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首页> 外文期刊>Medicine. >Target Therapy of Unresectable or Metastatic Dermatofibrosarcoma Protuberans With Imatinib Mesylate: An Analysis on 22 Chinese Patients
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Target Therapy of Unresectable or Metastatic Dermatofibrosarcoma Protuberans With Imatinib Mesylate: An Analysis on 22 Chinese Patients

机译:甲磺酸伊马替尼治疗无法切除或转移性皮肤纤维母细胞肉瘤的靶向治疗:22例中国患者分析

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摘要

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.
机译:隆突性皮肤皮肤肉瘤(DFSP)是一种罕见的皮肤组织斑块状肿瘤,发生在躯干上,多于四肢和颈部。超过95%的DFSP在17q22和22q13染色体区域出现异常,从而导致COL1A1和PDGFB基因融合。手术是DFSP的最佳治疗方法,但是对于局部晚期或转移性患者,效果不佳,就像化学疗法和放射疗法一样。这项研究的目的是回顾性评估伊马替尼在单一机构对22名患有局部无效或转移性DFSP的中国患者的治疗活性和安全性。在收集的367名中国DFSP患者的数据中,我们回顾性分析了22名局部晚期或转移性DFSP患者,他们均于2009年1月至2014年10月在一个中心接受过伊马替尼治疗。患者均以400的初始剂量接受伊马替尼治疗他们对伊马替尼产生抗药性后逐渐增加至每日200 mg,并逐步增加至每日800 mg。中位随访时间为36个月,中位治疗时间为15个月。结果显示,伊马替尼治疗了10例局部晚期DFSP患者和12例转移性DFSP患者。除1名发生原发伊马替尼耐药的患者外,还有15例患者达到部分缓解(PR),6例患者达到疾病稳定(SD)。纤维肉瘤DFSP和经典DFSP患者均表现出对伊马替尼的相似反应。 PFS中位数估计为19个月。尚未达到中位总体生存期(OS),估计的1年和3年OS率分别为95.5%(21/22)和77.3%(17/22)。在伊马替尼新辅助治疗后,每10例原发不可切除的DFSP患者中有4例接受了完全手术切除。伊马替尼疗法具有良好的安全性耐受性,是局部无效或转移性DFSP的治疗选择。伊马替尼对局部晚期或转移性DFSP的新辅助治疗可改善手术效果,并可能有助于切除难治的肿瘤。

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