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Erschienen in: Current Treatment Options in Oncology 2/2014

01.06.2014 | Skin Cancer (WH Sharfman, Section Editor)

Update on Vaccines for High-Risk Melanoma

verfasst von: Sarah A. Weiss, MD, Sunandana Chandra, MD, Anna C. Pavlick, DO

Erschienen in: Current Treatment Options in Oncology | Ausgabe 2/2014

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Opinion statement

The management of high-risk melanoma has historically included primary surgical resection with or without lymphadenectomy followed by an array of adjuvant options including radiation therapy or immunomodulatory therapies such as interferon-α, granulocyte macrophage colony-stimulating factor, and a multitude of vaccines. There has been a long-standing interest in the development of vaccines in high-risk and metastatic melanoma, and clinical trials have been ongoing for decades. Given that melanoma is identified as one of the most immunogenic solid tumors, there is continued hope that vaccine therapies will improve clinical outcomes. Despite intense interest in this field, few clinical trials to-date have demonstrated significant benefit from melanoma vaccines in high-risk disease. Several trials have even documented a detrimental effect on outcomes after vaccine administration. While the role of vaccines in the adjuvant setting of high-risk melanoma presently remains unclear, recent advances in immunotherapy for melanoma including development of cytotoxic T-lymphocyte antigen 4 (CTLA-4) and programmed cell death 1 (PD-1) monoclonal antibodies have demonstrated meaningful clinical responses. With further study and focus on mechanisms of immune regulation, there remains promise for the role of vaccines in combination with other immune-stimulatory agents in high-risk melanoma.
Literatur
1.
2.
4.
5.
Zurück zum Zitat Garbe C, Eigentler TK, Keilholz U, et al. Systematic review of medical treatment in melanoma: current status and future prospects. Oncologist. 2011;16:5–24.PubMedCentralPubMedCrossRef Garbe C, Eigentler TK, Keilholz U, et al. Systematic review of medical treatment in melanoma: current status and future prospects. Oncologist. 2011;16:5–24.PubMedCentralPubMedCrossRef
6.
Zurück zum Zitat Kirkwood JM, Ibrahim JG, Sondak VK, et al. High- and low-dose interferon alfa-2b in high-risk melanoma: first analysis of intergroup trial E1690/S9111/C9190. J Clin Oncol. 2000;18:2444–58.PubMed Kirkwood JM, Ibrahim JG, Sondak VK, et al. High- and low-dose interferon alfa-2b in high-risk melanoma: first analysis of intergroup trial E1690/S9111/C9190. J Clin Oncol. 2000;18:2444–58.PubMed
7.
Zurück zum Zitat Kirkwood JM, Manola J, Ibrahim J, et al. A pooled analysis of Eastern Cooperative Oncology Group and intergroup trials of adjuvant high-dose interferon for melanoma. Clin Cancer Res. 2004;10:1670–7.PubMedCrossRef Kirkwood JM, Manola J, Ibrahim J, et al. A pooled analysis of Eastern Cooperative Oncology Group and intergroup trials of adjuvant high-dose interferon for melanoma. Clin Cancer Res. 2004;10:1670–7.PubMedCrossRef
8.
Zurück zum Zitat Rietschel P, Chapman PB. Immunotherapy of Melanoma. Hematol Oncol Clin North Am. 2006;20:751–66.PubMedCrossRef Rietschel P, Chapman PB. Immunotherapy of Melanoma. Hematol Oncol Clin North Am. 2006;20:751–66.PubMedCrossRef
9.
Zurück zum Zitat Oble DA, Loewe R, Yu P, et al. Focus on TILs: prognostic significance of tumor infiltrating lymphocytes in human melanoma. Cancer Immun. 2009;9:1–20. Oble DA, Loewe R, Yu P, et al. Focus on TILs: prognostic significance of tumor infiltrating lymphocytes in human melanoma. Cancer Immun. 2009;9:1–20.
10.
11.
Zurück zum Zitat Zarour HM, Kirkwood JM. Melanoma vaccines: early progress and future promises. Semin Cutan Med Surg. 2003;22:68–75.PubMedCrossRef Zarour HM, Kirkwood JM. Melanoma vaccines: early progress and future promises. Semin Cutan Med Surg. 2003;22:68–75.PubMedCrossRef
12.
