成人急性非淋巴细胞白血病的联合化疗。

Cancer chemotherapy reports Pub Date : 1975-11-01
H Glucksberg, C D Buckner, A Fefer, Q DeMarsh, D Coleman, R B Dobrow, J Huff, C Kjobech, A S Hill, W Dittman, P E Neiman, M A Cheever, A B Einstein, E D Thomas
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摘要

1973年1月至1975年2月,在大学附属机构和私人机构中,77名急性非淋巴细胞白血病成人接受柔红霉素、阿糖胞嘧啶、6-硫鸟嘌呤、强的松和长春新碱联合治疗。31例患者接受治疗(方案1)后,所有药物的剂量均显著增加(方案2)。方案1和方案2的CR率分别为59%(29例患者中的17例)和70%(46例患者中的32例)。方案2的平均疗程数和达到CR的中位数天数分别从3天减少到1.4天和46天减少到29天。未能达到CR是由于方案1期间的持续性白血病和方案2期间的致命感染。在方案2中,20例大于50年的患者中有10例(50%)发生CR,而26例小于50年的患者中有22例(85%)发生CR。社区和大学机构的CR率相似。
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Combination chemotherapy for acute nonlymphoblastic leukemia in adults.

Between January 1973 and February 1975, 77 adults with acute nonlymphoblastic leukemia were treated with a combination of daunorubicin, cytosine arabinoside, 6-thioguanine, prednisone, and vincristine in university-affiliated and private institutions. After 31 patients were treated (regimen 1) the doses of all drugs were significantly increased (regimen 2). Regimes 1 and 2 yielded CR rates of 59% (17 of 29 patients) and 70% (32 of 46 patients) respectively. With regimens 2 the mean number of courses and the median number of days to CR decreased from 3 to 1.4 and from 46 to 29 respectively. Failure to achieve CR was due to persistent leukemia during regimen 1 and fatal infections during regimen 2. With regimen 2 ten of 20 patients (50%) greater than 50 years had CR compared to 22 of 26 patients (85%) less than 50 years. CR rates were similar in community and university institutions.

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PORFIROMYCIN. Phase I study of 5-azacytidine (NSC-102816) using 24-hour continuous infusion for 5 days. Bleomycin (NSC-125066) and CCNU (NSC-79037) in the combination chemotherapy of mopp-resistant hodgkin's disease. Combination chemotherapy with 5-fluorouracil (NSC-19893), methotrexate (NSC-740), and prednisolone (NSC-9900) (FAP protocol) for hepatoma. Cyclophosphamide (NSC-26271) maintenance therapy after a second remission of childhood acute lymphoblastic leukemia: comparative clinical trial (standard dose versus intermittent high dose versus cyclophosphamide plus cytosine arabinoside (NSC-63878)).
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