Evidence map›Paper›PMID 42504914›Full record

ReviewClinical pharmacology and therapeutics2026

Fecal Microbiota Transplantation and Microbiota-Based Therapeutics in Allogeneic Hematopoietic Stem Cell Transplantation: Current Evidence and Future Directions.

Bálint Gergely Szabó, Dorina Korózs, Michal Bator, Krisztina Jeszenszky, Viktor Lakatos, László Gopcsa, Péter Reményi, János Sinkó

Abstract readReview
In one paragraph

Review in Clinical pharmacology and therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Bálint Gergely Szabó *Department of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-1775-1356
Dorina Korózs *Doctoral College, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-1445-8739
Michal BatorDepartment of Hematology, Cellular Therapies, and Internal Medicine, Wroclaw Medical University, Wrocław, Poland.ORCID 0000-0001-6400-4922
Krisztina JeszenszkyDoctoral College, Semmelweis University, Budapest, Hungary.ORCID 0009-0008-1123-065X
Viktor LakatosNational Institute of Haematology and Infectious Diseases, South Pest Central Hospital, Budapest, Hungary.ORCID 0009-0009-0695-0289
László GopcsaDoctoral College, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-4930-7049
Péter ReményiNational Institute of Haematology and Infectious Diseases, South Pest Central Hospital, Budapest, Hungary.ORCID 0000-0002-6116-9745
János SinkóDepartment of Internal Medicine and Haematology, Semmelweis University, Budapest, Hungary.ORCID 0000-0001-7721-6828

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The intestinal microbiome is a key regulator of immune homeostasis, metabolism, and epithelial barrier integrity. In patients with malignant hematological diseases, particularly those undergoing hematopoietic stem cell transplantation, microbiome perturbations by reduced diversity, pathobiont expansion, and loss of beneficial metabolites are common as a consequence of exposure to cytotoxic therapy and broad-spectrum antimicrobials. Accordingly, enteral microbiome manipulation has emerged as a promising strategy. We performed a narrative review of the literature in PubMed/MEDLINE, Embase, and the Web of Science from inception to October 2025. We focused on adult hematology and HSCT populations and synthesized evidence across microbiome-directed interventions, including fecal microbiota transplantation (FMT) and emerging standardized microbiota products, as well as adjunctive strategies such as pre-, pro-, and postbiotics, dietary modulation, and microbiome-sparing antimicrobial practices. Available clinical evidence, predominantly from case series, small cohorts and a limited number of randomized trials, suggests that FMT is feasible in selected immunocompromised patients and may be beneficial for recurrent Clostridioides difficile infection, multidrug-resistant organism decolonization and steroid-refractory gastrointestinal GvHD. Mechanistic data support pleiotropic effects of microbiome restoration, including replenishment of immunoregulatory metabolites, improved colonization resistance and reinforcement of mucosal function. While most reported adverse events are mild, rare transmission events and product variability necessitate for rigorous donor screening, standardized manufacturing and regulatory oversight. Key knowledge gaps include patient selection, optimal timing, dosing strategies, durability of benefit and integration with concurrent medications. In conclusion, microbiome-based interventions may transition from rescue therapy toward a structured component of supportive care in hematologic malignancy management.

Indexed as

Fecal Microbiota TransplantationGastrointestinal MicrobiomeHematopoietic Stem Cell TransplantationAnimalsGraft vs Host DiseaseHumansTransplantation, Homologous

Identifiers

PMID42504914
PMCPMC13403382

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.