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Effect of the imatinib treatment regimen on the postoperative prognosis of patients with high-risk gastrointestinal stromal tumors

机译:伊马替尼治疗方案对高危胃肠道间质瘤患者术后预后的影响

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Background: Surgical resection is the standard treatment for localized and potentially resectable gastrointestinal stromal tumors (GISTs), If the postoperative pathology diagnosis indicates that patients are at high risk of recurrence, they should be treated with imatinib. Even though the introduction of imatinib substantially improved the outcome of GIST patients, it is unclear whether different imatinib treatment regimens affect patients’ survival. Methods: This retrospective study included 120 patients who underwent tumor resection for high-risk GISTs between January 2009 and October 2018. The patients were divided into three groups: one group of patients received postoperative imatinib adjuvant therapy regularly (regular treatment group); the second group was not treated with imatinib until they were found to have disease progression (observation group); the third group was treated with postoperative imatinib adjuvant therapy irregularly (irregularly treatment group). The progression-free survival (PFS) and overall survival (OS) were compared between the three groups, and the prognostic risk factors were analysed by the Cox regression model. Results: The median PFS was 45 months (range: 25–59). The 3- and 5-year PFS values were 71.3% and 49.9%, respectively. The PFS in the regular group was longer than in the observation group and irregular group ( P 0.001). The median OS was 59 months (range:47–78). The 3- and 5-year OS values were 91.6% and 84.2%, respectively. There were no differences in OS among the three groups ( P =0.150). The extent of radical resection ( P 0.001) and intraoperative tumor rupture ( P =0.005) were independent prognostic factors influencing OS. Conclusions: Irregular administration of imatinib was associated with a worse PFS, but it did not affect the OS of patients with high-risk GISTs. Avoiding intraoperative tumor rupture and R0 resection were associated with better survival.
机译:背景:手术切除是局部和潜在可切除的胃肠道间质瘤(GIST)的标准治疗方法,如果术后病理诊断表明患者有高复发风险,则应使用伊马替尼治疗。尽管伊马替尼的引入显着改善了GIST患者的预后,但尚不清楚不同的伊马替尼治疗方案是否会影响患者的生存。方法:这项回顾性研究包括120例于2009年1月至2018年10月期间因高危GIST进行肿瘤切除的患者。患者分为三组:一组患者定期接受伊马替尼术后辅助治疗(常规治疗组);另一组接受常规伊马替尼辅助治疗。第二组直到发现病情进展才接受伊马替尼治疗(观察组);第三组术后不规律接受伊马替尼辅助治疗(不规则治疗组)。比较三组的无进展生存期(PFS)和总生存期(OS),并通过Cox回归模型分析预后风险因素。结果:PFS中位数为45个月(范围:25-59)。 3年和5年PFS值分别为71.3%和49.9%。常规组的PFS长于观察组和不规则组的PFS(P <0.001)。中位OS为59个月(范围:47-78)。 3年和5年OS值分别为91.6%和84.2%。三组之间的OS无差异(P = 0.150)。根治性切除的程度(P <0.001)和术中肿瘤破裂(P = 0.005)是影响OS的独立预后因素。结论:伊马替尼的不规律给药与较差的PFS相关,但并不影响高危GIST患者的OS。避免术中肿瘤破裂和R0切除与更好的生存率相关。

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