4.8 Article

Microbiota as Predictor of Mortality in Allogeneic Hematopoietic-Cell Transplantation

Journal

NEW ENGLAND JOURNAL OF MEDICINE
Volume 382, Issue 9, Pages 822-834

Publisher

MASSACHUSETTS MEDICAL SOC
DOI: 10.1056/NEJMoa1900623

Keywords

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Funding

  1. National Cancer Institute [R01-CA228308, R01 CA203950-01, R01CA203950-01, P30 CA008748, P01-CA023766]
  2. National Heart, Lung, and Blood Institute [K08HL143189-01A1, 1R01HL124112]
  3. National Institute of Allergy and Infectious Diseases [U01 AI124275, R01 AI032135, AI095706, R01 AI137269-01, 9R01AI100288]
  4. National Institutes of Health [KL2 TR001115-03]
  5. Claude D. Pepper Older Americans Independence Center of the National Institute on Aging [2P30AG028716-11]
  6. Lymphoma Foundation
  7. Sawiris Foundation
  8. Society of MSK
  9. Empire Clinical Research Investigator Program
  10. Seres Therapeutics
  11. Japan Society for the Promotion of Science [17H04206, 17K09945]
  12. Japan Science and Technology Agency
  13. Mochida Memorial Foundation for Medical and Pharmaceutical Research
  14. Conquer Cancer Foundation
  15. Gilead Sciences
  16. Alfonso Martin Escudero Foundation
  17. MSK Cycle for Survival
  18. Collaborative Research Center Transregio 221
  19. Grants-in-Aid for Scientific Research [17K09945, 17H04206] Funding Source: KAKEN

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In this study, the gastrointestinal microbiome was serially monitored in patients undergoing allogeneic hematopoietic-cell transplantation at four centers. Lower microbial diversity was associated with poorer outcomes after HCT. Background Relationships between microbiota composition and clinical outcomes after allogeneic hematopoietic-cell transplantation have been described in single-center studies. Geographic variations in the composition of human microbial communities and differences in clinical practices across institutions raise the question of whether these associations are generalizable. Methods The microbiota composition of fecal samples obtained from patients who were undergoing allogeneic hematopoietic-cell transplantation at four centers was profiled by means of 16S ribosomal RNA gene sequencing. In an observational study, we examined associations between microbiota diversity and mortality using Cox proportional-hazards analysis. For stratification of the cohorts into higher- and lower-diversity groups, the median diversity value that was observed at the study center in New York was used. In the analysis of independent cohorts, the New York center was cohort 1, and three centers in Germany, Japan, and North Carolina composed cohort 2. Cohort 1 and subgroups within it were analyzed for additional outcomes, including transplantation-related death. Results We profiled 8767 fecal samples obtained from 1362 patients undergoing allogeneic hematopoietic-cell transplantation at the four centers. We observed patterns of microbiota disruption characterized by loss of diversity and domination by single taxa. Higher diversity of intestinal microbiota was associated with a lower risk of death in independent cohorts (cohort 1: 104 deaths among 354 patients in the higher-diversity group vs. 136 deaths among 350 patients in the lower-diversity group; adjusted hazard ratio, 0.71; 95% confidence interval [CI], 0.55 to 0.92; cohort 2: 18 deaths among 87 patients in the higher-diversity group vs. 35 deaths among 92 patients in the lower-diversity group; adjusted hazard ratio, 0.49; 95% CI, 0.27 to 0.90). Subgroup analyses identified an association between lower intestinal diversity and higher risks of transplantation-related death and death attributable to graft-versus-host disease. Baseline samples obtained before transplantation already showed evidence of microbiome disruption, and lower diversity before transplantation was associated with poor survival. Conclusions Patterns of microbiota disruption during allogeneic hematopoietic-cell transplantation were similar across transplantation centers and geographic locations; patterns were characterized by loss of diversity and domination by single taxa. Higher diversity of intestinal microbiota at the time of neutrophil engraftment was associated with lower mortality. (Funded by the National Cancer Institute and others.)

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