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Abstract B140: Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2

Publication ,  Journal Article
Wong, MKK; Morse, MA; McDermott, DF; Clark, JI; Kaufman, HL; Daniels, GA; Hua, H; Aung, S
Published in: Cancer Immunology Research
January 1, 2016

Background: The PROCLAIMSM registry (www.proclaimregistry.com), created in 2011, is the largest collection of IL-2 treated patients in the US and provides real-time insights into sequencing or combining IL-2 with new and old therapies and how this may affect patient outcomes. Previously, we reported a median overall survival (mOS) of 20 months with a median follow-up of 37 months in metastatic melanoma (mM) patients treated with high dose IL-2 (HD IL-2) between 2007 and 2012 from a retrospective cohort. These findings led to the hypothesis that improved mOS may have been a result of subsequent salvage therapies, including checkpoint inhibitors.Purpose: To report on the analysis of survival data from 26 sites.Methods: Patients must have received at least one dose of HD IL-2 for this analysis. Those that received checkpoint therapy prior to HD IL-2 were excluded. Statistics and survival analysis on prospectively entered patients were performed on datasets as of March 16th, 2015.Results: The median overall survival (mOS) for the 236 patients was 18.4 months with a median follow-up of 21.7 months. Patients were stratified into three groups; HD IL-2 only (n=123), HD IL-2 followed by ipilimumab (Post ipi, n=78), and HD IL-2 followed by PD-1 inhibitors (Post αPD-1, n=35). There were four patients in the Post αPD-1 group that received anti-PD-L1 treatment. Patients in the HD IL-2 only, Post ipi, and Post αPD-1 groups achieved a mOS of 14, 15.7, and 28.7 months, respectively. The estimated 12-month survival rates were 56%, 64%, and 97%, respectively. There were 10/78 (13%) and 3/35 (8.6%) post therapy treatment-related incidences of autoimmune events in the Post Ipi and Post αPD-1 groups, respectively. No treatment related deaths were reported.Conclusions: This is the first report of clinical data relating to HD IL-2 use followed by checkpoint blockade of the PD-1 pathway. Treatment with anti-PD-1 after initial therapy with HD IL-2 had significantly prolonged survival compared to patients treated with ipilimumab. Moreover, improved survival was not observed in patients treated with follow-on ipilimumab compared to patients treated only with HD IL-2. Anti-PD-1 therapy after HD IL-2, appears to be safe, is therapeutically active. These data support the concept of investigating IL-2 therapy in combination or sequence with newly developed immune checkpoint inhibitors.Citation Format: Michael K.K. Wong, Michael A. Morse, David F. McDermott, Joseph I. Clark, Howard L. Kaufman, Gregory A. Daniels, Hong Hua, Sandra Aung. Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2. [abstract]. In: Proceedings of the CRI-CIMT-EATI-AACR Inaugural International Cancer Immunotherapy Conference: Translating Science into Survival; September 16-19, 2015; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2016;4(1 Suppl):Abstract nr B140.

Duke Scholars

Published In

Cancer Immunology Research

DOI

EISSN

2326-6074

ISSN

2326-6066

Publication Date

January 1, 2016

Volume

4

Issue

1_Supplement

Start / End Page

B140 / B140

Publisher

American Association for Cancer Research (AACR)

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 3204 Immunology
  • 1115 Pharmacology and Pharmaceutical Sciences
  • 1112 Oncology and Carcinogenesis
  • 1107 Immunology
 

Citation

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Wong, M. K. K., Morse, M. A., McDermott, D. F., Clark, J. I., Kaufman, H. L., Daniels, G. A., … Aung, S. (2016). Abstract B140: Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2. Cancer Immunology Research, 4(1_Supplement), B140–B140. https://doi.org/10.1158/2326-6074.cricimteatiaacr15-b140
Wong, Michael K. K., Michael A. Morse, David F. McDermott, Joseph I. Clark, Howard L. Kaufman, Gregory A. Daniels, Hong Hua, and Sandra Aung. “Abstract B140: Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2.” Cancer Immunology Research 4, no. 1_Supplement (January 1, 2016): B140–B140. https://doi.org/10.1158/2326-6074.cricimteatiaacr15-b140.
Wong MKK, Morse MA, McDermott DF, Clark JI, Kaufman HL, Daniels GA, et al. Abstract B140: Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2. Cancer Immunology Research. 2016 Jan 1;4(1_Supplement):B140–B140.
Wong, Michael K. K., et al. “Abstract B140: Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2.” Cancer Immunology Research, vol. 4, no. 1_Supplement, American Association for Cancer Research (AACR), Jan. 2016, pp. B140–B140. Crossref, doi:10.1158/2326-6074.cricimteatiaacr15-b140.
Wong MKK, Morse MA, McDermott DF, Clark JI, Kaufman HL, Daniels GA, Hua H, Aung S. Abstract B140: Overall survival of metastatic melanoma patients treated with HD IL-2 followed by immune checkpoint blockade of the CTLA-4 or the PD-1 pathways: Analysis of data on the current use of HD IL-2. Cancer Immunology Research. American Association for Cancer Research (AACR); 2016 Jan 1;4(1_Supplement):B140–B140.

Published In

Cancer Immunology Research

DOI

EISSN

2326-6074

ISSN

2326-6066

Publication Date

January 1, 2016

Volume

4

Issue

1_Supplement

Start / End Page

B140 / B140

Publisher

American Association for Cancer Research (AACR)

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 3204 Immunology
  • 1115 Pharmacology and Pharmaceutical Sciences
  • 1112 Oncology and Carcinogenesis
  • 1107 Immunology