Tamoxifen

From Glioblastoma Treatments
Revision as of 09:48, 19 March 2024 by Lazy (talk | contribs) (Created page with "{{TreatmentInfo |drug_name=Tamoxifen |FDA_approval=Yes (for breast cancer treatment) |used_for=Investigational use in glioblastoma (GBM) treatment |clinical_trial_phase=Phase II clinical trials and retrospective studies |common_side_effects=Increased risk of blood clots, uterine cancer in women, impotence, and loss of libido in men, weight gain |OS_without=Not specified |OS_with=Varies; in gliomas, doses range from 160-240 mg per day showed tumor regression in 25% of pat...")
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Property Information
Drug Name Tamoxifen
FDA Approval Yes (for breast cancer treatment)
Used for Investigational use in glioblastoma (GBM) treatment
Clinical Trial Phase Phase II clinical trials and retrospective studies
Clinical Trial Explanation Not specified
Common Side Effects Increased risk of blood clots, uterine cancer in women, impotence, and loss of libido in men, weight gain
OS without Not specified
OS with Varies; in gliomas, doses range from 160-240 mg per day showed tumor regression in 25% of patients
PFS without Median survival time for GBM typically ranges from 3-7 months with second-line chemotherapy
PFS with Median survival of 16 months for Grade III tumors and 7.2 months for GBM with tamoxifen treatment
Usefulness Rating 3
Usefulness Explanation Not specified
Toxicity Level Not specified
Toxicity Explanation Not specified

Notes: Tamoxifen, a well-known breast cancer therapy, inhibits protein kinase C in gliomas, potentially slowing cancer cell growth and stimulating angiogenesis at high doses. Early studies indicate its promise in tumor regression and survival extension, with some patients experiencing major benefits. Its effectiveness and side effects, especially at high doses required for glioma treatment, highlight the need for further research to identify responsive patient groups and optimize treatment protocols.


From Ben Williams Book: Not specified

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