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伊马替尼治疗后初始不可切除的胃肠道间质瘤患者切除标本中CD117表达降低作为复发可能预后标志物的临床病理分析

Decrease of CD117 expression as possible prognostic marker for recurrence in the resected specimen after imatinib treatment in patients with initially unresectable gastrointestinal stromal tumors: a clinicopathological analysis.

作者信息

Mearadji Amir, den Bakker Michael A, van Geel Albertus N, Eggermont Alexander M M, Sleijfer Stefan, Verweij Jaap, de Wilt Johannes H W, Verhoef Cornelis

机构信息

Department of Surgical Oncology, Erasmus Medical Center, Daniel Den Hoed Cancer Center, Rotterdam, The Netherlands.

出版信息

Anticancer Drugs. 2008 Jul;19(6):607-12. doi: 10.1097/CAD.0b013e32830138f9.

Abstract

Gastrointestinal stromal tumors (GIST) are the most common malignant mesenchymal tumors of the gastrointestinal tract. The principal treatment modality for primary GIST is surgery whereas for metastatic GIST, imatinib has an established role. In patients with locally advanced and metastatic GIST, the role of surgery in the imatinib era is still unclear. Fifteen patients with locally advanced (n=9) and/or metastatic GIST (n=6) were treated with imatinib followed by resection. Detailed histopathological examination was performed before and after treatment with imatinib, which was given for a median of 11 months before surgery. Ten patients showed a radiographic partial response, four patients had stable disease, and one patient progressed. At the time of surgery, the median tumor diameter was 6.5 cm. In all the nine patients with locally advanced GIST, a R0 resection could be performed. Histopathological examination showed imatinib effects in all tumors, including the case with progressive disease. All patients with locally advanced disease (n=9) were alive after a median follow-up of 40 months (range: 18-59), of which seven patients were free of disease. Four of the six patients treated for metastatic GIST died of disease after 30, 45, 50, and 74 months of follow-up. Remarkably, in five of six patients in whom CD117 expression was diminished or lost in the resection specimen, disease recurrence was observed. In patients with retained CD117 expression, one of the nine patients had recurrent disease. In conclusion, preoperative imatinib treatment in patients with locally advanced GIST resulted in a decrease of tumor load in most patients, enabling complete surgical resection. For patients with metastatic GIST, the role of surgery remains less clear. Loss or decrease of CD117 expression in the resected specimen after imatinib treatment may be associated with disease recurrence.

摘要

胃肠道间质瘤(GIST)是胃肠道最常见的恶性间叶组织肿瘤。原发性GIST的主要治疗方式是手术,而对于转移性GIST,伊马替尼已确立其作用。在局部晚期和转移性GIST患者中,手术在伊马替尼时代的作用仍不明确。15例局部晚期(n = 9)和/或转移性GIST(n = 6)患者接受伊马替尼治疗后行手术切除。在伊马替尼治疗前后进行了详细的组织病理学检查,手术前伊马替尼的中位治疗时间为11个月。10例患者影像学检查显示部分缓解,4例患者病情稳定,1例患者病情进展。手术时,肿瘤中位直径为6.5 cm。在所有9例局部晚期GIST患者中,均可行R0切除。组织病理学检查显示伊马替尼对所有肿瘤均有作用,包括病情进展的病例。所有局部晚期疾病患者(n = 9)在中位随访40个月(范围:18 - 59个月)后均存活,其中7例患者无疾病。6例接受转移性GIST治疗的患者中有4例在随访30、45、50和74个月后死于疾病。值得注意的是,在6例切除标本中CD117表达降低或缺失的患者中有5例出现疾病复发。在保留CD117表达的患者中,9例患者中有1例出现复发性疾病。总之,局部晚期GIST患者术前接受伊马替尼治疗可使大多数患者肿瘤负荷降低,从而能够进行完整的手术切除。对于转移性GIST患者,手术的作用仍不太明确。伊马替尼治疗后切除标本中CD117表达的缺失或降低可能与疾病复发有关。

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