Cardeña-Gutiérrez Ana, López Barahona Mónica
MedicalOncologyDepartment, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.
Centro Estudios Biosanitarios, Madrid, Spain.
Front Med (Lausanne). 2022 Jun 14;9:908752. doi: 10.3389/fmed.2022.908752. eCollection 2022.
Immune checkpoint inhibitors (ICIs) have dramatically transformed oncology by prolonging overall survival and yielding better patient tolerance compared to other chemotherapeutic agents. However, numerous questions remain unanswered about the toxicity profile of ICIs, its relationship with the treatment response, and causes underlying the excellent treatment response in some patients, while recalcitrance in others. Research groups have continued to seek biomarkers that may permit the identification of treatment responders and predict toxicity to facilitate cessation of immunotherapy before the development of severe toxicity. However, some studies have found associations between serious adverse events and longer survivorship. The research question entailed determining whether a biomarker is needed to predict severe immune-related adverse events prior to their development or whether providing early treatment for toxicity would inhibit the immune system from attaining a long-lasting anti-tumor effect. Therefore, this review conducted an in-depth analysis into the molecular basis of these observations.
免疫检查点抑制剂(ICIs)通过延长总生存期并与其他化疗药物相比产生更好的患者耐受性,极大地改变了肿瘤学。然而,关于ICIs的毒性特征、其与治疗反应的关系以及一些患者治疗反应优异而另一些患者治疗抵抗的潜在原因,仍有许多问题未得到解答。研究团队一直在寻找生物标志物,这些生物标志物可能有助于识别治疗反应者并预测毒性,以便在严重毒性发生之前停止免疫治疗。然而,一些研究发现严重不良事件与更长生存期之间存在关联。该研究问题涉及确定是否需要一种生物标志物来在严重免疫相关不良事件发生之前预测它们,或者为毒性提供早期治疗是否会抑制免疫系统获得持久的抗肿瘤效果。因此,本综述对这些观察结果的分子基础进行了深入分析。