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细胞减灭手术为伊马替尼治疗后全身性进展的转移性胃肠间质瘤提供预后获益:单中心回顾性研究。

Cytoreductive surgery offers prognostic benefits in metastatic gastrointestinal stromal tumors with generalized progression following imatinib therapy: a single institute retrospective study.

机构信息

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Hepato-Pancreato-Biliary Surgery/Sarcoma Center, Peking University Cancer Hospital & Institute, No. 52 Fucheng Road, Haidian District, Beijing, People's Republic of China.

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Pathology, Peking University Cancer Hospital & Institute, Beijing, People's Republic of China.

出版信息

BMC Surg. 2023 Jul 4;23(1):189. doi: 10.1186/s12893-023-02087-3.

Abstract

BACKGROUND

Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal tumors of the gastrointestinal tract. Distant metastasis has been detected in approximately 50% of GIST patients at the first diagnosis. The surgical strategy for metastatic GIST with generalized progression (GP) after imatinib therapy remains unclear.

METHODS

We recruited 15 patients with imatinib-resistant metastatic GIST. They received cytoreductive surgery (CRS) for tumor rupture, intestinal obstruction and gastrointestinal bleeding. We collected clinical, pathological and prognostic data for analyses.

RESULTS

OS and PFS after R0/1 CRS were 56.88 ± 3.47 and 26.7 ± 4.12 months, respectively, when compared with 26 ± 5.35 and 5 ± 2.78 months after R2 CRS (P = 0.002 and P < 0.001, respectively). The OS of patients from the initiation of imatinib in the R0/1 group was 133.90 ± 15.40 months when compared with 59.80 ± 10.98 months in the R2 CRS group. There were two significant grade III complications after 15 operations (13.3%). No patient underwent reoperation. In addition, no perioperative death occurred.

CONCLUSIONS

R0/1 CRS is highly probable to provide prognostic benefits for patients with metastatic GIST who experience GP following imatinib treatment. An aggressive surgical strategy for achieving R0/1 CRS can be deemed safe. If applicable, R0/1 CRS should be carefully considered in imatinib-treated patients with GP metastatic GIST.

摘要

背景

胃肠道间质瘤(GIST)是胃肠道最常见的间叶性肿瘤。大约 50%的 GIST 患者在首次诊断时就已发生远处转移。对于接受伊马替尼治疗后出现广泛进展(GP)的转移性 GIST 患者,手术治疗策略仍不明确。

方法

我们招募了 15 例接受伊马替尼治疗后发生耐药性转移性 GIST 且发生肿瘤破裂、肠梗阻和胃肠道出血的患者。我们收集了这些患者的临床、病理和预后数据进行分析。

结果

与接受 R2 减瘤手术(CRS)后的 26 个月(5.35 年)相比,接受 R0/1 减瘤手术后患者的总生存期(OS)和无进展生存期(PFS)分别为 56.88±3.47 个月和 26.70±4.12 个月(P=0.002 和 P<0.001)。与 R2 CRS 组的 59.80±10.98 个月相比,从开始接受伊马替尼治疗到发生 R0/1 CRS 的患者的 OS 为 133.90±15.40 个月。在 15 次手术中有 2 例发生了严重的 III 级并发症(13.3%)。没有患者需要再次手术,且无围手术期死亡发生。

结论

对于接受伊马替尼治疗后发生 GP 的转移性 GIST 患者,R0/1 CRS 很可能会带来生存获益。对于实现 R0/1 CRS 的积极手术策略,可以认为是安全的。对于接受伊马替尼治疗后发生 GP 的转移性 GIST 患者,如果适用,应仔细考虑 R0/1 CRS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e5/10318709/549dbde39384/12893_2023_2087_Fig1_HTML.jpg

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