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88 Evidence of enhanced immune activation within the tumor microenvironment and the circulation of female patients with high-risk melanoma compared to males
  1. Mariam Saad1,
  2. Aik Choon Tan2,
  3. Issam El Naqa2,
  4. Sandra Lee3,
  5. F Stephen Hodi4,
  6. Lisa Butterfield5,
  7. William LaFramboise6,
  8. Walter Storkus7,
  9. Jose Conejo-Garcia2,
  10. Patrick Hwu2,
  11. Howard Streicher8,
  12. Vernon Sondak2,
  13. John Kirkwood9 and
  14. Ahmad Tarhini2
  1. 1American University of Beirut, Detroit, MI, USA
  2. 2H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA
  3. 3Harvard Medical School, Dana Farber Cancer Institute, ECOG-ACRIN Biostatistics Center, Boston, MA, USA
  4. 4Dana-Farber/Harvard Cancer Center, Boston, MA, USA
  5. 5Parker Institute for Cancer Immunotherapy, San Francisco, CA, USA
  6. 6Allegheny General Hospital, Pittsburgh, PA, USA
  7. 7University of Pittsburgh, Pittsburgh, PA, USA
  8. 8National Cancer Institute, Chevy Chase, MD, USA
  9. 9UPMC Hillman Cancer Center, Pittsburgh, PA, USA


Background Sex differences in tumor immunity and response to immunotherapy were shown in murine models and descriptive analyses from recent clinical trials. We recently reported that female gender is a favorable prognostic marker for survival benefit following ipilimumab and high dose interferon-alfa (HDI) adjuvant therapy of high-risk melanoma in the ECOG-ACRIN E1609 trial (N=1670). Therefore, we investigated differences in candidate immune biomarkers in the circulation and tumor microenvironment (TME) of female and male patients.

Methods Gene expression profiling (GEP) was performed on the tumor biopsies of 718 (454 male, 264 female) patients. The primary endpoint was mRNA expression profiling using U133A 2.0 Affymetrix gene chips. Raw microarray data sets were normalized by using the Robust Multi-array Average (RMA) method using Affymetrix Power Tools (APT) as previously published. Multiple probe sets representing the same genes were collapsed by using the probe with maximum gene expression. Gene set enrichment analysis (GSEA) was performed by comparing the female and male tumor samples, and gene sets with FDR q-value <0.1 were deemed as significant. Similarly, peripheral blood (serum and PBMC) samples were tested for soluble (Luminex) and cellular (multicolor flow cytometry) prognostic biomarkers in a subset of patients (N=321; 109 female and 212 male). All patients provided an IRB-approved written informed consent.

Results Among the subset of patients tested for circulating biomarkers, females were significantly younger than males (P=0.03). Testing PBMCs, the percentages of CD3+ T cells (P=0.04) and CD3+CD4+ helper T cells (P=0.0005) were significantly higher in female patients compared to males. Also, there were trends toward higher levels of proinflammatory cytokines IL1beta (P=0.07) and IL6 (P=0.06) in females. On the other hand, males had significantly higher percentages of monocytes (P=0.03). Further, there were trends toward higher percentages of CD3+/CD4+/CD25hi+/Foxp3+ (P=0.1) and CD3+/CD4+/CD25+/CD127low+ (P=0.1) T-reg in male patients compared to females. Among the cohort of patients (N=718) with tumor GEP data, females were significantly younger than males (P=0.0009). GEP identified pathways and genes related to immune cell infiltration and activation that were significantly enriched in the tumors of females compared to males (table 1).

Abstract 88 Table 1

Immune pathways significantly enriched in tumors of females

Conclusions Female gender was associated with adjuvant immunotherapeutic benefits and female patients were more likely to have evidence of immune activation within the TME and the circulation, supporting a potentially important role for female related factors in the immune response against melanoma, and these require further investigation.

Acknowledgements We are grateful to the patients and family members who participated in the E1609 trial and the E1609 trial investigators. This study was conducted by the ECOG-ACRIN Cancer Research Group (Peter J. O’Dwyer, MD and Mitchell D. Schnall, MD, PhD, Group Co-Chairs) and supported by the National Cancer Institute of the National Institutes of Health under the following award numbers: U10CA180794, U10CA180820, U10CA180888, UG1CA233180, UG1CA233184. Biomarkers studies were supported under the following award number: P50CA12197310 (Tarhini and Kirkwood). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Trial Registration NCT01274338

Ethics Approval The E1609 study protocol was approved by the institutional review board of each participating institution and conducted in accordance with Good Clinical Practice guidelines as defined by the International Conference on Harmonization. All patients provided an IRB-approved written informed consent.

Consent Not applicable.

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