Dartmouth-Hitchcock Medical Center, Norris Cotton Cancer Center, Lebanon, NH, USA.
Int J Cancer. 2011 Dec 1;129(11):2533-42. doi: 10.1002/ijc.26234.
Although surgery remains the mainstay for the treatment of primary gastrointestinal stromal tumors (GIST), a significant number of patients experience disease recurrence within 5 years of surgery. The emergence of imatinib therapy for the treatment of patients with advanced GIST has offered unprecedented improvements in clinical outcomes for these patients. Prospective clinical trials have supported the efficacy and safety of imatinib before and after surgical resection of GIST. The American College of Surgeons Oncology Group Z9001 pivotal trial revealed that 1 year of adjuvant imatinib therapy provides significantly superior recurrence-free survival in patients with GIST after surgical resection, when compared to placebo. Additional trials and case studies have also begun to define the potential clinical benefit of imatinib in the neoadjuvant setting. Optimized risk stratification paradigms will be required to ensure the appropriate selection of patients to undergo treatment with imatinib in these settings. Risk stratification schemes are evolving that potentially will include mutation status and tumor rupture, and predictive nomograms have recently been proposed. The recent European Society of Medical Oncology and National Comprehensive Cancer Network guidelines mention use of adjuvant imatinib for ≥ 1 year in patients with KIT(+) , resectable GIST at high risk of recurrence. Moreover, the guidelines support the use of neoadjuvant imatinib in cases of limited disease if it would facilitate less extensive surgery and organ sparing. This article reviews pivotal efficacy and safety data for adjuvant imatinib and explores the potential clinical benefit of neoadjuvant imatinib in patients with GIST.
尽管手术仍然是治疗原发性胃肠道间质瘤(GIST)的主要方法,但仍有相当数量的患者在手术后 5 年内出现疾病复发。伊马替尼治疗晚期 GIST 的出现为这些患者的临床结果带来了前所未有的改善。前瞻性临床试验支持 GIST 手术切除前后伊马替尼的疗效和安全性。美国外科医师学院肿瘤学组 Z9001 关键试验表明,与安慰剂相比,GIST 手术后接受 1 年辅助伊马替尼治疗可显著提高无复发生存率。此外,其他试验和病例研究也开始定义伊马替尼在新辅助治疗中的潜在临床获益。需要优化风险分层方案,以确保在这些情况下选择合适的患者接受伊马替尼治疗。风险分层方案正在不断发展,可能包括突变状态和肿瘤破裂,最近还提出了预测性列线图。最近的欧洲肿瘤内科学会和国家综合癌症网络指南提到,对于 KIT(+)、可切除、高复发风险的 GIST 患者,辅助伊马替尼治疗应持续 1 年以上。此外,如果新辅助伊马替尼治疗可促进手术范围缩小和器官保留,则支持在局限性疾病中使用。本文综述了辅助伊马替尼的关键疗效和安全性数据,并探讨了新辅助伊马替尼在 GIST 患者中的潜在临床获益。