Kemper Marcel, Reitnauer Lea Elisabeth, Lenz Georg, Evers Georg, Bleckmann Annalen
Department of Medicine A, University Hospital Muenster, 48149 Muenster, Germany.
West German Cancer Center, University Hospital Muenster, 48149 Muenster, Germany.
Cancers (Basel). 2025 Jul 7;17(13):2256. doi: 10.3390/cancers17132256.
Small cell lung cancer (SCLC) remains a highly aggressive malignancy with a poor prognosis. Despite multimodal standard therapies, most patients relapse within months, and second-line treatment options such as topotecan offer only limited benefit. Novel therapeutic strategies are therefore urgently needed. This narrative review is based on a selective literature search conducted via PubMed and ClinicalTrials.gov (last updated June 2025). Emerging treatment strategies include bispecific T-cell engagers (e.g., tarlatamab), antibody-drug conjugates (ADCs) such as sacituzumab govitecan, DS-7300, and ZL-1310, as well as targeted therapies. Among these, tarlatamab has demonstrated improved survival outcomes with an acceptable safety profile and is poised to become the new second-line standard. In contrast, ADCs and targeted agents have shown only modest efficacy and have yet to deliver meaningful survival benefits, often accompanied by increased toxicity. Additionally, the identification of molecular subtypes of SCLC has revealed subtype-specific differences in treatment response. However, clinical translation is challenged by intratumoral heterogeneity, plasticity, and the lack of standardized diagnostic assays. While tarlatamab represents a major therapeutic advancement, other agents remain in early clinical development and require validation in large, randomized trials. The clinical implementation of molecular subtyping remains limited, though it holds promise for future personalized treatment approaches. Despite recent progress, SCLC continues to pose substantial therapeutic challenges, emphasizing the need for improved treatment strategies and validated predictive biomarkers.
小细胞肺癌(SCLC)仍然是一种侵袭性很强的恶性肿瘤,预后较差。尽管有多种标准治疗方法,但大多数患者在数月内就会复发,而诸如拓扑替康等二线治疗选择仅能带来有限的益处。因此,迫切需要新的治疗策略。本叙述性综述基于通过PubMed和ClinicalTrials.gov(最后更新于2025年6月)进行的选择性文献检索。新兴的治疗策略包括双特异性T细胞衔接器(如tarlatamab)、抗体药物偶联物(ADC),如赛托珠单抗戈维汀、DS - 7300和ZL - 1310,以及靶向治疗。其中,tarlatamab已显示出改善的生存结果且安全性可接受,有望成为新的二线标准治疗药物。相比之下,ADC和靶向药物仅显示出适度的疗效,尚未带来有意义的生存益处,且常常伴随着毒性增加。此外,SCLC分子亚型的鉴定揭示了治疗反应中的亚型特异性差异。然而,临床转化受到肿瘤内异质性、可塑性以及缺乏标准化诊断检测方法的挑战。虽然tarlatamab代表了一项重大的治疗进展,但其他药物仍处于早期临床开发阶段,需要在大型随机试验中进行验证。分子亚型分类的临床应用仍然有限,尽管它为未来的个性化治疗方法带来了希望。尽管最近取得了进展,但SCLC仍然带来巨大的治疗挑战,这凸显了改进治疗策略和经过验证的预测生物标志物的必要性。