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Integrative multi-omics analysis uncovers tumor-immune-gut axis influencing immunotherapy outcomes in ovarian cancer

  • Spencer R. Rosario
  • , Mark D. Long
  • , Shanmuga Chilakapati
  • , Eduardo Cortes Gomez
  • , Sebastiano Battaglia
  • , Prashant K. Singh
  • , Jianmin Wang
  • , Katy Wang
  • , Kristopher Attwood
  • , Suzanne M. Hess
  • , AJ Robert McGray
  • , Kunle Odunsi
  • , Brahm H. Segal
  • , Gyorgy Paragh
  • , Song Liu
  • , Jennifer A. Wargo
  • , Emese Zsiros
  • Roswell Park Cancer Institute
  • Northeastern University
  • Janssen Pharmaceuticals
  • American College of Radiology
  • The University of Chicago
  • University of Texas MD Anderson Cancer Center

Research output: Contribution to journal › Article › peer-review

38 Scopus citations

Abstract

Recurrent ovarian cancer patients, especially those resistant to platinum, lack effective curative treatments. To address this, we conducted a phase 2 clinical trial (NCT02853318) combining pembrolizumab with bevacizumab, to increase T cell infiltration into the tumor, and oral cyclophosphamide, to reduce the number of regulatory T cells. The trial accrued 40 heavily pretreated recurrent ovarian cancer patients. The primary endpoint, progression free survival, was extended to a median of 10.2 months. The secondary endpoints demonstrated an objective response rate of 47.5%, and disease control in 30% of patients for over a year while maintaining a good quality of life. We performed comprehensive molecular, immune, microbiome, and metabolic profiling on samples of trial patients. Here, we show increased T and B cell clusters and distinct microbial patterns with amino acid and lipid metabolism are linked to exceptional clinical responses. This study suggests the immune milieu and host-microbiome can be leveraged to improve antitumor response in future immunotherapy trials.

Original languageEnglish
Article number10609
JournalNature Communications
Volume15
Issue number1
DOIs
StatePublished - Dec 2024

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