Skip to main content
Top
Published in: Cancer and Metastasis Reviews 1/2015

01-03-2015 | Clinical

Immunotherapy of melanoma: Present options and future promises

Authors: Anand Rotte, Madhuri Bhandaru, Youwen Zhou, Kevin J. McElwee

Published in: Cancer and Metastasis Reviews | Issue 1/2015

Login to get access

Abstract

Metastatic melanoma is notorious for its immune evasion and resistance to conventional chemotherapy. The recent success of ipilimumab, a human monoclonal antibody against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), in increasing the median survival time and stabilizing the disease progression renewed, hopes in treatment for melanoma. Currently, ipilimumab and high-dose interleukin-2 (IL-2; Aldesleukin) are approved as monotherapies for the treatment of patients with unresectable advanced melanoma, and pegylated interferon-α2b (p-IFN-α2b) is approved as an adjuvant for the treatment of patients with surgically resected high-risk melanoma. The present review describes the currently approved immune-modulators and the promising immune-based interventions that are currently in clinical trials. We present the four commonly used strategies to boost immune responses against the tumors; monoclonal antibodies, cytokines, cancer vaccines, and adoptive T cell transfer. The corresponding lists of ongoing clinical trials include details of the trial phase, target patients, intervention details, status of the study, and expected date of completion. Further, our review discusses the challenges faced by immunotherapy and the various strategies adopted to overcome them.
Literature
2.
4.
go back to reference Saranga-Perry, V., Ambe, C., Zager, J. S., & Kudchadkar, R. R. (2014). Recent developments in the medical and surgical treatment of melanoma. CA: A Cancer Journal for Clinicians, 64(3), 171–185. doi:10.3322/caac.21224. Saranga-Perry, V., Ambe, C., Zager, J. S., & Kudchadkar, R. R. (2014). Recent developments in the medical and surgical treatment of melanoma. CA: A Cancer Journal for Clinicians, 64(3), 171–185. doi:10.​3322/​caac.​21224.
6.
go back to reference Hodi, F. S., Oble, D. A., Drappatz, J., Velazquez, E. F., Ramaiya, N., Ramakrishna, N., et al. (2008). CTLA-4 blockade with ipilimumab induces significant clinical benefit in a female with melanoma metastases to the CNS. Nature Clinical Practice Oncology, 5(9), 557–561. doi:10.1038/ncponc1183.CrossRefPubMed Hodi, F. S., Oble, D. A., Drappatz, J., Velazquez, E. F., Ramaiya, N., Ramakrishna, N., et al. (2008). CTLA-4 blockade with ipilimumab induces significant clinical benefit in a female with melanoma metastases to the CNS. Nature Clinical Practice Oncology, 5(9), 557–561. doi:10.​1038/​ncponc1183.CrossRefPubMed
8.
go back to reference Robert, C., Thomas, L., Bondarenko, I., O’Day, S., Weber, J., Garbe, C., et al. (2011). Ipilimumab plus dacarbazine for previously untreated metastatic melanoma. New England Journal of Medicine, 364(26), 2517–2526. doi:10.1056/NEJMoa1104621.CrossRefPubMed Robert, C., Thomas, L., Bondarenko, I., O’Day, S., Weber, J., Garbe, C., et al. (2011). Ipilimumab plus dacarbazine for previously untreated metastatic melanoma. New England Journal of Medicine, 364(26), 2517–2526. doi:10.​1056/​NEJMoa1104621.CrossRefPubMed
11.
go back to reference Atkins, M. B., Lotze, M. T., Dutcher, J. P., Fisher, R. I., Weiss, G., Margolin, K., et al. (1999). High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993. Journal of Clinical Oncology, 17(7), 2105–2116.PubMed Atkins, M. B., Lotze, M. T., Dutcher, J. P., Fisher, R. I., Weiss, G., Margolin, K., et al. (1999). High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993. Journal of Clinical Oncology, 17(7), 2105–2116.PubMed
12.
