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Fecal microbiota transplant promotes response in immunotherapy-refractory melanoma patients

Erez N. BaruchDepartment of Clinical Immunology and Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, IsraelIlan YoungsterPediatric Division and the Microbiome Research Center, Shamir (Assaf Harofeh) Medical Center, Be’er Ya’akov, IsraelGuy Ben‐BetzalelThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelRona OrtenbergThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelAdi LahatDepartment of Gastroenterology, Sheba Medical Center, Tel HaShomer, IsraelLior H. KatzDepartment of Gastroenterology, Hadassah Medical Center, Jerusalem, IsraelKaterina AdlerDepartment of Mathematics, Bar Ilan University, Ramat Gan, IsraelDaniela Dick‐NeculaInstitute of Pathology, Sheba Medical Center, Tel-HaShomer, IsraelStephen RaskinRadiological Institute, Sheba Medical Center, Tel HaShomer, IsraelNaamah BlochAzrieli Faculty of Medicine, Bar Ilan University, Safed, IsraelД. Л. РотинInstitute of Pathology, Sheba Medical Center, Tel-HaShomer, IsraelLiat AnafiInstitute of Pathology, Sheba Medical Center, Tel-HaShomer, IsraelCamila AviviInstitute of Pathology, Sheba Medical Center, Tel-HaShomer, IsraelJenny MelnichenkoThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelYael Steinberg‐SilmanThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelRonac MamtaniDivision of Hematology and Oncology, University of Pennsylvania, Philadelphia, PA, USAHagit HaratiThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelNethanel AsherThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelRonnie Shapira‐FrommerThe Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, IsraelTal Brosh‐NissimovInfectious Diseases Unit, Assuta Ashdod University Hospital, Ashdod, IsraelYael EshetDepartment of Nuclear Medicine, Sheba Medical Center, Tel HaShomer, IsraelShira Ben-SimonAzrieli Faculty of Medicine, Bar Ilan University, Safed, IsraelZiv OrenAzrieli Faculty of Medicine, Bar Ilan University, Safed, IsraelMd Abdul Wadud KhanProgram for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USAMoran AmitDepartment of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USANadim J. AjamiProgram for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USAIris BarshackInstitute of Pathology, Sheba Medical Center, Tel-HaShomer, IsraelJacob SchachterSchool of Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, IsraelJennifer A. WargoDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USAOmry KorenAzrieli Faculty of Medicine, Bar Ilan University, Safed, IsraelGal MarkelDepartment of Clinical Immunology and Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, IsraelBen BoursiCenter for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA, USA
2020en
ABI

Аннотация

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.

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