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首页> 外文期刊>Journal of Clinical Oncology >Combination chemotherapy for metastatic or recurrent carcinoma of the breast--a randomized phase III trial comparing CAF versus VATH versus VATH alternating with CMFVP: Cancer and Leukemia Group B Study 8281.
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Combination chemotherapy for metastatic or recurrent carcinoma of the breast--a randomized phase III trial comparing CAF versus VATH versus VATH alternating with CMFVP: Cancer and Leukemia Group B Study 8281.

机译:组合化疗用于乳腺的转移性或复发癌 - 一种随机期III试验比较CAF与Vath与CMFV的vath交替:癌症和白血病组研究8281。

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PURPOSE: We sought to compare three doxorubicin-based therapies for metastatic breast cancer for response frequency, time to treatment failure (TTF), and survival. MATERIALS AND METHODS: Women with metastatic breast cancer who had measurable disease, required laboratory tests, had received no prior chemotherapy for metastases, had a Cancer and Leukemia Group B (CALGB) performance status < or = 2, and provided informed consent were eligible. Treatment included the following: arm I--cyclophosphamide, doxorubicin, and fluorouracil (CAF); arm II--vinblastine, doxorubicin, thiotepa, and halotestin (VATH); and arm III--VATH alternating with cyclophosphamide, methotrexate, fluorouracil, vincristine, and prednisone (CMFVP) on cycles 3, 5, 7, 9, etc. Doses were modified for toxicities. Standard CALGB response and toxicity criteria were used. RESULTS: Between August 1982 and February 1987, 497 women were entered and 491 were treated on study. Pretreatment characteristics were well balanced and the median follow-up duration was 79 months. There were no significant differences in response (complete [CR] plus partial [PR]) at 50% on arm I, 57% on arm II, and 51% on arm III. The median TTFs were 8, 8, and 9 months, respectively, in favor of arm III when compared with arm I (P = .028). The median survival times for treatment arms I, II, and III were 15, 17, and 17 months, respectively. After multivariate regression analyses, only estrogen receptors (ER), performance status, and number of metastatic sites influenced TTF and survival. Leukopenia was the most common grade 3 or 4 toxicity, occurring in 90%, 80%, and 92% of patients per arm, respectively. Lethal toxicities were seen in four, five, and six women, respectively. Overall, there were more grade > or = 3 toxicities on arm II than I, and most occurred on arm III (P = .02). CONCLUSION: The VATH regimen appears similarly effective to the CAF regimen as initial therapy. Alternating CMFVP with VATH did not improve response rate or survival. After accounting for other variables, treatment arm was not related to outcome. New therapeutic regimens are still needed.
机译:目的:我们试图比较三种基于多柔比蛋白的转移性乳腺癌治疗响应乳腺癌,治疗失败(TTF)和存活时间。材料和方法:患有可衡量疾病的转移性乳腺癌的妇女,所需的实验室测试,未经前期化学疗法进行转移,具有癌症和白血病组(Calgb)绩效状态<或= 2,并提供了知情同意。治疗包括:ARM I - 环磷酰胺,多柔比星和氟尿嘧啶; ARM II - 芳嗪,多柔比星,Thiotepa和Halotestin(VATH);和ARM III - 与环磷酰胺,甲氨蝶呤,氟尿嘧啶,长春螯列机和泼尼松(CMFVP)交替,用于循环3,5,7,9等剂量。毒性修饰剂量。使用标准CALGB响应和毒性标准。结果:1982年8月和1987年2月,进入497名妇女,491名妇女进行研究。预处理特征平衡良好,中位随访时间为79个月。响应没有显着差异(完整[Cr]加上部分[PR])在ARM I的50%,ARM II上57%,ARM III的51%。与ARM I相比,中位TTFS分别为8,8和9个月,有利于ARM III(P = .028)。治疗臂I,II和III的中位存活时间分别为15,17和17个月。在多变量回归分析后,只有雌激素受体(ER),性能状态和转移性位点的数量影响TTF和生存率。白细胞减少症是最常见的3或4级毒性,分别发生在90%,80%和92%的患者中。致命毒性分别在四个,五个和六名妇女中看到。总体而言,在ARM II上有更多的等级>或= 3个毒性,并且大部分发生在ARM III(P = .02)。结论:VATH方案看起来与CAF方案同样有效作为初始治疗。具有VATH的交替CMFVP没有提高响应率或生存。在核算其他变量后,治疗臂与结果无关。仍然需要新的治疗方案。

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