go back to reference Kaufman, H. L., Kirkwood, J. M., Hodi, F. S., Agarwala, S., Amatruda, T., Bines, S. D., et al. (2013). The society for immunotherapy of cancer consensus statement on tumour immunotherapy for the treatment of cutaneous melanoma. Nature Reviews. Clinical Oncology, 10(10), 588–598. doi:10.1038/nrclinonc.2013.153.CrossRefPubMed Kaufman, H. L., Kirkwood, J. M., Hodi, F. S., Agarwala, S., Amatruda, T., Bines, S. D., et al. (2013). The society for immunotherapy of cancer consensus statement on tumour immunotherapy for the treatment of cutaneous melanoma. Nature Reviews. Clinical Oncology, 10(10), 588–598. doi:10.​1038/​nrclinonc.​2013.​153.CrossRefPubMed
13.
go back to reference Okuyama, S., Gonzalez, R., & Lewis, K. D. (2010). Pegylated interferon alpha-2b as adjuvant treatment of Stage III malignant melanoma: an evidence-based review. Core Evidence, 5, 39–48.PubMedPubMedCentral Okuyama, S., Gonzalez, R., & Lewis, K. D. (2010). Pegylated interferon alpha-2b as adjuvant treatment of Stage III malignant melanoma: an evidence-based review. Core Evidence, 5, 39–48.PubMedPubMedCentral
14.
go back to reference Kirkwood, J. M., & Ernstoff, M. S. (1984). Interferons in the treatment of human cancer. Journal of Clinical Oncology, 2(4), 336–352.PubMed Kirkwood, J. M., & Ernstoff, M. S. (1984). Interferons in the treatment of human cancer. Journal of Clinical Oncology, 2(4), 336–352.PubMed
18.
go back to reference Dariavach, P., Mattei, M. G., Golstein, P., & Lefranc, M. P. (1988). Human Ig superfamily CTLA-4 gene: Chromosomal localization and identity of protein sequence between murine and human CTLA-4 cytoplasmic domains. European Journal of Immunology, 18(12), 1901–1905. doi:10.1002/eji.1830181206.CrossRefPubMed Dariavach, P., Mattei, M. G., Golstein, P., & Lefranc, M. P. (1988). Human Ig superfamily CTLA-4 gene: Chromosomal localization and identity of protein sequence between murine and human CTLA-4 cytoplasmic domains. European Journal of Immunology, 18(12), 1901–1905. doi:10.​1002/​eji.​1830181206.CrossRefPubMed
19.
go back to reference Karandikar, N. J., Vanderlugt, C. L., Walunas, T. L., Miller, S. D., & Bluestone, J. A. (1996). CTLA-4: a negative regulator of autoimmune disease. Journal of Experimental Medicine, 184(2), 783–788.CrossRefPubMed Karandikar, N. J., Vanderlugt, C. L., Walunas, T. L., Miller, S. D., & Bluestone, J. A. (1996). CTLA-4: a negative regulator of autoimmune disease. Journal of Experimental Medicine, 184(2), 783–788.CrossRefPubMed
20.
go back to reference Walunas, T. L., Bakker, C. Y., & Bluestone, J. A. (1996). CTLA-4 ligation blocks CD28-dependent T cell activation. Journal of Experimental Medicine, 183(6), 2541–2550.CrossRefPubMed Walunas, T. L., Bakker, C. Y., & Bluestone, J. A. (1996). CTLA-4 ligation blocks CD28-dependent T cell activation. Journal of Experimental Medicine, 183(6), 2541–2550.CrossRefPubMed
21.
go back to reference Phan, G. Q., Yang, J. C., Sherry, R. M., Hwu, P., Topalian, S. L., Schwartzentruber, D. J., et al. (2003). Cancer regression and autoimmunity induced by cytotoxic T lymphocyte-associated antigen 4 blockade in patients with metastatic melanoma. Proceedings of the National Academy of Sciences of the United States of America, 100(14), 8372–8377. doi:10.1073/pnas.1533209100.CrossRefPubMedPubMedCentral Phan, G. Q., Yang, J. C., Sherry, R. M., Hwu, P., Topalian, S. L., Schwartzentruber, D. J., et al. (2003). Cancer regression and autoimmunity induced by cytotoxic T lymphocyte-associated antigen 4 blockade in patients with metastatic melanoma. Proceedings of the National Academy of Sciences of the United States of America, 100(14), 8372–8377. doi:10.​1073/​pnas.​1533209100.CrossRefPubMedPubMedCentral
22.
