Podcast
Questions and Answers
In the context of intracranial tumors, differentiate between the mechanisms by which inflammation and compression contribute to neurological deficits.
In the context of intracranial tumors, differentiate between the mechanisms by which inflammation and compression contribute to neurological deficits.
- Inflammation induces apoptosis primarily in glial cells, leading to demyelination, while compression causes necrosis in neurons due to direct physical pressure.
- Inflammation exacerbates cerebral edema, leading to widespread neuronal dysfunction, while compression induces ischemia through vascular compromise. (correct)
- Inflammation directly damages neuronal cell bodies, while compression primarily affects axonal conduction and synaptic transmission.
- Inflammation primarily disrupts the blood-brain barrier, resulting in vasogenic edema, while compression causes cytotoxic edema due to cellular energy failure.
How does the histological grade of an astrocytoma, as determined through biopsy, influence the selection of chemotherapeutic agents and the overall prognosis for a patient?
How does the histological grade of an astrocytoma, as determined through biopsy, influence the selection of chemotherapeutic agents and the overall prognosis for a patient?
- The histological grade is irrelevant, as all astrocytomas are treated with the same standard chemotherapy regimen regardless of cellular differentiation or mitotic index.
- Higher-grade astrocytomas necessitate the inclusion of angiogenesis inhibitors such as bevacizumab, whereas lower-grade tumors are primarily managed with radiation and temozolomide.
- Lower-grade astrocytomas (Grades I and II) typically respond well to alkylating agents, while higher-grade tumors (Grades III and IV) require a combination of platinum-based and antimetabolite drugs.
- Histological grade dictates prognosis; lower-grade tumors have better overall survival, and therapy focuses on maintaining quality of life, while higher-grade tumors necessitate aggressive multimodal therapy. (correct)
What is the relative utility of Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) in differentiating between vasogenic and cytotoxic edema associated with brain tumors, and how does this distinction impact therapeutic decision-making?
What is the relative utility of Computed Tomography (CT) and Magnetic Resonance Imaging (MRI) in differentiating between vasogenic and cytotoxic edema associated with brain tumors, and how does this distinction impact therapeutic decision-making?
- Both CT and MRI can reliably distinguish between vasogenic and cytotoxic edema, but MRI offers higher resolution and greater anatomical detail, which is beneficial for surgical planning.
- CT is superior for detecting vasogenic edema due to its high sensitivity to changes in vascular permeability, while MRI is better for cytotoxic edema because of its ability to visualize intracellular swelling.
- CT is used for initial assessment due to its speed and availability, while MRI is reserved for cases where CT findings are inconclusive, irrespective of edema type.
- MRI is more sensitive in detecting both types of edema, allowing precise delineation of the edematous region; differentiation influences the use of corticosteroids (vasogenic) versus osmotic agents (cytotoxic). (correct)
In the context of surgical resection of brain tumors, what are the principal advantages and disadvantages of utilizing intraoperative brain mapping techniques compared to relying solely on preoperative imaging and anatomical landmarks?
In the context of surgical resection of brain tumors, what are the principal advantages and disadvantages of utilizing intraoperative brain mapping techniques compared to relying solely on preoperative imaging and anatomical landmarks?
What are the critical distinctions between the mechanisms of action and clinical applications of alkylating agents, antimetabolites, and plant alkaloids in the chemotherapy of brain tumors, and how do these differences inform combination therapy strategies?
What are the critical distinctions between the mechanisms of action and clinical applications of alkylating agents, antimetabolites, and plant alkaloids in the chemotherapy of brain tumors, and how do these differences inform combination therapy strategies?
In the management of brain tumors, how does the implementation of Positron Emission Tomography (PET) and Electroencephalogram (EEG) findings alter treatment strategies, and what are the limitations of each modality?
In the management of brain tumors, how does the implementation of Positron Emission Tomography (PET) and Electroencephalogram (EEG) findings alter treatment strategies, and what are the limitations of each modality?
