Advancements in Melanoma Treatment: A Review of PD-1 Inhibitors, T-VEC, mRNA Vaccines, and Tumor-Infiltrating Lymphocyte Therapy in an Evolving Landscape of Immunotherapy

被引:0
作者
Mehta, Apoorva [1 ]
Motavaf, Mateen [2 ]
Nebo, Ikenna [1 ]
Luyten, Sophia [1 ]
Osei-Opare, Kofi D. [1 ]
Gru, Alejandro A. [3 ]
机构
[1] Columbia Univ, Vagelos Coll Phys & Surg, 630 W 168th St, New York, NY 10032 USA
[2] Duke Univ, Sch Med, Durham, NC 27710 USA
[3] Columbia Univ Irving Med Ctr, Dept Dermatol, New York, NY 10032 USA
关键词
melanoma; treatment; mRNA vaccine; TIL; therapy; T-VEC; PD-1; inhibitors; PD-L1; CAR-T; T-cell; immunotherapy; advancement; HERPES-SIMPLEX-VIRUS; 5-YEAR SURVIVAL OUTCOMES; METASTATIC MELANOMA; ACQUIRED-RESISTANCE; COMBINED NIVOLUMAB; ADOPTIVE TRANSFER; CELL TRANSFER; IPILIMUMAB; BLOCKADE; PEMBROLIZUMAB;
D O I
10.3390/jcm14041200
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Melanoma, an aggressive skin cancer, presents significant therapeutic challenges. Consequently, innovative treatment strategies beyond conventional chemotherapy, radiation, and surgery are actively explored. This review discusses the evolution of immunotherapy in advanced melanoma, highlighting PD-1/PD-L1 inhibitors, mRNA vaccines, Talimogene Laherparepvec (T-VEC), and tumor-infiltrating lymphocyte (TIL) therapies. PD-1/PD-L1 inhibitors such as pembrolizumab and nivolumab block immune checkpoints, promoting T-cell cytotoxic activity and improving overall survival in patients with advanced melanoma. T-VEC, a modified oncolytic herpes virus, promotes a systemic anti-tumor response while simultaneously lysing malignant cells. mRNA vaccines, such as Moderna's mRNA-4157/V940, take advantage of malignant-cell-specific neoantigens to amplify the adaptive immune response while protecting healthy tissue. TIL therapy is a form of therapy involving ex vivo expansion and reinfusion of the patient's tumor-specific lymphocytes and has been shown to provide durable tumor control. While these therapies have demonstrated promising clinical outcomes, challenges such as tumor resistance, high financial burden, and limited accessibility pose challenges to their widespread use. This review explores combination therapies such as PD-L1 inhibitors with mRNA vaccines, or TIL therapy, which aim to enhance treatment through synergistic approaches. Further research is required to optimize these combinations, address barriers preventing their use, and control adverse events.
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页数:23
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  • [1] Boyd K.U., Wehrli B.M., Temple C.L.F., Intra-lesional interleukin-2 for the treatment of in-transit melanoma, J. Surg. Oncol, 104, pp. 711-717, (2011)
  • [2] Maverakis E., Cornelius L.A., Bowen G.M., Phan T., Fitzmaurice S., He Y., Burrall B., Duong C., Kloxin A.M., Sultani H., Et al., Metastatic Melanoma—A Review of Current and Future Treatment Options, Acta Derm. Venereol, 95, pp. 516-524, (2015)
  • [3] Berwick M., Wiggins C., The current epidemiology of cutaneous malignant melanoma, Front. Biosci, 11, pp. 1244-1254, (2006)
  • [4] Garbe C., Eigentler T.K., Keilholz U., Hauschild A., Kirkwood J.M., Systematic Review of Medical Treatment in Melanoma: Current Status and Future Prospects, Oncologist, 16, pp. 5-24, (2011)
  • [5] Overwijk W.W., Restifo N.P., B16 as a Mouse Model for Human Melanoma, CP Immunol, 39, (2000)
  • [6] Kakadia S., Yarlagadda N., Awad R., Kundranda M., Niu J., Naraev B., Mina L., Dragovich T., Gimbel M., Mahmoud F., Mechanisms of resistance to BRAF and MEK inhibitors and clinical update of US Food and Drug Administration-approved targeted therapy in advanced melanoma, Onco Targets Ther, 11, pp. 7095-7107, (2018)
  • [7] Shah V., Panchal V., Shah A., Vyas B., Agrawal S., Bharadwaj S., Immune checkpoint inhibitors in metastatic melanoma therapy (Review), Med. Int, 4, (2024)
  • [8] Hodi F.S., O'Day S.J., McDermott D.F., Weber R.W., Sosman J.A., Haanen J.B., Gonzalez R., Robert C., Schadendorf D., Hassel J.C., Et al., Improved survival with ipilimumab in patients with metastatic melanoma, N. Engl. J. Med, 363, pp. 711-723, (2010)
  • [9] Muller A.J., Manfredi M.G., Zakharia Y., Prendergast G.C., Inhibiting IDO pathways to treat cancer: Lessons from the ECHO-301 trial and beyond, Semin. Immunopathol, 41, pp. 41-48, (2019)
  • [10] Long G.V., Dummer R., Hamid O., Gajewski T.F., Caglevic C., Dalle S., Arance A., Carlino M.S., Grob J.-J., Kim T.M., Et al., Epacadostat plus pembrolizumab versus placebo plus pembrolizumab in patients with unresectable or metastatic melanoma (ECHO-301/KEYNOTE-252): A phase 3, randomised, double-blind study, Lancet Oncol, 20, pp. 1083-1097, (2019)