go back to reference Wolchok, J. D., Kluger, H., Callahan, M. K., Postow, M. A., Rizvi, N. A., Lesokhin, A. M., et al. (2013). Nivolumab plus ipilimumab in advanced melanoma. New England Journal of Medicine, 369(2), 122–133. doi:10.1056/NEJMoa1302369.CrossRefPubMed Wolchok, J. D., Kluger, H., Callahan, M. K., Postow, M. A., Rizvi, N. A., Lesokhin, A. M., et al. (2013). Nivolumab plus ipilimumab in advanced melanoma. New England Journal of Medicine, 369(2), 122–133. doi:10.​1056/​NEJMoa1302369.CrossRefPubMed
27.
go back to reference Inman, B. A., Sebo, T. J., Frigola, X., Dong, H., Bergstralh, E. J., Frank, I., et al. (2007). PD-L1 (B7-H1) expression by urothelial carcinoma of the bladder and BCG-induced granulomata: Associations with localized stage progression. Cancer, 109(8), 1499–1505. doi:10.1002/cncr.22588.CrossRefPubMed Inman, B. A., Sebo, T. J., Frigola, X., Dong, H., Bergstralh, E. J., Frank, I., et al. (2007). PD-L1 (B7-H1) expression by urothelial carcinoma of the bladder and BCG-induced granulomata: Associations with localized stage progression. Cancer, 109(8), 1499–1505. doi:10.​1002/​cncr.​22588.CrossRefPubMed
28.
go back to reference Thompson, R. H., Gillett, M. D., Cheville, J. C., Lohse, C. M., Dong, H., Webster, W. S., et al. (2004). Costimulatory B7-H1 in renal cell carcinoma patients: indicator of tumor aggressiveness and potential therapeutic target. Proceedings of the National Academy of Sciences of the United States of America, 101(49), 17174–17179. doi:10.1073/pnas.0406351101.CrossRefPubMedPubMedCentral Thompson, R. H., Gillett, M. D., Cheville, J. C., Lohse, C. M., Dong, H., Webster, W. S., et al. (2004). Costimulatory B7-H1 in renal cell carcinoma patients: indicator of tumor aggressiveness and potential therapeutic target. Proceedings of the National Academy of Sciences of the United States of America, 101(49), 17174–17179. doi:10.​1073/​pnas.​0406351101.CrossRefPubMedPubMedCentral
29.
go back to reference Nomi, T., Sho, M., Akahori, T., Hamada, K., Kubo, A., Kanehiro, H., et al. (2007). Clinical significance and therapeutic potential of the programmed death-1 ligand/programmed death-1 pathway in human pancreatic cancer. Clinical Cancer Research, 13(7), 2151–2157. doi:10.1158/1078-0432.CCR-06-2746.CrossRefPubMed Nomi, T., Sho, M., Akahori, T., Hamada, K., Kubo, A., Kanehiro, H., et al. (2007). Clinical significance and therapeutic potential of the programmed death-1 ligand/programmed death-1 pathway in human pancreatic cancer. Clinical Cancer Research, 13(7), 2151–2157. doi:10.​1158/​1078-0432.​CCR-06-2746.CrossRefPubMed
30.
go back to reference Hamanishi, J., Mandai, M., Iwasaki, M., Okazaki, T., Tanaka, Y., Yamaguchi, K., et al. (2007). Programmed cell death 1 ligand 1 and tumor-infiltrating CD8+ T lymphocytes are prognostic factors of human ovarian cancer. Proceedings of the National Academy of Sciences of the United States of America, 104(9), 3360–3365. doi:10.1073/pnas.0611533104.CrossRefPubMedPubMedCentral Hamanishi, J., Mandai, M., Iwasaki, M., Okazaki, T., Tanaka, Y., Yamaguchi, K., et al. (2007). Programmed cell death 1 ligand 1 and tumor-infiltrating CD8+ T lymphocytes are prognostic factors of human ovarian cancer. Proceedings of the National Academy of Sciences of the United States of America, 104(9), 3360–3365. doi:10.​1073/​pnas.​0611533104.CrossRefPubMedPubMedCentral
31.
