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阿霉素和顺铂联合胸部放疗治疗局限期小细胞肺癌的剂量递增研究。

Dose escalation study of amrubicin and cisplatin with concurrent thoracic radiotherapy for limited-disease small cell lung cancer.

机构信息

Department of Respiratory Medicine, Sasebo City General Hospital, Nagasaki, Japan.

Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

Cancer Chemother Pharmacol. 2019 Nov;84(5):1059-1064. doi: 10.1007/s00280-019-03940-0. Epub 2019 Sep 5.

Abstract

BACKGROUND

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.

PURPOSE

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 AND METHODS

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).

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

目的

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)。

方法

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。

结论

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。

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