Zurück zum Zitat Klein O, Schmidt C, Knights A, et al. Melanoma vaccines: developments over the past 10 years. Expert Rev Vaccines. 2011;10:853–73.PubMedCrossRef Klein O, Schmidt C, Knights A, et al. Melanoma vaccines: developments over the past 10 years. Expert Rev Vaccines. 2011;10:853–73.PubMedCrossRef
13.
Zurück zum Zitat Kawakami Y, Robbins PF, Wang RF, Parkhurst M, Kang X, Rosenberg SA. The use of melanosomal proteins in the immunotherapy of melanoma. J Immunother. 1998;21:237–46.PubMedCrossRef Kawakami Y, Robbins PF, Wang RF, Parkhurst M, Kang X, Rosenberg SA. The use of melanosomal proteins in the immunotherapy of melanoma. J Immunother. 1998;21:237–46.PubMedCrossRef
14.
Zurück zum Zitat Spitler LE, Grossbard ML, Ernstoff MS, et al. Adjuvant therapy of stage III and IV malignant melanoma using granulocyte-macrophage colony-stimulating factor. J Clin Oncol. 2000;18:1614–21.PubMed Spitler LE, Grossbard ML, Ernstoff MS, et al. Adjuvant therapy of stage III and IV malignant melanoma using granulocyte-macrophage colony-stimulating factor. J Clin Oncol. 2000;18:1614–21.PubMed
15.
Zurück zum Zitat Lawson DH, Lee SJ, Tarhini AA, et al. E4679: Phase III cooperative group study of yeast-derived granulocyte macrophage colony-stimulating factor (GM-CSF) vs placebo as adjuvant treatment of patients with completely resected stage III-IV melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2010;28:8504. Lawson DH, Lee SJ, Tarhini AA, et al. E4679: Phase III cooperative group study of yeast-derived granulocyte macrophage colony-stimulating factor (GM-CSF) vs placebo as adjuvant treatment of patients with completely resected stage III-IV melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2010;28:8504.
16.
Zurück zum Zitat Slingluff Jr CL, Petroni GR, Yamshchikov GV, et al. Clinical and immunologic results of a randomized phase II trial of vaccination using four peptides either administered in granulocyte-macrophage colony-stimulating factor in adjuvant or pulsed on dendritic cells. J Clin Oncol. 2003;21:4016–26.PubMedCrossRef Slingluff Jr CL, Petroni GR, Yamshchikov GV, et al. Clinical and immunologic results of a randomized phase II trial of vaccination using four peptides either administered in granulocyte-macrophage colony-stimulating factor in adjuvant or pulsed on dendritic cells. J Clin Oncol. 2003;21:4016–26.PubMedCrossRef
17.
Zurück zum Zitat Slingluff Jr CL, Petroni GR, Olson WC, et al. Effect of granulocyte/macrophage colony-stimulating factor on circulating CD8+ and CD4+ T-cell responses to a multi-peptide melanoma vaccine: outcome of a multicenter randomized trial. Clin Cancer Res. 2009;15:7036–44.PubMedCentralPubMedCrossRef Slingluff Jr CL, Petroni GR, Olson WC, et al. Effect of granulocyte/macrophage colony-stimulating factor on circulating CD8+ and CD4+ T-cell responses to a multi-peptide melanoma vaccine: outcome of a multicenter randomized trial. Clin Cancer Res. 2009;15:7036–44.PubMedCentralPubMedCrossRef
18.
Zurück zum Zitat Block MS, Suman VJ, Nevala WK, et al. Pilot study of granulocyte-macrophage colony-stimulating factor and interleukin-2 as immune adjuvants for a melanoma peptide vaccine. Melanoma Res. 2011;21:438–45.PubMedCrossRef Block MS, Suman VJ, Nevala WK, et al. Pilot study of granulocyte-macrophage colony-stimulating factor and interleukin-2 as immune adjuvants for a melanoma peptide vaccine. Melanoma Res. 2011;21:438–45.PubMedCrossRef
19.
