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晚期乳腺癌患者的联合化疗与阿霉素治疗。西南肿瘤学组研究。

Combination chemotherapy and adriamycin in patients with advanced breast cancer. A Southwest Oncology Group study.

作者信息

Hoogstraten B, George S L, Samal B, Rivkin S E, Costanzi J J, Bonnet J D, Thigpen T, Braine H

出版信息

Cancer. 1976 Jul;38(1):13-20. doi: 10.1002/1097-0142(197607)38:1<13::aid-cncr2820380104>3.0.co;2-5.

Abstract

In January, 1972, the Southwest Oncology Group initiated two randomized studies for patients with advanced breast cancer. The study for patients with prior chemotherapy showed a 33% response rate with adriamycin. The study for patients without previous chemotherapy consisted of three treatment regimens; a weekly repeated combination of cyclophosphamide, methotrexate, 5-fluorouracil, vincristine, and prednisone; these same five drugs given in courses of 5 days repeated every 4 weeks; and adriamycin as a single agent every 3 weeks. For the 283 evaluable patients, the response rates were: weekly combination 63/106 (59%); intermittent combination 39/98 (40%); and adriamycin 31/79 (39%). The median duration of response was 8 months for weekly combination, 10 months for intermittent therapy and only 4 months for adriamycin. Leukopenia was the dose-limiting toxicity with all three regimens. The weekly combination is the most effective therapy for patients with advanced disease. Extensive trails of combinations that include adriamycin are underway.

摘要

1972年1月,西南肿瘤协作组启动了两项针对晚期乳腺癌患者的随机研究。针对接受过先前化疗的患者开展的研究显示,阿霉素的有效率为33%。针对未接受过先前化疗的患者开展的研究包括三种治疗方案:每周重复使用环磷酰胺、甲氨蝶呤、5-氟尿嘧啶、长春新碱和泼尼松的联合方案;同样这五种药物每4周重复进行为期5天的疗程给药;以及每3周单独使用一次阿霉素。对于283例可评估患者,有效率分别为:每周联合方案63/106(59%);间歇联合方案39/98(40%);阿霉素方案31/79(39%)。每周联合方案的中位缓解持续时间为8个月,间歇疗法为10个月,阿霉素方案仅为4个月。白细胞减少是所有三种方案的剂量限制性毒性。每周联合方案是晚期疾病患者最有效的治疗方法。正在开展包括阿霉素在内的联合方案的广泛试验。

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