Venturino A, Comandini D, Simoni C, Merlini L, Naso C, Palumbo R, Fusco V, Porcile G, Pronzato P, Rosso R, Repetto L
Oncologia Medica 1 - Istituto Nazionale per la Ricerca sul Cancro, Genova.
Breast Cancer Res Treat. 2000 Apr;60(3):195-200. doi: 10.1023/a:1006350602108.
Metastatic breast cancer remains an incurable disease and the median overall survival has not significantly improved over the past two decades. Aims of the present randomized phase II trial were to analyse activity and toxicity of chemotherapies with single agent or with combination regimens in previously treated patients with advanced breast cancer. Ninety-nine eligible patients were randomized to receive the following chemotherapies: Arm A - vinorelbine 30 mg/m2 i.v. weekly; Arm B - leucovorin 100 mg/m2 i.v. followed by 5-fluorouracil 370 mg/m2 i.v. days 1 --> 5, q 28 days; Arm C - mitoxantrone 12 mg/m2 i.v. only day 1 + leucovorin 100 mg/m2 i.v. followed by 5-fluorouracil 370 mg/m2 i.v. days 1 --> 3, q 28 days. Patients characteristics are comparable in the three groups. The median number of chemotherapy courses administered was 7, 6 and 5 in arm A, B and C, respectively. Objective responses were 24%, 30% and 21% and the median duration of responses were 2, 2.5 and 5.5 months in the arm A, B and C, respectively. Median overall survivals were 9.5, 9 and 9 months in the three arms. No difference was noted comparing the survivals of responding or non responding patients. General toxicity was not mild, with 27.5% of patients experiencing WHO grade 3-4 toxicities. Our results are similar in the three groups of patients and comparable to those reported by other authors. Chemotherapy applied to patients with second or subsequent recurrence allow objective responses in a small percentage of patients. Moreover responders have a negligible prolongation of survival.
转移性乳腺癌仍然是一种无法治愈的疾病,在过去二十年中,其总体中位生存期并未显著改善。本随机II期试验的目的是分析单药化疗或联合化疗方案对先前接受过治疗的晚期乳腺癌患者的活性和毒性。99名符合条件的患者被随机分配接受以下化疗:A组——长春瑞滨30mg/m²静脉注射,每周一次;B组——亚叶酸钙100mg/m²静脉注射,随后5-氟尿嘧啶370mg/m²静脉注射,第1至5天,每28天重复一次;C组——米托蒽醌12mg/m²仅在第1天静脉注射 + 亚叶酸钙100mg/m²静脉注射,随后5-氟尿嘧啶370mg/m²静脉注射,第1至3天,每28天重复一次。三组患者的特征具有可比性。A、B和C组分别给予的化疗疗程中位数为7、6和5。客观缓解率分别为24%、30%和21%,A、B和C组的缓解持续时间中位数分别为2、2.5和5.5个月。三组的总体中位生存期分别为9.5、9和9个月。在比较缓解和未缓解患者的生存期时未发现差异。总体毒性并不轻微,27.5%的患者经历了WHO 3-4级毒性。我们在三组患者中的结果相似,并且与其他作者报道的结果相当。应用于第二次或后续复发患者的化疗仅能使一小部分患者获得客观缓解。此外,缓解者的生存期延长可忽略不计。