exist, no treatment based on these proposed mechanisms has led to acceptable intervention options [5,18]. According to ASCO and ESMO guidelines, there are no recommended or effective agents to prevent CIPN [20,21]. They suggest assessing patients regularly for the devel opment of CIPN and to be aware of patients at high risk with factors predisposing them to develop CIPN [20,21]. In terms of treatment, the only recommended agent proven to be efficacious against CIPN is duloxetine [20,21]. Clinical trials support that duloxetine treatment reduces the pain, numbness, and tingling symptoms patients experience with CIPN, but only to a moderate degree [22]. However, duloxetine still has limited benefit. It should be noted that it had the greatest effect on treating CIPN due to platinum-based drugs than other therapies like taxanes [21]. Other options such as tricyclic antidepressants or anti-seizure medications have been explored, but trials show mixed results [18,23]. ASCO currently makes no recommendations on these other therapies, but ESMO does endorse their consideration for treatment [20,21]. Additionally, rehabilitation via physical and/or occupational ther apy may be helpful in CIPN patients with reduced function [2]. There fore, there is still a need to explore and develop efficacious treatments for CIPN. This review aims to discuss CIPN, novel pharmacological and nonpharmacological treatment and prevention methods for CIPN, and future directions for this condition and its treatments. 2. Assessment, diagnosis, and epidemiology of chemotherapyinduced peripheral neuropathy The epidemiology of CIPN is complicated because of the many different scales used to assess CIPN [24]. One study reports a CIPN aggregate prevalence of 48%, with rates starting at 68.1% within one month after the conclusion of chemotherapy treatment and steadily declining with the duration of treatment [19]. Another study shows a one-year cumulative prevalence rate of around 28.7% [24]. One of the main determinants of whether patients will develop CIPN is their type of cancer, establishing the type of treatment they will undergo [25]. Solid tumor cancers are the most likely to be treated with the neurotoxic chemotherapy drugs previously mentioned, therefore increasing the risk of these patients developing CIPN [25]. Furthermore, the cumulative dose of the chemotherapy agent is recognized as the most important factor in CIPN development [25]. Currently, there is no standardized approach for assessing and diagnosing CIPN, as this has proven to be very difficult to quantify definitively [18,26–28]. Broadly, assessment techniques can be divided into objective and subjective approaches [18]. One effective objective assessment that can be used is a neurophysiological examination [5,29]. Nerve conduction studies (NCS) can help distinguish between demye lination vs. axonopathy pathologies useful in assessing CIPN because almost all cases are related to axonopathy [6,30]. NCS will show reduced amplitudes of sensory nerve action potentials (SNAPs) and compound muscle action potentials (CAMPs) with nearly unchanged conduction velocities in CIPN [3,5]. This contrasts with the decreased nerve conduction velocity you would see in a demyelinating disease [5]. An advantage to these tests is they are readily accessible in most hos pitals. However, they only assess large myelinated fibers [30]. CIPN preferentially damages small fibers, limiting the use of NCS [30]. Group assessments that study these small fibers are quantitative sensory testing (QST), which evaluate pain and temperature [30].asw One of the subjective assessments is the National Cancer InstituteCommon Terminology Criteria for Adverse Events (NCI-CTCAE), in which a medical professional uses a 1–5 scale to grade adverse events (including peripheral neuropathy) based on the severity of the symp toms [31]. Additional subjective tests include patient-reported assess ments of their neuropathy, which, compared to physician-reported evaluations, generally reported more severe symptoms and effects on their daily lives [32]. Physicians underreporting and underestimating the severity of patients’ CIPN shows a clear and needed importance of using patient-reported outcomes for assessing CIPN [32]. Given the limitations of both objective and subjective studies, com posite studies have become progressively favorable for assessing CIPN [5,33]. These studies combine objective and subjective studies to eval uate CIPN, with the most common one being the Total Neuropathy Score (TNS) [5,34]. This allows simultaneous assessment of graded physician-reported severity with objective sensibility measures and NCS [34]. A pitfall to this method is that it is more time-consuming than other studies and requires instrumentation, leading to issues of avail ability and standardization [33,34]. It has proven to be more sensitive than the NCI-CTCAE, and it is proposed as a reliable source for assessing both severity and changes following CIPN [34]. Since CIPN symptoms are highly subjective, it leaves for a chal lenging diagnosis [26]. The first step in diagnosing CIPN is to exclude other potential neuropathy causes such as preexisting conditions, asso ciation with surgery, and any other factors that would come with an 2 A.D. Desforges et al. Biomedicine & Pharmacotherapy 147 (2022) 112671 increased risk of developing peripheral neuropathy [18,26,35]. Following exclusion of other potential causes, clinical examination is usually used to diagnose CIPN [30,35]. This greatly relies on the pres ence of sensory abnormalities, which can be evaluated and graded via several different assessments previously discussed [30,35]. However, a clinical examination can only endorse abnormalities in the nervous system but cannot prove their origin [36]. Despite its disadvantages, clinical examination for the diagnosis of CIPN is cost-effective with easy administration making it very appealing [30]. pharmacotherapeutic option for the management of CIPN [50]. Like gabapentin, pregabalin is an anticonvulsant medication that binds to the alpha2-delta protein, which inhibits the presynaptic, voltage-gated calcium channel and is thus considered a first-line treatment option for neuropathic pain [51]. Despite these drugs’ seemingly identical mechanisms, a lower-cost generic version of gabapentin is available, making