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etoposide + ifosfamide + cisplatin + doxorubicin + bleomycin + vinblastine + dacarbazine

Development stage
Preclinical
Lead developer
Bristol Myers Squibb
Modality
Small Molecules
Administration
Intravenous, Oral, Intramuscular, Subcutaneous
01

Overview

This is a multi-agent chemotherapy regimen composed of seven cytotoxic drugs: etoposide, ifosfamide, cisplatin, doxorubicin, bleomycin, vinblastine, and dacarbazine. Each component has a distinct mechanism of action targeting rapidly dividing cancer cells through various pathways: - Etoposide inhibits topoisomerase II, leading to DNA strand breaks. - Ifosfamide is an alkylating agent that crosslinks DNA. - Cisplatin forms DNA adducts causing apoptosis. - Doxorubicin intercalates into DNA and inhibits topoisomerase II. - Bleomycin induces single and double-strand breaks in DNA via free radical formation. - Vinblastine disrupts microtubule assembly during mitosis. - Dacarbazine acts as an alkylating agent after metabolic activation. This combination does not correspond to a standard named regimen but includes drugs from regimens such as ABVD (doxorubicin, bleomycin, vinblastine, dacarbazine), VIP (etoposide, ifosfamide, cisplatin), and others used for lymphomas or germ cell tumors[1][2][3][4]. The rationale for combining these agents is to maximize antitumor efficacy by attacking cancer cells through multiple mechanisms while minimizing overlapping toxicities.

02

Targets

TOP2A (DNA topoisomerase II)TUBB (Tubulin (alpha and beta subunits))DNA

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