Evidence map›Paper›PMID 31597568›Full record

ArticleGenome medicine2019

Relating the gut metagenome and metatranscriptome to immunotherapy responses in melanoma patients.

Brandilyn A Peters, Melissa Wilson, Una Moran, Anna Pavlick, Allison Izsak, Todd Wechter, Jeffrey S Weber, Iman Osman, Jiyoung Ahn

Open access · goldAbstract read
In one paragraph

Article in Genome medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 169 papers, 14 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
169citing papers in PubMed, 14 pooled it
8.6field-weighted citation impact, top 1% of its field
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

169 citing papers in PubMed, 14 syntheses or guidelines pooled it, 267 citations in OpenAlex.

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109 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 1 country.

Brandilyn A PetersDepartment of Population Health, NYU School of Medicine, New York, NY, 10016, USA.ORCID 0000-0002-1534-2578
Melissa WilsonDepartment of Medicine, NYU School of Medicine, New York, NY, USA.
Una MoranNYU Perlmutter Cancer Center, New York, NY, USA.
Anna PavlickDepartment of Medicine, NYU School of Medicine, New York, NY, USA.
Allison IzsakThe Ronald O. Perelman Department of Dermatology, NYU School of Medicine, New York, NY, USA.
Todd WechterThe Ronald O. Perelman Department of Dermatology, NYU School of Medicine, New York, NY, USA.
Jeffrey S WeberDepartment of Medicine, NYU School of Medicine, New York, NY, USA.
Iman OsmanDepartment of Medicine, NYU School of Medicine, New York, NY, USA.
Jiyoung AhnDepartment of Population Health, NYU School of Medicine, New York, NY, 10016, USA. Jiyoung.Ahn@nyumc.org.
NYU Langone’s Laura and Isaac Perlmutter Cancer CenterNew York University · USNYU Langone Health · USSidney Kimmel Cancer Center · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Project 4P50CA225450 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KIRCHHOFF, TOMAS · 2019 to 2025
$12.5M
The Oral Microbiome and Upper Aerodigestive Squamous Cell CancerR01CA159036 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG, HAYES, RICHARD BERNARD · 2011 to 2024
$3.5M
Prospective Study of Human Oral Microbiome and Pancreatic Cancer RiskR01CA164964 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG · 2014 to 2017
$2.2M
NCI NIH HHS P30 CA016087NCI NIH HHS P30CA016087NCI NIH HHS P50 CA225450NCI NIH HHS P50CA225450NCI NIH HHS R01 CA159036NCI NIH HHS R01 CA164964NCI NIH HHS R01CA164964
6 · The paper itself

Abstract

backgroundRecent evidence suggests that immunotherapy efficacy in melanoma is modulated by gut microbiota. Few studies have examined this phenomenon in humans, and none have incorporated metatranscriptomics, important for determining expression of metagenomic functions in the microbial community.

methodsIn melanoma patients undergoing immunotherapy, gut microbiome was characterized in pre-treatment stool using 16S rRNA gene and shotgun metagenome sequencing (n = 27). Transcriptional expression of metagenomic pathways was confirmed with metatranscriptome sequencing in a subset of 17. We examined associations of taxa and metagenomic pathways with progression-free survival (PFS) using 500 × 10-fold cross-validated elastic-net penalized Cox regression.

resultsHigher microbial community richness was associated with longer PFS in 16S and shotgun data (p < 0.05). Clustering based on overall microbiome composition divided patients into three groups with differing PFS; the low-risk group had 99% lower risk of progression than the high-risk group at any time during follow-up (p = 0.002). Among the species selected in regression, abundance of Bacteroides ovatus, Bacteroides dorei, Bacteroides massiliensis, Ruminococcus gnavus, and Blautia producta were related to shorter PFS, and Faecalibacterium prausnitzii, Coprococcus eutactus, Prevotella stercorea, Streptococcus sanguinis, Streptococcus anginosus, and Lachnospiraceae bacterium 3 1 46FAA to longer PFS. Metagenomic functions related to PFS that had correlated metatranscriptomic expression included risk-associated pathways of L-rhamnose degradation, guanosine nucleotide biosynthesis, and B vitamin biosynthesis.

conclusionsThis work adds to the growing evidence that gut microbiota are related to immunotherapy outcomes, and identifies, for the first time, transcriptionally expressed metagenomic pathways related to PFS. Further research is warranted on microbial therapeutic targets to improve immunotherapy outcomes.

Indexed as

MetagenomeTranscriptomeAgedFecesFemaleGastrointestinal MicrobiomeHumansImmunotherapyMaleMelanomaMicrobiotaRNA, Ribosomal, 16SRNA, Ribosomal, 16SImmunotherapyMelanomaMetagenomeMetatranscriptomeMicrobiome

Identifiers

PMID31597568
PMCPMC6785875
OpenAlexW2979785336

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.