Immune-Related Colitis Is Associated with Fecal Microbial Dysbiosis and Can Be Mitigated by Fecal Microbiota Transplantation

Author:

Elkrief Arielle123ORCID,Waters Nicholas R.4ORCID,Smith Natalie4ORCID,Dai Angel4ORCID,Slingerland John4ORCID,Aleynick Nathan14ORCID,Febles Binita4ORCID,Gogia Pooja3ORCID,Socci Nicholas D.56ORCID,Lumish Melissa7ORCID,Giardina Paul A.4ORCID,Chaft Jamie E.38ORCID,Eng Juliana38ORCID,Motzer Robert J.89ORCID,Mendelsohn Robin B.78ORCID,Markey Kate A.1011ORCID,Zhuang Mingqiang14ORCID,Li Yanyun14ORCID,Yang Zhifan14ORCID,Hollmann Travis J.112ORCID,Rudin Charles M.38ORCID,van den Brink Marcel R.M.4813ORCID,Shia Jinru1ORCID,DeWolf Susan14ORCID,Schoenfeld Adam J.38ORCID,Hellmann Matthew D.38ORCID,Babady N. Esther1516ORCID,Faleck David M.817ORCID,Peled Jonathan U.813ORCID

Affiliation:

1. 1Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

2. 2Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.

3. 3Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

4. 4Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.

5. 5Bioinformatics Core Facility, Memorial Sloan Kettering Cancer Center, New York, New York.

6. 6Marie-Josée & Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.

7. 7Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

8. 8Weill Cornell Medical College, New York, New York.

9. 9Genitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

10. 10Fred Hutchinson Cancer Center, Seattle, Washington.

11. 11Division of Medical Oncology, University of Washington, Seattle, Washington.

12. 12Bristol Myers Squibb, Princeton, New Jersey.

13. 13Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

14. 14Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

15. 15Clinical Microbiology Service, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

16. 16Infectious Disease Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

17. 17Gastroenterology, Hepatology and Nutrition Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Abstract

Abstract Colitis induced by treatment with immune-checkpoint inhibitors (ICI), termed irColitis, is a substantial cause of morbidity complicating cancer treatment. We hypothesized that abnormal fecal microbiome features would be present at the time of irColitis onset and that restoring the microbiome with fecal transplant from a healthy donor would mitigate disease severity. Herein, we present fecal microbiota profiles from 18 patients with irColitis from a single center, 5 of whom were treated with healthy-donor fecal microbial transplantation (FMT). Although fecal samples collected at onset of irColitis had comparable α-diversity to that of comparator groups with gastrointestinal symptoms, irColitis was characterized by fecal microbial dysbiosis. Abundances of Proteobacteria were associated with irColitis in multivariable analyses. Five patients with irColitis refractory to steroids and biologic anti-inflammatory agents received healthy-donor FMT, with initial clinical improvement in irColitis symptoms observed in four of five patients. Two subsequently exhibited recurrence of irColitis symptoms following courses of antibiotics. Both received a second “salvage” FMT that was, again, followed by clinical improvement of irColitis. In summary, we observed distinct microbial community changes that were present at the time of irColitis onset. FMT was followed by clinical improvements in several cases of steroid- and biologic-agent-refractory irColitis. Strategies to restore or prevent microbiome dysbiosis in the context of immunotherapy toxicities should be further explored in prospective clinical trials.

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Immunology

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