米托蒽醌
医学
长春新碱
蒽环类
化疗
内科学
切碎
依托泊苷
环磷酰胺
非霍奇金淋巴瘤
淋巴瘤
肿瘤科
联合化疗
阿霉素
去甲柔比星
胃肠病学
癌症
阿糖胞苷
乳腺癌
作者
I Kimura,T Ohnoshi,T Masaoka,K Sampi,Kiyoshi Namba
出处
期刊:PubMed
日期:1986-10-01
卷期号:13 (10): 3034-9
被引量:1
摘要
Thirty-one patients with advanced non-Hodgkin's lymphoma were entered in a trial of a four-drug combination of mitoxantrone, cyclophosphamide, vincristine, and prednisolone (MCOP). This trial was intended to test the efficacy of substituting mitoxantrone for adriamycin in the CHOP combination, and to evaluate tumor response in patients who had received anthracycline antibiotic therapy. Of 31 patients, 25 were fully evaluated for tumor response and toxicity. There were 7 responses (4 complete, 3 partial) among 9 patients who had received radiation alone or chemotherapy not containing anthracycline antibiotics, whereas there were 7 responses (3 complete, 4 partial) in 16 patients who had been given anthracycline-containing chemotherapy. Median duration of response was 11+ weeks (range; 5 to 43+ weeks). The major toxicity was myelosuppression, although patients tolerated this well. This study suggested that mitoxantrone is not fully cross-resistant with anthracycline antibiotics and that MCOP is an effective regimen in patients with previously treated non-Hodgkin's lymphoma. However, when salvage chemotherapy for CHOP-failure is intended, cyclophosphamide and vincristine in MCOP should be further substituted by other agents such as etoposide and cis-platinum.
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