Faghfuri Elnaz, Faramarzi Mohammad Ali, Nikfar Shekoufeh, Abdollahi Mohammad
a 1 Department of Pharmaceutical Biotechnology and Biotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Expert Rev Anticancer Ther. 2015;15(9):981-93. doi: 10.1586/14737140.2015.1074862. Epub 2015 Jul 30.
Malignant melanoma is an important issue in oncology due to its high incidence, high mortality, and resistance to systemic therapy; however, targeted immunotherapy has noticeably improved the survival rates of melanoma patients. Promising targeted immunotherapies for malignant melanoma include the blockade of immune checkpoints with antibodies targeting cytotoxic T lymphocyte-associated antigen 4 and the programmed cell death protein 1 pathway. The US FDA-approved antibody ipilimumab targets cytotoxic T lymphocyte-associated antigen 4; however, it was limited by toxicity and a low response. Nivolumab and pembrolizumab (formerly lambrolizumab), the two FDA-approved anti-programmed death-1 monoclonal antibodies, show highly durable response rates and long-term safety, validating the importance of the programmed cell death protein 1 pathway blockade for treatment of malignant melanoma.
恶性黑色素瘤因其高发病率、高死亡率以及对全身治疗的耐药性,成为肿瘤学领域的一个重要问题;然而,靶向免疫疗法显著提高了黑色素瘤患者的生存率。针对恶性黑色素瘤有前景的靶向免疫疗法包括用靶向细胞毒性T淋巴细胞相关抗原4和程序性细胞死亡蛋白1途径的抗体阻断免疫检查点。美国食品药品监督管理局(FDA)批准的抗体伊匹单抗靶向细胞毒性T淋巴细胞相关抗原4;然而,它受到毒性和低反应率的限制。纳武单抗和派姆单抗(原名为兰布单抗)这两种FDA批准的抗程序性死亡-1单克隆抗体,显示出高度持久的反应率和长期安全性,证实了阻断程序性细胞死亡蛋白1途径对治疗恶性黑色素瘤的重要性。