Tarantino Paolo, Carmagnani Pestana Roberto, Corti Chiara, Modi Shanu, Bardia Aditya, Tolaney Sara M, Cortes Javier, Soria Jean-Charles, Curigliano Giuseppe
Division of New Drugs and Early Drug Development, European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
CA Cancer J Clin. 2022 Mar;72(2):165-182. doi: 10.3322/caac.21705. Epub 2021 Nov 12.
As distinct cancer biomarkers have been discovered in recent years, a need to reclassify tumors by more than their histology has been proposed, and therapies are now tailored to treat cancers based on specific molecular aberrations and immunologic markers. In fact, multiple histology-agnostic therapies are currently adopted in clinical practice for treating patients regardless of their tumor site of origin. In parallel with this new model for drug development, in the past few years, several novel antibody-drug conjugates (ADCs) have been approved to treat solid tumors, benefiting from engineering improvements in the conjugation process and the introduction of novel linkers and payloads. With the recognition that numerous surface targets are expressed across various cancer histologies, alongside the remarkable activity of modern ADCs, this drug class has been increasingly evaluated as suitable for a histology-agnostic expansion of indication. For illustration, the anti-HER2 ADC trastuzumab deruxtecan has demonstrated compelling activity in HER2-overexpressing breast, gastric, colorectal, and lung cancer. Examples of additional novel and potentially histology-agnostic ADC targets include trophoblast cell-surface antigen 2 (Trop-2) and nectin-4, among others. In the current review article, the authors summarize the current approvals of ADCs by the US Food and Drug Administration focusing on solid tumors and discuss the challenges and opportunities posed by the multihistological expansion of ADCs.
近年来,随着不同的癌症生物标志物被发现,有人提出需要超越组织学对肿瘤进行重新分类,现在的治疗方法是根据特定的分子异常和免疫标志物来量身定制以治疗癌症。事实上,目前临床实践中采用了多种不考虑组织学的治疗方法来治疗患者,而不考虑其肿瘤的起源部位。与这种新的药物开发模式并行的是,在过去几年里,几种新型抗体药物偶联物(ADC)已被批准用于治疗实体瘤,这得益于偶联过程中的工程改进以及新型连接子和有效载荷的引入。随着人们认识到多种癌症组织学中都表达大量表面靶点,再加上现代ADC具有显著活性,这类药物越来越被认为适合进行不考虑组织学的适应证扩展。例如,抗HER2 ADC德曲妥珠单抗已在HER2过表达的乳腺癌、胃癌、结直肠癌和肺癌中显示出令人信服的活性。其他新型且可能不考虑组织学的ADC靶点包括滋养层细胞表面抗原2(Trop-2)和nectin-4等。在当前这篇综述文章中,作者总结了美国食品药品监督管理局目前对用于实体瘤的ADC的批准情况,并讨论了ADC多组织学适应证扩展带来的挑战和机遇。