Zurück zum Zitat Slingluff Jr CL, Petroni GR, Chianese-Bullock KA, et al. Randomized multicenter trial of the effects of melanoma- associated helper peptides and cyclophosphamide on the immunogenicity of a multi-peptide melanoma vaccine. J Clin Oncol. 2011;29:2924–32.PubMedCentralPubMedCrossRef Slingluff Jr CL, Petroni GR, Chianese-Bullock KA, et al. Randomized multicenter trial of the effects of melanoma- associated helper peptides and cyclophosphamide on the immunogenicity of a multi-peptide melanoma vaccine. J Clin Oncol. 2011;29:2924–32.PubMedCentralPubMedCrossRef
20.•
Zurück zum Zitat Gibney GT, Weber JS, Kudchadkar RR, et al. Safety and efficacy of adjuvant anti-PD1 therapy (nivolumab) in combination with vaccine in resected high-risk metastatic melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2013;31:9056. This trial highlights the importance of investigating combinations vaccines and newer immunotherapies such as nivolumab. Patients on this regimen who did not relapse had an increase in T-regulatory cells. Gibney GT, Weber JS, Kudchadkar RR, et al. Safety and efficacy of adjuvant anti-PD1 therapy (nivolumab) in combination with vaccine in resected high-risk metastatic melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2013;31:9056. This trial highlights the importance of investigating combinations vaccines and newer immunotherapies such as nivolumab. Patients on this regimen who did not relapse had an increase in T-regulatory cells.
21.
Zurück zum Zitat Slingluff CL, Petroni GR, Chianese-Bullock KA, et al. A multi-peptide vaccine plus toll-like receptor agonists in melanoma patients, with evaluation of the vaccine site microenvironment and sentinel immunized node (Mel58; NCT01585350). ASCO Annual Meeting Abstracts. J Clin Oncol. 2013;31: [Abstract TPS3125]. Slingluff CL, Petroni GR, Chianese-Bullock KA, et al. A multi-peptide vaccine plus toll-like receptor agonists in melanoma patients, with evaluation of the vaccine site microenvironment and sentinel immunized node (Mel58; NCT01585350). ASCO Annual Meeting Abstracts. J Clin Oncol. 2013;31: [Abstract TPS3125].
22.
Zurück zum Zitat Ferrucci PF, Tosti G, di Pietro A, et al. Newly identified tumor antigens as promising cancer vaccine targets for malignant melanoma treatment. Curr Top Med Chem. 2012;12:11–31.PubMedCrossRef Ferrucci PF, Tosti G, di Pietro A, et al. Newly identified tumor antigens as promising cancer vaccine targets for malignant melanoma treatment. Curr Top Med Chem. 2012;12:11–31.PubMedCrossRef
23.
Zurück zum Zitat Kruit WH, van Ojik HH, Brichard VG, et al. Phase I/2 study of subcutaneous and intradermal immunization with a recombinant MAGE-3 protein in patients with detectable metastatic melanoma. Int J Cancer. 2005;117:596–604.PubMedCrossRef Kruit WH, van Ojik HH, Brichard VG, et al. Phase I/2 study of subcutaneous and intradermal immunization with a recombinant MAGE-3 protein in patients with detectable metastatic melanoma. Int J Cancer. 2005;117:596–604.PubMedCrossRef
24.
Zurück zum Zitat Kruit WH, Suciu S, Dreno B, et al. Selection of immunostimulant AS15 for active immunization with MAGE-A3 protein: results of a randomized phase II study of the European Organisation for Research and Treatment of Cancer Melanoma Group in metastatic melanoma. J Clin Oncol. 2013;31:2413–21.PubMedCrossRef Kruit WH, Suciu S, Dreno B, et al. Selection of immunostimulant AS15 for active immunization with MAGE-A3 protein: results of a randomized phase II study of the European Organisation for Research and Treatment of Cancer Melanoma Group in metastatic melanoma. J Clin Oncol. 2013;31:2413–21.PubMedCrossRef
26.••
Zurück zum Zitat Kirkwood JM, Dreno B, Hauschild A, et al. DERMA phase III trial of MAGE-A3 antigen-specific cancer immunotherapeutic (ASCI) as adjuvant therapy in patients with MAGE-A3-positive resected stage III melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2011;29. This phase III randomized trial known as the DERMA trial showed that MAGE-A3 vaccination in resected stage IIIB/C melanoma patients does not significantly extend DFS when compared with placebo. Kirkwood JM, Dreno B, Hauschild A, et al. DERMA phase III trial of MAGE-A3 antigen-specific cancer immunotherapeutic (ASCI) as adjuvant therapy in patients with MAGE-A3-positive resected stage III melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2011;29. This phase III randomized trial known as the DERMA trial showed that MAGE-A3 vaccination in resected stage IIIB/C melanoma patients does not significantly extend DFS when compared with placebo.
27.
Zurück zum Zitat Barrow C, Browning J, MacGregor D, et al. Tumor antigen expression in melanoma varies according to antigen and stage. Clin Cancer Res. 2006;12:764–71.PubMedCrossRef Barrow C, Browning J, MacGregor D, et al. Tumor antigen expression in melanoma varies according to antigen and stage. Clin Cancer Res. 2006;12:764–71.PubMedCrossRef
28.
