The MAP regimen is a standard chemotherapy protocol for osteosarcoma (high-grade bone sarcoma, usually in children, adolescents, and young adults).
Components of MAP
- M = Methotrexate (high-dose MTX with leucovorin rescue)
- A = Adriamycin (Doxorubicin)
- P = Platinum (Cisplatin)
Indications
- High-grade osteosarcoma (localized or metastatic)
- Often given in neoadjuvant setting (before surgery) → then adjuvant cycles post-surgery.
- Used in pediatric, adolescent, and young adult patients (standard of care).
Typical Schedule (Children’s Oncology Group / EURAMOS-1 trial)
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Pre-operative (neoadjuvant):
- High-dose methotrexate (12 g/m² IV) weekly × several doses
- Cisplatin (120 mg/m² IV, day 1) + Doxorubicin (75 mg/m² IV, days 1–2) every 3 weeks
- Surgery (resection of primary tumor ± metastases)
- Post-operative (adjuvant):
- Repeat cycles of MAP (total duration usually 6–9 months)
(Exact dosing varies by protocol, age, and institution — pediatric vs adult dosing is adjusted carefully.)
Toxicities
- Methotrexate (HD-MTX): nephrotoxicity, hepatotoxicity, mucositis, neurotoxicity, delayed clearance (requires leucovorin rescue + hydration/alkalinization).
- Doxorubicin: cardiotoxicity (cumulative dose-dependent), myelosuppression, alopecia.
- Cisplatin: nephrotoxicity, ototoxicity, neurotoxicity (peripheral neuropathy), severe nausea/vomiting.
Monitoring
- MTX serum levels + renal function (to guide leucovorin rescue).
- Cardiac monitoring (ECHO/MUGA) for doxorubicin.
- Renal and audiology tests for cisplatin.
- CBC for myelosuppression.
Summary for oncology pharmacist:
The MAP regimen (Methotrexate + Adriamycin [doxorubicin] + Cisplatin) is the backbone of curative chemotherapy for osteosarcoma. It is used both pre- and post-surgery to maximize tumor shrinkage and eradicate micrometastatic disease, but requires intensive monitoring for renal, cardiac, and auditory toxicities.