it more commonly prescribed than pregabalin in treating neuropathic pain. However, studies have shown that patients who respond poorly to gabapentin may experience a clinically significant improvement in pain when switching to pregabalin [52]. The varied response to these medications is likely due to their different pharma cokinetic profiles. Compared to gabapentin, pregabalin has a faster ab sorption rate, a higher maximum absorption rate, and a higher bioavailability [53]. Additional studies should further examine the varying efficacy of these medications to treat CIPN symptoms, especially pain. 3. Treatments 3.1. Nerve-protective therapy Erythropoietin (EPO) is a cytokine that is involved in hematopoiesis regulation. It also possesses neuroprotective effects, such as enhancing nerve regeneration and recovery following peripheral nerve injury [37, 38]. As chemotherapeutic agents are thought to induce peripheral neuropathy through the impairment of the peripheral nerves, this neu roprotective effect makes EPO a seemingly ideal candidate for CIPN [39]. However, the utilization of EPO for the treatment of CIPN is highly contraindicated and should be approached with caution as EPO is associated with tumor cell growth [40]. 3.3. Anti-inflammatory therapies Some studies suggest that the best treatment approach for CIPN in cludes non-steroidal anti-inflammatory drugs (NSAIDs) that can reduce pain symptoms and the underlying inflammation associated with pain [54]. However, studies involving NSAIDs in the treatment of CIPN are limited and require further evaluation. 3.2. Ion channel-targeted therapies 3.4. Neurotransmitter-based therapy One of the many pathophysiological characteristics associated with CIPN is the alteration of ion channel expression in primary afferent sensory neurons [41]. Therefore, researchers have postulated that these ion channels may serve as a potential target in the treatment of CIPN. These ion channels can be targeted through substances that can bind to them, such as lidocaine, or through the direct administration of these ions, such as calcium and magnesium. Lidocaine is a sodium channel blocker that prevents the flow of so dium ions through the channel pore [42]. It effectively relieves various causes of neuropathic pain, including CIPN [43,44]. Intravenous (IV) lidocaine produced a significant, moderate long-term (average of 23 days) analgesic effect in 8 out of 9 patients with CIPN [45]. These results are very promising, especially since the most common adverse effects associated with IV lidocaine include irritation at the injection site. To overcome this side effect and perhaps increase the intended duration of action, oral sodium channel blockers, such as mexiletine, may be administered instead of IV lidocaine [45]. These promising results demonstrate the need for larger clinical trials to further investigate the role of sodium channel blockers in the treat ment of CIPN. Magnesium infusion has also been postulated as a potential thera peutic option for CIPN. Researchers found a direct negative correlation between magnesium intake and CIPN severity. The magnesium supple mentation during chemotherapy is proposed to decrease oxaliplatininduced hyper-excitability of neurons and overall neuron damage. Increased magnesium administration levels were associated with a lower prevalence of CIPN and less severe symptoms in individuals who did experience CIPN [46]. However, other studies have failed to demonstrate any efficacy in using magnesium infusions to treat CIPN [47]. Similarly, calcium infusions failed to reduce CIPN in multiple studies, including those that combined calcium and magnesium in fusions in hopes of achieving an additive effect [48]. Gabapentin is an anticonvulsant medication that inhibits the release of excitatory neurotransmitters. To achieve this, gabapentin crosses the blood-brain barrier and binds with high affinity to the alpha2-delta protein, a subunit to the presynaptic voltage-gated calcium channels of neurons[43]. Multiple studies have shown that gabapentin adminis tration may alleviate the symptoms associated with CIPN, including neuropathic pain and neurologic deficits [49]. Furthermore, gabapentin has a mild side effect profile, making it a promising Venlafaxine (Effexor XR®) and duloxetine (Cymbalta®) belong to a class of medications called selective serotonin and norepinephrine re uptake inhibitors (SNRIs). These medications, primarily used to treat major depressive disorder (MDD), increase serotonin and norepineph rine levels in the neuronal synapse by blocking their subsequent reup take [55]. SNRIs are also the first and only FDA-approved drug class for treating pain caused by diabetic peripheral neuropathy [56]. The side effects of venlafaxine and duloxetine are generally mild and include nausea, changes in sleeping patterns, constipation, sexual dysfunction, and increased heart rate and blood pressure. Additionally, these medi cations can cause an increase in bleeding risk among patients taking anticoagulants (e.g., warfarin and aspirin) [57]. A recent meta-analysis that included ten different studies (both controlled studies and observational studies) evaluated the potential use of SNRIs for the treatment of CIPN. SNRIs demonstrated substantial ef ficacy and excellent tolerability for the treatment of CIPN [58]. Although these studies emphasized the therapeutic potential of both venlafaxine and duloxetine in CIPN, further studies revealed that duloxetine possesses a higher efficacy in reducing the grade and severity of neuropathic pain [55,59,60]. Duloxetine is often considered a first-line treatment option for CIPN [61]. Despite these exciting results, other studies could not identify a significant reduction in acute or chronic CIPN symptoms following venlafaxine treatment [62]. However, these differences are likely due to alterations in venlafaxine dose, as lower doses (i.e., 37.5 mg once daily) were administered in these subsequent studies, and patients with neu ropathy generally require higher doses of venlafaxine (i.e., 75 mg twice daily) [62,63]. A closer look at the underlying mechanisms of ven lafaxine reveals a potential mechanism for this dose-related efficacy. Venlafaxine has a 30-fold greater affinity for serotonin transporters compared to norepinephrine transporters. Hence, venlafaxine acts pri marily on