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PMID: 18765555 Published · ppublish English Journal Article

Treatment of metastatic melanoma using interleukin-2 alone or in conjunction with vaccines.

Smith FO, Downey SG, Klapper JA, Yang JC, Sherry RM, Royal RE, Kammula US, Hughes MS, Restifo NP, Levy CL, White DE, Steinberg SM, Rosenberg SA

Abstract

To identify prognostic factors associated with survival beyond 4 years and overall response in patients with metastatic melanoma treated with high-dose bolus i.v. interleukin-2 (IL-2) given either alone or in combination with a variety of melanoma vaccines. 684 consecutive patients with metastatic melanoma received high-dose bolus i.v. IL-2 either alone or in conjunction with a variety of melanoma vaccines. Treatments occurred between August 1, 1985 and January 1, 2006. The overall objective response rate was 13% for patients receiving IL-2 alone and 16% for patients who received IL-2 with vaccine. In patients treated with IL-2 alone (n=305) and IL-2 with vaccine (n=379), having an objective response was associated with survival beyond 4 years (P<0.0001). No pretreatment factors could be identified that were strongly associated with increased rate of objective response or long-term survival in patients receiving IL-2 alone. In patients receiving IL-2 with vaccines, there were increased response rates in patients with s.c. or cutaneous disease only and lower response rates with visceral disease only. Patients who received the gp100:209-217(210M) peptide plus IL-2 showed a strong trend to increased objective responses compared with IL-2 alone (22% versus 12.8%; P=0.01) and also compared with patients who received a variety of vaccines that did not include this immunogenic peptide (13.8%; P=0.009). IL-2 can produce a modest response rate in patients with metastatic melanoma including patients with durable complete responses. S.c. or cutaneous disease only and vaccination with gp100:209-217(210M) peptide was associated with significant increase in response rates.

