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Modified MACOP-B chemotherapy for intermediate and high grade non Hodgkins lymphomas
1Dept. of Medical Oncology, Tata Memorial Hospital, Parel, Bombay.
The Journal of the Association of Physicians of India
|October 1, 1994
Summary
This study assessed the feasibility and efficacy of the MACOP-B chemotherapy regimen for Non-Hodgkin Lymphoma patients in India. While outpatient administration was feasible, the high response rates originally reported could not be confirmed.
Area of Science:
- Oncology
- Hematology
- Clinical Trials
Background:
- The MACOP-B (methotrexate with leucovorin rescue, doxorubicin, cyclophosphamide, vincristine, prednisolone, and bleomycin) regimen is a standard treatment for Non-Hodgkin Lymphoma.
- Previous studies have reported varying efficacy of the MACOP-B regimen.
- Assessing outpatient administration feasibility and confirming efficacy in a specific population is crucial.
Purpose of the Study:
- To evaluate the feasibility of administering the MACOP-B chemotherapy regimen on an outpatient basis.
- To confirm the efficacy of the MACOP-B regimen in treating intermediate- and high-grade lymphoma.
- To identify clinical features predicting treatment response and disease-free survival.
Main Methods:
- A single-institute study treated 51 patients with intermediate- and high-grade lymphoma using the MACOP-B regimen.
- Patients received chemotherapy on an outpatient basis.
- Clinical features, response rates, disease-free survival, and toxicity were analyzed.
Main Results:
- Complete remission was achieved in 65% of patients.
- At 40 months follow-up, 40% of patients were alive, and 60% of complete responders were disease-free.
- Hematological toxicity occurred in 90% of patients, with 14% experiencing Grade IV toxicity. Severe mucositis affected 40%.
Conclusions:
- Outpatient administration of aggressive chemotherapy (MACOP-B) is feasible in India.
- The study failed to confirm the high response rates previously reported for the MACOP-B regimen.
- Patients with absence of B symptoms, non-bulky disease, and diffuse large cell histology showed better remission rates.