serotonin reuptake at low doses, making it act similarly to a selective serotonin reuptake inhibitor (SSRI) rather than an SNRI. This key difference likely accounts for its ineffectiveness in treating CIPN at lower doses [62,64]. Additional studies should be done to determine the appropriate dose of SNRIs in the treatment of CIPN to ensure efficacy while minimizing adverse effects. Tricyclic antidepressants (TCAs), which also block the reuptake of norepinephrine and serotonin, have long been recognized for their use in 3 A.D. Desforges et al. Biomedicine & Pharmacotherapy 147 (2022) 112671 treating neuropathic pain [65]. Although these drugs have demon strated efficacy in reducing neuropathic pain, studies have found these drugs to be ineffective in treating pain associated with CIPN [66–68]. TCAs also present a high incidence of adverse effects and should be avoided until more conclusive studies can be conducted [69]. these treatment regimens have only produced a modest effect, if any. When researchers applied a topical mixture of amitriptyline and keta mine to patients experiencing numbness, tingling, and/or pain associ ated with CIPN three times per day for three weeks, they did not see any significant improvement in symptoms compared to placebo [85]. In another similar study, a topical mixture of amitriptyline, ketamine, and baclofen was applied to the area associated with pain twice daily for four weeks. However, even with the addition of baclofen, patients only re ported a slight improvement of symptoms [86]. Prior studies have shown that activating transient receptor potential melastatin 8 (TRPM8), the primary cold sensor in humans, can suppress the mechanical sensitization associated with CIPN [87]. Moreover, these molecular receptors are upregulated in neuropathic pain models, sug gesting they may provide an easy and efficient target in the treatment of CIPN [88]. Although some studies have illuminated the possible benefits of menthol in treating CIPN, further studies need to be done to strengthen this very limited data [89]. The transient receptor potential (TRP) channel family is credited with being the most important ion channel family involved in detecting and transmitting noxious stimuli [90]. Among these TRP channels is the transient receptor potential vanilloid receptor (TRPV1), which initiates neurogenic inflammation and pain sensation and is thought to be involved in the CIPN-associated pain pathology [91]. Topical capsaicin is a TRPV1 agonist that has demonstrated efficacy in treating neuro pathic pain, including that associated with CIPN [92–94]. Although capsaicin, which is the active component found in chili peppers, may cause a burning sensation, none of the patients within these studies found this side effect to be intolerable. 3.5. Antioxidants The manganese chelates and superoxide dismutase mimetic man gafodipir is a widely used diagnostic tool that enhances contrast during magnetic resonance imaging (MRI). Its side effects, including cardio vascular effects and facial flushing, can be prevented with an adequate rate of intravenous injection [70]. Both preclinical and clinical studies have provided evidence for the use of mangafodipir in treating CIPN, where individuals experienced a significant reduction in pain [71]. Importantly, mangafodipir is an efficacious inhibitor of CIPN without interfering with the tumoricidal activity of chemotherapy [72]. One proposed mechanism of CIPN is the increased production of reactive oxygen species (ROS) in patients receiving chemotherapy, as an increase in ROS can cause direct damage to nerves through enhanced oxidative stress. Additionally, several chemotherapy agents cause a depletion of certain elements that make nerves more susceptible to injury (e.g., glutathione), therefore contributing to the observed neurotoxicity [73]. Although the underlying mechanisms responsible for the ability of mangafodipir to treat CIPN are not entirely elucidated, studies have suggested its antioxidant properties may be neuro- and/or myelin-protective and prevent this ROS-mediated injury [71,74]. Man gafodipir also acts as a superoxide dismutase (SOD) mimetic and pos sesses catalase-, and glutathione reductase–like properties, therefore targeting and preventing multiple steps of the ROS cascade that induce CIPN. Specifically, mangafodipir inhibits cellular oxidative stress by catalyzing the dismutation of superoxide and disarming redox-active iron [72]. Unfortunately, mangafodipir was removed from the U.S. market in 2003 and the European market in 2012 due to commercial reasons from the manufacturer [75]. 3.8. Non-drug treatments A meta-analysis of 12 studies was conducted to evaluate the efficacy of non-pharmacologic interventions in treating CIPN. These studies found that acupuncture, massage, and foot bath independently pro duced a significant reduction in CIPN symptoms [95]. Another systemic review found that two out of three studies revealed acupuncture notably alleviated CIPN pain, although the third study did not reveal a signifi cant effect [38]. Further studies have shown the effectiveness of acupuncture in treating CIPN-associated pain and numbness, all pre senting with little to minimal side effects [96–99]. Physical therapy is an established and highly effective treatment option for neuropathic pain and thus has been evaluated for its potential use in the treatment of CIPN. A home physical therapy program that included exercise in patients with breast cancer revealed less pain and decreased pain over time in the treatment group compared to the sedentary group [100]. A systemic review that evaluated physical therapy for CIPN found similar results, whereas patients reported a significant reduction in CIPN symptoms, including pain and paresthesia [101]. Another promising noninvasive treatment strategy for CIPN includes scrambler therapy, whereby a machine is used to block the transmission of pain signals by emitting synthetic, non-pain information to C fiber surface receptors, which normally receive pain messages [102]. Pilot evaluations revealed a significant reduction in pain symptoms associ ated with CIPN, and these results were long-lasting as they were still present throughout ten weeks of follow-up [103,104]. Notably, no adverse events were reported in these studies. Unfortunately, these studies neglected to incorporate