How does the presence of a brain tumor influence intracranial pressure (ICP), and what compensatory mechanisms are initially engaged to maintain normal ICP before decompensation occurs?
How does the presence of a brain tumor influence intracranial pressure (ICP), and what compensatory mechanisms are initially engaged to maintain normal ICP before decompensation occurs?
When managing seizures associated with brain tumors, how do tumor location and histology guide the selection of antiepileptic drugs (AEDs), and what are the implications of enzyme-inducing AEDs on chemotherapy efficacy?
When managing seizures associated with brain tumors, how do tumor location and histology guide the selection of antiepileptic drugs (AEDs), and what are the implications of enzyme-inducing AEDs on chemotherapy efficacy?
Differentiate between the indications and contraindications for employing brachytherapy versus external beam radiation therapy in the treatment of localized brain tumors, considering factors such as tumor size, location, and histology.
Differentiate between the indications and contraindications for employing brachytherapy versus external beam radiation therapy in the treatment of localized brain tumors, considering factors such as tumor size, location, and histology.
Critically evaluate the premise that 'non-functioning' pituitary adenomas are clinically benign, considering their potential mass effects and insidious endocrine consequences.
Critically evaluate the premise that 'non-functioning' pituitary adenomas are clinically benign, considering their potential mass effects and insidious endocrine consequences.
When managing a patient with a suspected brain tumor, what are the relative merits and limitations of relying solely on clinical symptoms versus integrating advanced diagnostic imaging techniques (MRI, CT, PET) for early detection and accurate characterization?
When managing a patient with a suspected brain tumor, what are the relative merits and limitations of relying solely on clinical symptoms versus integrating advanced diagnostic imaging techniques (MRI, CT, PET) for early detection and accurate characterization?
How does the concept of 'brain shift' during craniotomy influence the accuracy of neuronavigational systems, and what strategies can be employed to mitigate this phenomenon and ensure precise tumor resection?
How does the concept of 'brain shift' during craniotomy influence the accuracy of neuronavigational systems, and what strategies can be employed to mitigate this phenomenon and ensure precise tumor resection?
What are the ethical considerations surrounding the use of experimental therapies, such as gene therapy or immunotherapy, in patients with recurrent high-grade gliomas who have exhausted standard treatment options, and how should these considerations inform clinical decision-making?
What are the ethical considerations surrounding the use of experimental therapies, such as gene therapy or immunotherapy, in patients with recurrent high-grade gliomas who have exhausted standard treatment options, and how should these considerations inform clinical decision-making?
How do the principles of radiation oncology dictate the fractionation scheme (dose per fraction and total treatment duration) for external beam radiation therapy in patients with brain tumors?
How do the principles of radiation oncology dictate the fractionation scheme (dose per fraction and total treatment duration) for external beam radiation therapy in patients with brain tumors?
Discuss the impact of anti-angiogenic therapies, such as bevacizumab, on the tumor microenvironment and the resulting implications for drug delivery and radiation sensitivity in glioblastoma multiforme.
Discuss the impact of anti-angiogenic therapies, such as bevacizumab, on the tumor microenvironment and the resulting implications for drug delivery and radiation sensitivity in glioblastoma multiforme.
How does the disruption of the blood-brain barrier (BBB) in brain tumors influence the delivery and efficacy of chemotherapeutic agents, and what strategies are being developed to overcome this barrier?
How does the disruption of the blood-brain barrier (BBB) in brain tumors influence the delivery and efficacy of chemotherapeutic agents, and what strategies are being developed to overcome this barrier?
In the palliative care of patients with end-stage brain tumors, how should clinicians balance the competing goals of maximizing symptom control, preserving cognitive function, and respecting patient autonomy in the face of declining neurological status?
In the palliative care of patients with end-stage brain tumors, how should clinicians balance the competing goals of maximizing symptom control, preserving cognitive function, and respecting patient autonomy in the face of declining neurological status?