Zurück zum Zitat Davis ID, Chen W, Jackson H, et al. Recombinant NY-ESO-1 protein with ISCOMATRIX adjuvant induces broad integrated antibody and CD4+ and CD8+ T cell responses in humans. PNAS. 2004;101:10697–702.PubMedCentralPubMedCrossRef Davis ID, Chen W, Jackson H, et al. Recombinant NY-ESO-1 protein with ISCOMATRIX adjuvant induces broad integrated antibody and CD4+ and CD8+ T cell responses in humans. PNAS. 2004;101:10697–702.PubMedCentralPubMedCrossRef
29.
Zurück zum Zitat Nicholaou T, Chen W, Davis ID, et al. Immunoediting and persistence of antigen-specific immunity in patients who have previously been vaccinated with NY-ESO-1 protein formulated in ISCOMATRIX™. Cancer Immunol Immunother. 2011;60:1625–37.PubMedCrossRef Nicholaou T, Chen W, Davis ID, et al. Immunoediting and persistence of antigen-specific immunity in patients who have previously been vaccinated with NY-ESO-1 protein formulated in ISCOMATRIX™. Cancer Immunol Immunother. 2011;60:1625–37.PubMedCrossRef
31.
Zurück zum Zitat Sabado RL, Pavlick AC, Gnjatic S, et al. Phase I/II study of resiquimod as an immunologic adjuvant for NY-ESO-1 protein vaccination in patients with melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2012;30: [Abstract 2589]. Sabado RL, Pavlick AC, Gnjatic S, et al. Phase I/II study of resiquimod as an immunologic adjuvant for NY-ESO-1 protein vaccination in patients with melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2012;30: [Abstract 2589].
32.
Zurück zum Zitat Livingston PO, Wong GYC, Adluri S, et al. Improved survival in stage III melanoma patients with GM2 antibodies: a randomized trial of adjuvant vaccination with GM2 ganglioside. J Clin Oncol. 1994;12:1036–44.PubMed Livingston PO, Wong GYC, Adluri S, et al. Improved survival in stage III melanoma patients with GM2 antibodies: a randomized trial of adjuvant vaccination with GM2 ganglioside. J Clin Oncol. 1994;12:1036–44.PubMed
33.•
Zurück zum Zitat Eggermont AMM, Suciu S, Rutkowski P, et al. Adjuvant ganglioside GM2-KLH/QS-21 vaccination vs observation after resection of primary tumor 1.5 mm in patients with stage II melanoma: results of the EORTC 18961 randomized phase III trial. J Clin Oncol. 2013;31:3831–40. A phase III trial (EORTC 18961) studied the efficacy of the adjuvant ganglioside GM2-KLH/QS-21 vaccine in resected stage II melanoma patients and found that the vaccine did not improve RFS, but actually demonstrated a trend toward decreased OS, for which the trial was closed early.PubMedCrossRef Eggermont AMM, Suciu S, Rutkowski P, et al. Adjuvant ganglioside GM2-KLH/QS-21 vaccination vs observation after resection of primary tumor 1.5 mm in patients with stage II melanoma: results of the EORTC 18961 randomized phase III trial. J Clin Oncol. 2013;31:3831–40. A phase III trial (EORTC 18961) studied the efficacy of the adjuvant ganglioside GM2-KLH/QS-21 vaccine in resected stage II melanoma patients and found that the vaccine did not improve RFS, but actually demonstrated a trend toward decreased OS, for which the trial was closed early.PubMedCrossRef
34.
Zurück zum Zitat Neller MA, Lopez JA, Schmidt CW. Antigens for cancer immunotherapy. Semin Immunol. 2008;20:286–95.PubMedCrossRef Neller MA, Lopez JA, Schmidt CW. Antigens for cancer immunotherapy. Semin Immunol. 2008;20:286–95.PubMedCrossRef
35.
Zurück zum Zitat Motl SE. Technology evaluation: Canvaxin, John Wayne Cancer Institute/CancerVax. Curr Opin Mol Ther. 2004;6:104–11.PubMed Motl SE. Technology evaluation: Canvaxin, John Wayne Cancer Institute/CancerVax. Curr Opin Mol Ther. 2004;6:104–11.PubMed
36.
