Department of Medical Oncology, Azienda Socio Sanitaria Territoriale of Cremona, Cremona, Italy.
Division of Molecular Pathology, The Institute of Cancer Research, London, UK.
Expert Opin Ther Targets. 2021 Aug;25(8):677-683. doi: 10.1080/14728222.2021.1978070. Epub 2021 Sep 16.
Despite the efforts of the scientific community, the prognosis of metastatic colorectal cancer (mCRC) remains poor. Actionable gene fusions such as Neurotrophic Tropomyosin Receptor Kinases rearrangements are rare but might represent a new target to improve outcomes in this setting. The first-generation TRK inhibitors, larotrectinib and entrectinib, have demonstrated efficacy and safety in mCRC cancer patients exhibiting pathogenic fusions. Moreover, second-generation molecules are emerging, able to overcome the acquired resistance to blocking.
This review aims to report the current knowledge and the available evidence on fusion in mCRC, with a focus on molecular bases, clinical characteristics, prognostic meaning, and new therapeutic approaches, from the perspective of the clinical oncologist.
Considering the limited options associated with the treatment of mCRC patients, the possibility of identifying new molecular biomarkers is an urgent clinical need. The availability of new molecular targets and the combinations of different agents might represent the true breakthrough point, allowing for change in the clinical course of colorectal cancer patients.
尽管科学界付出了努力,但转移性结直肠癌(mCRC)的预后仍然不佳。神经生长因子受体激酶重排等可操作的基因融合虽然罕见,但可能代表改善这一情况下结局的新靶点。第一代 TRK 抑制剂拉罗替尼和恩曲替尼在表现出致病性融合的 mCRC 癌症患者中显示出疗效和安全性。此外,第二代药物正在出现,能够克服对阻断的获得性耐药。
本综述旨在从临床肿瘤学家的角度报告 mCRC 中融合的现有知识和证据,重点介绍分子基础、临床特征、预后意义和新的治疗方法。
考虑到 mCRC 患者治疗相关选择有限,识别新的分子生物标志物是迫切的临床需求。新的分子靶点的出现和不同药物的联合应用可能代表着真正的突破点,使结直肠癌患者的临床病程发生改变。