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甲磺酸伊马替尼对不可切除或转移性隆突性皮肤纤维肉瘤的靶向治疗:22例中国患者的分析

Target therapy of unresectable or metastatic dermatofibrosarcoma protuberans with imatinib mesylate: an analysis on 22 Chinese patients.

作者信息

Wang Chunmeng, Luo Zhiguo, Chen Jie, Zheng Biqiang, Zhang Ruming, Chen Yong, Shi Yingqiang

机构信息

Form the Department of Gastric Cancer and Soft Tissue Sarcomas, Fudan University Shanghai Cancer Center (CW, JC, BZ, RZ, YC, YS); Department of Oncology, Shanghai Medical College, Fudan University (CW, ZL, JC, BZ, RZ, YC, YS); and Department of Medical Oncology (ZL), Fudan University Shanghai Cancer Center, Shanghai, PR China.

出版信息

Medicine (Baltimore). 2015 May;94(17):e773. doi: 10.1097/MD.0000000000000773.

Abstract

Dermatofibrosarcoma protuberans (DFSP) is a rare, plaque-like tumor of the cutaneous tissue occurring more on the trunk than the extremities and neck. More than 95% of DFSP present anomalies on the 17q22 and 22q13 chromosomal regions leading to the fusion of COL1A1 and PDGFB genes. Surgery is the optimal treatment for DFSP, but less effective in locally advanced or metastatic patients, as is the case with chemotherapy and radiotherapy. The aim of this study was to assess retrospectively the therapeutic activity and safety of imatinib on 22 Chinese patients with locally inoperative or metastatic DFSP at a single institution.In the collected data of 367 Chinese patients with DFSP, we analyzed retrospectively 22 patients with locally advanced or metastatic DFSP, all of whom received imatinib therapy at 1 center from January 2009 to October 2014. Patients were administered with imatinib at an initial dose of 400 mg and escalated to 800 mg daily after they developed imatinib resistance. The median follow-up time was 36 months, and the median treatment time was 15 months.The results showed that 10 locally advanced DFSP patients and 12 metastatic DFSP patients received imatinib therapy. Apart from 1 patient who developed primary imatinib resistance, 15 patients achieved partial remission (PR), and 6 patients achieved stable disease (SD). Both fibrosarcomatous DFSP and classic DFSP patients demonstrated similar response to imatinib. Median PFS was estimated to be 19 months. Median overall survival (OS) has not been reached, and estimated 1- and 3-year OS rates were 95.5% (21/22) and 77.3% (17/22), respectively. Four out of 10 patients with primarily unresectable DFSP received complete surgical resection after neoadjuvant treatment of imatinib.Imatinib therapy is well tolerated with a safety profile and is the therapy of choice in locally inoperative or metastatic DFSP. Neoadjuvant treatment of locally advanced or metastatic DFSP with imatinib improves surgical outcomes and may facilitate resection of difficult tumors.

摘要

隆突性皮肤纤维肉瘤(DFSP)是一种罕见的皮肤组织斑块状肿瘤,多见于躯干,而非四肢和颈部。超过95%的DFSP在17q22和22q13染色体区域存在异常,导致COL1A1和PDGFB基因融合。手术是DFSP的最佳治疗方法,但对于局部晚期或转移性患者效果较差,化疗和放疗也是如此。本研究的目的是回顾性评估伊马替尼对一家机构中22例局部无法手术或转移性DFSP中国患者的治疗活性和安全性。在收集的367例中国DFSP患者的数据中,我们回顾性分析了22例局部晚期或转移性DFSP患者,所有患者在2009年1月至2014年10月期间均在1个中心接受伊马替尼治疗。患者初始剂量为400mg伊马替尼,出现伊马替尼耐药后剂量增至每日800mg。中位随访时间为36个月,中位治疗时间为15个月。结果显示,10例局部晚期DFSP患者和12例转移性DFSP患者接受了伊马替尼治疗。除1例出现原发性伊马替尼耐药的患者外,15例患者实现部分缓解(PR),6例患者病情稳定(SD)。纤维肉瘤样DFSP患者和经典DFSP患者对伊马替尼的反应相似。中位无进展生存期(PFS)估计为19个月。中位总生存期(OS)尚未达到,估计1年和3年OS率分别为95.5%(21/22)和77.3%(17/22)。10例原发性不可切除DFSP患者中有4例在接受伊马替尼新辅助治疗后接受了完整的手术切除。伊马替尼治疗耐受性良好,具有安全特征,是局部无法手术或转移性DFSP的首选治疗方法。用伊马替尼对局部晚期或转移性DFSP进行新辅助治疗可改善手术结果,并可能有助于切除困难肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ebc/4603059/ff3b411547fc/medi-94-e773-g001.jpg

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