a control group for comparison. Ran domized, double-blind clinical trials that included a sham group found no significant difference between CIPN patients receiving scrambler versus sham therapy [105]. Further studies should be conducted to determine if scrambler therapy is a viable treatment option for those suffering from CIPN symptoms, such as pain. Neurofeedback (NF) is a non-invasive treatment that targets brain activity to reduce the severity and impact of chronic pain. NF therapy is performed in conjunction with an electroencephalogram (EEG) or 3.6. Other drugs Another proposed mechanism of CIPN is the ability of chemotherapy agents to sensitize neurons in the spinal cord responsible for receiving and analyzing pain signals. Cannabinoids activate both the 5-HT1A re ceptor system and the CB1 receptors to suppress this mechanical sensi tization and thus have been elucidated for the potential treatment of CIPN [76,77]. Studies have shown that endocannabinoid deficiencies are prevalent during CIPN, and researchers hypothesize that by replenishing this deficit with cannabinoids, patients may experience pain relief [78]. A pilot trial investigated nabiximols, which CIPN. Un fortunately, nabiximols did not significantly reduce CIPN. However, the researchers did emphasize that 5 out of 16 responders reported a sig nificant reduction in CIPN that was far greater than anyone in the pla cebo group [79]. Therefore, further studies should be done to identify individuals who may benefit from cannabinoid treatment for CIPN, especially since side effects from these medications have been rarely reported [80]. Glutamine is an amino acid naturally produced by the body and plays an important role in our immune system and intestinal health [81]. Although studies have supported the efficacy of oral glutamine therapy in alleviating CIPN symptoms, these studies were limited by small sample sizes and the lack of a control group [82,83]. As oral glutamine lacks clear evidence to support its efficacy in treating CIPN, it is not recommended to treat CIPN symptoms in patients [84]. 3.7. Topical treatments Multiple studies have examined potential topical treatments, both alone and in combination, for the treatment of CIPN. However, most of 4 A.D. Desforges et al. Biomedicine & Pharmacotherapy 147 (2022) 112671 functional magnetic resonance imaging (fMRI), which allows for the accurate measurement of brain activity [106]. A randomized controlled trial found that EEG NF significantly reduced CIPN symptoms compared to control, suggesting NF may be a productive treatment option for patients suffering from CIPN [107]. to assess and diagnose. There are several different assessments and diagnosis methods available, but currently, there is no standardization on which one to use. Part of the issue in finding a treatment for CIPN is that the pathophysiology is not well understood. This has led to many different pharmacological and non-pharmacological agents being used in trials to try and find prevention and treatment methods for CIPN. Many agents show great promise in their use but need larger studies conducted on them, such as IV lidocaine, cannabinoids, oral glutamine, cryotherapy, acupuncture, massage therapy, and exercise. In contrast, others were found to show no real efficacy or need for further trials because of the poor outcomes such as calcium, magnesium, TCAs, and nabiximols. Furthermore, certain therapies can increase the risk and severity of CIPN and should be avoided, including EPO and acetyl-L-carnitine (ALC). The future direction for the treatment and prevention of CIPN is aiming to better understand the pathophysiology and, as a result, hopefully, find a therapy that can help treat this condition. Until then, duloxetine is currently the only recommended agent for CIPN treatment. Non-pharmacological therapies have proven to be helpful in some pa tients and may provide relief in certain individuals. 3.9. Future directions in treatment of chemotherapy-induced peripheral neuropathy Many prevention and treatment agents, both pharmacological and not, have been discussed throughout this paper. While several therapies look promising, few have proven to definitively prevent and/or treat CIPN. Currently, duloxetine is the only agent endorsed by the ASCO and ESMO guidelines for treatment for CIPN [20,21]. It is well tolerated and has recently been found to not interfere with the effects of chemother apeutic agents resulting in it being supported as the first standardized drug to treat CIPN [20,108]. While no other agent has proven to treat and prevent CIPN with the same efficacy and safety as duloxetine, many have shown great promise and will be further discussed below. One of the more recent pharmacological agents being explored is MR309, a selective antagonist of the sigma 1 receptor [109,110]. The sigma 1 receptor is found in the endoplasmic reticulum and modulates nociception and sensitization signaling pathways [109]. A phase II trial found patients treated with MR309 had a significant reduction in chronic neuropathic pain compared to the placebo group [109]. In addition, MR309 was found to be safe and allowed patients to receive a higher cumulative dose of the chemotherapeutic agent they were being treated with [109,110]. Scrambler therapy is another commonly studied technique to reduce CIPN symptoms. This treatment works by sending “non-pain” signals to replace “pain” signals perceived by the nerves [111–113]. The goal is to essentially block pain information’s effects, thereby reducing the pain felt by the patient [112]. Scrambler therapy can drastically relieve acute and chronically CIPN pain with no toxicity [111,112]. Another treatment being tried is topical menthol [114]. Derived from mint, menthol activates the TRPM-8 receptor, responsible for detecting cold stimuli in peripheral nerves [114]. It was found to have a significant therapeutic response in CIPN when administered twice a day to affected skin areas and tolerated well [114]. Integrative and behavioral approaches focus on pain that deals with the complex processing of cognition and emotion to influence pain perception [115]. Studies have shown that patients’ increased cata strophizing was associated with more severe pain symptoms [116]. The following complementary therapies focus on psychological and behav ioral strategies and