Gladieff L, Houyau P, Mihura J, Martinez M, Caunes N, Chevreau C, Bugat R, Roché H
Département d'oncologie médicale, centre Claudius-Regaud, Toulouse, France.
Bull Cancer. 1996 Sep;83(9):703-6.
To assess efficacy and toxicity of less toxic analogs for advanced breast cancer in elderly women, we performed a phase II study using the combination mitoxantrone (MTZ)-vinorelbine (VNR). From January 1991 to May 1993, 25 women older than 70 years received a chemotherapy consisting in 10 mg/m2 of MTZ on day 1, followed by 20 mg/m2 of VNR on day 1 and 8. Cycles were repeated every 21 days for a maximum of ten cycles in the case of an objective response. Sixteen women previously received first line hormonotherapy, eight with only one metastatic site. Twenty-three patients are evaluable for response and toxicity. An objective response was observed in five cases (22%), with a median time to progression of 13 months. More than 75% of the planned dose-intensity, for MTZ and VNR was received by 90 and 57.2% of patients, respectively. Dose-limiting toxicity was myelosuppression but no febrile neutropenia was observed. Extra haematologic toxicities were unfrequent. This combination is well tolerated by elderly women, but best results could be achieved by increasing delivered dose intensity.
为评估毒性较低的类似物对老年女性晚期乳腺癌的疗效和毒性,我们进行了一项使用米托蒽醌(MTZ)-长春瑞滨(VNR)联合方案的II期研究。1991年1月至1993年5月,25名70岁以上的女性接受了化疗,具体方案为第1天给予10mg/m²的MTZ,随后在第1天和第8天给予20mg/m²的VNR。每21天重复一个周期,若出现客观缓解则最多进行十个周期。16名女性先前接受过一线激素治疗,其中8名仅有一个转移部位。23名患者可评估疗效和毒性。观察到5例(22%)出现客观缓解,中位进展时间为13个月。分别有90%和57.2%的患者接受了超过计划剂量强度75%的MTZ和VNR。剂量限制性毒性为骨髓抑制,但未观察到发热性中性粒细胞减少。血液学外毒性不常见。老年女性对该联合方案耐受性良好,但通过提高给药剂量强度可能会取得更好的结果。