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Minimal residual disease negativity in multiple myeloma is associated with intestinal microbiota composition
- Source :
- Blood Advances. 3:2040-2044
- Publication Year :
- 2019
- Publisher :
- American Society of Hematology, 2019.
-
Abstract
- Patients with multiple myeloma (MM) who achieve minimal residual disease (MRD) negativity after upfront treatment have superior outcomes compared with those who remain MRD+. Recently, associations have been shown between specific commensal microbes and development of plasma cell disorders. Here, we report the association between intestinal microbiota composition and treatment outcome in MM. Microbiota composition of fecal samples collected from 34 MM patients after induction therapy and at the time of flow cytometry–based bone marrow MRD testing was determined by 16S ribosomal RNA sequencing. We observed a higher relative abundance of Eubacterium hallii in the 16 MRD− patients relative to the 18 MRD+ patients. No association was observed between microbial relative abundance and autologous stem cell transplantation history or MM paraprotein isotype. No differences in microbiota α diversity were observed between MRD− and MRD+ patients. The potential association of microbiota composition with treatment response in MM patients is an important parameter for additional correlative and clinical investigation.
- Subjects :
- Adult
Male
Neoplasm, Residual
Biopsy
Plasma cell
Autologous stem-cell transplantation
Bone Marrow
hemic and lymphatic diseases
Humans
Medicine
Eubacterium
Microbiome
Multiple myeloma
Aged
Neoplasm Staging
Aged, 80 and over
Lymphoid Neoplasia
biology
business.industry
Hematology
Minimal Residual Disease Negativity
Middle Aged
biology.organism_classification
medicine.disease
Combined Modality Therapy
Minimal residual disease
Gastrointestinal Microbiome
body regions
Treatment Outcome
medicine.anatomical_structure
Immunology
Female
Bone marrow
Multiple Myeloma
business
Subjects
Details
- ISSN :
- 24739537 and 24739529
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- Blood Advances
- Accession number :
- edsair.doi.dedup.....34f0b526c940de4c3d093ca71899c30f
- Full Text :
- https://doi.org/10.1182/bloodadvances.2019032276