What critical role does the tumor microenvironment play in mediating resistance to chemotherapy and radiation therapy in glioblastoma, and how can this knowledge be leveraged to develop more effective therapeutic strategies?
What critical role does the tumor microenvironment play in mediating resistance to chemotherapy and radiation therapy in glioblastoma, and how can this knowledge be leveraged to develop more effective therapeutic strategies?
When planning surgical resection of a brain tumor located in close proximity to eloquent cortex, how do the principles of neuroplasticity inform the decision to perform preoperative 'eloquent cortex mapping' and intraoperative monitoring?
When planning surgical resection of a brain tumor located in close proximity to eloquent cortex, how do the principles of neuroplasticity inform the decision to perform preoperative 'eloquent cortex mapping' and intraoperative monitoring?
Elucidate the mechanisms by which primary brain tumors induce secondary cerebral edema, and how does the specific type of edema (vasogenic vs. cytotoxic) influence the selection of therapeutic interventions aimed at mitigating intracranial pressure?
Elucidate the mechanisms by which primary brain tumors induce secondary cerebral edema, and how does the specific type of edema (vasogenic vs. cytotoxic) influence the selection of therapeutic interventions aimed at mitigating intracranial pressure?
What are the principal challenges associated with delivering targeted therapies, such as monoclonal antibodies or small molecule inhibitors, across the blood-brain barrier (BBB) to treat brain tumors, and what strategies are under development to overcome these challenges?
What are the principal challenges associated with delivering targeted therapies, such as monoclonal antibodies or small molecule inhibitors, across the blood-brain barrier (BBB) to treat brain tumors, and what strategies are under development to overcome these challenges?
How does the classification of brain tumors based on cellular origin (e.g., glial cells, meninges, Schwann cells) correlate with their propensity for local invasion versus distant metastasis, and how does this influence treatment planning?
How does the classification of brain tumors based on cellular origin (e.g., glial cells, meninges, Schwann cells) correlate with their propensity for local invasion versus distant metastasis, and how does this influence treatment planning?
Explain how intraoperative magnetic resonance imaging (iMRI) enhances the extent of resection (EOR) in surgical management of high-grade gliomas, and discuss its limitations in terms of cost, availability, and potential for prolonging anesthesia time.
Explain how intraoperative magnetic resonance imaging (iMRI) enhances the extent of resection (EOR) in surgical management of high-grade gliomas, and discuss its limitations in terms of cost, availability, and potential for prolonging anesthesia time.
In the context of stereotactic radiosurgery (SRS) for brain metastases, discuss the trade-offs between delivering a single high-dose fraction versus multiple smaller fractions in terms of local tumor control, risk of radiation necrosis, and impact on surrounding normal brain tissue.
In the context of stereotactic radiosurgery (SRS) for brain metastases, discuss the trade-offs between delivering a single high-dose fraction versus multiple smaller fractions in terms of local tumor control, risk of radiation necrosis, and impact on surrounding normal brain tissue.
Evaluate the evidence supporting the use of tumor-treating fields (TTFields) as an adjunct to standard chemotherapy in glioblastoma multiforme (GBM), considering their mechanism of action, clinical efficacy, and potential side effects.
Evaluate the evidence supporting the use of tumor-treating fields (TTFields) as an adjunct to standard chemotherapy in glioblastoma multiforme (GBM), considering their mechanism of action, clinical efficacy, and potential side effects.
When managing patients with brain tumors who are receiving corticosteroids to reduce cerebral edema, how should clinicians monitor for and mitigate potential side effects, such as hyperglycemia, immunosuppression, and myopathy, while optimizing therapeutic benefits?
When managing patients with brain tumors who are receiving corticosteroids to reduce cerebral edema, how should clinicians monitor for and mitigate potential side effects, such as hyperglycemia, immunosuppression, and myopathy, while optimizing therapeutic benefits?
Describe the unique challenges associated with diagnosing and treating brain tumors in pediatric patients compared to adults, focusing on differences in tumor histology, location, and response to therapy.
