Ellis G K, Green S, Schulman S, Coltman C A, Hynes H E, Rivkin S, Livingston R B
Puget Sound Oncology Consortium, Seattle, Washington.
Cancer. 1991 Sep 1;68(5):934-9. doi: 10.1002/1097-0142(19910901)68:5<934::aid-cncr2820680504>3.0.co;2-n.
Twenty-seven women with metastatic breast cancer were treated with doxorubicin (Adriamycin, Adria Laboratories, Columbus, OH) every other week, alternating with 5-fluorouracil (5FU) and high-dose calcium leucovorin, for a 12-week induction regimen, followed by weekly doxorubicin and oral daily cyclophosphamide. Twenty-five women were eligible and evaluable. Of these, complete response occurred in two patients (8%) and partial response in six patients (24%), for a total response rate of 32%. Toxicity was similar to that seen in previous Southwest Oncology Group (SWOG) trials in this patient population. Response rates in this study were inferior, with comparable median survivals to those of previous SWOG studies that are reviewed. Additional, more dose-intensive approaches incorporating newer approaches to the administration of cancer chemotherapeutic agents are planned.
27名转移性乳腺癌女性患者接受了如下治疗:每两周使用一次阿霉素(阿霉素,阿德里亚实验室,俄亥俄州哥伦布市),并与5-氟尿嘧啶(5FU)和高剂量亚叶酸钙交替使用,进行为期12周的诱导治疗方案,随后每周使用阿霉素并每日口服环磷酰胺。25名女性符合条件且可评估。其中,2名患者(8%)出现完全缓解,6名患者(24%)出现部分缓解,总缓解率为32%。毒性与先前西南肿瘤学组(SWOG)在该患者群体中的试验所见相似。本研究中的缓解率较低,中位生存期与之前回顾的SWOG研究相当。计划采用更多剂量密集型方法,并结合癌症化疗药物给药的新方法。