are all safe, inexpensive, and come without adverse effects [115]. Although there are mixed reviews, acupuncture may have its role in CIPN management [117]. Acupuncture stimulation suppresses nociception in peripheral sites by increasing endogenous opioid release [118]. While some studies report reduced pain and improved quality of life in CIPN patients, others have shown no benefit in either of these areas with acupuncture therapy [117]. Because this treatment is deemed safe and could alleviate some patients’ symptoms, it can be considered at the clinician’s discretion [117]. Another explored approach is massage therapy to manage cancer pain [115]. The basis of this is that calming the body calms the mind, which relaxes the body [115]. Massage ther apy reduces pain, anxiety, nausea, and fatigue [115]. Lastly, mind-body techniques can manage cancer pain, including CIPN [115]. These combine educating the patient that psychological factors can influence pain (and vice versa) with training in cognitive (hypnosis, imagery, etc.) or behavioral coping skills [115]. Funding Diana Cruz-Topete, PhD, Heart, Lung, and Blood Institute (NHBLI) 5K01HL144882-0(D.C.-T.); Center for Redox Biology and Cardiovascu lar Disease (D.C.-T. and H.A.D.). CRediT authorship contribution statement Elyse M. Cornett: Conceptualization, Methodology, Software, Writing – review & editing. Alan David Kaye: Conceptualization, Methodology, Software, Supervision, Writing – review & editing. Diana Cruz-Topete: Conceptualization, Methodology, Software, Writing – re view & editing. Ivan Urits: Conceptualization, Methodology, Software, Writing – review & editing. Omar Viswanathb: Conceptualization, Methodology, Software, Omar Viswanat. Hemangini A. Dhaibar: Data curation, Writing – original draft. Allison D. Desforges: Data curation, Writing – original draft, Writing – review & editing. Chance M. Her bert: Data curation, Writing – original draft, Writing – review & editing. Allyson L. Spence: Visualization, Investigation, Writing – review & editing. Hemangini A. Dhaibar: Software, Validation. Bailey Reid: Visualization, Investigation, Writing – review & editing. Hemangini Dhaibar: Writing – review & editing. Conflict of interest statement None References [1] K. Barrell, A.G. Smith, Peripheral neuropathy, Med. Clin. North Am. 103 (2) (2019) 383–397. [2] T.J. Brown, R. Sedhom, A. Gupta, Chemotherapy-induced peripheral neuropathy, JAMA Oncol. 5 (5) (2019) 750. [3] N.C. Miltenburg, W. Boogerd, Chemotherapy-induced neuropathy: a comprehensive survey, Cancer Treat. Rev. 40 (7) (2014) 872–882. [4] M.D. Stubblefield, H.J. Burstein, A.W. Burton, C.M. Custodio, G.E. Deng, M. Ho, L. Junck, G.S. Morris, J.A. Paice, S. Tummala, J.H. Von Roenn, NCCN task force report: management of neuropathy in cancer, JNCCN J. Natl. Compr. Cancer Netw. 7 (SUPPL. 5) (2009) 1–26. [5] G. Cavaletti, P. Marmiroli, Chemotherapy-induced peripheral neurotoxicity, Nat. Rev. Neurol. 6 (12) (2010) 657–666. [6] D.L. Hershman, C. Lacchetti, R.H. Dworkin, E.M. Lavoie Smith, J. Bleeker, G. Cavaletti, C. Chauhan, P. Gavin, A. Lavino, M.B. Lustberg, J. Paice, B. Schneider, M.L. Smith, T. Smith, S. Terstriep, N. Wagner-Johnston, K. Bak, C. L. Loprinzi, O. American Society of Clinical, Prevention and management of chemotherapy-induced peripheral neuropathy in survivors of adult cancers: American society of clinical oncology clinical practice guideline, J. Clin. Oncol. 32 (18) (2014) 1941–1967. [7] N.P. Ezendam, B. Pijlman, C. Bhugwandass, J.F. Pruijt, F. Mols, M.C. Vos, J. M. Pijnenborg, L.V. van de Poll-Franse, Chemotherapy-induced peripheral 4. Conclusion CIPN is a possible adverse effect of chemotherapy. In addition to having to live with the pain, it also can affect patients’ ability to work and is associated with a greater financial burden than in patients who do not experience CIPN. CIPN is not only hard to treat, but it is also difficult 5 A.D. Desforges et al. [8] [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22] [23] [24] [25] [26] [27] [28] [29] [30] [31] Biomedicine & Pharmacotherapy 147 (2022) 112671 neuropathy and its impact on health-related quality of life among ovarian cancer survivors: results from the population-based PROFILES registry, Gynecol. Oncol. 135 (3) (2014) 510–517. N.R. Zanville, K.N.H. Nudelman, D.J. Smith, A.H.D. Von, B.C. McDonald, V. L. Champion, et al., Evaluating the impact of chemotherapy-induced peripheral neuropathy symptoms (CIPN-sx) on perceived ability to work in breast cancer survivors during the first year post-treatment, Support. Care Cancer 24 (11) (2016) 4779–4789. C.T. Pike, H.G. Birnbaum, C.E. Muehlenbein, G.M. Pohl, R.B. Natale, Healthcare costs and workloss burden of patients with chemotherapy-associated peripheral neuropathy in breast, ovarian, head and neck, and nonsmall cell lung cancer, Chemother. Res. Pract. 2012 (2012) 1–10. A. Badros, O. Goloubeva, J.S. Dalal, I. Can, J. Thompson, A.P. Rapoport, M. Heyman, G. Akpek, R.G. Fenton, Neurotoxicity of bortezomib therapy in multiple myeloma: a single-center experience and review of the literature, Cancer 110 (5) (2007) 1042–1049. W. Grisold, G. Cavaletti, A.J. Windebank, Peripheral neuropathies from chemotherapeutics and targeted agents: diagnosis, treatment, and prevention, Neuro Oncol. 14 (SUPPL.4) (2012) 45–54. N. Kerckhove, A. Collin, S. Condé, C. Chaleteix, D. Pezet, D. Balayssac, Long-term effects, pathophysiological mechanisms, and risk factors of chemotherapyinduced peripheral neuropathies: a comprehensive literature review, Front. Pharmacol. 