Neoantigen responses, immune correlates, and favorable outcomes after ipilimumab treatment of patients with prostate cancer

Author:

Subudhi Sumit K.1ORCID,Vence Luis2ORCID,Zhao Hao2ORCID,Blando Jorge2,Yadav Shalini S.2,Xiong Qing2,Reuben Alexandre3ORCID,Aparicio Ana1ORCID,Corn Paul G.1ORCID,Chapin Brian F.4,Pisters Louis L.4,Troncoso Patricia5,Tidwell Rebecca Slack6ORCID,Thall Peter6,Wu Chang-Jiun7ORCID,Zhang Jianhua7ORCID,Logothetis Christopher L.1ORCID,Futreal Andrew7ORCID,Allison James P.28ORCID,Sharma Padmanee128ORCID

Affiliation:

1. Department of Genitourinary Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

2. Immunotherapy Platform, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

3. Department of Thoracic Head and Neck Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

4. Department of Urology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

5. Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

6. Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

7. Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

8. Department of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Abstract

Low–tumor mutational burden prostate tumors express neoantigens that elicit T cell responses associated with favorable clinical outcomes to ipilimumab.

Funder

Prostate Cancer Foundation

University of Texas MD Anderson Cancer Center

Stand Up To Cancer

Parker Institute for Cancer Immunotherapy

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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