Ribas A, Albanell J, Bellmunt J, Bermejo B, Gallardo E, Vera R, Bodi R, Solé-Calvo L A
Medical Oncology Service, Hospital General Universitari Vall d'Hebron, Barcelona, Spain.
Acta Oncol. 1997;36(7):701-4. doi: 10.3109/02841869709001340.
Doxorubicin for four cycles plus cyclophosphamide, methotrexate and 5-fluorouracil (CMF) for eight cycles is an effective adjuvant regimen for breast cancer patients with more than three involved axillary lymph nodes. We reviewed the incidence of dose delays and growth factor requirements when this regimen is administered to patients receiving concurrent irradiation. Thirty-six patients with more than three involved axillary lymph nodes were treated with the sequential regimen doxorubicin-CMF and irradiation. Patients with two or more dose delays received G-CSF treatment. Seventy-five percent of the patients required dose delays for day-22 neutropenia, and growth factors were needed for half of the patients in order to maintain a received dose intensity of 0.940. The first delayed cycle occurred in 74% of the patients while receiving concomitant chemoradiotherapy. Frequent dose delays were required when the sequential regimen doxorubicin-CMF was administered along with radiotherapy. Growth factors are needed to maintain dose intensity similar to that achieved in the original trial.
对于有三个以上腋窝淋巴结受累的乳腺癌患者,四个周期的多柔比星加八个周期的环磷酰胺、甲氨蝶呤和5-氟尿嘧啶(CMF)是一种有效的辅助治疗方案。我们回顾了该方案用于接受同步放疗的患者时剂量延迟和生长因子需求的发生率。36例有三个以上腋窝淋巴结受累的患者接受了多柔比星-CMF序贯方案及放疗。有两次或更多次剂量延迟的患者接受了粒细胞集落刺激因子(G-CSF)治疗。75%的患者因第22天中性粒细胞减少需要剂量延迟,为维持0.940的接受剂量强度,一半的患者需要生长因子。74%的患者在接受同步放化疗时出现了第一个延迟周期。当多柔比星-CMF序贯方案与放疗同时进行时,需要频繁的剂量延迟。需要生长因子来维持与原试验相似的剂量强度。