Describe the unique challenges associated with diagnosing and treating brain tumors in pediatric patients compared to adults, focusing on differences in tumor histology, location, and response to therapy.
How do molecular biomarkers, such as MGMT methylation status and IDH1/2 mutations, influence prognosis and treatment decision-making in patients with glioblastoma, and what are the limitations of relying solely on these markers?
How do molecular biomarkers, such as MGMT methylation status and IDH1/2 mutations, influence prognosis and treatment decision-making in patients with glioblastoma, and what are the limitations of relying solely on these markers?
Outline the key steps involved in performing a stereotactic brain biopsy for diagnosis of deep-seated brain tumors, and discuss the potential risks and benefits compared to open surgical resection.
Outline the key steps involved in performing a stereotactic brain biopsy for diagnosis of deep-seated brain tumors, and discuss the potential risks and benefits compared to open surgical resection.
In the management of brain tumor-related fatigue, how should clinicians differentiate between primary fatigue caused by the tumor itself versus secondary fatigue resulting from treatment-related side effects or comorbid conditions, and how should this distinction guide therapeutic interventions?
In the management of brain tumor-related fatigue, how should clinicians differentiate between primary fatigue caused by the tumor itself versus secondary fatigue resulting from treatment-related side effects or comorbid conditions, and how should this distinction guide therapeutic interventions?
What is the significance of assessing cognitive function in patients undergoing treatment for brain tumors, and what neuropsychological tests are most sensitive to detect subtle cognitive changes associated with tumor progression or treatment-related neurotoxicity?
What is the significance of assessing cognitive function in patients undergoing treatment for brain tumors, and what neuropsychological tests are most sensitive to detect subtle cognitive changes associated with tumor progression or treatment-related neurotoxicity?
Evaluate the effectiveness of prophylactic antiepileptic drug (AED) administration in patients undergoing craniotomy for supratentorial brain tumors, considering the potential benefits of seizure prevention versus the risks of adverse drug effects and drug interactions.
Evaluate the effectiveness of prophylactic antiepileptic drug (AED) administration in patients undergoing craniotomy for supratentorial brain tumors, considering the potential benefits of seizure prevention versus the risks of adverse drug effects and drug interactions.
How do genetic mutations promote tumor creation, and what is the difference between primary and secondary brain tumors?
How do genetic mutations promote tumor creation, and what is the difference between primary and secondary brain tumors?
A patient presents with symptoms suggestive of a suprasellar tumor. What is the most likely clinical manifestation based on the tumor's location, and which imaging modality is the most effective for confirming the diagnosis?
A patient presents with symptoms suggestive of a suprasellar tumor. What is the most likely clinical manifestation based on the tumor's location, and which imaging modality is the most effective for confirming the diagnosis?
A researcher is investigating new therapeutic targets for glioblastoma. Which molecular characteristic of glioblastoma cells offers the most promising avenue for targeted drug development?
A researcher is investigating new therapeutic targets for glioblastoma. Which molecular characteristic of glioblastoma cells offers the most promising avenue for targeted drug development?
A patient undergoing radiation therapy for a brain tumor develops cognitive deficits. What intervention is most appropriate for managing these deficits?
A patient undergoing radiation therapy for a brain tumor develops cognitive deficits. What intervention is most appropriate for managing these deficits?
Flashcards
Brain Tumors
Brain Tumors
Occupies space within the skull, growing as a spherical mass or diffuse infiltrating tissue.
Primary Brain Tumors
Primary Brain Tumors
Originate from cells within the brain and progress locally. Rarely metastasize.
Secondary Brain Tumors
Secondary Brain Tumors
Develop from structures outside the brain and are twice as common as primary brain tumors.
