Funasaka Chikako, Kanemasa Yusuke, Kageyama Akihiko, Shimoyama Tatsu, Omuro Yasushi
Dept. of Medical Oncology, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital.
Gan To Kagaku Ryoho. 2020 Aug;47(8):1205-1208.
Standard regimens for extrapulmonary neuroendocrine carcinomas(EPNEC)are not established. Treatment used for small cell lung cancer is also used for EPNECs. Amrubicin(AMR) monotherapy is used as salvage therapy for small cell lung cancer, but its efficacy in EPNEC is not clear. The aim of this study was to estimate the efficacy of AMR monotherapy in EPNEC. We retrospectively investigated patients with EPNEC who received first-line platinum-based chemotherapy between April 2007 and March 2019. The time to treatment failure(TTF)and the efficacy and toxicity was analyzed in the patients who received AMR monotherapy. Among 43 patients with EPNEC, 14(13 males, one female; median age, 58 years)received AMR monotherapy. Primary site included the pancreas(n=3), stomach(n=3), rectum(n=1), anal canal(n=1), salivary glands(n= 1), urothelial(n=1), bladder(n=1), prostate(n=1), and 2 patients had primary unknown cancer. Pathological type included small cell(n=4), large cell(n=2), and other types(n=8). Prior chemotherapy comprised CDDP plus CPT-11(n =5), CDDP plus ETP(n=2), and CBDCA plus ETP(n=6). The median TTF was 49(20-61)days. One patient had a partial response and the disease control rate was 33%. The common adverse events of >Grade 3 were leukopenia(69%), neutropenia(62%), and febrile neutropenia(23%). AMR monotherapy was clinically effective and safe for EPNEC.
肺外神经内分泌癌(EPNEC)的标准治疗方案尚未确立。用于小细胞肺癌的治疗方法也用于EPNEC。氨柔比星(AMR)单药疗法用作小细胞肺癌的挽救治疗,但其在EPNEC中的疗效尚不清楚。本研究的目的是评估AMR单药疗法在EPNEC中的疗效。我们回顾性调查了2007年4月至2019年3月期间接受一线铂类化疗的EPNEC患者。对接受AMR单药疗法的患者的治疗失败时间(TTF)、疗效和毒性进行了分析。在43例EPNEC患者中,14例(13例男性,1例女性;中位年龄58岁)接受了AMR单药疗法。原发部位包括胰腺(n = 3)、胃(n = 3)、直肠(n = 1)、肛管(n = 1)、唾液腺(n = 1)、尿路上皮(n = 1)、膀胱(n = 1)、前列腺(n = 1),2例患者原发癌不明。病理类型包括小细胞(n = 4)、大细胞(n = 2)和其他类型(n = 8)。既往化疗方案包括顺铂加伊立替康(n = 5)、顺铂加依托泊苷(n = 2)、卡铂加依托泊苷(n = 6)。中位TTF为49(20 - 61)天。1例患者部分缓解,疾病控制率为33%。3级以上常见不良事件为白细胞减少(69%)、中性粒细胞减少(62%)和发热性中性粒细胞减少(23%)。AMR单药疗法对EPNEC临床有效且安全。