| Literature DB >> 33303685 |
Gal Markel1,2,3, Ben Boursi4,5,6, Erez N Baruch1,2, Ilan Youngster7,4, Guy Ben-Betzalel8, Rona Ortenberg8, Adi Lahat9, Lior Katz10, Katerina Adler11, Daniela Dick-Necula12, Stephen Raskin4,13, Naamah Bloch14, Daniil Rotin12, Liat Anafi12, Camila Avivi12, Jenny Melnichenko8, Yael Steinberg-Silman8, Ronac Mamtani15, Hagit Harati8, Nethanel Asher8, Ronnie Shapira-Frommer8, Tal Brosh-Nissimov16, Yael Eshet4,12,17, Shira Ben-Simon14, Oren Ziv14, Md Abdul Wadud Khan18, Moran Amit19, Nadim J Ajami18, Iris Barshack4,12, Jacob Schachter8,4, Jennifer A Wargo18,20, Omry Koren14.
Abstract
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.Entities:
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Year: 2020 PMID: 33303685 DOI: 10.1126/science.abb5920
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728