Evidence map›Paper›PMID 41967083›Full record

ReviewThe oncologist2026

Immunotherapy with guts: a review of microbial therapeutic adjuncts for immunotherapy in solid tumors.

Kelly Pum, Emil Lou, Paolo Goffredo, Cyrus Jahansouz, Subbaya Subramanian, Ajay Prakash

Abstract readReview
In one paragraph

Review in The oncologist, 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

6 authors.

Kelly PumCollege of Biological Sciences, University of Minnesota, Minneapolis, MN, 55108, United States.ORCID 0009-0004-4707-6317
Emil LouDivision of Hematology, Oncology, and Transplantation, University of Minnesota Medical School, Minneapolis, MN, 55455, United States.ORCID 0000-0002-1607-1386
Paolo GoffredoMasonic Cancer Center, University of Minnesota Medical School, Minneapolis, MN, 55455, United States.ORCID 0000-0001-7078-6625
Cyrus JahansouzMasonic Cancer Center, University of Minnesota Medical School, Minneapolis, MN, 55455, United States.ORCID 0000-0002-7884-2799
Subbaya SubramanianDivision of Hematology, Oncology, and Transplantation, University of Minnesota Medical School, Minneapolis, MN, 55455, United States.ORCID 0000-0002-2544-480X
Ajay PrakashDivision of Hematology, Oncology, and Transplantation, University of Minnesota Medical School, Minneapolis, MN, 55455, United States.ORCID 0000-0003-3895-040X

Funding

Microbiome-derived regulators of therapy-resistant colorectal tumorsR21CA267707 · NCI · UNIVERSITY OF MINNESOTA · PI GRIFFIN, TIMOTHY J., JAGTAP, PRATIK D · 2022 to 2023
$397k
Minnesota Colorectal Cancer Foundation and The Mezin-Koats FoundationNCI NIH HHS R21 CA267707
6 · The paper itself

Abstract

backgroundImmunotherapy has transformed the management of some solid tumor types, but its impact has been limited to the subset of cancer patients who have "hot" or immunogenic tumors. Num2erous studies are based on strategies for turning "cold," or immune-unresponsive, tumors into a "hot" state. The gut microbiome has emerged as a potential co-therapy for standard immune checkpoint inhibitors (ICIs) to achieve this goal. Recent approaches have primarily focused on the use of probiotics, microbial consortia, or fecal microbiota transplantations in combination with anti-PD-1 and anti-CTLA-4 antibodies.

methodsThis review highlights the current status of microbiome modulation and its potential impact on clinical practice. Probiotics, such as CMB588, and microbial consortia have been selected following successful preclinical studies. These taxa may initiate T cell infiltration and are commonly found in the microbial profiles of individuals who have previously responded to immunotherapy.

resultsSeveral trials with these therapies have had success and noted minimal safety concerns compared to monotherapy treatments. Fecal microbiota transplantation (FMT), originally used to treat Clostridium difficile infections, has also demonstrated promising results in increasing immune checkpoint inhibitor (ICI) efficacy across various cancer types and is being utilized in multiple ongoing trials.

conclusionThese therapeutics form the foundation for exciting possibilities in immunotherapy and improving patient outcomes.

Indexed as

Fecal Microbiota TransplantationGastrointestinal MicrobiomeImmune Checkpoint InhibitorsImmunotherapyNeoplasmsProbioticsHumansImmune Checkpoint Inhibitorsclinical trialsimmune checkpoint inhibitorsimmunotherapymicrobial modulationsolid tumorstumor microenvironment

Identifiers

PMID41967083
PMCPMC13167794

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.