Department of Medical Oncology, Centre Léon-Bérard, Lyon, France.
Ann Oncol. 2012 Jul;23(7):1659-65. doi: 10.1093/annonc/mdr622. Epub 2012 Feb 21.
Imatinib is the standard of care for patients with advanced gastrointestinal stromal tumors (GIST).
This article reviews recent data on the impact of imatinib treatment interruption and subsequent rechallenge in patients with advanced GIST.
The randomized BFR14 trial showed that (i) interruption of imatinib after 1, 3, or 5 years of treatment in patients with nonprogressive GIST was associated with a high risk of progression even in patients with a complete response; (ii) rechallenge with imatinib restored tumor control in most patients, but the tumor response seldom reached that before treatment interruption; (iii) patients receiving continuous imatinib had a high rate of prolonged tumor control, which increased with longer imatinib treatment. The findings in the metastatic setting have important implications regarding the duration of adjuvant imatinib in GIST.
Discontinuation of imatinib in responding patients with advanced GIST is associated with a high risk of progression and is therefore not recommended. Although rechallenge is a strategy for treating patients who relapse after stopping imatinib, suboptimal tumor response indicates that continuous kinase suppression is necessary to achieve the best clinical outcome. Three-year adjuvant imatinib is recommended for patients with resected 'high-risk' GIST; however, a longer duration may provide additional benefits.
伊马替尼是晚期胃肠道间质瘤(GIST)患者的标准治疗方法。
本文回顾了伊马替尼治疗中断及其随后重新挑战对晚期 GIST 患者影响的最新数据。
随机 BFR14 试验表明:(i)非进展性 GIST 患者在治疗 1、3 或 5 年后中断伊马替尼治疗与进展风险升高相关,即使在完全缓解的患者中也是如此;(ii)伊马替尼重新挑战恢复了大多数患者的肿瘤控制,但肿瘤反应很少达到治疗中断前的水平;(iii)接受持续伊马替尼治疗的患者具有较高的肿瘤控制延长率,随着伊马替尼治疗时间的延长而增加。转移性疾病中的发现对 GIST 辅助伊马替尼的持续时间具有重要意义。
在晚期 GIST 中,对有反应的患者停止伊马替尼治疗与进展风险升高相关,因此不建议这样做。虽然重新挑战是治疗停止伊马替尼后复发的患者的一种策略,但肿瘤反应不佳表明需要持续的激酶抑制才能获得最佳临床结果。对于切除的“高危”GIST 患者推荐使用 3 年的辅助伊马替尼治疗;然而,更长的持续时间可能会带来额外的益处。