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Multiple Myeloma DREAM Challenge reveals epigenetic regulator PHF19 as marker of aggressive disease.
Mason, Mike J; Schinke, Carolina; Eng, Christine L P; Towfic, Fadi; Gruber, Fred; Dervan, Andrew; White, Brian S; Pratapa, Aditya; Guan, Yuanfang; Chen, Hongjie; Cui, Yi; Li, Bailiang; Yu, Thomas; Chaibub Neto, Elias; Mavrommatis, Konstantinos; Ortiz, Maria; Lyzogubov, Valeriy; Bisht, Kamlesh; Dai, Hongyue Y; Schmitz, Frank; Flynt, Erin; Danziger, Samuel A; Ratushny, Alexander; Dalton, William S; Goldschmidt, Hartmut; Avet-Loiseau, Herve; Samur, Mehmet; Hayete, Boris; Sonneveld, Pieter; Shain, Kenneth H; Munshi, Nikhil; Auclair, Daniel; Hose, Dirk; Morgan, Gareth; Trotter, Matthew; Bassett, Douglas; Goke, Jonathan; Walker, Brian A; Thakurta, Anjan; Guinney, Justin.
Affiliation
  • Mason MJ; Sage Bionetworks, Seattle, WA, USA. michael.mason@sagebase.org.
  • Schinke C; Myeloma Center, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  • Eng CLP; Computational & Systems Biology, Genome Institute of Singapore, Singapore, Singapore.
  • Towfic F; Celgene Corporation, Summit, NJ, USA.
  • Gruber F; GNS Healthcare, Cambridge, MA, USA.
  • Dervan A; Celgene, Seattle, WA, USA.
  • White BS; Sage Bionetworks, Seattle, WA, USA.
  • Pratapa A; Department of Computer Science, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.
  • Guan Y; Department of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, MI, USA.
  • Chen H; Shanghai Jiao Tong University, Shanghai, China.
  • Cui Y; Stanford University School of Medicine, Palo Alto, CA, USA.
  • Li B; Department of Radiation Oncology, Stanford University School of Medicine, Palo Alto, CA, USA.
  • Yu T; Sage Bionetworks, Seattle, WA, USA.
  • Chaibub Neto E; Sage Bionetworks, Seattle, WA, USA.
  • Mavrommatis K; Celgene Corporation, Summit, NJ, USA.
  • Ortiz M; Predictive Sciences, Celgene Corporation, Seville, Spain.
  • Lyzogubov V; University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  • Bisht K; Celgene Corporation, Summit, NJ, USA.
  • Dai HY; M2Gen, Tampa, FL, USA.
  • Schmitz F; Celgene, Seattle, WA, USA.
  • Flynt E; Celgene Corporation, Summit, NJ, USA.
  • Dan Rozelle; Rancho BioSciences, San Diego, CA, USA.
  • Danziger SA; Celgene, Seattle, WA, USA.
  • Ratushny A; Celgene, Seattle, WA, USA.
  • Dalton WS; Department of Malignant Hematology, Moffitt Cancer Center & Research Institute, Tampa, FL, USA.
  • Goldschmidt H; Medizinische Klinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
  • Avet-Loiseau H; Nationales Centrum für Tumorerkrankungen, Heidelberg, Germany.
  • Samur M; Institut Universitaire du Cancer Oncopole, Toulouse, France.
  • Hayete B; Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Sonneveld P; Department of Biostatistics, Harvard TH Chan School of Public Health, Boston, MA, USA.
  • Shain KH; GNS Healthcare, Cambridge, MA, USA.
  • Munshi N; Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
  • Auclair D; Department of Malignant Hematology, Moffitt Cancer Center, Tampa, FL, USA.
  • Hose D; Tumor Biology Department, Moffitt Cancer Center, Tampa, FL, USA.
  • Morgan G; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Trotter M; VA Boston Healthcare System, Boston, MA, USA.
  • Bassett D; Multiple Myeloma Research Foundation, Norwalk, CT, USA.
  • Goke J; Medizinische Klinik V, Universitätsklinikum Heidelberg, Heidelberg, Germany.
  • Walker BA; Labor für Myelomforschung, Universitätsklinikum Heidelberg, Heidelberg, Germany.
  • Thakurta A; University of Arkansas for Medical Sciences, Little Rock, AR, USA.
  • Guinney J; Predictive Sciences, Celgene Corporation, Seville, Spain.
Leukemia ; 34(7): 1866-1874, 2020 07.
Article in En | MEDLINE | ID: mdl-32060406
ABSTRACT
While the past decade has seen meaningful improvements in clinical outcomes for multiple myeloma patients, a subset of patients does not benefit from current therapeutics for unclear reasons. Many gene expression-based models of risk have been developed, but each model uses a different combination of genes and often involves assaying many genes making them difficult to implement. We organized the Multiple Myeloma DREAM Challenge, a crowdsourced effort to develop models of rapid progression in newly diagnosed myeloma patients and to benchmark these against previously published models. This effort lead to more robust predictors and found that incorporating specific demographic and clinical features improved gene expression-based models of high risk. Furthermore, post-challenge analysis identified a novel expression-based risk marker, PHF19, which has recently been found to have an important biological role in multiple myeloma. Lastly, we show that a simple four feature predictor composed of age, ISS, and expression of PHF19 and MMSET performs similarly to more complex models with many more gene expression features included.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Biomarkers, Tumor / Gene Expression Regulation, Neoplastic / Clinical Trials as Topic / Models, Statistical / Epigenesis, Genetic / DNA-Binding Proteins / Multiple Myeloma Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Leukemia Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Biomarkers, Tumor / Gene Expression Regulation, Neoplastic / Clinical Trials as Topic / Models, Statistical / Epigenesis, Genetic / DNA-Binding Proteins / Multiple Myeloma Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Leukemia Journal subject: HEMATOLOGIA / NEOPLASIAS Year: 2020 Document type: Article Affiliation country: United States