go back to reference Wintterle, S., Schreiner, B., Mitsdoerffer, M., Schneider, D., Chen, L., Meyermann, R., et al. (2003). Expression of the B7-related molecule B7-H1 by glioma cells: a potential mechanism of immune paralysis. Cancer Research, 63(21), 7462–7467.PubMed Wintterle, S., Schreiner, B., Mitsdoerffer, M., Schneider, D., Chen, L., Meyermann, R., et al. (2003). Expression of the B7-related molecule B7-H1 by glioma cells: a potential mechanism of immune paralysis. Cancer Research, 63(21), 7462–7467.PubMed
32.
go back to reference Topalian, S. L., Sznol, M., McDermott, D. F., Kluger, H. M., Carvajal, R. D., Sharfman, W. H., et al. (2014). Survival, durable tumor remission, and long-term safety in patients with advanced melanoma receiving nivolumab. Journal of Clinical Oncology, 32(10), 1020–1030. doi:10.1200/JCO.2013.53.0105.CrossRefPubMedPubMedCentral Topalian, S. L., Sznol, M., McDermott, D. F., Kluger, H. M., Carvajal, R. D., Sharfman, W. H., et al. (2014). Survival, durable tumor remission, and long-term safety in patients with advanced melanoma receiving nivolumab. Journal of Clinical Oncology, 32(10), 1020–1030. doi:10.​1200/​JCO.​2013.​53.​0105.CrossRefPubMedPubMedCentral
33.
go back to reference Robert, C., Ribas, A., Wolchok, J. D., Hodi, F. S., Hamid, O., Kefford, R., et al. (2014). Anti-programmed-death-receptor-1 treatment with pembrolizumab in ipilimumab-refractory advanced melanoma: a randomised dose-comparison cohort of a phase 1 trial. Lancet, 384(9948), 1109–1117. doi:10.1016/S0140-6736(14)60958-2.CrossRefPubMed Robert, C., Ribas, A., Wolchok, J. D., Hodi, F. S., Hamid, O., Kefford, R., et al. (2014). Anti-programmed-death-receptor-1 treatment with pembrolizumab in ipilimumab-refractory advanced melanoma: a randomised dose-comparison cohort of a phase 1 trial. Lancet, 384(9948), 1109–1117. doi:10.​1016/​S0140-6736(14)60958-2.CrossRefPubMed
36.
go back to reference Schaer, D. A., Hirschhorn-Cymerman, D., & Wolchok, J. D. (2014). Targeting tumor-necrosis factor receptor pathways for tumor immunotherapy. Journal of Immunotherapy Cancer, 2, 7. doi:10.1186/2051-1426-2-7.CrossRef Schaer, D. A., Hirschhorn-Cymerman, D., & Wolchok, J. D. (2014). Targeting tumor-necrosis factor receptor pathways for tumor immunotherapy. Journal of Immunotherapy Cancer, 2, 7. doi:10.​1186/​2051-1426-2-7.CrossRef
37.
go back to reference Vitale, L. A., He, L. Z., Thomas, L. J., Widger, J., Weidlick, J., Crocker, A., et al. (2012). Development of a human monoclonal antibody for potential therapy of CD27-expressing lymphoma and leukemia. Clinical Cancer Research, 18(14), 3812–3821. doi:10.1158/1078-0432.CCR-11-3308.CrossRefPubMed Vitale, L. A., He, L. Z., Thomas, L. J., Widger, J., Weidlick, J., Crocker, A., et al. (2012). Development of a human monoclonal antibody for potential therapy of CD27-expressing lymphoma and leukemia. Clinical Cancer Research, 18(14), 3812–3821. doi:10.​1158/​1078-0432.​CCR-11-3308.CrossRefPubMed
39.
