Suppr超能文献

转移性乳腺癌强化与中度化疗方案的随机研究。

A randomized study of intensive versus moderate chemotherapy programs in metastatic breast cancer.

作者信息

Rosner D, Nemoto T, Lane W W

出版信息

Cancer. 1987 Mar 1;59(5):874-83. doi: 10.1002/1097-0142(19870301)59:5<874::aid-cncr2820590503>3.0.co;2-o.

Abstract

Two intensive chemotherapy regimens CFPMV (Cytoxan [cyclophosphamide], 5-fluorouracil, prednisone, methotrexate, vincristine) and CA (Cytoxan, Adriamycin [doxorubicin]) were tested against a moderate regimen, CFP, in a prospective three-arm, randomized study with crossover when relapse or failure occurred, in order to assess whether the response, duration of remission, and survival can be altered by using more intensive regimens as first-line or as rescue therapy. All three regimens were equally effective as initial chemotherapy: CFP 26/46 (57%); CFPMV 31/48 (65%) and CA 26/47 (55%) (P = 0.61) with the least toxicity for the CFP regimen. Median duration of remission were 9.5, 11, and 9 months, respectively. Complete responses were almost identical in all three regimens: 4/46 (9%); 6/48 (12%) and 5/47 (11%) (P = 0.94). CFPMV was an effective regimen as second-line therapy: 11/33 (33%) or third-line therapy: 7/21 (33%). The CA regimen was equally effective as second-line therapy: 8/25 (32%), suggesting that intensive regimens provide an effective rescue therapy, as well in previous responders as in nonresponders. Initial intensive regimens have not substantially altered long-term survival in the whole group of treated patients, Arm II (CFPMV----CA----CFP) 17.6 months; Arm III (CA----CFP----CFPMV) 12.3 months when compared with initial moderate regimens Arm I (CFP----CFPMV----CA) 16.6 months (P = 0.24). The same lack of difference in survival was noticed in responder patients in each arm: Arm II 19.0 months; Arm III 16.0 months versus Arm I 22.0 months (P = 0.13). Our data suggest that a moderate regimen is as effective as more intense regimens for induction therapy in metastatic breast cancer, with less toxicity, preserving the opportunity for an effective rescue therapy with intensive regimens in second or third-line chemotherapy.

摘要

在一项前瞻性三臂随机研究中,对两种强化化疗方案CFPMV(环磷酰胺、5-氟尿嘧啶、泼尼松、甲氨蝶呤、长春新碱)和CA(环磷酰胺、阿霉素)与一种中度方案CFP进行了对比试验,当出现复发或治疗失败时采用交叉治疗,以评估使用更强化的方案作为一线治疗或挽救治疗是否能改变缓解率、缓解持续时间和生存率。所有三种方案作为初始化疗的效果相同:CFP组26/46例(57%);CFPMV组31/48例(65%);CA组26/47例(55%)(P = 0.61),其中CFP方案的毒性最小。缓解的中位持续时间分别为9.5个月、11个月和9个月。所有三种方案的完全缓解率几乎相同:4/46例(9%);6/48例(12%);5/47例(11%)(P = 0.94)。CFPMV作为二线治疗方案有效:11/33例(33%),作为三线治疗方案也有效:7/21例(33%)。CA方案作为二线治疗同样有效:8/25例(32%),这表明强化方案无论是对既往有反应者还是无反应者,都能提供有效的挽救治疗。初始强化方案在整个治疗患者组中并未显著改变长期生存率,与初始中度方案相比,II组(CFPMV→CA→CFP)为17.6个月;III组(CA→CFP→CFPMV)为12.3个月,而I组(CFP→CFPMV→CA)为16.6个月(P = 0.24)。在各治疗组的反应者中也观察到生存率无差异:II组为19.0个月;III组为16.0个月,而I组为22.0个月(P = 0.13)。我们的数据表明,在转移性乳腺癌的诱导治疗中,中度方案与更强化的方案效果相同,且毒性更小,同时保留了在二线或三线化疗中使用强化方案进行有效挽救治疗的机会。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验