Rager Taylor, Eckburg Adam, Patel Meet, Qiu Rong, Gantiwala Shahina, Dovalovsky Katrina, Fan Kelly, Lam Katie, Roesler Claire, Rastogi Aayush, Gautam Shruti, Dube Namrata, Morgan Bridget, Nasifuzzaman S M, Ramaswami Dhruv, Gnanasekar Varun, Smith Jeffrey, Merchant Aftab, Puri Neelu
College of Medicine, University of Illinois, Rockford, IL 61107, USA.
Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Cancers (Basel). 2022 Aug 3;14(15):3779. doi: 10.3390/cancers14153779.
Melanoma possesses invasive metastatic growth patterns and is one of the most aggressive types of skin cancer. In 2021, it is estimated that 7180 deaths were attributed to melanoma in the United States alone. Once melanoma metastasizes, traditional therapies are no longer effective. Instead, immunotherapies, such as ipilimumab, pembrolizumab, and nivolumab, are the treatment options for malignant melanoma. Several biomarkers involved in tumorigenesis have been identified as potential targets for molecularly targeted melanoma therapy, such as tyrosine kinase inhibitors (TKIs). Unfortunately, melanoma quickly acquires resistance to these molecularly targeted therapies. To bypass resistance, combination treatment with immunotherapies and single or multiple TKIs have been employed and have been shown to improve the prognosis of melanoma patients compared to monotherapy. This review discusses several combination therapies that target melanoma biomarkers, such as BRAF, MEK, RAS, c-KIT, VEGFR, c-MET and PI3K. Several of these regimens are already FDA-approved for treating metastatic melanoma, while others are still in clinical trials. Continued research into the causes of resistance and factors influencing the efficacy of these combination treatments, such as specific mutations in oncogenic proteins, may further improve the effectiveness of combination therapies, providing a better prognosis for melanoma patients.
黑色素瘤具有侵袭性转移生长模式,是最具侵袭性的皮肤癌类型之一。据估计,仅在2021年,仅在美国就有7180人死于黑色素瘤。一旦黑色素瘤发生转移,传统疗法就不再有效。相反,免疫疗法,如伊匹木单抗、帕博利珠单抗和纳武利尤单抗,是恶性黑色素瘤的治疗选择。一些参与肿瘤发生的生物标志物已被确定为分子靶向黑色素瘤治疗的潜在靶点,如酪氨酸激酶抑制剂(TKIs)。不幸的是,黑色素瘤很快就会对这些分子靶向疗法产生耐药性。为了绕过耐药性,已采用免疫疗法与单一或多种TKIs的联合治疗,并且与单一疗法相比,已证明这种联合治疗可改善黑色素瘤患者的预后。本综述讨论了几种针对黑色素瘤生物标志物的联合疗法,如BRAF、MEK、RAS、c-KIT、VEGFR、c-MET和PI3K。其中一些方案已获得美国食品药品监督管理局(FDA)批准用于治疗转移性黑色素瘤,而其他方案仍在临床试验中。对耐药原因以及影响这些联合治疗疗效的因素(如致癌蛋白中的特定突变)的持续研究,可能会进一步提高联合疗法的有效性,为黑色素瘤患者提供更好的预后。