Inoue Akira, Sugawara Shunichi, Yamazaki Koichi, Maemondo Makoto, Suzuki Toshiro, Gomi Kazunori, Takanashi Shingo, Inoue Chieko, Inage Minoru, Yokouchi Hiroshi, Watanabe Hiroshi, Tsukamoto Toumei, Saijo Yasuo, Ishimoto Osamu, Hommura Fumihiro, Nukiwa Toshihiro
Department of Respiratory Medicine, Sendai Kousei Hospital, Sendai, Japan.
J Clin Oncol. 2008 Nov 20;26(33):5401-6. doi: 10.1200/JCO.2008.18.1974. Epub 2008 Oct 14.
Amrubicin, a new anthracycline agent, and topotecan are both active for previously treated small-cell lung cancer (SCLC). No comparative study of these agents has been reported. This randomized phase II study was conducted to select amrubicin or topotecan for future evaluation.
Patients with SCLC previously treated with platinum-containing chemotherapy were randomly assigned to receive amrubicin (40 mg/m(2) on days 1 through 3) or topotecan (1.0 mg/m(2) on days 1 through 5). Patients were stratified by Eastern Cooperative Oncology Group performance status (0, 1, or 2) and type of relapse (chemotherapy sensitive or refractory). The primary end point was overall response rate (ORR), and secondary end points were progression-free survival (PFS), overall survival, and toxicity profile.
From February 2004 to July 2007, 60 patients were enrolled, and 59 patients (36 patients with sensitive and 23 patients with refractory relapse) were assessable for efficacy and safety evaluation. Neutropenia was severe, and one treatment-related death owing to infection was observed in the amrubicin arm. ORRs were 38% (95% CI, 20% to 56%) for the amrubicin arm and 13% (95% CI, 1% to 25%) for the topotecan arm. In sensitive relapse, ORRs were 53% for the amrubicin arm and 21% for the topotecan arm. In refractory relapse, ORRs were 17% for the amrubicin arm and 0% for the topotecan arm. Median PFS was 3.5 months for patients in the amrubicin arm and 2.2 months for patients in the topotecan arm. Multivariate analysis revealed that amrubicin has more influence than topotecan on overall survival.
Amrubicin may be superior to topotecan with acceptable toxicity for previously treated patients with SCLC. Further evaluation of amrubicin for relapsed SCLC is warranted.
氨柔比星是一种新型蒽环类药物,拓扑替康对既往接受过治疗的小细胞肺癌(SCLC)均有活性。尚未有关于这两种药物的比较研究报道。本随机II期研究旨在选择氨柔比星或拓扑替康以供未来评估。
既往接受含铂化疗的SCLC患者被随机分配接受氨柔比星(第1至3天,40mg/m²)或拓扑替康(第1至5天,1.0mg/m²)。患者按东部肿瘤协作组体能状态(0、1或2)和复发类型(化疗敏感或难治)进行分层。主要终点为总缓解率(ORR),次要终点为无进展生存期(PFS)、总生存期和毒性特征。
2004年2月至2007年7月,共入组60例患者,59例患者(36例敏感复发和23例难治复发)可进行疗效和安全性评估。中性粒细胞减少严重,在氨柔比星组观察到1例因感染导致的治疗相关死亡。氨柔比星组的ORR为38%(95%CI,20%至56%),拓扑替康组为13%(95%CI,1%至25%)。在敏感复发中,氨柔比星组的ORR为53%,拓扑替康组为21%。在难治复发中,氨柔比星组的ORR为17%,拓扑替康组为0%。氨柔比星组患者的中位PFS为3.5个月,拓扑替康组为2.2个月。多变量分析显示,氨柔比星对总生存期的影响大于拓扑替康。
对于既往接受过治疗的SCLC患者,氨柔比星可能优于拓扑替康,且毒性可接受。有必要对氨柔比星用于复发性SCLC进行进一步评估。