Zurück zum Zitat Morton DL, Hseuh EC, Essner R, et al. Prolonged survival of patients receiving active immunotherapy with canvaxin therapeutic polyvalent vaccine after complete resection of melanoma metastatic to regional lymph nodes. Ann Surg. 2002;236:438–49.PubMedCentralPubMedCrossRef Morton DL, Hseuh EC, Essner R, et al. Prolonged survival of patients receiving active immunotherapy with canvaxin therapeutic polyvalent vaccine after complete resection of melanoma metastatic to regional lymph nodes. Ann Surg. 2002;236:438–49.PubMedCentralPubMedCrossRef
37.
Zurück zum Zitat Hsueh EC, Essner R, Foshag LJ, et al. Prolonged survival after complete resection of disseminated melanoma and active immunotherapy with a therapeutic cancer vaccine. J Clin Oncol. 2002;20:4549–54.PubMedCrossRef Hsueh EC, Essner R, Foshag LJ, et al. Prolonged survival after complete resection of disseminated melanoma and active immunotherapy with a therapeutic cancer vaccine. J Clin Oncol. 2002;20:4549–54.PubMedCrossRef
38.
Zurück zum Zitat Hseuh EC, Gupta RK, Qi K, Yee R, Leopoldo ZC, Morton DL. TA90 immune complex predicts survival following surgery and adjuvant vaccine immunotherapy for stage IV melanoma. Cancer J Sci Am. 1997;3:364–70. Hseuh EC, Gupta RK, Qi K, Yee R, Leopoldo ZC, Morton DL. TA90 immune complex predicts survival following surgery and adjuvant vaccine immunotherapy for stage IV melanoma. Cancer J Sci Am. 1997;3:364–70.
39.
Zurück zum Zitat Tsioulias GJ, Gupta RK, Tisman G, et al. Serum TA90 Antigen-antibody complex as a surrogate marker for the efficacy of a polyvalent allogeneic whole-cell vaccine (CancerVax) in Melanoma. Ann Surg Oncol. 2001;8:198–203.PubMedCrossRef Tsioulias GJ, Gupta RK, Tisman G, et al. Serum TA90 Antigen-antibody complex as a surrogate marker for the efficacy of a polyvalent allogeneic whole-cell vaccine (CancerVax) in Melanoma. Ann Surg Oncol. 2001;8:198–203.PubMedCrossRef
40.
Zurück zum Zitat Kelland L. Discontinued drugs in 2005: oncology drugs. Expert Opin Invest Drugs. 2006;15:1309–18.CrossRef Kelland L. Discontinued drugs in 2005: oncology drugs. Expert Opin Invest Drugs. 2006;15:1309–18.CrossRef
41.•
Zurück zum Zitat CancerVax announces results of phase 3 clinical trials of canvaxin™ in patients with stage III and stage IV melanoma. Available at: http://www.marketwired.com/press-release/-675445.htm. Accessed December 29, 2013. This press release reports that the two large randomized Phase III trials evaluating Canvaxin plus BCG vs placebo plus BCG for completely resected stage III and IV melanoma was discontinued prematurely because there was found to be no difference in survival outcomes. CancerVax announces results of phase 3 clinical trials of canvaxin™ in patients with stage III and stage IV melanoma. Available at: http://​www.​marketwired.​com/​press-release/​-675445.​htm. Accessed December 29, 2013. This press release reports that the two large randomized Phase III trials evaluating Canvaxin plus BCG vs placebo plus BCG for completely resected stage III and IV melanoma was discontinued prematurely because there was found to be no difference in survival outcomes.
42.
Zurück zum Zitat Eggermont AMM. Immunotherapy: vaccine trials in melanoma—time for reflection. Nat Rev Clin Oncol. 2009;6:256–8.PubMedCrossRef Eggermont AMM. Immunotherapy: vaccine trials in melanoma—time for reflection. Nat Rev Clin Oncol. 2009;6:256–8.PubMedCrossRef
43.•
Zurück zum Zitat Mackiewic A, Mackiewicz J, Wysocki PJ, et al. Long-term survival of high-risk melanoma patients immunized with a Hyper-IL-6-modified allogeneic whole-cell vaccine after complete resection. Expert Opin Invest Drugs. 2012;21:773–83. This is the first report of an adjuvant allogeneic gene-modified melanoma vaccine studied in two phase II trials as adjuvant therapy in resected stage IIIB, IIIC, and IV melanoma that was found to have a DFS and OS survival advantage when compared with non-treated historical controls.CrossRef Mackiewic A, Mackiewicz J, Wysocki PJ, et al. Long-term survival of high-risk melanoma patients immunized with a Hyper-IL-6-modified allogeneic whole-cell vaccine after complete resection. Expert Opin Invest Drugs. 2012;21:773–83. This is the first report of an adjuvant allogeneic gene-modified melanoma vaccine studied in two phase II trials as adjuvant therapy in resected stage IIIB, IIIC, and IV melanoma that was found to have a DFS and OS survival advantage when compared with non-treated historical controls.CrossRef
44.
