Aisner J, Cirrincione C, Perloff M, Perry M, Budman D, Abrams J, Panasci L, Muss H, Citron M, Holland J
University of Maryland Cancer Center, Baltimore, USA.
J Clin Oncol. 1995 Jun;13(6):1443-52. doi: 10.1200/JCO.1995.13.6.1443.
We sought to compare three doxorubicin-based therapies for metastatic breast cancer for response frequency, time to treatment failure (TTF), and survival.
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.
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).
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.
我们试图比较三种基于阿霉素的转移性乳腺癌治疗方案在缓解频率、治疗失败时间(TTF)和生存率方面的差异。
符合条件的转移性乳腺癌女性患者需具备可测量的病灶、需要实验室检查、未曾接受过转移性疾病的化疗、癌症与白血病B组(CALGB)体能状态≤2且签署了知情同意书。治疗方案如下:第一组——环磷酰胺、阿霉素和氟尿嘧啶(CAF);第二组——长春花碱、阿霉素、噻替派和氟羟甲睾酮(VATH);第三组——在第3、5、7、9等周期,VATH与环磷酰胺、甲氨蝶呤、氟尿嘧啶、长春新碱和泼尼松(CMFVP)交替使用。根据毒性调整剂量。采用标准的CALGB缓解和毒性标准。
1982年8月至1987年2月期间,497名女性患者入组,491名患者接受研究治疗。治疗前特征均衡,中位随访时间为79个月。第一组的缓解率(完全缓解[CR]加部分缓解[PR])为50%,第二组为57%,第三组为51%,三组之间无显著差异。三组的中位TTF分别为8、8和9个月,与第一组相比,第三组更具优势(P = 0.028)。治疗组I、II和III的中位生存时间分别为15、17和17个月。多因素回归分析后,只有雌激素受体(ER)、体能状态和转移部位数量影响TTF和生存率。白细胞减少是最常见的3级或4级毒性反应,每组患者的发生率分别为90%、80%和92%。分别有4名、5名和6名女性出现致命毒性反应。总体而言,第二组的≥3级毒性反应比第一组多,且大多发生在第三组(P = 0.02)。
VATH方案作为初始治疗方案,疗效似乎与CAF方案相似。VATH与CMFVP交替使用并未提高缓解率或生存率。在考虑其他变量后,治疗组与预后无关。仍需要新的治疗方案。