Fecal microbiota transplant promotes response in immunotherapy-refractory melanoma patients.
Adult
Antineoplastic Agents, Immunological
/ therapeutic use
CD8-Positive T-Lymphocytes
/ immunology
Fecal Microbiota Transplantation
/ adverse effects
Female
Gastrointestinal Microbiome
Humans
Immunotherapy
Intestinal Mucosa
/ immunology
Lymphocytes, Tumor-Infiltrating
/ immunology
Male
Melanoma
/ therapy
Middle Aged
Nivolumab
/ therapeutic use
Programmed Cell Death 1 Receptor
/ antagonists & inhibitors
Skin Neoplasms
/ therapy
Transcriptome
Tumor Microenvironment
/ genetics
Journal
Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511
Informations de publication
Date de publication:
05 02 2021
05 02 2021
Historique:
received:
06
03
2020
accepted:
01
12
2020
pubmed:
12
12
2020
medline:
24
2
2021
entrez:
11
12
2020
Statut:
ppublish
Résumé
The gut microbiome has been shown to influence the response of tumors to anti-PD-1 (programmed cell death-1) immunotherapy in preclinical mouse models and observational patient cohorts. However, modulation of gut microbiota in cancer patients has not been investigated in clinical trials. In this study, we performed a phase 1 clinical trial to assess the safety and feasibility of fecal microbiota transplantation (FMT) and reinduction of anti-PD-1 immunotherapy in 10 patients with anti-PD-1-refractory metastatic melanoma. We observed clinical responses in three patients, including two partial responses and one complete response. Notably, treatment with FMT was associated with favorable changes in immune cell infiltrates and gene expression profiles in both the gut lamina propria and the tumor microenvironment. These early findings have implications for modulating the gut microbiota in cancer treatment.
Identifiants
pubmed: 33303685
pii: science.abb5920
doi: 10.1126/science.abb5920
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Programmed Cell Death 1 Receptor
0
Nivolumab
31YO63LBSN
Types de publication
Clinical Trial, Phase I
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
602-609Commentaires et corrections
Type : CommentIn
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Informations de copyright
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.