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Preoperative adjuvant therapy for locally advanced and recurrent/metastatic gastrointestinal stromal tumors: a retrospective study

机译:术前佐剂治疗局部晚期和复发性/转移性胃肠道间质瘤:回顾性研究

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摘要

Abstract Background Preoperative imatinib mesylate therapy for gastrointestinal stromal tumors (GISTs) is controversial. This study aimed to explore the clinical efficacy and optimal duration of preoperative imatinib mesylate (IM) therapy in patients with locally advanced and recurrent/metastatic GISTs. Methods We retrospectively examined patients who received preoperative imatinib mesylate therapy from January 2013 to December 2018 at Xiangya Hospital, Central South University and the Second Xiangya Hospital of Central South University, China. Clinical data, including the results of tests for mutations in KIT and PDGFR, findings from regularly conducted re-examinations, abdominal-enhanced computed tomography/magnetic resonance imaging data, responses to imatinib, progression-free survival, and overall cancer-specific survival, were recorded. Results A total of 25 patients were enrolled in our study, including 18 with a locally advanced GIST and 7 with recurrent or metastatic GISTs. Their ages ranged from 22 to 70 years (M:F = 1.6:0.9), with a mean age of 50.48 ± 12.51 years. The tumor locations included the stomach (56.0%), rectum (16.0%), enterocoelic/retroperitoneal sites (12.0%), and the small intestine (12.0%). Based on testing for mutations in KIT and PDGFR, 22 patients received 400 mg/day KIT, and 3 patients received 600 mg/day PDGFR. The median duration of preoperative IM therapy was 8.96 ± 4.81 months, ranging from 3 to 26 months. According to the Choi criteria, 24 patients achieved a partial response (PR), and 1 patient had stable disease (SD). All patients underwent surgery after preoperative IM therapy, and no postoperative complications appeared. The 2-year PFS and 5-year PFS were 92% and 60%, respectively, and the total 5-year cancer-specific survival (CSS) was 92%. Conclusion Preoperative imatinib therapy is feasible for locally advanced and recurrent/metastatic GISTs and can effectively shrink the tumor size, allow organ sparing, and avoid extensive organ resection. Moreover, the optimal duration of preoperative IM therapy in patients with locally advanced and recurrent/metastatic GISTs was 8.96 ± 4.81 months, ranging from 3 to 26 months, and gastric GISTs had a better response to preoperative IM therapy than did non-gastric GISTs.
机译:摘要背景术前伊替尼甲磺酸盐治疗胃肠道肿瘤(GIST)是有争议的。本研究旨在探讨局部先进和复发性/转移性的患者术前伊替尼甲磺酸盐(IM)治疗的临床疗效和最佳持续时间。方法回顾性研究,从2013年1月到2018年1月到2018年12月,中南大学湘雅医院,中国中南大学第二襄加医院,回顾性地检查了术前伊马替尼甲磺酸盐治疗的患者。临床资料,包括试验和PDGFR中突变的试验结果,从定期进行再试检查,腹部增强的计算机断层摄影/磁共振成像数据,对伊马替尼,无进展生存和整体癌症特异性存活的调查结果,被记录了。结果我们研究共有25名患者,其中包括18名局部先进的GIST和7名,其中7名具有复发或转移性的GIST。他们的年龄范围从22到70岁(M:F = 1.6:0.9),平均年龄为50.48±12.51岁。肿瘤位置包括胃(56.0%),直肠(16.0%),肠内裂/腹膜腹部位点(12.0%)和小肠(12.0%)。基于试剂盒和PDGFR中突变的测试,22例患者接受了400毫克/天的套件,3例患者接受600毫克/天PDGFR。术前IM疗法的中位数持续时间为8.96±4.81个月,范围为3至26个月。根据CHOI标准,24名患者达到了部分反应(PR),1例患者稳定(SD)。所有患者在术前IM治疗后接受手术,均未出现术后并发症。为期2年的PFS和5年的PFS分别为92%和60%,分别为5年的癌症特异性生存(CSS)为92%。结论术前伊马替尼治疗可用于局部先进和复发/转移性,可以有效地缩小肿瘤大小,允许器官备件,避免大量器官切除。此外,众所周期和复发/转移性或转移性患者术前IM治疗的最佳持续时间为8.96±4.81个月,范围为3〜26个月,胃部的GIST比非胃部的术前疗法更好地反应。

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