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External Beam Radiation Therapy With or Without Brachytherapy Boost in Men With Very-High-Risk Prostate Cancer: A Large Multicenter International Consortium Analysis.
Patel, Sagar A; Ma, Ting Martin; Wong, Jessica K; Stish, Bradley J; Dess, Robert T; Pilar, Avinash; Reddy, Chandana; Wedde, Trude B; Lilleby, Wolfgang A; Fiano, Ryan; Merrick, Gregory S; Stock, Richard G; Demanes, D Jeffrey; Moran, Brian J; Tran, Phuoc T; Krauss, Daniel J; Abu-Isa, Eyad I; Pisansky, Thomas M; Choo, C Richard; Song, Daniel Y; Greco, Stephen; Deville, Curtiland; DeWeese, Theodore L; Tilki, Derya; Ciezki, Jay P; Karnes, R Jeffrey; Nickols, Nicholas G; Rettig, Matthew B; Feng, Felix Y; Berlin, Alejandro; Tward, Jonathan D; Davis, Brian J; Reiter, Robert E; Boutros, Paul C; Romero, Tahmineh; Horwitz, Eric M; Tendulkar, Rahul D; Steinberg, Michael L; Spratt, Daniel E; Xiang, Michael; Kishan, Amar U.
Afiliação
  • Patel SA; Department of Radiation Oncology, Emory University, Atlanta, Georgia. Electronic address: sagar.patel@emory.edu.
  • Ma TM; Department of Radiation Oncology, University of California, Los Angeles, California.
  • Wong JK; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
  • Stish BJ; Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
  • Dess RT; Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
  • Pilar A; Radiation Medicine Program, Princess Margaret Cancer Centre, Ontario, Canada; Department of Radiation Oncology, University of Toronto, Ontario, Canada.
  • Reddy C; Department of Radiation Oncology, Cleveland Clinic, Cleveland Ohio.
  • Wedde TB; Oslo University Hospital, Oslo, Norway.
  • Lilleby WA; Oslo University Hospital, Oslo, Norway.
  • Fiano R; Urologic Research Institute, Ohio University School of Medicine, Athens Ohio.
  • Merrick GS; Urologic Research Institute, Ohio University School of Medicine, Athens Ohio.
  • Stock RG; Department of Radiation Oncology, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Demanes DJ; Department of Radiation Oncology, University of California, Los Angeles, California.
  • Moran BJ; Chicago Prostate Cancer Center, Westmont, Illinois.
  • Tran PT; Department of Radiation Oncology, University of Maryland, Baltimore Maryland.
  • Krauss DJ; William Beaumont School of Medicine, Royal Oak, Michigan.
  • Abu-Isa EI; Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.
  • Pisansky TM; Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
  • Choo CR; Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
  • Song DY; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Greco S; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Deville C; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • DeWeese TL; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Tilki D; Martini-Klinik Prostate Cancer Center, University Hospital Hamburg Eppendorf, Hamburg, Germany.
  • Ciezki JP; Department of Radiation Oncology, Cleveland Clinic, Cleveland Ohio.
  • Karnes RJ; Department of Urology, Mayo Clinic, Rochester, Minnesota.
  • Nickols NG; Department of Radiation Oncology, University of California, Los Angeles, California.
  • Rettig MB; Division of Medical Oncology, Ronald Reagan UCLA Medical Center, University of California, Los Angeles, California.
  • Feng FY; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, California.
  • Berlin A; Radiation Medicine Program, Princess Margaret Cancer Centre, Ontario, Canada.
  • Tward JD; Department of Radiation Therapy Oncology, Huntsman Cancer Institute at the University of Utah, Salt Lake City, Utah.
  • Davis BJ; Department of Radiation Oncology, Mayo Clinic, Rochester, Minnesota.
  • Reiter RE; Department of Urology, University of California, Los Angeles, California.
  • Boutros PC; Department of Urology, University of California, Los Angeles, California.
  • Romero T; Division of General Internal Medicine and Health Services Research, University of California, Los Angeles, California.
  • Horwitz EM; Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
  • Tendulkar RD; Department of Radiation Oncology, Cleveland Clinic, Cleveland Ohio.
  • Steinberg ML; Department of Radiation Oncology, University of California, Los Angeles, California.
  • Spratt DE; Seidman Cancer Center, Case Western Reserve University, Cleveland, Ohio.
  • Xiang M; Department of Radiation Oncology, University of California, Los Angeles, California.
  • Kishan AU; Department of Radiation Oncology, University of California, Los Angeles, California.
Int J Radiat Oncol Biol Phys ; 115(3): 645-653, 2023 03 01.
Article em En | MEDLINE | ID: mdl-36179990
ABSTRACT

PURPOSE:

Very-high-risk (VHR) prostate cancer (PC) is an aggressive subgroup with high risk of distant disease progression. Systemic treatment intensification with abiraterone or docetaxel reduces PC-specific mortality (PCSM) and distant metastasis (DM) in men receiving external beam radiation therapy (EBRT) with androgen deprivation therapy (ADT). Whether prostate-directed treatment intensification with the addition of brachytherapy (BT) boost to EBRT with ADT improves outcomes in this group is unclear. METHODS AND MATERIALS This cohort study from 16 centers across 4 countries included men with VHR PC treated with either dose-escalated EBRT with ≥24 months of ADT or EBRT + BT boost with ≥12 months of ADT. VHR was defined by National Comprehensive Cancer Network (NCCN) criteria (clinical T3b-4, primary Gleason pattern 5, or ≥2 NCCN high-risk features), and results were corroborated in a subgroup of men who met Systemic Therapy in Advancing or Metastatic Prostate Cancer Evaluation of Drug Efficacy (STAMPEDE) trials inclusion criteria (≥2 of the following clinical T3-4, Gleason 8-10, or PSA ≥40 ng/mL). PCSM and DM between EBRT and EBRT + BT were compared using inverse probability of treatment weight-adjusted Fine-Gray competing risk regression.

RESULTS:

Among the entire cohort, 270 underwent EBRT and 101 EBRT + BT. After a median follow-up of 7.8 years, 6.7% and 5.9% of men died of PC and 16.3% and 9.9% had DM after EBRT and EBRT + BT, respectively. There was no significant difference in PCSM (sHR, 1.47 [95% CI, 0.57-3.75]; P = .42) or DM (sHR, 0.72, [95% CI, 0.30-1.71]; P = .45) between EBRT + BT and EBRT. Results were similar within the STAMPEDE-defined VHR subgroup (PCSM sHR, 1.67 [95% CI, 0.48-5.81]; P = .42; DM sHR, 0.56 [95% CI, 0.15-2.04]; P = .38).

CONCLUSIONS:

In this VHR PC cohort, no difference in clinically meaningful outcomes was observed between EBRT alone with ≥24 months of ADT compared with EBRT + BT with ≥12 months of ADT. Comparative analyses in men treated with intensified systemic therapy are warranted.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Braquiterapia Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Próstata / Braquiterapia Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article