Gliomas
Gliomas
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Tumors Arising from Supporting Structures
Tumors Arising from Supporting Structures
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Developmental Tumors
Developmental Tumors
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Clinical Manifestations of Brain Tumors
Clinical Manifestations of Brain Tumors
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Computed Tomography (CT) Scan with Dye
Computed Tomography (CT) Scan with Dye
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Magnetic Resonance Imaging (MRI)
Magnetic Resonance Imaging (MRI)
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Computer-Assisted Stereotactic Biopsy
Computer-Assisted Stereotactic Biopsy
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Brain Mapping Technology
Brain Mapping Technology
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Positron Emission Tomography (PET)
Positron Emission Tomography (PET)
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Electroencephalogram (EEG)
Electroencephalogram (EEG)
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Cytologic Studies
Cytologic Studies
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Treating Secreting Tumors
Treating Secreting Tumors
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Hormone Replacement
Hormone Replacement
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Brain tumor surgical objective
Brain tumor surgical objective
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Radiation Therapy
Radiation Therapy
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External Radiation
External Radiation
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Internal Radiation (Brachytherapy)
Internal Radiation (Brachytherapy)
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Chemotherapy
Chemotherapy
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Intrathecal Chemotherapy
Intrathecal Chemotherapy
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Alkylating Agents
Alkylating Agents
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Antimetabolites
Antimetabolites
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Plant Alkaloids
Plant Alkaloids
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Mitotic Inhibitors
Mitotic Inhibitors
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Antitumor Antibiotic
Antitumor Antibiotic
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Topoisomerase Inhibitors
Topoisomerase Inhibitors
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Study Notes
- Brain tumors occupy space within the skull.
- Brain tumors grow as either a spherical mass or as a diffuse, infiltrating tissue.
- Brain tumor effects are caused by inflammation, compression, and infiltration of tissue.
Primary Brain Tumors
- Originate from cells within the brain.
- Progress locally and rarely metastasize
- Common sites for primary brain tumors are glial cells and the supratentorial region.
Secondary Brain Tumors
- Also known as metastatic brain tumors.
- Develop from structures outside the brain.
- Secondary brain tumors are twice as common as primary brain tumors.
- Can occur from lung, breast, lower GIT, pancreas, kidney, or skin neoplasms.
Intracerebral Tumors
- Gliomas infiltrate any portion of the brain.
- Gliomas are the most common type of brain tumor.
- Types of Gliomas:
- Astrocytomas (Grades I and II)
- Glioblastoma (Astrocytoma Grades III and IV)
- Oligodendroglioma (Low and High Grades)
- Ependymoma (Grades I - IV)
- Medulloblastoma
Other Brain Tumors Types
- Tumors Arising from Supporting Structures: Meningiomas, Neuromas (Acoustic Neuroma, Schwannoma), and Pituitary Adenomas
- Developmental Tumors: Angiomas, Dermoid, epidermoid, teratoma, and craniopharyngioma
- Metastatic Lesions
Clinical Manifestations
- Increased intracranial pressure.
- Headache.
- Vomiting.
- Visual disturbances.
- Seizures.
- Localized symptoms.
Diagnostic Tests
- Computed Tomography (CT) Scan with Dye: Gives information on the number, size, and density of lesions, and the extent of secondary cerebral edema, also provides info about the ventricular system.
- Magnetic Resonance Imaging (MRI): Most helpful diagnostic tool for detecting brain tumors, particularly smaller lesions and brainstem and pituitary region tumors where bone is thick., and Useful for monitoring response to treatment.
- Computer-Assisted Stereotactic (3D) Biopsy: Used to diagnose deep-seated brain tumors and provide a basis for treatment and prognosis.
- Uses a three-dimensional frame for precise tumor location.
- Stereotactic frame and multiple imaging studies (X-ray, CT Scan, MRI) are used to localize the tumor and verify its position.
- Brain Mapping Technology: Helps determine the proximity of diseased brain areas to structures essential for normal brain function.
- Positron Emission Tomography (PET): Used to supplement MRI.
- Low-grade tumors are associated with hypometabolism.
- High-grade tumors are associated with hypermetabolism.
