Zhang Chenlu, Wang Zhiming, Zhuang Rongyuan, Guo Xi, Feng Yi, Shen Feng, Liu Wenshuai, Zhang Yong, Tong Hanxing, Sun Wending, Liu Jun, Wang Guan, Dai Chun, Lu Weiqi, Zhou Yuhong
Department of Medical Oncology, Zhongshan Hospital, Fudan University, Shanghai, People's Republic of China.
Department of General Surgery, Shanghai Public Health Clinical Center, Shanghai, People's Republic of China.
Onco Targets Ther. 2020 Oct 13;13:10335-10342. doi: 10.2147/OTT.S270481. eCollection 2020.
We report two inflammatory myofibroblastic tumor (IMT) patients with ALK fusions (RRBP-ALK and TNS1-ALK, respectively). They both received tumor resection surgery and treatment with ALK inhibitors crizotinib followed by alectinib, and upon receiving each of the drugs, showed a brief response, then experienced recurrence or progression of the disease. During the treatment, whole exome sequencing (WES) and RNA sequencing (RNA-Seq) were applied to monitor potential drug-induced gene mutation and expression changes. A novel, secondary mutation in ALK exon 23 (L1196Q) was identified in patient 1 after alectinib resistance developed. Guided by this result, a newer ALK inhibitor, ceritinib was prescribed. The patient was able to achieve a partial response (PR) and is in good condition as of the manuscript date. On the contrary, there was no secondary mutation identified in ALK in patient 2 after drug resistance. While the expression of PTCH1, a negative regulator of the sonic hedgehog (SHH) signaling pathway, was significantly reduced at the time after the treatment with crizotinib before that of alectinib. The expression of PTCH1 was also reduced after the treatment with alectinib. It was reported that ALK can exert its biological functions partially by activating SHH signaling pathway. The down-regulation of PTCH1 suggests the compensatory activation of SHH pathway may cause resistance to ALK inhibitors in IMT. Going forward, monitoring gene mutation and expression changes through DNA and RNA sequencing will be able to offer opportunities to investigate potential mechanisms of drug resistance and will help to achieve precise prescription for better treatment outcomes.
我们报告了两名患有间变性淋巴瘤激酶(ALK)融合(分别为RRBP-ALK和TNS1-ALK)的炎性肌成纤维细胞瘤(IMT)患者。他们均接受了肿瘤切除手术,并先后接受了ALK抑制剂克唑替尼和阿来替尼治疗,在使用每种药物后均出现了短暂反应,随后疾病复发或进展。在治疗过程中,应用全外显子组测序(WES)和RNA测序(RNA-Seq)来监测潜在的药物诱导基因突变和表达变化。在患者1出现阿来替尼耐药后,在ALK外显子23中发现了一种新的继发性突变(L1196Q)。基于这一结果,给予了一种更新的ALK抑制剂色瑞替尼。该患者能够实现部分缓解(PR),截至撰写本文时情况良好。相反,患者2在耐药后未在ALK中发现继发性突变。虽然在使用阿来替尼之前,在使用克唑替尼治疗后,音猬因子(SHH)信号通路的负调节因子PTCH1的表达显著降低。使用阿来替尼治疗后,PTCH1的表达也降低。据报道,ALK可部分通过激活SHH信号通路发挥其生物学功能。PTCH1的下调表明SHH通路的代偿性激活可能导致IMT对ALK抑制剂产生耐药性。展望未来,通过DNA和RNA测序监测基因突变和表达变化将能够为研究耐药性的潜在机制提供机会,并有助于实现精准用药以获得更好的治疗效果。