Skip to main content

Phase 2 study of the g209-2M melanoma peptide vaccine and low-dose interleukin-2 in advanced melanoma: Cancer and Leukemia Group B 509901.

Publication ,  Journal Article
Roberts, JD; Niedzwiecki, D; Carson, WE; Chapman, PB; Gajewski, TF; Ernstoff, MS; Hodi, FS; Shea, C; Leong, SP; Johnson, J; Zhang, D ...
Published in: J Immunother
2006

High-dose interleukin-2 (IL-2) is the only approved immunologic therapy for advanced melanoma, but response rates are low and significant toxicities limit treatment to otherwise healthy patients. g209-2M is a nanopeptide engineered to mimic an epitope of the gp100 melanocyte differentiation protein that is recognized in a human leukocyte antigen (HLA)-restricted manner by melanoma tumor-infiltrating lymphocytes in some patients. Previous reports indicated that administration of the g209-2M peptide could induce g209-reactive circulating T cells in patients with melanoma and that the combination of g209-2M and high-dose IL-2 might be a more active treatment than high-dose IL-2 alone. Low-dose IL-2 is not active but has significant biologic effects, and because of a different toxicity profile, it can be offered to most patients. The primary objective of this cooperative group phase 2 study was to determine the activity of the combination of g209-2M and low-dose IL-2 in advanced melanoma. Twenty-six HLA appropriate patients with advanced melanoma received subcutaneous g209-2M peptide once every 3 weeks and subcutaneous IL-2 (5 million IU/m) daily for 5 days during the first and second weeks. Patients were monitored for tumor response, toxicity, and induction of g209-reactive circulating T cells. There were no objective responses. There were no toxic deaths and no grade 4 toxicities. More than half of the patients experienced some grade 2 toxicity and one quarter experienced grade 3 toxicity. There was no convincing evidence by enzyme-linked immunospot or tetramer analysis of induction of g209-reactive circulating T cells. The combination of g209-2M and low-dose IL-2 is safe and tolerable but inactive against advanced melanoma. Absence of evidence of immunization raises concerns for peptide-based immunization strategies with concurrent IL-2.

Duke Scholars

Published In

J Immunother

DOI

ISSN

1524-9557

Publication Date

2006

Volume

29

Issue

1

Start / End Page

95 / 101

Location

United States

Related Subject Headings

  • gp100 Melanoma Antigen
  • Skin Neoplasms
  • Peptides
  • Peptide Fragments
  • Neoplasm Recurrence, Local
  • Middle Aged
  • Membrane Glycoproteins
  • Melanoma
  • Male
  • Leukocytes, Mononuclear
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Roberts, J. D., Niedzwiecki, D., Carson, W. E., Chapman, P. B., Gajewski, T. F., Ernstoff, M. S., … Cancer and Leukemia Group B, . (2006). Phase 2 study of the g209-2M melanoma peptide vaccine and low-dose interleukin-2 in advanced melanoma: Cancer and Leukemia Group B 509901. J Immunother, 29(1), 95–101. https://doi.org/10.1097/01.cji.0000195295.74104.ad
Roberts, John D., Donna Niedzwiecki, William E. Carson, Paul B. Chapman, Thomas F. Gajewski, Marc S. Ernstoff, F Stephen Hodi, et al. “Phase 2 study of the g209-2M melanoma peptide vaccine and low-dose interleukin-2 in advanced melanoma: Cancer and Leukemia Group B 509901.J Immunother 29, no. 1 (2006): 95–101. https://doi.org/10.1097/01.cji.0000195295.74104.ad.
Roberts JD, Niedzwiecki D, Carson WE, Chapman PB, Gajewski TF, Ernstoff MS, et al. Phase 2 study of the g209-2M melanoma peptide vaccine and low-dose interleukin-2 in advanced melanoma: Cancer and Leukemia Group B 509901. J Immunother. 2006;29(1):95–101.
Roberts, John D., et al. “Phase 2 study of the g209-2M melanoma peptide vaccine and low-dose interleukin-2 in advanced melanoma: Cancer and Leukemia Group B 509901.J Immunother, vol. 29, no. 1, 2006, pp. 95–101. Pubmed, doi:10.1097/01.cji.0000195295.74104.ad.
Roberts JD, Niedzwiecki D, Carson WE, Chapman PB, Gajewski TF, Ernstoff MS, Hodi FS, Shea C, Leong SP, Johnson J, Zhang D, Houghton A, Haluska FG, Cancer and Leukemia Group B. Phase 2 study of the g209-2M melanoma peptide vaccine and low-dose interleukin-2 in advanced melanoma: Cancer and Leukemia Group B 509901. J Immunother. 2006;29(1):95–101.

Published In

J Immunother

DOI

ISSN

1524-9557

Publication Date

2006

Volume

29

Issue

1

Start / End Page

95 / 101

Location

United States

Related Subject Headings

  • gp100 Melanoma Antigen
  • Skin Neoplasms
  • Peptides
  • Peptide Fragments
  • Neoplasm Recurrence, Local
  • Middle Aged
  • Membrane Glycoproteins
  • Melanoma
  • Male
  • Leukocytes, Mononuclear