- Useful in making treatment decisions.
- Electroencephalogram (EEG):Can detect abnormal brain waves in area or adjacent to tumors.
- Used to evaluate temporal lobe seizures and assist in ruling out other disorders.
- Cytologic Studies: CSF samples can be used to detect malignant cells shed from CNS tumors, indicating metastasis.
Medical Management
- Secreting tumors respond to medications that suppress hormones.
- Non-functioning tumors may or may not affect pituitary function.
- Hormone replacement may be required to restore normal endocrine function.
Nursing Management
- Assess the characteristics of headaches.
- Use upright positioning and pain medications to manage pain.
- Nurses should evaluate the effectiveness of pain management interventions.
- Educate family about the possibility of seizures and adherence to medications.
- Medications to alleviate nausea and prevent vomiting should be considered.
- Caregiving family members should be included in the plan of care.
Surgical Management
- Objective: To remove as much tumor as possible without increasing neurological deficits and to relieve symptoms by partial removal (decompression).
- Surgery allows surgeons to obtain tissue to establish a definitive diagnosis.
- The specific surgical approach depends on the type of tumor, its location, and accessibility.
- Types of Surgeries:
- Craniotomy (Traditional)
- Craniotomy (Microscope and Microsurgical Instrumentation)
- Transsphenoidal Surgery
Radiation Therapy
- Also called radiotherapy.
- The use of high-powered rays to damage cancer cells and stop them from growing.
- Used to destroy tumor tissue that cannot be removed with surgery, kill remaining cancer cells after surgery, or when surgery is not possible.
External Radiation
- Comes from a large machine and given five days a week for several weeks.
- Treatment schedule determined by tumor type, size, and patient age.
- Delivers radiation over an extended period to protect healthy tissue.
- Radiation can be directed at the tumor, surrounding tissue, or the entire brain.
- Radiation may also be directed to the spinal cord.
- When whole brain is treated, an extra dose of radiation can be given to the tumor area, via external radiation or an implant.
Internal Radiation
- Also called brachytherapy.
- Uses an implant (small wire or pellet) placed in an applicator and inserted into the body near the tumor.
- Radiation from the implant has localized effects.
- Used after surgical tumor removal.
- Implants may be permanent or removed after treatment.
- Radiation exposure from permanent implants poses a minuscule risk to others.
Chemotherapy
- Uses drugs to kill cancer cells.
- A single drug or drug combination may be administered orally or via injection.
- Intrathecal chemotherapy involves injecting drugs into the cerebrospinal fluid.
- Treatment is given in cycles of treatment periods followed by recovery periods.
- Patients may be treated in a doctor’s office or clinic for their treatments
Commonly Used Chemo Drug Classes
- Alkylating Agents:interfere with cellular function, killing cells in various phases of the cycle.
- Altretamine.
- Busulfan.
- Carboplatin.
- Carmustine.
- Chlorambucil.
- Cisplatin.
- Cyclophosphamide.
- Dacarbazine.
- Antimetabolites: replace natural substances in the DNA
- azathioprine, mercaptopurine, and thioguanine, fluorouracil and floxuridine
- Plant Alkaloids: prevent cells from reproduction.
- Mitotic Inhibitors: prevent cell division.
- aclitaxel, docetaxel, vinblastine, vincristine, and vinorelbine
- Antitumor Antibiotic: prevent cells from reproducing.
- Anthracyclines: Doxorubicin, Daunorubicin, Epirubicin, Mitoxantrone, and Idarubicin.
- Chromomycin: Dactinomycin and Plicamycin.
- Miscellaneous: Mitomycin and Bleomycin.
- Topoisomerase Inhibitors: block critical enzymes for cell reproduction.
- Eukaryotic type II topoisomerase inhibitors (topo II): amsacrine, etoposide, etoposide phosphate, teniposide and doxorubicin.
- bacterial type II topoisomerase inhibitors (gyrase and topo IV): fluoroquinolones.
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