Zurück zum Zitat Markowicz S, Nowecki ZI, Rutkowski P, et al. Adjuvant vaccination with melanoma antigen-pulsed dendritic cells in stage III melanoma patients. Med Oncol. 2012;29:2966–77.PubMedCrossRef Markowicz S, Nowecki ZI, Rutkowski P, et al. Adjuvant vaccination with melanoma antigen-pulsed dendritic cells in stage III melanoma patients. Med Oncol. 2012;29:2966–77.PubMedCrossRef
45.
Zurück zum Zitat Petenko NN, Mikhaylova IN, Chkadua GZ, et al. Adjuvant dendritic cell (DC)-based vaccine therapy of melanoma patients. ASCO Annual Meeting Abstracts. J Clin Oncol. 2012;30: [Abstract 2524]. Petenko NN, Mikhaylova IN, Chkadua GZ, et al. Adjuvant dendritic cell (DC)-based vaccine therapy of melanoma patients. ASCO Annual Meeting Abstracts. J Clin Oncol. 2012;30: [Abstract 2524].
46.
Zurück zum Zitat Hu JC, Coffin RS, Davis CJ, et al. A phase I study of OncoVEXGM-CSF, a second generation oncolytic herpes simplex virus expressing granulocyte macrophage colony-stimulating factor. Clin Cancer Res. 2006;15:6737–47.CrossRef Hu JC, Coffin RS, Davis CJ, et al. A phase I study of OncoVEXGM-CSF, a second generation oncolytic herpes simplex virus expressing granulocyte macrophage colony-stimulating factor. Clin Cancer Res. 2006;15:6737–47.CrossRef
47.
Zurück zum Zitat Senzer NN, Kaufman HL, Amatruda T, et al. Phase II clinical trial of a granulocyte-macrophage colony-stimulating factor-encoding, second-generation oncolytic herpes virus in patients with unresectable metastatic melanoma. J Clin Oncol. 2009;27:5763–71.PubMedCrossRef Senzer NN, Kaufman HL, Amatruda T, et al. Phase II clinical trial of a granulocyte-macrophage colony-stimulating factor-encoding, second-generation oncolytic herpes virus in patients with unresectable metastatic melanoma. J Clin Oncol. 2009;27:5763–71.PubMedCrossRef
48.••
Zurück zum Zitat Andtbacka RHI, Collichio F, Amatruda T, et al. OPTIM: a randomized phase 3 trial of talimogene laherparepvec (T-VEC) vs subcutaneous granulocyte-macrophage colony-stimulating factor for the treatment of unresectable stage IIIB/C and IV melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2013;31: [Abstract LBA9008]. This is a prospective phase III trial (OPTIM) that studied patients with stage IIIB, IIIC or IV melanoma that compared administration of an oncolytic vaccine with GM-CSF and a trend toward improved OS vaccine arm. Andtbacka RHI, Collichio F, Amatruda T, et al. OPTIM: a randomized phase 3 trial of talimogene laherparepvec (T-VEC) vs subcutaneous granulocyte-macrophage colony-stimulating factor for the treatment of unresectable stage IIIB/C and IV melanoma. ASCO Annual Meeting Abstracts. J Clin Oncol. 2013;31: [Abstract LBA9008]. This is a prospective phase III trial (OPTIM) that studied patients with stage IIIB, IIIC or IV melanoma that compared administration of an oncolytic vaccine with GM-CSF and a trend toward improved OS vaccine arm.
Metadaten
Titel
Update on Vaccines for High-Risk Melanoma
verfasst von
Sarah A. Weiss, MD
Sunandana Chandra, MD
Anna C. Pavlick, DO
Publikationsdatum
01.06.2014
Verlag
Springer US
Erschienen in
Current Treatment Options in Oncology / Ausgabe 2/2014
Print ISSN: 1527-2729
Elektronische ISSN: 1534-6277
DOI
https://doi.org/10.1007/s11864-014-0283-7

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