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Immune-Related Colitis Is Associated with Fecal Microbial Dysbiosis and Can Be Mitigated by Fecal Microbiota Transplantation.
Elkrief, Arielle; Waters, Nicholas R; Smith, Natalie; Dai, Angel; Slingerland, John; Aleynick, Nathan; Febles, Binita; Gogia, Pooja; Socci, Nicholas D; Lumish, Melissa; Giardina, Paul A; Chaft, Jamie E; Eng, Juliana; Motzer, Robert J; Mendelsohn, Robin B; Markey, Kate A; Zhuang, Mingqiang; Li, Yanyun; Yang, Zhifan; Hollmann, Travis J; Rudin, Charles M; van den Brink, Marcel R M; Shia, Jinru; DeWolf, Susan; Schoenfeld, Adam J; Hellmann, Matthew D; Babady, N Esther; Faleck, David M; Peled, Jonathan U.
Afiliação
  • Elkrief A; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Waters NR; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Smith N; Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Dai A; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Slingerland J; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Aleynick N; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Febles B; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Gogia P; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Socci ND; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Lumish M; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Giardina PA; Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Chaft JE; Bioinformatics Core Facility, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Eng J; Marie-Josée & Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Motzer RJ; Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Mendelsohn RB; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Markey KA; Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Zhuang M; Weill Cornell Medical College, New York, New York.
  • Li Y; Thoracic Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Yang Z; Weill Cornell Medical College, New York, New York.
  • Hollmann TJ; Weill Cornell Medical College, New York, New York.
  • Rudin CM; Genitourinary Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • van den Brink MRM; Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Shia J; Weill Cornell Medical College, New York, New York.
  • DeWolf S; Fred Hutchinson Cancer Center, Seattle, Washington.
  • Schoenfeld AJ; Division of Medical Oncology, University of Washington, Seattle, Washington.
  • Hellmann MD; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Babady NE; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Faleck DM; Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Peled JU; Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, New York.
Cancer Immunol Res ; 12(3): 308-321, 2024 03 04.
Article em En | MEDLINE | ID: mdl-38108398
ABSTRACT
Colitis induced by treatment with immune-checkpoint inhibitors (ICI), termed irColitis, is a substantial cause of morbidity complicating cancer treatment. We hypothesized that abnormal fecal microbiome features would be present at the time of irColitis onset and that restoring the microbiome with fecal transplant from a healthy donor would mitigate disease severity. Herein, we present fecal microbiota profiles from 18 patients with irColitis from a single center, 5 of whom were treated with healthy-donor fecal microbial transplantation (FMT). Although fecal samples collected at onset of irColitis had comparable α-diversity to that of comparator groups with gastrointestinal symptoms, irColitis was characterized by fecal microbial dysbiosis. Abundances of Proteobacteria were associated with irColitis in multivariable analyses. Five patients with irColitis refractory to steroids and biologic anti-inflammatory agents received healthy-donor FMT, with initial clinical improvement in irColitis symptoms observed in four of five patients. Two subsequently exhibited recurrence of irColitis symptoms following courses of antibiotics. Both received a second "salvage" FMT that was, again, followed by clinical improvement of irColitis. In summary, we observed distinct microbial community changes that were present at the time of irColitis onset. FMT was followed by clinical improvements in several cases of steroid- and biologic-agent-refractory irColitis. Strategies to restore or prevent microbiome dysbiosis in the context of immunotherapy toxicities should be further explored in prospective clinical trials.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Colite / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Produtos Biológicos / Colite / Microbioma Gastrointestinal Idioma: En Ano de publicação: 2024 Tipo de documento: Article