8 (FEB) (2017) 1–17. A.J. Windebank, W. Grisold, Chemotherapy-induced neuropathy, J. Peripher. Nerv. Syst. JPNS 46 (2008) 27–46. Gordon-Williams R., Farquhar-Smith P. Recent advances in understanding chemotherapy-induced peripheral neuropathy. F1000Res. 2020 Mar 11;9:F1000 Faculty Rev-177. M.J. McKeage, T. Hsu, D. Screnci, G. Haddad, B.C. Baguley, Nucleolar damage correlates with neurotoxicity induced by different platinum drugs, Br. J. Cancer 85 (8) (2001) 1219–1225. R. Gordon-Williams, P. Farquhar-Smith, Recent advances in understanding chemotherapy-induced peripheral neuropathy, F1000Res 9 (2020) 177. M. Koyanagi, S. Imai, M. Matsumoto, Y. Iguma, N. Kawaguchi-Sakita, T. Kotake, Y. Iwamitsu, M. Ntogwa, R. Hiraiwa, K. Nagayasu, M. Saigo, T. Ogihara, A. Yonezawa, T. Omura, S. Nakagawa, T. Nakagawa, K. Matsubara, Pronociceptive roles of schwann cell-derived galectin-3 in taxane-induced peripheral neuropathy, Cancer Res. 81 (8) (2021) 2207–2219. M. Stillman, J.P. Cata, Management of chemotherapy-induced peripheral neuropathy, Curr. Pain. Headache Rep. 10 (4) (2006) 279–287. M. Seretny, G.L. Currie, E.S. Sena, S. Ramnarine, R. Grant, M.R. Macleod, L. A. Colvin, M. Fallon, Incidence, prevalence, and predictors of chemotherapyinduced peripheral neuropathy: a systematic review and meta-analysis, Pain 155 (12) (2014) 2461–2470. C.L. Loprinzi, C. Lacchetti, J. Bleeker, G. Cavaletti, C. Chauhan, D.L. Hertz, M. R. Kelley, A. Lavino, M.B. Lustberg, J.A. Paice, B.P. Schneider, E.M. Lavoie Smith, M.L. Smith, T.J. Smith, N. Wagner-Johnston, D.L. Hershman, Prevention and management of chemotherapy-induced peripheral neuropathy in survivors of adult cancers: ASCO guideline update, J. Clin. Oncol. 38 (28) (2020) 3325–3348. B. Jordan, A. Margulies, F. Cardoso, G. Cavaletti, H.S. Haugnes, P. Jahn, E. Le Rhun, F. Scotté, M.J.B Taphoorn, ESMO Guidelines Committee. Electronic address: [email protected], EONS Education Working Group. Electronic address: [email protected], EANO Guideline Committee. Electronic address: [email protected], Systemic anticancer therapyinduced peripheral and central neurotoxicity: ESMO–EONS–EANO Clinical Practice Guidelines for diagnosis, prevention, treatment and follow-up, Ann. Oncol. 31 (10) (2020) 1306–1319. E.M.L. Smith, Effect of duloxetine on pain, function, and quality of life among patients with chemotherapy-induced painful peripheral neuropathy: a randomized clinical trial, JAMA J. Am. Med. Assoc. 309 (13) (2014) 1359–1367. K.S. Y, Managing peripheral neuropathy, Coping Cancer 22 (5) (2008) 30, 1p. A. Molassiotis, H.L. Cheng, V. Lopez, J.S.K. Au, A. Chan, A. Bandla, K.T. Leung, Y. C. Li, K.H. Wong, L. Suen, C.W. Chan, J. Yorke, C. Farrell, R. Sundar, Are we misestimating chemotherapy-induced peripheral neuropathy? Analysis of assessment methodologies from a prospective, multinational, longitudinal cohort study of patients receiving neurotoxic chemotherapy, BMC Cancer 19 (1) (2019) 1–19. G. Cavaletti, P. Alberti, A.A. Argyriou, M. Lustberg, N.P. Staff, S. Tamburin, Chemotherapy-induced peripheral neurotoxicity: a multifaceted, still unsolved issue, J. Peripher. Nerv. Syst. 24 (S2) (2019) S6–S12. F.H. Hausheer, R.L. Schilsky, S. Bain, E.J. Berghorn, F. Lieberman, Diagnosis, management, and evaluation of chemotherapy-induced peripheral neuropathy, Semin. Oncol. 33 (1) (2006) 15–49. D. Iżycki, A.A. Niezgoda, M. Kaźmierczak, T. Piorunek, N. Iżycka, B. Karaszewska, E. Nowak-Markwitz, Chemotherapy-induced peripheral neuropathy - diagnosis, evolution and treatment, Ginekol. Pol. 87 (7) (2016) 516–521. S.J.L. Flatters, P.M. Dougherty, L.A. Colvin, Clinical and preclinical perspectives on Chemotherapy-Induced Peripheral Neuropathy (CIPN): a narrative review, Br. J. Anaesth. 119 (4) (2017) 737–749. N.C. Miltenburg, W. Boogerd, Chemotherapy-induced neuropathy: a comprehensive survey, Cancer Treat. Rev. 40 (7) (2014) 872–882. G. Gutiérrez-Gutiérrez, M. Sereno, A. Miralles, E. Casado-Sáenz, E. GutiérrezRivas, Chemotherapy-induced peripheral neuropathy: clinical features, diagnosis, prevention and treatment strategies, Clin. Transl. Oncol. 12 (2) (2010) 81–91. E.N. Gathogo, S. Shah, F.A. Post, Common terminology criteria for adverse events (CTCAE), Aids 31 (8) (2017) 1199–1201. [32] K. Shimozuma, Y. Ohashi, A. Takeuchi, T. Aranishi, S. Morita, K. Kuroi, S. Ohsumi, H. Makino, H. Mukai, N. Katsumata, Y. Sunada, T. Watanabe, F. H. Hausheer, Feasibility and validity of the Patient Neurotoxicity Questionnaire during taxane chemotherapy in a phase III randomized trial in patients with breast cancer: N-SAS BC 02, Support. Care Cancer 17 (12) (2009) 1483–1491. [33] G. Cavaletti, B. Frigeni, F. Lanzani, L. Mattavelli, E. Susani, P. Alberti, D. Cortinovis, P. Bidoli, Chemotherapy-Induced Peripheral Neurotoxicity assessment: A critical revision of the currently available tools, Eur. J. Cancer 46 (3) (2010) 479–494. [34] G. Cavaletti, B. Frigeni, F. Lanzani, M. Piatti, S. Rota, C. Briani, G. Zara, R. Plasmati, F. Pastorelli, A. Caraceni, A. Pace, M. Manicone, A. Lissoni, N. Colombo, G. Bianchi, C. Zanna, G. Italian NETox, The Total Neuropathy Score as an assessment tool for grading the course of chemotherapy-induced peripheral neurotoxicity: comparison with the National Cancer Institute-Common Toxicity Scale, J. Peripher. Nerv. Syst. 12 (3) (2007) 210–215. [35] P. Hansson, Neuropathic pain: clinical characteristics and diagnostic workup, Eur. J. Pain. 6 (SUPPL. 1) (2002) 47–50. [36] M. Haanpää, N. Attal, M. Backonja, R. Baron, M. Bennett, D. Bouhassira, G. Cruccu, P. Hansson, J.A. Haythornthwaite, G.D. Iannetti, T.S. Jensen, T. Kauppila, T.J. Nurmikko, A. Rice, M. Rowbotham, J. Serra, C. Sommer, B. H. Smith, R.D. Treede, NeuPSIG guidelines on neuropathic pain assessment, Pain 152 (1) (2011) 14–27. [37] Z.S. Yin, H. Zhang, W. Gao, Erythropoietin promotes functional recovery and enhances nerve regeneration after peripheral nerve injury in rats, Am. J. Neuroradiol. 31 (2010) 509–515. [38] L.-Y. Hu, W.-L. Mi, G.-C. Wu, Y.-Q. Wang, Q.-L. Mao-Ying, Prevention and treatment for chemotherapy-induced peripheral neuropathy: therapies based on CIPN mechanisms, Curr. Neuropharmacol. 16 (2018) 1254. [39] M. Sisignano, R. Baron, K. Scholich, G. Geisslinger, Mechanism-based treatment for chemotherapy-induced peripheral neuropathic pain, Nat. Rev. Neurol. 10 (2014) 694–707. [40] S. Pradeep, J. Huang, E.M. Mora, A.M. Nick, M.S. Cho, S.Y. Wu, K. Noh, C. V. Pecot, R. Rupaimoole, M.A. Stein, S. Brock, Y. Wen, C. Xiong, K. Gharpure, J. M. Hansen, A.S. Nagaraja, R.A. Previs, P. Vivas-Mejia, H.D. Han, W. Hu, L. S. Mangala, B. Zand, L.J. Stagg, J.E. Ladbury, B. Ozpolat, S.N. Alpay, M. Nishimura, R.L. Stone, K. Matsuo, G.N. Armaiz-Peña, H.J. Dalton, C. Danes, B. Goodman, C. Rodriguez-Aguayo, C. Kruger, A. Schneider, S. Haghpeykar, P. Jaladurgam, M.C. Hung, R.L. Coleman, J. Liu, C. Li, D. Urbauer, G. LopezBerestein, D.B. Jackson, A.K. Sood, Erythropoietin stimulates tumor growth via EphB4, Cancer Cell 28 (2015) 610–622. [41] K.A. Aromolaran, P.A. Goldstein, Ion channels and neuronal hyperexcitability in chemotherapy-induced peripheral neuropathy: cause and effect? Mol. Pain. (2017). [42] T.R. Cummins, Setting up for the block: the mechanism underlying lidocaine’s use-dependent inhibition of sodium channels, J. Physiol. 