Enteric Microbiome Markers as Early Predictors of Clinical Outcome in Allogeneic Hematopoietic Stem Cell Transplant: Results of a Prospective Study in Adult Patients

Author:

Mancini Nicasio12,Greco Raffaella3,Pasciuta Renée1,Barbanti Maria Chiara3,Pini Giacomo1,Morrow Olivia Beatrice1,Morelli Mara3,Vago Luca3,Clementi Nicola2,Giglio Fabio3,Lupo Stanghellini Maria Teresa3,Forcina Alessandra3,Infurnari Laura1,Marktel Sarah3,Assanelli Andrea3,Carrabba Matteo3,Bernardi Massimo3,Corti Consuelo3,Burioni Roberto12,Peccatori Jacopo3,Sormani Maria Pia4,Banfi Giuseppe5,Ciceri Fabio36,Clementi Massimo12

Affiliation:

1. Laboratory of Microbiology and Virology, San Raffaele Scientific Institute, Milan, Italy

2. Department of Microbiology and Virology, University “Vita-Salute” San Raffaele, Milan, Italy

3. Hematology and Bone Marrow Transplantation Unit, Division of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, Milan, Italy

4. Department of Health Sciences (DISSAL) University of Genoa, Italy

5. Galeazzi Scientific Institute and University “Vita-Salute” San Raffaele, Milan, Italy

6. Department of Hematology and Bone Marrow Transplantation, University “Vita-Salute” San Raffaele, Milan, Italy

Abstract

Abstract Background Infections and graft-vs-host disease (GvHD) still represent major, not easily predictable complications in allogeneic hematopoietic stem cell transplant (allo-HSCT). Both conditions have been correlated to altered enteric microbiome profiles during the peritransplant period. The main objective of this study was to identify possible early microbiome-based markers useful in pretransplant risk stratification. Methods Stool samples were collected from 96 consecutive patients at the beginning of the pretransplant conditioning regimen (T0) and at 10 (T1) and 30 (T2) days following transplant. When significant in univariate analysis, the identified microbiome markers were used in multivariate regression analyses, together with other significant clinical variables for allo-HSCT-related risk stratification. Four main outcomes were addressed: (1) septic complications, (2) GvHD, (3) relapse of the underlying disease, and (4) mortality. Results The presence of >5% proinflammatory Enterobacteriaceae at T0 was the only significant marker for the risk of microbiologically confirmed sepsis. Moreover, ≤10% Lachnospiraceae at T0 was the only significant factor for increased risk of overall mortality, including death from both infectious and noninfectious causes. Finally, a low bacterial alpha-diversity (Shannon index ≤ 1.3) at T1 was the only variable significantly correlating with an increased risk of GvHD within 30 days. Conclusions Microbiome markers can be useful in the very early identification of patients at risk for major transplant-related complications, offering new tools for individualized preemptive or therapeutic strategies to improve allo-HSCT outcomes.

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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