go back to reference Leitner, J., Klauser, C., Pickl, W. F., Stockl, J., Majdic, O., Bardet, A. F., et al. (2009). B7-H3 is a potent inhibitor of human T-cell activation: No evidence for B7-H3 and TREML2 interaction. European Journal of Immunology, 39(7), 1754–1764. doi:10.1002/eji.200839028.CrossRefPubMedPubMedCentral Leitner, J., Klauser, C., Pickl, W. F., Stockl, J., Majdic, O., Bardet, A. F., et al. (2009). B7-H3 is a potent inhibitor of human T-cell activation: No evidence for B7-H3 and TREML2 interaction. European Journal of Immunology, 39(7), 1754–1764. doi:10.​1002/​eji.​200839028.CrossRefPubMedPubMedCentral
40.
go back to reference Chapoval, A. I., Ni, J., Lau, J. S., Wilcox, R. A., Flies, D. B., Liu, D., et al. (2001). B7-H3: a costimulatory molecule for T cell activation and IFN-gamma production. Nature Immunology, 2(3), 269–274. doi:10.1038/85339.CrossRefPubMed Chapoval, A. I., Ni, J., Lau, J. S., Wilcox, R. A., Flies, D. B., Liu, D., et al. (2001). B7-H3: a costimulatory molecule for T cell activation and IFN-gamma production. Nature Immunology, 2(3), 269–274. doi:10.​1038/​85339.CrossRefPubMed
41.
go back to reference Loo, D., Alderson, R. F., Chen, F. Z., Huang, L., Zhang, W., Gorlatov, S., et al. (2012). Development of an Fc-enhanced anti-B7-H3 monoclonal antibody with potent antitumor activity. Clinical Cancer Research, 18(14), 3834–3845. doi:10.1158/1078-0432.CCR-12-0715.CrossRefPubMed Loo, D., Alderson, R. F., Chen, F. Z., Huang, L., Zhang, W., Gorlatov, S., et al. (2012). Development of an Fc-enhanced anti-B7-H3 monoclonal antibody with potent antitumor activity. Clinical Cancer Research, 18(14), 3834–3845. doi:10.​1158/​1078-0432.​CCR-12-0715.CrossRefPubMed
43.
45.
go back to reference Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998). Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF. Journal of Clinical Investigation, 101(4), 890–898. doi:10.1172/JCI1112.CrossRefPubMedPubMedCentral Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998). Macrophages that have ingested apoptotic cells in vitro inhibit proinflammatory cytokine production through autocrine/paracrine mechanisms involving TGF-beta, PGE2, and PAF. Journal of Clinical Investigation, 101(4), 890–898. doi:10.​1172/​JCI1112.CrossRefPubMedPubMedCentral
46.
go back to reference Gerber, D. E., Stopeck, A. T., Wong, L., Rosen, L. S., Thorpe, P. E., Shan, J. S., et al. (2011). Phase I safety and pharmacokinetic study of bavituximab, a chimeric phosphatidylserine-targeting monoclonal antibody, in patients with advanced solid tumors. Clinical Cancer Research, 17(21), 6888–6896. doi:10.1158/1078-0432.CCR-11-1074.CrossRefPubMed Gerber, D. E., Stopeck, A. T., Wong, L., Rosen, L. S., Thorpe, P. E., Shan, J. S., et al. (2011). Phase I safety and pharmacokinetic study of bavituximab, a chimeric phosphatidylserine-targeting monoclonal antibody, in patients with advanced solid tumors. Clinical Cancer Research, 17(21), 6888–6896. doi:10.​1158/​1078-0432.​CCR-11-1074.CrossRefPubMed
47.
go back to reference Kaufman, H. L., Ruby, C. E., Hughes, T., & Slingluff, C. L., Jr. (2014). Current status of granulocyte-macrophage colony-stimulating factor in the immunotherapy of melanoma. Journal of Immunotherapy Cancer, 2, 11. doi:10.1186/2051-1426-2-11.CrossRef Kaufman, H. L., Ruby, C. E., Hughes, T., & Slingluff, C. L., Jr. (2014). Current status of granulocyte-macrophage colony-stimulating factor in the immunotherapy of melanoma. Journal of Immunotherapy Cancer, 2, 11. doi:10.​1186/​2051-1426-2-11.CrossRef
48.
