Skip to content

Advertisement

  • Poster presentation
  • Open Access

Relationship between immune gene signatures and clinical response to PD-1 blockade with pembrolizumab (MK-3475) in patients with advanced solid tumors

  • Mark Ayers1,
  • Jared Lunceford1,
  • Michael Nebozhyn1,
  • Erin Murphy2,
  • Andrey Loboda1,
  • Andrew Albright1,
  • Jonathan Cheng1,
  • S Peter Kang1,
  • Scot Ebbinghaus1,
  • Jennifer Yearley1,
  • Veena Shankaran3,
  • Tanguy Seiwert4,
  • Antoni Ribas5 and
  • Terri McClanahan1
Journal for ImmunoTherapy of Cancer20153(Suppl 2):P80

https://doi.org/10.1186/2051-1426-3-S2-P80

Published: 4 November 2015

Keywords

Gastric CancerMelanomaImmune CheckpointAdvanced Solid TumorImmune Signature

Background

Immune checkpoint inhibition with anti–PD-1 monoclonal antibodies such as pembrolizumab has demonstrated robust, durable anti-tumor activity against many advanced malignancies. We analyzed immune-related gene expression profiles in pembrolizumab-treated patients with advanced solid tumors to identify immune gene signatures correlated with clinical benefit.

Methods

RNA was extracted from formalin-fixed, paraffin-embedded sections of baseline tumor samples and analyzed using a custom 680-gene set on the NanoString nCounter platform. A 10-gene preliminary “interferon-gamma” (IFN-γ) signature was developed in a discovery set of 19 patients with melanoma treated with pembrolizumab in the Phase 1b KEYNOTE-001 study (NCT01295827) and was later complemented with a 28-gene preliminary “expanded immune” signature. These 2 signatures were subsequently tested and refined in an independent cohort of 62 additional patients with melanoma treated in KEYNOTE-001. Further evaluation of the refined signatures was performed in 43 patients with head and neck squamous cell carcinoma (HNSCC) and 33 patients with gastric cancer enrolled in the Phase 1b KEYNOTE-012 study (NCT01848834).

Results

In the melanoma validation set, the IFN-γ and expanded immune signatures were significantly correlated with ORR (P=0.047 and 0.027) and PFS (P=0.016 and 0.015). The IFN-γ signature was refined from 10 genes to 6, and the expanded immune signature from 28 genes to 18. Two new signatures enriched in T cell markers and MHC class I and II genes were enumerated based on analysis of top-ranked genes on the platform in melanoma samples: “TCR signaling” (13 genes) and “de novo” (33 genes). All signatures were independently tested in HNSCC and gastric cancer and found to be significantly correlated with clinical benefit (Table 1). Tumors lacking an immune phenotype, as suggested by low values of signature scores, did not respond to pembrolizumab. Some non-responders had scores similar to those of responders, suggesting an immune phenotype is necessary but not sufficient for response.
Table 1

Nominal 1-sided P values for ORR and PFS calculated from logistic and Cox regression, respectively, using signature score as a continuous variable.

Signature

HNSCC

Gastric Cancer

 

ORR

PFS

ORR

PFS

IFN-λ

0.005

<0.001

0.077

0.032

TCR signaling

0.071

0.002

0.034

0.024

Expanded immune

0.015

<0.001

0.062

0.049

De novo

0.018

<0.001

0.068

0.037

Conclusions

Immune-related gene expression signatures composed of genes associated with T cell cytotoxic function, antigen presentation machinery, and IFN-γ signaling represent reproducible and sensitive tools that define common features of the immune microenvironment associated with response to pembrolizumab across multiple tumor types.

Authors’ Affiliations

(1)
Merck & Co., Inc., Kenilworth, USA
(2)
Merck & Co., Inc., Palo Alto, USA
(3)
University of Washington, Seattle, USA
(4)
The University of Chicago, Chicago, USA
(5)
University of California at Los Angeles Medical Center, Los Angeles, USA

Copyright

© Ayers et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Advertisement