Kalra Anjali, Rashdan Sawsan
Harold C Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical School, Dallas, TX, United States.
Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Front Oncol. 2023 Apr 14;13:1158417. doi: 10.3389/fonc.2023.1158417. eCollection 2023.
Latest advances in non-small cell lung cancer (NSCLC) therapies have revolutionized the treatment regimens utilized for NSCLCs with or without a driver mutation. Molecular targeted treatments such as tyrosine kinase inhibitors (TKIs) are utilized to prevent tumor progression and improve survival. Despite the great benefit of immunotherapy in NSCLC tumors with no driver mutation, the use of immune checkpoint inhibitors (ICIs) in NSCLC tumors harboring a driver mutation has been under debate. Furthermore, several trials have been conducted investigating the use of these therapies with TKIs. A few trials were halted due to growing concerns of increased toxicity with the combination of TKI and immunotherapy. The adverse events ranged from low grade dermatologic complaints to fatal interstitial lung diseases. These toxicities occur with both concurrent and sequential administration of treatment. Thus, recommendations for the safest method of combination treatment have not yet been described. This review paper discusses recent views on combination treatment, previous clinical trials reporting grade 3-4 toxicities, and guidelines for a safe timeline of administration of treatment based on past evidence.
非小细胞肺癌(NSCLC)治疗的最新进展彻底改变了用于有或没有驱动基因突变的NSCLC的治疗方案。诸如酪氨酸激酶抑制剂(TKIs)之类的分子靶向治疗被用于预防肿瘤进展并提高生存率。尽管免疫疗法对没有驱动基因突变的NSCLC肿瘤有很大益处,但在携带驱动基因突变的NSCLC肿瘤中使用免疫检查点抑制剂(ICIs)一直存在争议。此外,已经进行了几项试验来研究这些疗法与TKIs联合使用的情况。由于对TKI与免疫疗法联合使用毒性增加的担忧日益增加,一些试验被中止。不良事件范围从轻度皮肤不适到致命的间质性肺病。这些毒性在同时和序贯给药时都会出现。因此,尚未描述联合治疗最安全方法的建议。这篇综述文章讨论了关于联合治疗的最新观点、先前报告3-4级毒性的临床试验以及基于过去证据的安全给药时间指南。