Hersey Peter, Kakavand Hojabr, Wilmott James, van der Westhuizen Andre, Gallagher Stuart, Gowrishankar Kavitha, Scolyer Richard
Kolling Institute, Royal North Shore Hospital, St Leonards, NSW 2065, Australia.
Melanoma Institute of Australia, Rocklands Road, North Sydney, NSW, Australia.
Melanoma Manag. 2014 Nov;1(2):165-172. doi: 10.2217/mmt.14.14. Epub 2014 Dec 4.
The introduction of immunotherapy based on the blockade of the PD1/PD-L1 checkpoints has been associated with high response rates and durable remissions of disease in patients with metastatic melanoma, to the extent that it is now considered the standard of care for a wide range of patients, irrespective of their or mutation status. In addition, more frequent follow-up of patients who are at high risk of recurrence after surgical treatment appears to be justified, as does neoadjuvant treatments in order to render patients treatable by surgery. The limitations of this treatment include failure of some patients to respond, a low rate of complete responses and relapses of the disease during treatment. New initiatives in order to overcome these limitations include the identification of biomarkers for the selection responders and evaluations of treatment combinations that will increase responses and their durability. The latter includes combinations with antibodies against other checkpoints on T cells and cotreatments with inhibitors of resistance pathways in melanoma.
基于阻断PD1/PD-L1检查点的免疫疗法的引入,已与转移性黑色素瘤患者的高缓解率和持久疾病缓解相关联,以至于现在它被认为是广泛患者的标准治疗方法,无论其 或 突变状态如何。此外,对手术治疗后复发风险高的患者进行更频繁的随访似乎是合理的,新辅助治疗以使患者能够接受手术治疗也是如此。这种治疗的局限性包括一些患者无反应、完全缓解率低以及治疗期间疾病复发。为克服这些局限性而采取的新举措包括识别用于选择反应者的生物标志物以及评估可增加反应及其持久性的联合治疗。后者包括与针对T细胞上其他检查点的抗体联合以及与黑色素瘤耐药途径抑制剂联合治疗。