Division of Medical Oncology, Medical Oncology Department, Hospital Clínic Barcelona, Villarroel 170, 08036, Barcelona, Spain.
Translational Genomics and Targeted Therapeutics in Solid Tumours, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Drugs. 2020 Feb;80(3):241-262. doi: 10.1007/s40265-019-01240-8.
Small-cell lung cancer has defied our scientific community for decades. Chemotherapy has been the mainstay treatment for small-cell lung cancer (SCLC) and unlike its counterpart, non-small cell lung cancer, no significant therapeutic breakthroughs have been made since the 1970s. Among the reasons for this slow-paced therapeutic development, one that stands out is the distinctive and almost universal loss of function of the tumour suppressor genes TP53 and RB1 in this disease, for which pharmacological activation has yet to be achieved, despite having been highly sought after. Although no molecularly targeted approach has been approved for clinical practice thus far, several strategies are currently exploring the potential to drug the tumour's "Achilles heel" that stems from essential pathways regulating DNA-damage response. Most recently, we have witnessed newfound reasons to hope, as the combination of immunotherapy and systemic chemotherapy has improved survival outcomes, representing the first landmark achievement in decades and a new standard of care for patients with extensive disease SCLC. However, continuous efforts are still needed towards a better understanding of the molecular pathways that singularise this tumour to eventually identify the predictive biomarkers that might result in the development of a more rational therapeutic approach, including the use of immunotherapy combinations. In this review we aim to uncover critical aspects of the immune microenvironment and biology of SCLC and provide an overview of the current and future landscape of promising therapeutic opportunities. The challenge still stands, but regardless, we are living in exciting times to finally check SCLC off the "bucket list" of our scientific community.
小细胞肺癌几十年来一直令我们的科学界感到困惑。化疗一直是小细胞肺癌(SCLC)的主要治疗方法,与非小细胞肺癌不同,自 20 世纪 70 年代以来,这种治疗方法没有取得重大的治疗突破。在这种治疗发展缓慢的原因中,有一个突出的原因是这种疾病中肿瘤抑制基因 TP53 和 RB1 的功能几乎普遍丧失,尽管人们一直高度追求,但尚未实现药理学激活。尽管迄今为止还没有批准任何一种针对小细胞肺癌的分子靶向治疗方法,但目前有几种策略正在探索针对肿瘤“阿喀琉斯之踵”的药物潜力,这些肿瘤源自调节 DNA 损伤反应的基本途径。最近,我们有了新的希望,因为免疫疗法和全身化疗的联合使用改善了生存结果,这是几十年来的第一个里程碑式成就,也是广泛期 SCLC 患者的新护理标准。然而,仍然需要继续努力,以更好地了解使这种肿瘤具有独特性的分子途径,最终确定可能导致更合理治疗方法发展的预测性生物标志物,包括免疫疗法联合应用。在这篇综述中,我们旨在揭示 SCLC 的免疫微环境和生物学的关键方面,并概述当前和未来有希望的治疗机会的前景。挑战仍然存在,但无论如何,我们正生活在一个激动人心的时代,可以最终将 SCLC 从我们科学界的“待办事项”清单中划掉。