Márquez-Rodas Ivan, Cerezuela Pablo, Soria Ainara, Berrocal Alfonso, Riso Aldo, González-Cao María, Martín-Algarra Salvador
1 Servicio de Oncología Médica, Hospital General Universitario Gregorio Marañon, Madrid, Spain ; 2 Spanish Melanoma Group (GEM); 3 Servicio Oncología Médica, Hospital General Universitario Santa Lucía, Cartagena, Spain ; 4 Servicio de Oncología Médica, Universitario Ramon y Cajal, Madrid, Spain ; 5 Servicio de Oncología Médica, Hospital General Universitario de Valencia, Valencia, Spain ; 6 Translational Cancer Research Unit, Instituto Oncológico Dr Rosell, Quirón Dexeus University Hospital, Barcelona, Spain ; 7 Servicio de Oncología Médica, Clínica Universitaria de Navarra, Pamplona, Spain.
Ann Transl Med. 2015 Oct;3(18):267. doi: 10.3978/j.issn.2305-5839.2015.10.27.
In recent years, new strategies for treating melanoma have been introduced, improving the outlook for this challenging disease. One of the most important advances has been the development of immunotherapy. The better understanding of the role of the immunological system in tumor control has paved the way for strategies to enhance the immune response against cancer cells. Monoclonal antibodies (mAbs) against the immune checkpoints cytotoxic T-lymphocyte antigen-4 (CTLA-4) and programmed cell death protein 1 (PD-1) and its ligand (PD-L1) have demonstrated high activity in melanoma and other tumors. Ipilimumab, an anti CTLA-4 antibody, was the first drug of this class that was approved. Although the response rate with ipilimumab is low (less than 20% of patients have objective responses), 20% of patients have long survival, with similar results in the first and second line settings. Nivolumab and pembrolizumab, both anti PD-1 inhibitors, have been approved for the treatment of melanoma, with response rates of 40% and a demonstrated survival advantage in phase III trials. This has marked a new era in the treatment of metastatic melanoma and much research is now ongoing with other drugs targeting checkpoint inhibitors. In addition, the agonist of activating molecules on T cells and their combinations are being investigated. Herein we review the clinical development of checkpoint inhibitors and their approval for treatment of metastatic melanoma.
近年来,已引入治疗黑色素瘤的新策略,改善了这种具有挑战性疾病的预后。最重要的进展之一是免疫疗法的发展。对免疫系统在肿瘤控制中作用的更好理解为增强针对癌细胞的免疫反应的策略铺平了道路。针对免疫检查点细胞毒性T淋巴细胞抗原4(CTLA-4)、程序性细胞死亡蛋白1(PD-1)及其配体(PD-L1)的单克隆抗体(mAb)已在黑色素瘤和其他肿瘤中显示出高活性。抗CTLA-4抗体伊匹单抗是该类获批的首个药物。尽管伊匹单抗的缓解率较低(不到20%的患者有客观缓解),但20%的患者生存期长,一线和二线治疗结果相似。纳武单抗和派姆单抗这两种抗PD-1抑制剂均已获批用于治疗黑色素瘤,缓解率为40%,并在III期试验中显示出生存优势。这标志着转移性黑色素瘤治疗的新时代,目前针对其他靶向检查点抑制剂的药物有大量研究正在进行。此外,T细胞上激活分子的激动剂及其联合用药也在研究中。在此我们综述检查点抑制剂的临床研发及其获批用于治疗转移性黑色素瘤的情况。