582 (2007) 11. [43] V. Challapalli, I.W. Tremont-Lukats, E.D. Mcnicol, J. Lau, D.B. Carr, Systemic administration of local anesthetic agents to relieve neuropathic pain, Cochrane Database Syst. Rev. (2005), 003345. [44] I.W. Tremont-Lukats, V. Challapalli, E.D. McNicol, J. Lau, D.B. Carr, Systemic administration of local anesthetics to relieve neuropathic pain: a systematic review and meta-analysis, Anesth. Analg. 101 (2005) 1738–1749. [45] S. van den Heuvel, S. van der Wal, L.A. Smedes, S.A. Radema, N. van Alfen, K.C. P. Vissers, M. Steegers, Intravenous lidocaine: old-school drug, new purposereduction of intractable pain in patients with chemotherapy induced peripheral neuropathy, Pain. Res. Manag. 2017 (2017), 8053474. [46] E. Wesselink, R.M. Winkels, H. Van Baar, A.J.M.R. Geijsen, M. Van Zutphen, H. K. Van Halteren, B. Hansson, S.A. Radema, J. de Wilt, E. Kampman, D. Kok, Dietary intake of magnesium or calcium and chemotherapy-induced peripheral neuropathy in colorectal cancer patients, Nutrients 10 (2018). [47] C.L. Loprinzi, R. Qin, S.R. Dakhil, L. Fehrenbacher, K.A. Flynn, P. Atherton, D. Seisler, R. Qamar, G.C. Lewis, A. Grothey, Phase III randomized, placebocontrolled, double-blind study of intravenous calcium and magnesium to prevent oxaliplatin-induced sensory neurotoxicity (N08CB/Alliance), J. Clin. Oncol. 32 (2014) 997–1005. [48] B. Jordan, F. Jahn, J. Beckmann, S. Unverzagt, C. Müller-Tidow, K. Jordan, Calcium and magnesium infusions for the prevention of oxaliplatin-induced peripheral neurotoxicity: a systematic review, Oncology 24 (2016) 4617–4625. [49] M. Magnowska, N. Iżycka, J. Kapoła-Czyż, A. Romała, J. Lorek, M. Spaczyński, E. Nowak-Markwitz, Effectiveness of gabapentin pharmacotherapy in chemotherapy-induced peripheral neuropathy, Ginekol. Pol. 89 (2018) 200–204. [50] R. Yasaei, S. Katta, A. Saadabadi, Gabapentin. StatPearls, StatPearls Publishing, Treasure Island (FL), 2020. [51] S. Derry, R.F. Bell, S. Straube, P.J. Wiffen, D. Aldington, R.A. Moore, Pregabalin for neuropathic pain in adults, Cochrane Database Syst. Rev. 1 (2019), 007076. [52] J.D. Markman, T.S. Jensen, D. Semel, C. Li, B. Parsons, R. Behar, A.B. Sadosky, Effects of pregabalin in patients with neuropathic pain previously treated with gabapentin: a pooled analysis of parallel-group, randomized, placebo-controlled clinical trials, Pain. Pract. 17 (2017) 718–728. [53] H.N. Bockbrader, D. Wesche, R. Miller, S. Chapel, N. Janiczek, P. Burger, A comparison of the pharmacokinetics and pharmacodynamics of pregabalin and gabapentin, Clin. Pharmacokinet. 49 (2010) 661–669. [54] T.J. Kaley, L.M. Deangelis, Therapy of chemotherapy-induced peripheral neuropathy, Br. J. Haematol. 145 (2009) 3–14. [55] N. Farshchian, A. Alavi, S. Heydarheydari, N. Moradian, Comparative study of the effects of venlafaxine and duloxetine on chemotherapy-induced peripheral neuropathy, Cancer Chemother. Pharmacol. 82 (2018) 787–793. 6 A.D. Desforges et al. Biomedicine & Pharmacotherapy 147 (2022) 112671 [56] Center for Drug Evaluation and Research (CDER), U.S. Food and Drug Administration (FDA). The Voice of the Patient: Neuropathic Pain Associated with Peripheral Neuropathy. 2017;(February). [57] D. Santarsieri, T.L. Schwartz, Antidepressant efficacy and side-effect burden: a quick guide for clinicians, Drugs Context 4 (2015), 212290. [58] S.Y. Song, Y.B. Ko, H. Kim, G.W. Lee, J.B. Yang, H.K. Chang, S.M. Kwak, J. Jung, S. Lee, S.Y. Lee, H.J. Yoo, Effect of serotonin-norepinephrine reuptake inhibitors for patients with chemotherapy-induced painful peripheral neuropathy: a metaanalysis, Medicine 99 (1) (2020), e18653. [59] M.T. Aziz, B.L. Good, D.K. Lowe, Serotonin-norepinephrine reuptake inhibitors for the management of chemotherapy-induced peripheral neuropathy, Ann. Pharmacother. 48 (2014) 626–632. [60] E.M.L. Smith, H. Pang, C. Cirrincione, S. Fleishman, E.D. Paskett, T. Ahles, L. R. Bressler, C.E. Fadul, C. Knox, N. Le-Lindqwister, P.B. Gilman, C.L. Shapiro, f Alliance for Clinical Trials in Oncology, Effect of duloxetine on pain, function, and quality of life among patients with chemotherapy-induced painful peripheral neuropathy: a randomized clinical trial, JAMA J. Am. Med. Assoc. 309 (2013) 1359. [61] J. Piccolo, J.M. Kolesar, Prevention and treatment of chemotherapy-induced peripheral neuropathy, Am. J. Health-Syst. Pharm. 71 (2014) 19–25. [62] C. Zimmerman, P.J. Atherton, D. Pachman, D. Seisler, N. Wagner-Johnston, S. Dakhil, J.M. Lafky, R. Qin, A. Grothey, C.L. Loprinzi, MC11C4: a pilot randomized, placebo-controlled, double-blind study of venlafaxine to prevent oxaliplatin-induced neuropathy, Support. Care Cancer 24 (2016) 1071–1078. [63] R.H. Dworkin, A.B. O’connor, J. Audette, R. Baron, G.K. Gourlay, M.L. Haanpää, J.L. Kent, E.J. Krane, A.A. Lebel, R.M. Levy, S.C. Mackey, J. Mayer, C. Miaskowski, S.N. Raja, A.S. Rice, K.E. Schmader, B. Stacey, S. Stanos, R. D. Treede, D.C. Turk, G.A. Walco, C.D. Wells, Recommendations for the pharmacological management of neuropathic pain: an overview and literature update, Mayo Clin. Proc. 85 (2010) 3–14. [64] L.A.M.L.M. Antidepressant, Therapy with milnacipran and venlafaxine, Neuropsychiatr. Dis. Treat. (2010). [65] R.A. Sansone, L.A. Sansone, Pain, pain, go away: antidepressants and pain management, Psychiatry (2008). [66] S.H. Chu, Y.J. Lee, E.S. Lee, Y. Geng, X.S. Wang, C.S. Cleeland, Current use of drugs affecting the central nervous system for chemotherapy-induced peripheral neuropathy in cancer patients: a systematic review, Support. Care Cancer 23 (2015) 513–524. [67] A.L. Kautio, M. Haanpää, T. Saarto, E. Kalso, Amitriptyline in the treatment of chemotherapy-induced neuropathic symptoms, J. Pain. Symptom Manag. 35 (2008) 31–39. [68] J.E. Hammack, J.C. Michalak, C.L. Loprinzi, J.A. Sloan, P.J. Novotny, G.S. Soori, M.T. Tirona, Jr Rowland KM, P.J. Stella, J.A. Johnson, Phase III evaluation of nortriptyline for alleviation of symptoms of cis-platinum-induced peripheral neuropathy, Pain 98 (2002) 195–203. [69] E.P. Baltenberger, W.M. Buterbaugh, B.S. Martin, C.J. Thomas, Review of antidepressants in the treatment of neuropathic pain, Ment. Health Clin. 5 (3) (2015) 123–133. [70] S.N. Gandhi, M.A. Brown, J.G. Wong, D.A. Aguirre, C.B. Sirlin, MR contrast agents for liver imaging: what, when, how, Radiographics 26 (2006) 1621–1636. [71] R. Coriat, J. Alexandre, C. Nicco, L. Quinquis, E. Benoit, C. Chéreau, H. Lemaréchal, O. Mir, D. Borderie, J.M. Tréluyer, B. Weill, J. Coste, F. Goldwasser, F. Batteux, Treatment of oxaliplatin-induced peripheral neuropathy by intravenous mangafodipir, J. Clin. Investig. 