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Artificial Intelligence Predictive Model for Hormone Therapy Use in Prostate Cancer.
Spratt, Daniel E; Tang, Siyi; Sun, Yilun; Huang, Huei-Chung; Chen, Emmalyn; Mohamad, Osama; Armstrong, Andrew J; Tward, Jonathan D; Nguyen, Paul L; Lang, Joshua M; Zhang, Jingbin; Mitani, Akinori; Simko, Jeffry P; DeVries, Sandy; van der Wal, Douwe; Pinckaers, Hans; Monson, Jedidiah M; Campbell, Holly A; Wallace, James; Ferguson, Michelle J; Bahary, Jean-Paul; Schaeffer, Edward M; Sandler, Howard M; Tran, Phuoc T; Rodgers, Joseph P; Esteva, Andre; Yamashita, Rikiya; Feng, Felix Y.
Afiliación
  • Spratt DE; Department of Radiation Oncology, University Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland.
  • Tang S; Department of Electrical Engineering, Stanford University, Stanford, CA.
  • Sun Y; Artera, Inc., Los Altos, CA.
  • Huang HC; Department of Radiation Oncology, University Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland.
  • Chen E; Department of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland.
  • Mohamad O; Artera, Inc., Los Altos, CA.
  • Armstrong AJ; Artera, Inc., Los Altos, CA.
  • Tward JD; Department of Radiation Oncology, University of California, San Francisco, San Francisco.
  • Nguyen PL; Duke Cancer Institute Center for Prostate and Urologic Cancer, Division of Medical Oncology, Department of Medicine, Duke University, Durham, NC.
  • Lang JM; Department of Radiation Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City.
  • Zhang J; Department of Radiation Oncology, Dana-Farber/Brigham Cancer Center, Boston.
  • Mitani A; Division of Hematology/Medical Oncology, University of Wisconsin, Madison, WI.
  • Simko JP; Artera, Inc., Los Altos, CA.
  • DeVries S; Artera, Inc., Los Altos, CA.
  • van der Wal D; Department of Radiation Oncology, University of California, San Francisco, San Francisco.
  • Pinckaers H; NRG Oncology Biospecimen Bank, University of California, San Francisco, San Francisco.
  • Monson JM; Artera, Inc., Los Altos, CA.
  • Campbell HA; Artera, Inc., Los Altos, CA.
  • Wallace J; Department of Radiation Oncology, Saint Agnes Medical Center, Fresno, CA.
  • Ferguson MJ; Department of Radiation Oncology, Saint John Regional Hospital, Saint John, NB, Canada.
  • Bahary JP; University of Chicago Medicine Medical Group, Chicago.
  • Schaeffer EM; Department of Radiation Oncology, Allan Blair Cancer Centre, Regina, SK, Canada.
  • Sandler HM; Department of Radiation Oncology, Centre Hospitalier de l'Universite de Montreal, Montreal.
  • Tran PT; Department of Urology, Northwestern University Feinberg School of Medicine, Chicago.
  • Rodgers JP; Department of Radiation Oncology, Cedars-Sinai Medical Center, Los Angeles.
  • Esteva A; Department of Radiation Oncology, University of Maryland School of Medicine, Baltimore.
  • Yamashita R; Statistics and Data Management Center, NRG Oncology, Philadelphia.
  • Feng FY; Statistics and Data Management Center, American College of Radiology, Philadelphia.
NEJM Evid ; 2(8): EVIDoa2300023, 2023 Aug.
Article en En | MEDLINE | ID: mdl-38320143
ABSTRACT

BACKGROUND:

Androgen deprivation therapy (ADT) with radiotherapy can benefit patients with localized prostate cancer. However, ADT can negatively impact quality of life, and there remain no validated predictive models to guide its use.

METHODS:

We used digital pathology images from pretreatment prostate tissue and clinical data from 5727 patients enrolled in five phase 3 randomized trials, in which treatment was radiotherapy with or without ADT, as our data source to develop and validate an artificial intelligence (AI)­derived predictive patient-specific model that would determine which patients would develop the primary end point of distant metastasis. The model used baseline data to provide a binary output that a given patient will likely benefit from ADT or not. After the model was locked, validation was performed using data from NRG Oncology/Radiation Therapy Oncology Group (RTOG) 9408 (n=1594), a trial that randomly assigned men to radiotherapy plus or minus 4 months of ADT. Fine­Gray regression and restricted mean survival times were used to assess the interaction between treatment and the predictive model and within predictive model­positive, i.e., benefited from ADT, and ­negative subgroup treatment effects.

RESULTS:

Overall, in the NRG/RTOG 9408 validation cohort (14.9 years of median follow-up), ADT significantly improved time to distant metastasis. Of these enrolled patients, 543 (34%) were model positive, and ADT significantly reduced the risk of distant metastasis compared with radiotherapy alone. Of 1051 patients who were model negative, ADT did not provide benefit.

CONCLUSIONS:

Our AI-based predictive model was able to identify patients with a predominantly intermediate risk for prostate cancer likely to benefit from short-term ADT. (Supported by a grant [U10CA180822] from NRG Oncology Statistical and Data Management Center, a grant [UG1CA189867] from NCI Community Oncology Research Program, a grant [U10CA180868] from NRG Oncology Operations, and a grant [U24CA196067] from NRG Specimen Bank from the National Cancer Institute and by Artera, Inc. ClinicalTrials.gov numbers NCT00767286, NCT00002597, NCT00769548, NCT00005044, and NCT00033631.)
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: NEJM Evid Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de la Próstata Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans / Male Idioma: En Revista: NEJM Evid Año: 2023 Tipo del documento: Article