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Predicting cancer immunotherapy response from gut microbiomes using machine learning models.
Liang, Hai; Jo, Jay-Hyun; Zhang, Zhiwei; MacGibeny, Margaret A; Han, Jungmin; Proctor, Diana M; Taylor, Monica E; Che, You; Juneau, Paul; Apolo, Andrea B; McCulloch, John A; Davar, Diwakar; Zarour, Hassane M; Dzutsev, Amiran K; Brownell, Isaac; Trinchieri, Giorgio; Gulley, James L; Kong, Heidi H.
Affiliation
  • Liang H; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Jo JH; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Zhang Z; Biostatistics Branch, Division of Cancer Treatment and Diagnostics, National Cancer Institute, NIH, Bethesda, MD 20892, USA.
  • MacGibeny MA; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Han J; Department of Medical Education, West Virginia University, Morgantown, WV 26506, USA.
  • Proctor DM; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Taylor ME; Translational and Functional Genomics Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Che Y; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Juneau P; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Apolo AB; NIH Library, Division of Library Services, Office of Research Services, NIH, Bethesda, MD 20892, USA.
  • McCulloch JA; Zimmerman Associates Inc., Fairfax, VA 22030, USA.
  • Davar D; Genitourinary Malignancies Branch, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
  • Zarour HM; Genetics and Microbiome Core, Laboratory of Integrative Cancer Immunology, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
  • Dzutsev AK; Department of Medicine and UPMC Hillman Cancer Center University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Brownell I; Department of Medicine and UPMC Hillman Cancer Center University of Pittsburgh, Pittsburgh, PA 15213, USA.
  • Trinchieri G; Laboratory of Integrative Cancer Immunology, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
  • Gulley JL; Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
  • Kong HH; Center for Immuno-Oncology, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
Oncotarget ; 13: 876-889, 2022.
Article in En | MEDLINE | ID: mdl-35875611
ABSTRACT
Cancer immunotherapy has significantly improved patient survival. Yet, half of patients do not respond to immunotherapy. Gut microbiomes have been linked to clinical responsiveness of melanoma patients on immunotherapies; however, different taxa have been associated with response status with implicated taxa inconsistent between studies. We used a tumor-agnostic approach to find common gut microbiome features of response among immunotherapy patients with different advanced stage cancers. A combined meta-analysis of 16S rRNA gene sequencing data from our mixed tumor cohort and three published immunotherapy gut microbiome datasets from different melanoma patient cohorts found certain gut bacterial taxa correlated with immunotherapy response status regardless of tumor type. Using multivariate selbal analysis, we identified two separate groups of bacterial genera associated with responders versus non-responders. Statistical models of gut microbiome community features showed robust prediction accuracy of immunotherapy response in amplicon sequencing datasets and in cross-sequencing platform validation with shotgun metagenomic datasets. Results suggest baseline gut microbiome features may be predictive of clinical outcomes in oncology patients on immunotherapies, and some of these features may be generalizable across different tumor types, patient cohorts, and sequencing platforms. Findings demonstrate how machine learning models can reveal microbiome-immunotherapy interactions that may ultimately improve cancer patient outcomes.
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Full text: 1 Database: MEDLINE Main subject: Gastrointestinal Microbiome / Melanoma Type of study: Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Oncotarget Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Database: MEDLINE Main subject: Gastrointestinal Microbiome / Melanoma Type of study: Prognostic_studies / Systematic_reviews Limits: Humans Language: En Journal: Oncotarget Year: 2022 Type: Article Affiliation country: United States