MeSH Terms
Adolescent Adult Aged Antigens, Neoplasm/immunology,therapeutic use Cancer Vaccines/therapeutic use Child Combined Modality Therapy Female Humans Interleukin-2/administration & dosage Male Melanoma/mortality,therapy Membrane Glycoproteins/immunology,therapeutic use Middle Aged Neoplasm Metastasis Prognosis Skin Neoplasms/mortality,therapy Survival Analysis Treatment Outcome gp100 Melanoma Antigen
Chemicals
Antigens, Neoplasm Cancer Vaccines Interleukin-2 Membrane Glycoproteins PMEL protein, human gp100 Melanoma Antigen
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Smith Franz O
Surgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland 20892-1201, USA. franz_smith@nih.gov
Downey Stephanie G
Klapper Jacob A
Yang James C
Sherry Richard M
Royal Richard E
Kammula Udai S
Hughes Marybeth S
Restifo Nicholas P
Levy Catherine L
White Donald E
Steinberg Seth M
Rosenberg Steven A
References (26)
26 references, click to expand
  1. Functional analysis of antigen-specific T lymphocytes by serial measurement of gene expression in peripheral blood mononuclear cells and tumor specimens.
    J Immunol. 1999 Dec 15;163(12):6867-75 PMID: 10586088
  2. An evidence-based staging system for cutaneous melanoma.
    CA Cancer J Clin. 2004 May-Jun;54(3):131-49; quiz 182-4 PMID: 15195788
  3. Inability to immunize patients with metastatic melanoma using plasmid DNA encoding the gp100 melanoma-melanocyte antigen.
    Hum Gene Ther. 2003 May 20;14(8):709-14 PMID: 12804135
  4. High-dose regimen of interleukin-2 and interferon-alpha in combination with lymphokine-activated killer cells in patients with metastatic renal cell cancer.
    J Immunother. 1997 Jul;20(4):312-20 PMID: 9220321
  5. Immunizing patients with metastatic melanoma using recombinant adenoviruses encoding MART-1 or gp100 melanoma antigens.
    J Natl Cancer Inst. 1998 Dec 16;90(24):1894-900 PMID: 9862627
  6. Durability of complete responses in patients with metastatic cancer treated with high-dose interleukin-2: identification of the antigens mediating response.
    Ann Surg. 1998 Sep;228(3):307-19 PMID: 9742914
  7. Thyroid dysfunction in 281 patients with metastatic melanoma or renal carcinoma treated with interleukin-2 alone.
    J Immunother Emphasis Tumor Immunol. 1995 Nov;18(4):272-8 PMID: 8680655
  8. Guidelines for the safe administration of high-dose interleukin-2.
    J Immunother. 2001 Jul-Aug;24(4):287-93 PMID: 11565830
  9. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada.
    J Natl Cancer Inst. 2000 Feb 2;92(3):205-16 PMID: 10655437
  10. Immunization against epitopes in the human melanoma antigen gp100 following patient immunization with synthetic peptides.
    Cancer Res. 1996 Oct 15;56(20):4749-57 PMID: 8840994
  11. Effects of route and formulation on clinical pharmacokinetics of interleukin-2.
    Clin Pharmacokinet. 1994 Jul;27(1):19-31 PMID: 7955769
  12. Immunologic and therapeutic evaluation of a synthetic peptide vaccine for the treatment of patients with metastatic melanoma.
    Nat Med. 1998 Mar;4(3):321-7 PMID: 9500606
  13. Identification of new melanoma epitopes on melanosomal proteins recognized by tumor infiltrating T lymphocytes restricted by HLA-A1, -A2, and -A3 alleles.
    J Immunol. 1998 Dec 15;161(12):6985-92 PMID: 9862734
  14. Treatment of 283 consecutive patients with metastatic melanoma or renal cell cancer using high-dose bolus interleukin 2.
    JAMA. 1994 Mar 23-30;271(12):907-13 PMID: 8120958
  15. High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: analysis of 270 patients treated between 1985 and 1993.
    J Clin Oncol. 1999 Jul;17(7):2105-16 PMID: 10561265
  16. Factors associated with response to high-dose interleukin-2 in patients with metastatic melanoma.
    J Clin Oncol. 2001 Aug 1;19(15):3477-82 PMID: 11481353
  17. Correlates of response to IL-2 therapy in patients treated for metastatic renal cancer and melanoma.
    Cancer J Sci Am. 1996 Mar-Apr;2(2):91-8 PMID: 9166506
  18. Reporting results of cancer treatment.
    Cancer. 1981 Jan 1;47(1):207-14 PMID: 7459811
  19. Low-dose subcutaneous recombinant interleukin-2 in advanced human malignancy: a phase II outpatient study.
    Mol Biother. 1990 Mar;2(1):18-26 PMID: 2334534
  20. Cancer immunotherapy: moving beyond current vaccines.
    Nat Med. 2004 Sep;10(9):909-15 PMID: 15340416
  21. Low-dose intravenous bolus interleukin-2 with interferon-alpha therapy for metastatic melanoma and renal cell carcinoma.
    J Immunother. 1998 Jan;21(1):56-61 PMID: 9456437
  22. Daily low-dose subcutaneous recombinant interleukin-2 by alternate weekly administration: antitumor activity and immunomodulatory effects.
    Am J Clin Oncol. 1998 Feb;21(1):48-53 PMID: 9499257
  23. Improved induction of melanoma-reactive CTL with peptides from the melanoma antigen gp100 modified at HLA-A*0201-binding residues.
    J Immunol. 1996 Sep 15;157(6):2539-48 PMID: 8805655
  24. Interleukin-2: clinical applications.
    Semin Oncol. 2002 Jun;29(3 Suppl 7):12-7 PMID: 12068383
  25. Cancer statistics, 2007.
    CA Cancer J Clin. 2007 Jan-Feb;57(1):43-66 PMID: 17237035
  26. Recombinant fowlpox viruses encoding the anchor-modified gp100 melanoma antigen can generate antitumor immune responses in patients with metastatic melanoma.
    Clin Cancer Res. 2003 Aug 1;9(8):2973-80 PMID: 12912944
Article Info
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Abbr.
Clin Cancer Res
ISSN
1078-0432
Published
2008-09-01
Pages
5610-8
Language
English
Region
United States
NLM ID
9502500
PMCID
PMC2656367
Subset
IM
Grants
Intramural NIH HHS · Z01 SC003811-33 · United States
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