Evidence map›Paper›PMID 41760690›Full record

ArticleNPJ breast cancer2026

The landscape of the intestinal microbiome among patients with newly diagnosed invasive breast cancer and ductal carcinoma in situ (DCIS).

Sarah L Sammons, Thomas M Kuntz, Molly DiLullo, Xochitl C Morgan, Alyssa Martin, Melissa E Hughes, Tasnim Rahman, Romualdo Barroso-Sousa, Esther Ritah Ogayo, Julia Giordano and 8 more

Abstract read
In one paragraph

Article in NPJ breast cancer, 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

18 authors.

Sarah L SammonsMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Thomas M KuntzMicrobiome Analysis Core, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Molly DiLulloMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Xochitl C MorganMicrobiome Analysis Core, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Alyssa MartinMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Melissa E HughesMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Tasnim RahmanMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Romualdo Barroso-SousaDASA Oncology, Brasilia Hospital, Brasília, Brazil.
Esther Ritah OgayoMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Julia GiordanoPerelman School of Medicine, Philadelphia, PA, USA.
Sean RyanMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Adrienne G WaksMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Ilana SchlamMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jennifer LigibelMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Nancy U LinMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Ana C Garrido-CastroMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Elizabeth A MittendorfBreast Oncology Program, Dana-Farber Brigham Cancer Center, Boston, MA, USA.
Sara M TolaneyMedical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA. Sara_Tolaney@DFCI.HARVARD.EDU.ORCID http://orcid.org/0000-0002-5940-8671

Funding

Massachusetts Life Sciences Center Dana-Farber Cancer Institute project number 6395601National Cancer Institute (NCI) Breast Cancer SPORE P50CA168504 to DF/HCC
6 · The paper itself

Abstract

The intestinal microbiome shapes immune responses and is associated with patient outcomes in cancer following immunotherapy. We evaluated differences between the intestinal microbiome profiles of patients with early-stage invasive breast cancer (BC) and ductal carcinoma in situ (DCIS) by subtype using whole genome metagenomic sequencing. There were no significant differences in microbiome composition between DCIS and invasive BC as measured by alpha diversity (p = 0.20, ANOVA) or beta diversity (p = 0.52, PERMANOVA). Within invasive BC, patients with hormone receptor-positive (HR + )/HER2 + BC differed significantly in beta diversity relative to other subtypes (p < 0.05), with differences in six species (q < 0.25). Bacteroides ovatus was significantly more abundant in patients with stage III BC vs. stage I (p = 0.0003). Functional pathway analysis using HUMAnN3 revealed stage-specific enrichment of amino acid biosynthesis and nucleotide-related pathways. Altogether, these findings highlight potential microbial signatures associated with BC subtype and stage.

Identifiers

PMID41760690
PMCPMC13066469

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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.