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