go back to reference Shi, Y., Liu, C. H., Roberts, A. I., Das, J., Xu, G., Ren, G., et al. (2006). Granulocyte-macrophage colony-stimulating factor (GM-CSF) and T-cell responses: what we do and don’t know. Cell Research, 16(2), 126–133. doi:10.1038/sj.cr.7310017.CrossRefPubMed Shi, Y., Liu, C. H., Roberts, A. I., Das, J., Xu, G., Ren, G., et al. (2006). Granulocyte-macrophage colony-stimulating factor (GM-CSF) and T-cell responses: what we do and don’t know. Cell Research, 16(2), 126–133. doi:10.​1038/​sj.​cr.​7310017.CrossRefPubMed
50.
go back to reference Traversari, C., van der Bruggen, P., Luescher, I. F., Lurquin, C., Chomez, P., Van Pel, A., et al. (1992). A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E. Journal of Experimental Medicine, 176(5), 1453–1457.CrossRefPubMed Traversari, C., van der Bruggen, P., Luescher, I. F., Lurquin, C., Chomez, P., Van Pel, A., et al. (1992). A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E. Journal of Experimental Medicine, 176(5), 1453–1457.CrossRefPubMed
51.
go back to reference van der Bruggen, P., Traversari, C., Chomez, P., Lurquin, C., De Plaen, E., Van den Eynde, B., et al. (1991). A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. Science, 254(5038), 1643–1647.CrossRefPubMed van der Bruggen, P., Traversari, C., Chomez, P., Lurquin, C., De Plaen, E., Van den Eynde, B., et al. (1991). A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. Science, 254(5038), 1643–1647.CrossRefPubMed
53.
go back to reference Murakami, T., & Sunada, Y. (2011). Plasmid DNA gene therapy by electroporation: Principles and recent advances. Current Gene Therapy, 11(6), 447–456.CrossRefPubMed Murakami, T., & Sunada, Y. (2011). Plasmid DNA gene therapy by electroporation: Principles and recent advances. Current Gene Therapy, 11(6), 447–456.CrossRefPubMed
55.
go back to reference Bergman, P. J., Camps-Palau, M. A., McKnight, J. A., Leibman, N. F., Craft, D. M., Leung, C., et al. (2006). Development of a xenogeneic DNA vaccine program for canine malignant melanoma at the Animal Medical Center. Vaccine, 24(21), 4582–4585. doi:10.1016/j.vaccine.2005.08.027.CrossRefPubMed Bergman, P. J., Camps-Palau, M. A., McKnight, J. A., Leibman, N. F., Craft, D. M., Leung, C., et al. (2006). Development of a xenogeneic DNA vaccine program for canine malignant melanoma at the Animal Medical Center. Vaccine, 24(21), 4582–4585. doi:10.​1016/​j.​vaccine.​2005.​08.​027.CrossRefPubMed
56.
go back to reference Bergman, P. J., McKnight, J., Novosad, A., Charney, S., Farrelly, J., Craft, D., et al. (2003). Long-term survival of dogs with advanced malignant melanoma after DNA vaccination with xenogeneic human tyrosinase: a phase I trial. Clinical Cancer Research, 9(4), 1284–1290.PubMed Bergman, P. J., McKnight, J., Novosad, A., Charney, S., Farrelly, J., Craft, D., et al. (2003). Long-term survival of dogs with advanced malignant melanoma after DNA vaccination with xenogeneic human tyrosinase: a phase I trial. Clinical Cancer Research, 9(4), 1284–1290.PubMed
60.
go back to reference Kobayashi, M., Suzuki, K., Yashi, M., Yuzawa, M., Takayashiki, N., & Morita, T. (2007). Tumor infiltrating dendritic cells predict treatment response to immunotherapy in patients with metastatic renal cell carcinoma. Anticancer Research, 27(2), 1137–1141.PubMed Kobayashi, M., Suzuki, K., Yashi, M., Yuzawa, M., Takayashiki, N., & Morita, T. (2007). Tumor infiltrating dendritic cells predict treatment response to immunotherapy in patients with metastatic renal cell carcinoma. Anticancer Research, 27(2), 1137–1141.PubMed
61.
