Department of Surgery, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital (NCI-AVL), Amsterdam, The Netherlands.
Department of Medical Oncology, Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital (NCI-AVL), Amsterdam, The Netherlands.
Ann Surg Oncol. 2023 Dec;30(13):8660-8668. doi: 10.1245/s10434-023-14346-x. Epub 2023 Oct 9.
Neoadjuvant imatinib is considered for gastrointestinal stromal tumors (GISTs) when decreased tumor size provides less extensive surgery and higher R0 resection rates. This study evaluates the effectivity and safety of neoadjuvant imatinib for large or locally advanced GIST.
From the prospective database of the Dutch GIST Consortium, all patients who underwent surgery after neoadjuvant imatinib at our center between 2009 and 2022 were selected. Independent and blinded assessment of surgical strategy was performed by two surgeons, based on anonymized computed tomography (CT) scans before and after neoadjuvant imatinib.
Of 113 patients that received neoadjuvant imatinib, 108 (95%) [mean age 61.6, standard deviation (SD) 11.5, 54% male] underwent a GIST resection. Of all GISTs, 67% was localized in the stomach and 25% in the duodenum or small intestine. In 74% of the patients with GIST, a KIT exon 11 mutation was found. Decreased tumor size was seen in 95 (88%) patients. Having a KIT exon 11 mutation [odds ratio (OR) 5.64, 95% confidence interval (CI) 1.67-19.1, p < 0.01] or not having a mutation (OR 0.19, 95% CI 0.04-0.89, p = 0.04) were positive and negative predictive values for partial response, respectively. In 55 (51%) patients, there was deescalation of surgical strategy after neoadjuvant imatinib. Surgical complications were documented in 16 (15%) patients (n = 8, grade II; n = 5, grade IIIa; n = 3, grade IIIb) and R0 resection was accomplished in 95 (89%) patients. The 5-year disease-free and overall survival were 80% and 91%, respectively.
This study shows that neoadjuvant imatinib is effective and safe for patients with large or locally advanced GIST.
新辅助伊马替尼被认为适用于胃肠道间质瘤(GIST),因为肿瘤缩小可以减少手术范围并提高 R0 切除率。本研究评估了新辅助伊马替尼治疗大型或局部晚期 GIST 的有效性和安全性。
从荷兰 GIST 联合会的前瞻性数据库中,选择了 2009 年至 2022 年间在我们中心接受新辅助伊马替尼治疗后接受手术的所有患者。两名外科医生根据新辅助伊马替尼前后的匿名计算机断层扫描(CT)进行独立和盲法手术策略评估。
在接受新辅助伊马替尼治疗的 113 例患者中,有 108 例(95%)[平均年龄 61.6,标准差(SD)11.5,54%为男性]接受了 GIST 切除术。所有 GIST 中,67%位于胃,25%位于十二指肠或小肠。在 74%的患者中发现了 KIT 外显子 11 突变。95 例(88%)患者的肿瘤体积缩小。KIT 外显子 11 突变(比值比(OR)5.64,95%置信区间(CI)1.67-19.1,p < 0.01)或无突变(OR 0.19,95%CI 0.04-0.89,p = 0.04)分别是部分缓解的阳性和阴性预测值。在 55 例(51%)患者中,新辅助伊马替尼治疗后手术策略降级。记录了 16 例(15%)患者的手术并发症(n = 8,II 级;n = 5,IIIa 级;n = 3,IIIb 级),95 例(89%)患者实现了 R0 切除。5 年无病生存率和总生存率分别为 80%和 91%。
本研究表明,新辅助伊马替尼治疗大型或局部晚期 GIST 是有效且安全的。