Sato Yuki, Saito Go, Fujimoto Daichi
Department of Respiratory Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
Department of Respirology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Ther Adv Med Oncol. 2022 Oct 14;14:17588359221130503. doi: 10.1177/17588359221130503. eCollection 2022.
Histologic transformation (HT) is a major cause of drug resistance to therapy in patients with lung cancer. HTs to small-cell lung cancer (SCLC) have been reported frequently in patients with epidermal growth factor receptor ()-mutated lung cancer. Although HTs have an impact on the clinical outcomes in patients owing to a high refractoriness to treatments, there is limited data on the prevalence, causes, mechanisms, treatment efficacy, and future treatment strategies. In this review, we assess the literature regarding HTs comprehensively, including those describing EGFR-tyrosine kinase inhibitors, other molecular targeted drugs, and immune checkpoint inhibitors. Furthermore, we discuss the mechanisms of HTs and the lineage plasticity to SCLC and squamous cell carcinoma in lung cancer. In addition, we summarize the treatment efficacy and future perspectives of HTs in patients with lung cancer, and propose better management strategies for this group of patients.
组织学转化(HT)是肺癌患者治疗耐药的主要原因。在表皮生长因子受体(EGFR)突变的肺癌患者中,向小细胞肺癌(SCLC)的组织学转化已被频繁报道。尽管由于对治疗的高度难治性,组织学转化会影响患者的临床结局,但关于其发生率、原因、机制、治疗效果及未来治疗策略的数据有限。在本综述中,我们全面评估了有关组织学转化的文献,包括那些描述EGFR酪氨酸激酶抑制剂、其他分子靶向药物和免疫检查点抑制剂的文献。此外,我们讨论了组织学转化的机制以及肺癌向SCLC和鳞状细胞癌的谱系可塑性。另外,我们总结了肺癌患者组织学转化的治疗效果和未来前景,并为这组患者提出了更好的管理策略。