Serrano César, George Suzanne
Sarcoma Translational Research Laboratory, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
Department of Medical Oncology, Vall d'Hebron University Hospital, Barcelona, Spain.
Clin Cancer Res. 2020 Oct 1;26(19):5078-5085. doi: 10.1158/1078-0432.CCR-20-1706. Epub 2020 Jun 29.
Gastrointestinal stromal tumor (GIST) provides a paradigm to evaluate new molecularly targeted therapies and to identify structural and functional mechanisms for drug response and resistance. Drug development in GIST has successfully exploited the high reliance on KIT/PDGFRA oncogenic signaling as a therapeutic vulnerability. The recent arrival of avapritinib and ripretinib to the GIST arena has aimed to further improve on precision kinase inhibition and address tumor heterogeneity in imatinib-resistant GIST. The two main clinical challenges for the forthcoming years entail tumor eradication in patients with early-stage GIST, and maximization of tumor response in late-stage disease. To succeed, we will need to better understand the mechanisms behind adaptation to KIT inhibition and apoptosis evasion, tumor evolution after successive lines of treatment, and to explore clinically novel creative therapeutic strategies, with the overarching goal to tackle the intrinsic oncogenic complexity while minimizing adverse events.
胃肠道间质瘤(GIST)为评估新的分子靶向疗法以及确定药物反应和耐药性的结构和功能机制提供了一个范例。GIST的药物开发成功地利用了对KIT/PDGFRA致癌信号的高度依赖作为治疗靶点。阿伐替尼和瑞派替尼最近进入GIST领域,旨在进一步提高精准激酶抑制作用,并解决伊马替尼耐药GIST中的肿瘤异质性问题。未来几年的两个主要临床挑战是根除早期GIST患者的肿瘤,以及使晚期疾病的肿瘤反应最大化。为了取得成功,我们需要更好地理解适应KIT抑制和逃避凋亡背后的机制、连续治疗后肿瘤的演变,并探索临床上新颖的创新治疗策略,总体目标是应对内在的致癌复杂性,同时尽量减少不良事件。