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对14例连续接受舒尼替尼治疗的不可切除或转移性肺泡软组织肉瘤中国患者进行回顾性分析。

A retrospective analysis of 14 consecutive Chinese patients with unresectable or metastatic alveolar soft part sarcoma treated with sunitinib.

作者信息

Li Ting, Wang Lei, Wang Huijie, Zhang Shujuan, Zhang Xiaowei, Luo Zhiguo, Wang Chunmeng

机构信息

Department of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.

出版信息

Invest New Drugs. 2016 Dec;34(6):701-706. doi: 10.1007/s10637-016-0390-3. Epub 2016 Sep 8.

Abstract

Background The study was aim to assess the efficacy and safety of sunitinib on 14 Chinese patients with locally unresectable or metastatic Alveolar Soft Part Sarcoma (ASPS) at two institutions retrospectively. Methods Patients were treated with 37.5 mg of sunitinib once daily continuously without a scheduled off-treatment period. Dose holds or reductions were recommended for grade 3 AEs but were required for grade 4 AEs. Restarting treatment of sunitinib was allowed when AEs returned back to grade 1 or disappeared. The treatment was continued until progression disease (PD), unacceptable toxicity or death. Results From January 2011 to December 2015, 14 patients with unresectable or metastatic ASPS received sunitinib treatment. Among them, 4 patients achieved partial remission (PR), and 10 patients achieved stable disease (SD). Median progression free survival (PFS) was 41.0 months (95 % CI: 7.7 to 74.4 month). Median overall survival (OS) was not reached. The 1- and 4-year OS rates were 90.0 % and 60.0 % respectively. Two patients with primarily unresectable ASPS received complete surgical resection after neoadjuvant treatment of sunitinib. The majority of toxicities encountered were grade 1 or 2 and manageable. The most common adverse events (AEs) were bleeding (35.7 %), hair & skin color change (37.5 %) and mucositis (28.6 %). Conclusions Sunitinib is effective in locally unresectable or metastatic ASPS with a good safety profile. Neoadjuvant treatment with sunitinib improves the chance of resection for patients with locally advanced ASPS.

摘要

背景

本研究旨在回顾性评估舒尼替尼对两家机构的14例局部不可切除或转移性肺泡软组织肉瘤(ASPS)中国患者的疗效和安全性。方法:患者接受每日一次37.5mg舒尼替尼持续治疗,无预定停药期。3级不良事件(AE)建议剂量暂停或减量,但4级AE则需要。当AE恢复到1级或消失时允许重新开始舒尼替尼治疗。治疗持续至疾病进展(PD)、不可接受的毒性或死亡。结果:2011年1月至2015年12月,14例不可切除或转移性ASPS患者接受了舒尼替尼治疗。其中,4例患者达到部分缓解(PR),10例患者达到疾病稳定(SD)。中位无进展生存期(PFS)为41.0个月(95%CI:7.7至74.4个月)。中位总生存期(OS)未达到。1年和4年OS率分别为90.0%和60.0%。2例原发性不可切除ASPS患者在舒尼替尼新辅助治疗后接受了完整的手术切除。遇到的大多数毒性为1级或2级且可控制。最常见的不良事件(AE)是出血(35.7%)、毛发和皮肤颜色改变(37.5%)和粘膜炎(28.6%)。结论:舒尼替尼对局部不可切除或转移性ASPS有效,安全性良好。舒尼替尼新辅助治疗可提高局部晚期ASPS患者的切除机会。

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