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First-in-class Microbial Ecosystem Therapeutic 4 (MET4) in combination with immune checkpoint inhibitors in patients with advanced solid tumors (MET4-IO trial).
Spreafico, A; Heirali, A A; Araujo, D V; Tan, T J; Oliva, M; Schneeberger, P H H; Chen, B; Wong, M K; Stayner, L-A; Hansen, A R; Saibil, S D; Wang, B X; Cochrane, K; Sherriff, K; Allen-Vercoe, E; Xu, W; Siu, L L; Coburn, B.
Afiliação
  • Spreafico A; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto; Tumor Immunotherapy Program, Princess Margaret Cancer Centre, University Health Network, Toronto. Electronic address: anna.spreafico@uhn.ca.
  • Heirali AA; Toronto General Hospital Research Institute, University Health Network, Toronto, Canada.
  • Araujo DV; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto; Department of Medical Oncology, Hospital de Base, Sao Paulo, Brazil.
  • Tan TJ; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto; Division of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
  • Oliva M; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto; Department of Medical Oncology, Institut Catala d' Oncologia, L'Hospitalet de Llobregat, Barcelona; Universitat de Barcelona, Barcelona, Spain.
  • Schneeberger PHH; Toronto General Hospital Research Institute, University Health Network, Toronto, Canada; Swiss Tropical and Public Health Institute, Department of Medical Parasitology and Infection Biology, Allschwil; University of Basel, Basel, Switzerland.
  • Chen B; Biostatistics Department, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Wong MK; Department of Immunology, University of Toronto, Toronto.
  • Stayner LA; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Hansen AR; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Saibil SD; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Wang BX; Tumor Immunotherapy Program, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Cochrane K; Nubiyota LLP, Guelph, Canada.
  • Sherriff K; Nubiyota LLP, Guelph, Canada.
  • Allen-Vercoe E; Nubiyota LLP, Guelph, Canada.
  • Xu W; Biostatistics Department, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Siu LL; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto; Tumor Immunotherapy Program, Princess Margaret Cancer Centre, University Health Network, Toronto.
  • Coburn B; Toronto General Hospital Research Institute, University Health Network, Toronto, Canada. Electronic address: Bryan.Coburn@uhn.ca.
Ann Oncol ; 34(6): 520-530, 2023 06.
Article em En | MEDLINE | ID: mdl-36863483
BACKGROUND: The intestinal microbiome has been associated with response to immune checkpoint inhibitors (ICIs) in humans and causally implicated in ICI responsiveness in animal models. Two recent human trials demonstrated that fecal microbiota transplant (FMT) from ICI responders can rescue ICI responses in refractory melanoma, but FMT has specific limitations to scaled use. PATIENTS AND METHODS: We conducted an early-phase clinical trial of a cultivated, orally delivered 30-species microbial consortium (Microbial Ecosystem Therapeutic 4, MET4) designed for co-administration with ICIs as an alternative to FMT and assessed safety, tolerability and ecological responses in patients with advanced solid tumors. RESULTS: The trial achieved its primary safety and tolerability outcomes. There were no statistically significant differences in the primary ecological outcomes; however, differences in MET4 species relative abundance were evident after randomization that varied by patient and species. Increases in the relative abundance of several MET4 taxa, including Enterococcus and Bifidobacterium, taxa previously associated with ICI responsiveness, were observed and MET4 engraftment was associated with decreases in plasma and stool primary bile acids. CONCLUSIONS: This trial is the first report of the use of a microbial consortium as an alternative to FMT in advanced cancer patients receiving ICI and the results justify the further development of microbial consortia as a therapeutic co-intervention for ICI treatment in cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores de Checkpoint Imunológico / Melanoma Limite: Animals / Humans Idioma: En Ano de publicação: 2023

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores de Checkpoint Imunológico / Melanoma Limite: Animals / Humans Idioma: En Ano de publicação: 2023