Song Zizheng, Ren Guanying, Hu Ling, Wang Xiaolei, Song Jin, Jia Youchao, Zhao Guofa, Zang Aimin, Du Haiwei, Sun Ying, Zhao Xiaopeng
Department of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, China.
Department of Data Science, Burning Rock Biotech, Guangzhou, China.
Ann Transl Med. 2022 Jun;10(12):719. doi: 10.21037/atm-22-2436.
Acquired resistance is inevitable in non-small cell lung cancer (NSCLC) patients treated with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs). The emergence of exon 20 C797S is one of the major resistance mechanisms to osimertinib as a third-generation EGFR-TKI. To date, there is no standard of care for NSCLC patients after acquiring C797S. Immune checkpoint inhibitors (ICIs) have revolutionized the treatment of various types of cancers in the last decade. Whether NSCLC patients with acquired C797S could benefit from ICIs remains elusive.
Herein, we reported two cases of -mutant NSCLC patients who acquired a tertiary mutation C797S benefited from ICIs. A 28-year-old woman presented with anepithymia and nausea. Chest computed tomography (CT) revealed a mass in the right lung. She was diagnosed with stage IV lung adenocarcinoma (LUAD) with exon 19 deletion (19del) based on imaging and next-generation sequencing (NGS) findings. She received icotinib followed by osimertinib, then acquired T790M--C797S. She had low tumor mutation burden (TMB) and achieved partial response (PR) to a programmed cell death-1 (PD-1) inhibitor sintilimab combined with platinum-based doublet chemotherapy as late-line treatment lasting more than 5 months. A 66-year-old man complained with chest tightness, hemoptysis, and back pain. CT scans revealed a mass in the right lung and metastases to the bilateral lungs, liver, adrenal gland, mediastinal lymph nodes, and bone. He was also diagnosed with 19del-positive LUAD and treated with icotinib followed by osimertinib. He also acquired T790M--C797S. The patient had low TMB also and benefited from a PD-1 inhibitor camrelizumab combined with platinum-based doublet chemotherapy as late-line treatment with a progression-free survival (PFS) of 8 months. Two cases had no treatment-related adverse events leading to discontinuation of PD-1 inhibitors.
Our study provides the first clinical evidence that ICIs combined with platinum-based doublet chemotherapy may be effective treatment options for overcoming resistance mediated by T790M--C797S. Clinical trials are needed to evaluate the efficacy and safety of PD-1 inhibitors in the treatment of NSCLC patients harboring T790M--C797S.
在接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)治疗的非小细胞肺癌(NSCLC)患者中,获得性耐药不可避免。外显子20 C797S的出现是第三代EGFR-TKI奥希替尼主要耐药机制之一。迄今为止,NSCLC患者获得C797S后的治疗尚无标准治疗方案。免疫检查点抑制剂(ICIs)在过去十年中彻底改变了各类癌症的治疗方式。NSCLC患者获得C797S后是否能从ICIs中获益仍不明确。
在此,我们报告了两例携带三重突变C797S的EGFR突变NSCLC患者从ICIs中获益的病例。一名28岁女性出现食欲不振和恶心症状。胸部计算机断层扫描(CT)显示右肺有一个肿块。根据影像学和下一代测序(NGS)结果,她被诊断为IV期肺腺癌(LUAD)伴外显子19缺失(19del)。她接受了埃克替尼治疗,随后使用奥希替尼,之后出现T790M-C797S突变。她的肿瘤突变负荷(TMB)较低,作为晚期治疗,接受程序性细胞死亡蛋白1(PD-1)抑制剂信迪利单抗联合铂类双药化疗后获得部分缓解(PR),持续时间超过5个月。一名66岁男性主诉胸闷、咯血和背痛。CT扫描显示右肺有一个肿块,并伴有双侧肺、肝、肾上腺、纵隔淋巴结和骨转移。他也被诊断为19del阳性LUAD,接受了埃克替尼治疗,随后使用奥希替尼。他也出现了T790M-C797S突变。该患者TMB也较低,作为晚期治疗,接受PD-1抑制剂卡瑞利珠单抗联合铂类双药化疗后获益,无进展生存期(PFS)为8个月。两例患者均未出现导致停用PD-1抑制剂的治疗相关不良事件。
我们的研究提供了首个临床证据,表明ICIs联合铂类双药化疗可能是克服T790M-C797S介导的耐药的有效治疗选择。需要进行临床试验来评估PD-1抑制剂治疗携带T790M-C797S的NSCLC患者的疗效和安全性。