Yang Meng-Hang, Yu Jia, Cai Chen-Lei, Li Wei
Department of Oncology, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.
Front Oncol. 2022 Dec 7;12:1029282. doi: 10.3389/fonc.2022.1029282. eCollection 2022.
Histological transformation from non-small cell lung cancer (NSCLC) to small cell lung cancer (SCLC) is one of mechanisms of the acquired resistance to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKI). However, SCLC transformation and tumor heterogeneity have never been reported in sequential targeted therapy and immunotherapy.
Here, we described a patient with advanced EGFR-mutant NSCLC, who received erlotinib and underwent the resistance with EGFR T790M (-). The patient then received chemotherapy plus immunotherapy of programmed cell death 1 (PD-1) inhibitor, encountered progression with pathological transformation from NSCLC to SCLC that was overcome by chemotherapy of etoposide plus carboplatin (EC) with the main lesion significantly shrinking while metastatic nodules increasing. The pathology of the metastatic nodule showed NSCLC with EGFR T790M (+). Based on the tumor heterogeneity, EC chemotherapy combined with osimertinib was used, and patients responded well. The patient experienced four lung biopsies in all, which helped to provide the patient with precise treatment.
This case suggested that SCLC transformation and tumor heterogeneity should be paid attention to when disease progression occurred in advanced NSCLC whether receiving targeted therapy or immunotherapy.
非小细胞肺癌(NSCLC)向小细胞肺癌(SCLC)的组织学转化是对表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKI)获得性耐药的机制之一。然而,在序贯靶向治疗和免疫治疗中,SCLC转化和肿瘤异质性从未被报道过。
在此,我们描述了一名晚期EGFR突变型NSCLC患者,该患者接受了厄洛替尼治疗,并出现了EGFR T790M(-)耐药。该患者随后接受了化疗加程序性细胞死亡蛋白1(PD-1)抑制剂免疫治疗,出现了从NSCLC向SCLC的病理转化进展,而依托泊苷加卡铂(EC)化疗克服了这一进展,主要病灶显著缩小,而转移结节增加。转移结节的病理显示为EGFR T790M(+)的NSCLC。基于肿瘤异质性,使用了EC化疗联合奥希替尼,患者反应良好。该患者总共进行了四次肺活检,这有助于为患者提供精确的治疗。
该病例表明,晚期NSCLC无论是接受靶向治疗还是免疫治疗,当疾病进展时,都应注意SCLC转化和肿瘤异质性。