Ahmann F R, Pugh R
Cancer. 1987 Jan 15;59(2):239-44. doi: 10.1002/1097-0142(19870115)59:2<239::aid-cncr2820590211>3.0.co;2-c.
A Southwest Oncology Group pilot study was designed to evaluate a brief, 4.5-month induction course of chemotherapy with three presumably non-cross resistant regimens in poor-prognosis metastatic breast cancer. Sixty-three patients were treated with doxorubicin, cyclophosphamide, plus vincristine on day 1, methotrexate followed 30 minutes later by 5-fluorouracil (5-FU) on day 22, and mitomycin C plus 3 days of vinblastine on day 43. All three sequential regimens were repeated once and therapy was then discontinued in responding patients. The same chemotherapy was reinstituted at the time of relapse. The overall response rate to the induction chemotherapy was 35% and included only one complete response (2%). Median response duration was 9 months. Respondents were off all therapy for a median of 5 months (range, 1-12+ months) and were followed without evidence of progressive disease. Response to retreatment was 30% with no complete responses seen. Overall median survival from the data of diagnosis of metastatic disease was 24 months, with a median survival of 14 months from the date of initiation of therapy. Toxicity for this induction regimen was moderate with two treatment-related deaths secondary to myelosuppression. While the results of this pilot study fail to support the use of non-cross resistant regimens in breast cancer, short-term therapy appears to have no adverse effect on survival and resulted in significant periods during which no therapy was given, resulting in a reduction in overall toxicity.
西南肿瘤协作组开展了一项初步研究,旨在评估针对预后较差的转移性乳腺癌患者,采用三种可能无交叉耐药性的方案进行为期4.5个月的简短诱导化疗效果。63例患者在第1天接受阿霉素、环磷酰胺加长春新碱治疗,第22天接受甲氨蝶呤,30分钟后再接受5-氟尿嘧啶(5-FU)治疗,第43天接受丝裂霉素C加3天长春花碱治疗。所有三个序贯方案均重复一次,然后对有反应的患者停止治疗。复发时重新采用相同的化疗方案。诱导化疗的总缓解率为35%,仅包括1例完全缓解(2%)。中位缓解持续时间为9个月。有反应的患者停止所有治疗的中位时间为5个月(范围1至12个多月),之后随访未发现疾病进展迹象。再次治疗的缓解率为30%,未见完全缓解。从转移性疾病诊断数据来看,总体中位生存期为24个月,从开始治疗之日起的中位生存期为14个月。该诱导方案的毒性为中度,有两例与治疗相关的死亡,原因是骨髓抑制。虽然这项初步研究的结果不支持在乳腺癌中使用无交叉耐药性的方案,但短期治疗似乎对生存期没有不利影响,并且导致了相当长一段时间无需治疗,从而降低了总体毒性。