Lyu Heng-Xu, Ma Wen-Hua, Zhang Yong-Qian, Jin Hui, Wang Yu-Dong, Zhao Min
Department of Oncology, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Department of Medical Oncology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Front Med (Lausanne). 2024 Sep 25;11:1406515. doi: 10.3389/fmed.2024.1406515. eCollection 2024.
This research reports a case of histological transformation from non-small cell lung cancer (NSCLC) to transformed small cell lung cancer (T-SCLC) in a patient undergoing EGFR-tyrosine kinase inhibitors (TKIs). The aggressive characteristics of the tumor diverged significantly from those commonly associated with lung adenocarcinomas, leading to further histological analysis. The subsequent histological examination confirmed the transformation to SCLC, consistent with established mechanisms of acquired resistance in NSCLC. Given the limited therapeutic options, the patient was administered a serplulimab-based immunochemotherapy regimen, achieving a progression-free survival (PFS) of 6 months post-transformation. The study underscores the potential of PD-1 inhibitors, particularly serplulimab, in the treatment landscape for T-SCLC and highlights the need for future comprehensive research.
本研究报告了1例在接受表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)治疗的患者中,非小细胞肺癌(NSCLC)组织学转化为转化型小细胞肺癌(T-SCLC)的病例。肿瘤的侵袭性特征与肺腺癌通常相关的特征有显著差异,因此进行了进一步的组织学分析。随后的组织学检查证实已转化为小细胞肺癌,这与非小细胞肺癌获得性耐药的既定机制一致。鉴于治疗选择有限,对该患者给予了基于赛帕利单抗的免疫化疗方案,转化后无进展生存期(PFS)达到6个月。该研究强调了PD-1抑制剂,尤其是赛帕利单抗,在T-SCLC治疗领域的潜力,并突出了未来进行全面研究的必要性。