124 (2014) 262–272. [72] J.O.G. Karlsson, R.G. Andersson, P. Jynge, Mangafodipir a selective cytoprotectant — with special reference to oxaliplatin and its association to chemotherapy-induced peripheral neuropathy (CIPN), Transl. Oncol. 10 (2017) 641–649. [73] H.S. Shim, C. Bae, J. Wang, K.H. Lee, K.M. Hankerd, H.K. Kim, J.M. Chung, J. H. La, Peripheral and central oxidative stress in chemotherapy-induced neuropathic pain, Mol. Pain. 15 (2019), 1744806919840098. [74] D.R. Pachman, C.L. Loprinzi, A. Grothey, L.E. Ta, The search for treatments to reduce chemotherapy-induced peripheral neuropathy, J. Clin. Investig. 124 (2014) 72–74. [75] U.S. Food and Drug Administration (FDA). FDA-Approved Drugs: MANGAFODIPIR TRISODIUM [Internet]. 2020 [cited 2020 May 11]. Available from: 〈https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=over view.process&ApplNo=020652〉. [76] S.J. Ward, S.D. McAllister, R. Kawamura, R. Murase, H. Neelakantan, E. A. Walker, Cannabidiol inhibits paclitaxel-induced neuropathic pain through 5HT 1A receptors without diminishing nervous system function or chemotherapy efficacy, Br. J. Pharmacol. 171 (2014) 636–645. [77] Y. Mulpuri, V.N. Marty, J.J. Munier, K. Mackie, B.L. Schmidt, H.H. Seltzman, I. Spigelman, Synthetic peripherally-restricted cannabinoid suppresses chemotherapy-induced peripheral neuropathy pain symptoms by CB1 receptor activation, Neuropharmacology 139 (2018) 85–97. [78] J. Guindon, Y. Lai, S.M. Takacs, H.B. Bradshaw, A.G. Hohmann, Alterations in endocannabinoid tone following chemotherapy-induced peripheral neuropathy: effects of endocannabinoid deactivation inhibitors targeting fatty-acid amide hydrolase and monoacylglycerol lipase in comparison to reference analgesics following cisplatin treatment, Pharmacol. Res. 67 (2013) 94–109. [79] M.E. Lynch, P. Cesar-Rittenberg, A.G. Hohmann, A double-blind, placebocontrolled, crossover pilot trial with extension using an oral mucosal cannabinoid extract for treatment of chemotherapy-induced neuropathic pain, J. Pain. Symptom Manag. 47 (2014) 166–173. [80] M. Russo, C. Rifici, E. Sessa, G. D’Aleo, P. Bramanti, R.S. Calabrò, Sativex-induced neurobehavioral effects: causal or concausal? A practical advice! DARU, J. Pharm. Sci. (2015). [81] B.I. Labow, W.W. Souba, Glutamine, World J. Surg. 24 (2000) 1503–1513. [82] S. Amara, Oral glutamine for the prevention of chemotherapy-induced peripheral neuropathy, Ann. Pharmacother. 42 (2008) 1481–1485. [83] S. Wolf, D. Barton, L. Kottschade, A. Grothey, C. Loprinzi, Chemotherapy-induced peripheral neuropathy: prevention and treatment strategies, Eur. J. Cancer 44 (2008) 1507–1515. [84] W.N. Sun, J.W. Su, Z.P. Shen, H.T. Hsu, Effect of oral glutamine on chemotherapy-induced peripheral neuropathy in cancer patients: an evidencebased appraisal, J. Nurs. 65 (2018) 61–69. [85] M.E. Lynch, A.J. Clark, J. Sawynok, M.J.L. Sullivan, Topical 2% amitriptyline and 1% ketamine in neuropathic pain syndromes: a randomized, double-blind, placebo-controlled trial, Anesthesiology 103 (2005) 140–146. [86] D.L. Barton, E.J. Wos, R. Qin, B.I. Mattar, N.B. Green, K.S. Lanier, J.D. Bearden, J. W. Kugler, K.L. Hoff, P.S. Reddy, Jr Rowland KM, M. Riepl, B. Christensen, C. L. Loprinzi, A double-blind, placebo-controlled trial of a topical treatment for chemotherapy-induced peripheral neuropathy: NCCTG trial N06CA, Support. Care Cancer 19 (2011) 833–841. [87] C.J. Proudfoot, E.M. Garry, D.F. Cottrell, R. Rosie, H. Anderson, D.C. Robertson, S.M. Fleetwood-Walker, R. Mitchell, Analgesia mediated by the TRPM8 cold receptor in chronic neuropathic pain, Curr. Biol. 16 (2006) 1591–1605. [88] Y. Liu, N. Qin, TRPM8 in health and disease: cold sensing and beyond, Adv. Exp. Med. Biol. 704 (2011) 185–208. [89] A. Cortellini, L. Verna, K. Cannita, L. Napoleoni, A. Parisi, C. Ficorella, G. Porzio, Topical menthol for treatment of chemotherapy-induced peripheral neuropathy, Indian J. Palliat. Care 23 (2017) 350–352. [90] D. Julius, TRP channels and pain, Annu. Rev. Cell Dev. Biol. 29 (2013) 355–384. [91] M.J. Caterina, A. Leffler, A.B. Malmberg, W.J. Martin, J. Trafton, K.R. PetersenZeitz, M. Koltzenburg, A.I. Basbaum, D. Julius, Impaired nociception and pain sensation in mice lacking the capsaicin receptor, Science 288 (2000) 306–313. [92] T. Wagner, C. Poole, A. Roth-Daniek, The capsaicin 8% patch for neuropathic pain in clinical practice: a retrospective analysis, Pain. Med. (U. S. ) 14 (2013) 1202–1211. [93] D.M. Simpson, S. Brown, J. Tobias, Controlled trial of high-concentration capsaicin patch for treatment of painful HIV neuropathy, Neurology 70 (2008) 2305–2313. [94] I. Filipczak-Bryniarska, R.M. Krzyzewski, J. Kucharz, A. MichalowskaKaczmarczyk, J. Kleja, J. Woron, K. Strzepek, L. Kazior, J. Wordliczek, T. Grodzicki, K. Krzemieniecki, High-dose 8% capsaicin patch in treatment of chemotherapy-induced peripheral neuropathy: single-center experience, Med. Oncol. 34 (2017) 162. [95] P.J. Oh, Y.L. Kim, Effectiveness of non-pharmacologic interventions in chemotherapy induced peripheral neuropathy: a systematic review and metaanalysis, J. Korean Acad. Nurs. 48 (2018) 123–142. [96] D.R. Pachman, J.C. Watson, M.B. Lustberg, N.D. Wagner-Johnston, A. Chan, L. Broadfield, Y.T. Cheung, C. Steer, D.J. Storey, K.D. Chandwani, J. Paice, P. Jean-Pierre, J. Oh, J. Kamath, M. Fallon, H. Strik, S. Koeppen, C.L. Loprinzi, Management options for established chemotherapy-induced peripheral neuropathy, Support. Care Cancer 22 (2014) 2281–2295. [97] S. Schroeder, G. Meyer-Hamme, S. Epplée, Acupuncture for chemotherapyinduced peripheral neuropathy (CIPN): A pilot study using neurography, Acupunct. Med. 30 (2012) 4–7. [98] C. Visovsky, Acupuncture for the management of chemotherapy-induced peripheral neuropathy, J. Adv. Pract. Oncol. 3 (2012) 178–181. [99] M. Jung, N. Rein, B. Fuchs, Physical therapy for chemotherapy-i

Treatment and Diagnosis of Chemotherapy-Induced Peripheral Neuropathy (CIPN) PDF

Document Details

Tags

Related

Summary

Full Transcript

Upgrade to continue