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一线伊马替尼治疗耐药的转移性胃肠道间质瘤(GIST)患者的治疗模式、预后和生存情况。二线舒尼替尼治疗。

Patterns of care, prognosis, and survival in patients with metastatic gastrointestinal stromal tumors (GIST) refractory to first-line imatinib and second-line sunitinib.

机构信息

Institut Bergonié, Bordeaux, France.

出版信息

Ann Surg Oncol. 2012 May;19(5):1551-9. doi: 10.1245/s10434-011-2120-6. Epub 2011 Nov 8.

Abstract

BACKGROUND

Data regarding the management and outcome of patients with metastatic gastrointestinal stromal tumors (GIST) refractory to 1st-line imatinib and 2nd-line sunitinib are limited.

METHODS

Medical records of 223 imatinib-resistant and sunitinib-resistant GIST who were treated in 11 major referral centers were reviewed.

RESULTS

The three most frequent drugs used in the 3rd-line setting were: nilotinib n = 67 (29.5%), sorafenib n = 55 (24.5%), and imatinib n = 40 (17.5%). There were 18 patients (8%) who received best supportive care (BSC) only. The median progression-free survival (PFS) and overall survival (OS) on 3rd-line treatment were 3.6 months [95% confidence interval (95% CI), 3.1-4.1] and 9.2 months (95% CI, 7.5-10.9), respectively. Multivariate analysis showed that, in the 3rd-line setting, albumin level and KIT/PDGFRA mutational status were significantly associated with PFS, whereas performance status and albumin level were associated with OS. After adjustment for prognostic factors, nilotinib and sorafenib provided the best PFS and OS. Rechallenge with imatinib was also associated with improved OS in comparison with BSC.

CONCLUSION

In the 3rd-line setting, rechallenge with imatinib provided limited clinical benefit but was superior to BSC. Sorafenib and nilotinib have significant clinical activity in imatinib-resistant and sunitinib-resistant GIST and may represent an alternative for rechallenge with imatinib.

摘要

背景

对于一线伊马替尼和二线舒尼替尼耐药的转移性胃肠道间质瘤(GIST)患者的治疗和预后数据有限。

方法

回顾了 11 家主要转诊中心治疗的 223 例伊马替尼耐药和舒尼替尼耐药 GIST 患者的病历。

结果

三线治疗中最常使用的三种药物是:尼洛替尼 n = 67(29.5%)、索拉非尼 n = 55(24.5%)和伊马替尼 n = 40(17.5%)。有 18 名患者(8%)仅接受最佳支持治疗(BSC)。三线治疗的中位无进展生存期(PFS)和总生存期(OS)分别为 3.6 个月[95%置信区间(95%CI),3.1-4.1]和 9.2 个月(95%CI,7.5-10.9)。多变量分析显示,在三线治疗中,白蛋白水平和 KIT/PDGFRA 突变状态与 PFS 显著相关,而表现状态和白蛋白水平与 OS 相关。在调整了预后因素后,尼洛替尼和索拉非尼提供了最佳的 PFS 和 OS。与 BSC 相比,伊马替尼的再挑战也与 OS 的改善相关。

结论

在三线治疗中,伊马替尼的再挑战提供的临床获益有限,但优于 BSC。索拉非尼和尼洛替尼在伊马替尼耐药和舒尼替尼耐药的 GIST 中具有显著的临床活性,可能是伊马替尼再挑战的替代方案。

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