go back to reference Simonetti, O., Goteri, G., Lucarini, G., Rubini, C., Stramazzotti, D., Lo Muzio, L., et al. (2007). In melanoma changes of immature and mature dendritic cell expression correlate with tumor thickness: an immunohistochemical study. International Journal of Immunopathology and Pharmacology, 20(2), 325–333.PubMed Simonetti, O., Goteri, G., Lucarini, G., Rubini, C., Stramazzotti, D., Lo Muzio, L., et al. (2007). In melanoma changes of immature and mature dendritic cell expression correlate with tumor thickness: an immunohistochemical study. International Journal of Immunopathology and Pharmacology, 20(2), 325–333.PubMed
63.
go back to reference Weber, J., Atkins, M., Hwu, P., Radvanyi, L., Sznol, M., & Yee, C. (2011). White paper on adoptive cell therapy for cancer with tumor-infiltrating lymphocytes: a report of the CTEP subcommittee on adoptive cell therapy. Clinical Cancer Research, 17(7), 1664–1673. doi:10.1158/1078-0432.CCR-10-2272.CrossRefPubMed Weber, J., Atkins, M., Hwu, P., Radvanyi, L., Sznol, M., & Yee, C. (2011). White paper on adoptive cell therapy for cancer with tumor-infiltrating lymphocytes: a report of the CTEP subcommittee on adoptive cell therapy. Clinical Cancer Research, 17(7), 1664–1673. doi:10.​1158/​1078-0432.​CCR-10-2272.CrossRefPubMed
67.
go back to reference Boni, A., Cogdill, A. P., Dang, P., Udayakumar, D., Njauw, C. N., Sloss, C. M., et al. (2010). Selective BRAFV600E inhibition enhances T-cell recognition of melanoma without affecting lymphocyte function. Cancer Research, 70(13), 5213–5219. doi:10.1158/0008-5472.CAN-10-0118.CrossRefPubMed Boni, A., Cogdill, A. P., Dang, P., Udayakumar, D., Njauw, C. N., Sloss, C. M., et al. (2010). Selective BRAFV600E inhibition enhances T-cell recognition of melanoma without affecting lymphocyte function. Cancer Research, 70(13), 5213–5219. doi:10.​1158/​0008-5472.​CAN-10-0118.CrossRefPubMed
68.
go back to reference Wilmott, J. S., Long, G. V., Howle, J. R., Haydu, L. E., Sharma, R. N., Thompson, J. F., et al. (2012). Selective BRAF inhibitors induce marked T-cell infiltration into human metastatic melanoma. Clinical Cancer Research, 18(5), 1386–1394. doi:10.1158/1078-0432.CCR-11-2479.CrossRefPubMed Wilmott, J. S., Long, G. V., Howle, J. R., Haydu, L. E., Sharma, R. N., Thompson, J. F., et al. (2012). Selective BRAF inhibitors induce marked T-cell infiltration into human metastatic melanoma. Clinical Cancer Research, 18(5), 1386–1394. doi:10.​1158/​1078-0432.​CCR-11-2479.CrossRefPubMed
70.
go back to reference Eggermont, A. M., Suciu, S., Testori, A., Santinami, M., Kruit, W. H., Marsden, J., et al. (2012). Long-term results of the randomized phase III trial EORTC 18991 of adjuvant therapy with pegylated interferon alfa-2b versus observation in resected stage III melanoma. Journal of Clinical Oncology, 30(31), 3810–3818. doi:10.1200/JCO.2011.41.3799.CrossRefPubMed Eggermont, A. M., Suciu, S., Testori, A., Santinami, M., Kruit, W. H., Marsden, J., et al. (2012). Long-term results of the randomized phase III trial EORTC 18991 of adjuvant therapy with pegylated interferon alfa-2b versus observation in resected stage III melanoma. Journal of Clinical Oncology, 30(31), 3810–3818. doi:10.​1200/​JCO.​2011.​41.​3799.CrossRefPubMed
77.
