Immunotherapy in Melanoma: Recent Advances and Future Directions

被引:64
|
作者
Knight, Andrew [1 ]
Karapetyan, Lilit [2 ]
Kirkwood, John M. [3 ,4 ]
机构
[1] Univ Pittsburgh, Med Ctr, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15213 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Cutaneous Oncol, Tampa, FL 33612 USA
[3] Univ Pittsburgh, Hillman Canc Ctr, Dept Med, Div Hematol Oncol,Med Ctr, Pittsburgh, PA 15213 USA
[4] UPMC Hillman Canc Ctr, Tumor Microenvironm Ctr, Pittsburgh, PA 15232 USA
关键词
melanoma; immunotherapy; immune checkpoint blockade; LAG-3; TLR-9; STING; T-VEC; fecal microbiota transplant; adoptive cell therapy; TUMOR-INFILTRATING LYMPHOCYTES; STAGE-III MELANOMA; NIVOLUMAB PLUS IPILIMUMAB; ADOPTIVE CELL THERAPY; RANDOMIZED PHASE-III; METASTATIC MELANOMA; IV MELANOMA; ADJUVANT NIVOLUMAB; DOUBLE-BLIND; TALIMOGENE LAHERPAREPVEC;
D O I
10.3390/cancers15041106
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Immunotherapy has demonstrated the ability to reduce the risk of recurrence for melanoma following surgical resection and improve survival in patients with unresectable disease. Despite the significant advances made in the treatment of patients with melanoma, many patients will have recurrence or progression of disease despite currently available treatments. It is, therefore, critical to identify additional immunotherapy agents that will provide clinical benefit on their own or in combination with existing therapies. In this review, we explore the recent history of immunotherapy development, highlight landmark trials, and discuss promising treatments for patients refractory to current therapies. The use of immunotherapy in the treatment of advanced and high-risk melanoma has led to a striking improvement in outcomes. Although the incidence of melanoma has continued to rise, median survival has improved from approximately 6 months to nearly 6 years for patients with advanced inoperable stage IV disease. Recent understanding of the tumor microenvironment and its interplay with the immune system has led to the explosive development of novel immunotherapy treatments. Since the approval of the therapeutic cytokines interleukin-2 and interferon alfa-2 in the 1990s, the development of novel immune checkpoint inhibitors (ICIs), oncolytic virus therapy, and modulators of the tumor microenvironment have given way to a new era in melanoma treatment. Monoclonal antibodies directed at programmed cell death protein 1 receptor (PD-1) and its ligand (PDL-1), cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), and lymphocyte-activation gene 3 (LAG-3) have provided robust activation of the adaptive immune system, restoring immune surveillance leading to host tumor recognition and destruction. Multiple other immunomodulatory therapeutics are under investigation to overcome resistance to ICI therapy, including the toll-like receptor-9 (TLR-9) and 7/8 (TLR-7/8) agonists, stimulator of interferon genes (STING) agonists, and fecal microbiota transplantation. In this review, we focus on the recent advances in immunotherapy for the treatment of melanoma and provide an update on novel therapies currently under investigation.
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页数:18
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