Department of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.
Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Cancer Chemother Pharmacol. 2019 Nov;84(5):1059-1064. doi: 10.1007/s00280-019-03940-0. Epub 2019 Sep 5.
Amrubicin and cisplatin is one of the active regimens used to treat patients with extensive-disease (ED)-small cell lung cancer (SCLC), whereas combined therapy involving chemotherapy and concurrent thoracic radiotherapy is the standard treatment for limited-disease (LD)-SCLC.
This study aimed to determine the maximum tolerated dose (MTD) and dose-limiting toxicities (DLT) of amrubicin and cisplatin with concurrent thoracic radiotherapy (TRT) for LD-SCLC.
Patients that fulfilled the following eligibility criteria were enrolled: being aged ≤ 75 years and chemotherapy-naïve and having a performance status (PS) of 0-1, LD-SCLC, and adequate organ function. The patients received escalating doses of amrubicin on days 1, 2, and 3, and a fixed 60-mg/m dose of cisplatin on day 1. Four cycles of chemotherapy were administered, with each cycle lasting 4 weeks. TRT involving 2 Gy/day, once daily, commenced on day 2 of the first cycle of chemotherapy. The initial dose of amrubicin was 20 mg/m (level 1), and the dose was escalated to 25 mg/m (level 2) and then 30 mg/m (level 3).
Eight patients from three institutions were enrolled at three dose levels. The patients' characteristics were as follows: male/female: 3/5; median age (range): 68.5 (60-73); PS 0/1: 4/4; stage IIIA/IIIB disease: 3/5. Both level 3 patients experienced DLT (grade 4 neutropenia and/or leukopenia lasting > 4 days). Level 3 was defined as the MTD, and level 2 was recommended as the dose for this regimen. Seven patients exhibited partial responses, and 1 displayed progressive disease (response rate: 88%). The median progression-free survival and overall survival periods were 11.1 and 39.5 months, respectively. No treatment-related deaths occurred.
When this regimen was combined with TRT for LD-SCLC, the MTD was 30 mg/m for amrubicin and 60 mg/m for cisplatin. In addition, neutropenia and leukopenia were DLT, and doses of 25 mg/m for amrubicin and 60 mg/m for cisplatin are recommended for this regimen.
氨柔比星联合顺铂是治疗广泛期(ED)小细胞肺癌(SCLC)患者的有效方案之一,而化疗联合同期胸部放疗是局限期(LD)SCLC 的标准治疗方法。
本研究旨在确定氨柔比星联合顺铂联合同期胸部放疗(TRT)治疗 LD-SCLC 的最大耐受剂量(MTD)和剂量限制性毒性(DLT)。
符合以下纳入标准的患者入组:年龄≤75 岁,初治,体力状态(PS)0-1 分,LD-SCLC,器官功能良好。患者接受氨柔比星 20mg/m(1 级)、25mg/m(2 级)和 30mg/m(3 级)递增剂量,顺铂 60mg/m 固定剂量(1 级),于第 1、2、3 天给药,第 1 天给药。每 4 周为 1 个周期,共 4 个周期。第 1 周期化疗第 2 天开始行 2Gy/天,每日 1 次的 TRT。患者来自 3 家机构,共 8 例,分为 3 个剂量水平。患者特征如下:男/女:3/5;中位年龄(范围):68.5(60-73)岁;PS 0/1:4/4 分;ⅢA/ⅢB 期疾病:3/5 例。2 个剂量水平(3 级)患者均出现 DLT(4 级中性粒细胞减少和/或白细胞减少持续时间>4 天)。3 级为 MTD,2 级为该方案推荐剂量。7 例患者部分缓解,1 例进展(缓解率:88%)。中位无进展生存期和总生存期分别为 11.1 和 39.5 个月。无治疗相关死亡。
该方案联合 TRT 治疗 LD-SCLC 时,氨柔比星 MTD 为 30mg/m,顺铂为 60mg/m。此外,中性粒细胞减少和白细胞减少是 DLT,氨柔比星推荐剂量为 25mg/m,顺铂推荐剂量为 60mg/m。