go back to reference Fellner, C. (2012). Ipilimumab (yervoy) prolongs survival in advanced melanoma: Serious side effects and a hefty price tag may limit its use. P T, 37(9), 503–530.PubMedPubMedCentral Fellner, C. (2012). Ipilimumab (yervoy) prolongs survival in advanced melanoma: Serious side effects and a hefty price tag may limit its use. P T, 37(9), 503–530.PubMedPubMedCentral
78.
go back to reference Jonsson, B., & Wilking, N. (2012). Cancer vaccines and immunotherapeutics: Challenges for pricing, reimbursement and market access. Human Vaccin Immunotherapy, 8(9), 1360–1363. doi:10.4161/hv.21921.CrossRef Jonsson, B., & Wilking, N. (2012). Cancer vaccines and immunotherapeutics: Challenges for pricing, reimbursement and market access. Human Vaccin Immunotherapy, 8(9), 1360–1363. doi:10.​4161/​hv.​21921.CrossRef
79.
go back to reference Ma, C., & Armstrong, A. W. (2014). Severe adverse events from the treatment of advanced melanoma: a systematic review of severe side effects associated with ipilimumab, vemurafenib, interferon alfa-2b, dacarbazine and interleukin-2. The Journal of Dermatological Treatment, 25(5), 401–408. doi:10.3109/09546634.2013.813897.CrossRefPubMed Ma, C., & Armstrong, A. W. (2014). Severe adverse events from the treatment of advanced melanoma: a systematic review of severe side effects associated with ipilimumab, vemurafenib, interferon alfa-2b, dacarbazine and interleukin-2. The Journal of Dermatological Treatment, 25(5), 401–408. doi:10.​3109/​09546634.​2013.​813897.CrossRefPubMed
81.
go back to reference Lacouture, M. E., Wolchok, J. D., Yosipovitch, G., Kahler, K. C., Busam, K. J., & Hauschild, A. (2014). Ipilimumab in patients with cancer and the management of dermatologic adverse events. Journal of the American Academy of Dermatology, 71(1), 161–169. doi:10.1016/j.jaad.2014.02.035.CrossRefPubMed Lacouture, M. E., Wolchok, J. D., Yosipovitch, G., Kahler, K. C., Busam, K. J., & Hauschild, A. (2014). Ipilimumab in patients with cancer and the management of dermatologic adverse events. Journal of the American Academy of Dermatology, 71(1), 161–169. doi:10.​1016/​j.​jaad.​2014.​02.​035.CrossRefPubMed
82.
go back to reference Minkis, K., Garden, B. C., Wu, S., Pulitzer, M. P., & Lacouture, M. E. (2013). The risk of rash associated with ipilimumab in patients with cancer: a systematic review of the literature and meta-analysis. Journal of the American Academy of Dermatology, 69(3), e121–e128. doi:10.1016/j.jaad.2012.12.963.CrossRefPubMed Minkis, K., Garden, B. C., Wu, S., Pulitzer, M. P., & Lacouture, M. E. (2013). The risk of rash associated with ipilimumab in patients with cancer: a systematic review of the literature and meta-analysis. Journal of the American Academy of Dermatology, 69(3), e121–e128. doi:10.​1016/​j.​jaad.​2012.​12.​963.CrossRefPubMed
84.
go back to reference Hinds, A. M., Ahmad, D. S., Muenster, J. E., Berg, Z. M., Lopez, K. T., Holly, J. S., et al. (2014). Ipilimumab-induced colitis: a rare but serious side effect. Endoscopy, 46(Suppl 1 UCTN), E308–E309. doi:10.1055/s-0034-1377209.PubMed Hinds, A. M., Ahmad, D. S., Muenster, J. E., Berg, Z. M., Lopez, K. T., Holly, J. S., et al. (2014). Ipilimumab-induced colitis: a rare but serious side effect. Endoscopy, 46(Suppl 1 UCTN), E308–E309. doi:10.​1055/​s-0034-1377209.PubMed
Metadata
Title
Immunotherapy of melanoma: Present options and future promises
Authors
Anand Rotte
Madhuri Bhandaru
Youwen Zhou
Kevin J. McElwee
Publication date
01-03-2015
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 1/2015
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-014-9542-0

Other articles of this Issue 1/2015

Cancer and Metastasis Reviews 1/2015 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine