Evidence map›Paper›PMID 42263665›Full record

Trial reportBlood advances2026

Plant-based whole-food diets are feasible during auto-HCT and are associated with dose-dependent microbiome modulation.

Katherine Ueland, Taara Elahi, Mary Rasmussen, Alex E Wolfe, Hayley Purcell, Saranya Rani Chakka, Mercy Mirimo-Martinez, Heather Persinger, Karen Johnson, Alanna Boynton and 18 more

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06559709 (Implementing a Plant-Based Whole-Foods Meal Delivery Service for Patients Undergoing Autologous Hematopoietic Cell Transplantation for Multiple Myeloma), which is not on this 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.

NCT06559709 nacompletednot on this map

Implementing a Plant-Based Whole-Foods Meal Delivery Service for Patients Undergoing Autologous Hematopoietic Cell Transplantation for Multiple Myeloma: A Pilot Study

TypeinterventionalSponsorFred Hutchinson Cancer CenterRan2024 to 2025Enrolled26ConditionsMultiple MyelomaArmsBiospecimen Collection, Dietary Intervention, Medical Chart Review, Questionnaire Administration
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

5 · Who and what money

Authors and funding

28 authors.

Katherine UelandFred Hutchinson Cancer Center, Seattle, WA.
Taara ElahiFred Hutchinson Cancer Center, Seattle, WA.
Mary RasmussenFred Hutchinson Cancer Center, Seattle, WA.
Alex E WolfeFred Hutchinson Cancer Center, Seattle, WA.
Hayley PurcellNorthwest Metabolomics Research Center, University of Washington, Seattle, WA.
Saranya Rani ChakkaFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-3945-2496
Mercy Mirimo-MartinezFred Hutchinson Cancer Center, Seattle, WA.
Heather PersingerFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-4398-8616
Karen JohnsonFred Hutchinson Cancer Center, Seattle, WA.
Alanna BoyntonFred Hutchinson Cancer Center, Seattle, WA.
Kerry McMillenFred Hutchinson Cancer Center, Seattle, WA.
Mariia ByelykhUniversity of Washington, Seattle, WA.
Melinda A BiernackiFred Hutchinson Cancer Center, Seattle, WA.
Albert C YehFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-3455-7360
Naveed AliFred Hutchinson Cancer Center, Seattle, WA.
Shivaprasad ManjappaFred Hutchinson Cancer Center, Seattle, WA.
Natalie WulijiFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-1010-4589
David N FredricksFred Hutchinson Cancer Center, Seattle, WA.
Marie BleakleyFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-7018-8702
Leona A HolmbergFred Hutchinson Cancer Center, Seattle, WA.
Jonathan U PeledMemorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0002-4029-7625
Jeannette M SchenkFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-4865-7813
Daniel RafteryNorthwest Metabolomics Research Center, University of Washington, Seattle, WA.
Jing MaFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0001-6294-227X
Geoffrey R HillFred Hutchinson Cancer Center, Seattle, WA.
Marian L NeuhouserFred Hutchinson Cancer Center, Seattle, WA.
Stephanie J LeeFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-2600-6390
Kate A MarkeyFred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-7064-2362

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Propagation of graft vs. host disease through CD4+ T-cell cognate recognition of gastrointestinal microbiotaK08HL167161 · NHLBI · FRED HUTCHINSON CANCER CENTER · PI Albert Chia-Chun Yeh · 2023 to 2026
$650k
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA015704NHLBI NIH HHS K08 HL167161
6 · The paper itself

Abstract

abstractPlant-based whole food diets may represent a tractable approach to mitigating microbiome disruption and improving outcomes in patients undergoing autologous hematopoietic cell transplantation (auto-HCT) for multiple myeloma, a population in whom intestinal dysbiosis has been linked with inferior survival. We conducted a single-arm clinical trial at our center, in which participants undergoing auto-HCT (n = 22) received fresh, pre-prepared, plant-based meals for 5 weeks spanning conditioning, neutropenia, and early recovery, with the goal of supporting the consumption of nutrient-dense, high-fiber foods. The primary end points were feasibility and tolerability, defined by successful enrollment and patient-reported intake of study meals. Dietary intake was quantified using prospective food diaries and 24-hour dietary recall surveys. Secondary end points included changes in gut microbiome composition and function assessed by shotgun metagenomic sequencing and stool short-chain fatty acid (SCFA) measurements. The intervention was feasible and generally well tolerated, with all participants consuming delivered meals to some degree, with adherence sufficient to support planned dietary and correlative analyses. Greater intake of study meals was associated with more pronounced shifts in gut microbial communities, including enrichment of SCFA-producing taxa and compositional changes consistent with a fiber-responsive microbiome. Stool SCFA concentrations increased from baseline to the end of the intervention, suggesting a potential influence of the dietary strategy on microbial metabolite production during the peritransplant period. These findings demonstrate that a plant-based meal delivery intervention is implementable during auto-HCT and suggest dose-dependent modulation of the gut microbiome and its metabolic output. The trial was registered at ClinicalTrials.gov as NCT06559709.

Indexed as

Gastrointestinal MicrobiomeHematopoietic Stem Cell TransplantationMicrobiotaAdultAgedDiet, Plant-BasedFemaleHumansMaleMiddle AgedTransplantation, Autologous

Identifiers

PMID42263665
PMCPMC13486820

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Registered trials

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.