Hernández de Córdoba Irene, Mielgo-Rubio Xabier, Cejas Paloma, Palomar Ramos Jorge, Garrido-Rubiales Beatriz, Falagán Martínez Sandra, Rubio Romero Gustavo, Morales Parga María, Moll Taltavull Laura, Fernández González Andrea, Casado Sáenz Enrique, Sereno María
Department of Medical Oncology, Hospital Universitario Infanta Sofía, San Sebastián de los Reyes, 28702 Madrid, Spain.
Departamento de Oncología Médica, Hospital Universitario Cruces, 48903 Barakaldo, Spain.
Int J Mol Sci. 2025 May 26;26(11):5096. doi: 10.3390/ijms26115096.
Neuroendocrine transformation in non-small-cell lung cancer (NSCLC) is an uncommon but clinically significant resistance mechanism to targeted therapy, immunotherapy, and chemotherapy. This phenomenon, primarily observed in adenocarcinoma (ADC) with EGFR mutations under tyrosine kinase inhibitor (TKI) treatment, leads to histological transformation into small-cell lung cancer (SCLC), commonly associated with an aggressive clinical course and poor prognosis. Standard platinum-etoposide chemotherapy provides only transient disease control, highlighting the urgent need for improved therapeutic strategies. Early identification of transformation through biopsy, liquid biopsy, or biomarkers like neuron-specific enolase (NSE) and pro-gastrin-releasing peptide (pro-GRP) may allow for early intervention. As targeted therapies continue to develop, understanding the molecular drivers of neuroendocrine transformation is crucial for optimizing treatment. Further research into novel treatment approaches, including combination therapies with TKIs, chemotherapy, immunotherapy, and epigenetic modulators, is required to improve outcomes for these patients.
非小细胞肺癌(NSCLC)中的神经内分泌转化是一种罕见但临床上具有重要意义的对靶向治疗、免疫治疗和化疗的耐药机制。这种现象主要在酪氨酸激酶抑制剂(TKI)治疗下的伴有EGFR突变的腺癌(ADC)中观察到,会导致组织学转化为小细胞肺癌(SCLC),通常与侵袭性临床病程和不良预后相关。标准的铂类-依托泊苷化疗仅能提供短暂的疾病控制,凸显了对改进治疗策略的迫切需求。通过活检、液体活检或神经元特异性烯醇化酶(NSE)和胃泌素释放肽前体(pro-GRP)等生物标志物早期识别转化,可能有助于早期干预。随着靶向治疗的不断发展,了解神经内分泌转化的分子驱动因素对于优化治疗至关重要。需要进一步研究新的治疗方法,包括与TKI、化疗、免疫治疗和表观遗传调节剂的联合疗法,以改善这些患者的治疗效果。