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新辅助伊马替尼治疗胃肠道间质瘤(GIST):墨西哥人群的首次分析。

Neoadjuvant Imatinib in Gastrointestinal Stromal Tumors (GIST): The First Analysis of a Mexican Population.

作者信息

Medrano Guzman Rafael, Lopez Lara Xavier, Arias Rivera Atl Simon, Garcia Rios Luis E, Brener Chaoul Moises

机构信息

Surgical Oncology, Centro Médico Nacional Siglo XXI, Mexico City, MEX.

General Surgery, Hospital Angeles Lomas, Huixquilucan, MEX.

出版信息

Cureus. 2024 Jul 20;16(7):e65001. doi: 10.7759/cureus.65001. eCollection 2024 Jul.

DOI:10.7759/cureus.65001
PMID:39161479
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11333017/
Abstract

Introduction Gastrointestinal stromal tumors (GISTs) are neoplasms originating from the interstitial cells of Cajal, pacemaker cells responsible for intestinal motility. Patients with locally advanced GISTs and those with borderline resections due to the proximity of vital anatomical structures, which could result in unacceptable post-surgical morbidity, require special therapeutic consideration. Imatinib, a tyrosine kinase inhibitor, has demonstrated significant success in the non-surgical management of metastatic GIST, and its favorable impact on overall survival in the adjuvant setting makes it logical to speculate on the benefit it could provide as a neoadjuvant medication in patients with locally advanced disease. Methods Patients aged 18-90 years with a diagnosis of GIST confirmed by immunohistochemistry (CD117 positivity) who were treated at the Oncology Hospital of Centro Médico Nacional Siglo XXI in Mexico City from January 2012 to December 2016 were included in the study. It is a retrospective study with a duration of four years. Clinical data were collected from the medical records, which included sex, age, tumor location, initial resectability, reason for unresectability, initial tumor size, and mitotic rate. In the case of unresectable disease, patients who were evaluated by medical oncology and who had received treatment with 400 mg of imatinib daily were evaluated. Results A total of 312 patients diagnosed with GIST were analyzed. One hundred thirty-one were men (42%) with a mean age of 57 years, and 181 were women (58%) with a mean age of 59 years. The most frequent anatomical location was the stomach (n=185, 59.2%). At the time of diagnosis, 210 patients (67.3%) presented with resectable disease, while n=102 patients (32.7%) had unresectable disease. A total of 102 patients with unresectable disease received therapy with 400 mg of imatinib per day. Sixteen patients (15.7%) presented a reduction in tumor dimensions and underwent surgery. Conclusion The study highlights the importance of complete surgical resection and the potential benefit of neoadjuvant imatinib therapy in converting unresectable to resectable disease. The results suggest that imatinib can be effective in converting unresectable GISTs to resectable ones, allowing for a complete resection to be performed and obtaining an R0 resection in 93.7% of these cases.

摘要

引言

胃肠道间质瘤(GIST)是起源于 Cajal 间质细胞的肿瘤,Cajal 间质细胞是负责肠道蠕动的起搏细胞。局部晚期 GIST 患者以及因重要解剖结构临近而导致手术切除边缘不确定、可能导致不可接受的术后发病率的患者,需要特殊的治疗考量。伊马替尼是一种酪氨酸激酶抑制剂,已在转移性 GIST 的非手术治疗中取得显著成功,并且其在辅助治疗中对总生存期的有利影响使得推测其作为新辅助药物对局部晚期疾病患者可能带来的益处具有合理性。

方法

纳入 2012 年 1 月至 2016 年 12 月在墨西哥城国家医学中心 Siglo XXI 肿瘤医院接受治疗、年龄在 18 - 90 岁、经免疫组织化学确诊(CD117 阳性)为 GIST 的患者。这是一项为期四年的回顾性研究。从病历中收集临床数据,包括性别、年龄、肿瘤位置、初始可切除性、不可切除原因、初始肿瘤大小和有丝分裂率。对于不可切除疾病的患者,评估接受医学肿瘤学评估且每日接受 400mg 伊马替尼治疗的患者。

结果

共分析了 312 例诊断为 GIST 的患者。其中 131 例为男性(42%),平均年龄 57 岁,181 例为女性(58%),平均年龄 59 岁。最常见的解剖位置是胃(n = 18

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/67785c87e2d6/cureus-0016-00000065001-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/cf43c14c80d8/cureus-0016-00000065001-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/7965981d80ff/cureus-0016-00000065001-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/68d2dbb3ced9/cureus-0016-00000065001-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/67785c87e2d6/cureus-0016-00000065001-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/cf43c14c80d8/cureus-0016-00000065001-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/7965981d80ff/cureus-0016-00000065001-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/68d2dbb3ced9/cureus-0016-00000065001-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8655/11333017/67785c87e2d6/cureus-0016-00000065001-i04.jpg

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