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Testosterone Recovery Following Androgen Suppression and Prostate Radiotherapy (TRANSPORT): A Pooled Analysis of Five Randomized Trials from the Meta-Analysis of Randomized Trials in Cancer of the Prostate (MARCAP) Consortium.
Ong, Wee Loon; Romero, Tahmineh; Roy, Soumyajit; Nikitas, John; Joseph, David; Zapatero, Almudena; Malone, Shawn; Morgan, Scott C; Steinberg, Michael L; Valle, Luca F; Zaorsky, Nicholas G; Martin Ma, Ting; Rettig, Matthew B; Nickols, Nicholas; Jiang, Tommy; Reiter, Robert E; Eleswarapu, Sriram V; Maldonado, Xavier; Sun, Yilun; Nguyen, Paul L; Millar, Jeremy L; Martin, Jarad M; Spratt, Daniel E; Kishan, Amar U.
Afiliação
  • Ong WL; Alfred Health Radiation Oncology, Monash University, Melbourne, Australia.
  • Romero T; Division of General Internal Medicine and Health Services Research, University of California-Los Angeles, Los Angeles, CA, USA.
  • Roy S; Department of Radiation Oncology, Rush University Medical Centre, Chicago, IL, USA.
  • Nikitas J; Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Joseph D; Department of Medicine and Surgery, University of Western Australia, Perth, Australia.
  • Zapatero A; Department of Radiation Oncology, Health Research Institute, Hospital Universitario de la Princesa, Madrid, Spain.
  • Malone S; Department of Radiology, Radiation Oncology and Medical Physics, Ottawa Hospital Cancer Centre, University of Ottawa, Ottawa, Canada.
  • Morgan SC; Department of Radiation Oncology, University Hospitals Seidman Cancer Centre, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
  • Steinberg ML; Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Valle LF; Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Zaorsky NG; Department of Radiation Oncology, University Hospitals Seidman Cancer Centre, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
  • Martin Ma T; Department of Radiation Oncology, University of Washington, Seattle, WA, USA.
  • Rettig MB; Department of Medical Oncology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Nickols N; Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Jiang T; Department of Urology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Reiter RE; Department of Urology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Eleswarapu SV; Department of Urology, University of California-Los Angeles, Los Angeles, CA, USA.
  • Maldonado X; Hospital Universitari Vall d'Hebron, Barcelona, Spain.
  • Sun Y; Department of Radiation Oncology, University Hospitals Seidman Cancer Centre, Case Western Reserve University School of Medicine, Cleveland, OH, USA; Department of Population Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, USA.
  • Nguyen PL; Department of Radiation Oncology, Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Millar JL; Alfred Health Radiation Oncology, Monash University, Melbourne, Australia.
  • Martin JM; Department of Radiation Oncology, Calvary Mater Newcastle Hospital, University of Newcastle, Newcastle, Australia.
  • Spratt DE; Department of Radiation Oncology, University Hospitals Seidman Cancer Centre, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
  • Kishan AU; Department of Radiation Oncology, University of California-Los Angeles, Los Angeles, CA, USA. Electronic address: aukishan@mednet.ucla.edu.
Eur Urol ; 2024 Sep 19.
Article em En | MEDLINE | ID: mdl-39304428
ABSTRACT
BACKGROUND AND

OBJECTIVE:

Time to testosterone recovery (TR) following androgen deprivation therapy (ADT) with gonadotropin-releasing hormone agonists varies widely. We evaluate TR kinetics and the oncological impact of an effective castration period in patients receiving definitive radiotherapy and ADT for prostate cancer.

METHODS:

We obtained individual patient data from randomized controlled trials of radiotherapy with ADT and prospectively collected serial testosterone data from the MARCAP Consortium. We estimated the times to noncastrate TR (>1.7 nmol/l) and nonhypogonadal TR (>8.0 nmol/l) were estimated for each prescribed ADT duration, and developed corresponding nomograms. The association between effective castration period and metastasis-free survival (MFS) for any given ADT duration was evaluated via multivariable Cox regression. We conducted cubic spline analyses to assess nonlinear associations. KEY FINDINGS AND

LIMITATIONS:

We included 1444 men from five trials in the analysis, of whom 115 received 4 mo, 880 received 6 mo, 353 received 18 mo, 36 received 28 mo, and 60 received 36 mo of ADT. Times to noncastrate TR and to nonhypogonadal TR varied considerably by ADT duration. Higher baseline testosterone and lower age were associated with a higher likelihood of TR (p < 0.001 for both). Effective castration period was not linearly associated with MFS for any ADT duration on Cox regression. Cubic spline analysis revealed that the optimal effective castration period for an MFS benefit was 10.6 mo for men who received 6 mo of ADT and 18 mo for men who received 18 mo of ADT. CONCLUSIONS AND CLINICAL IMPLICATIONS Time to TR varies according to the ADT duration, baseline testosterone, and age. The relationship between effective castration period and MFS may be nonlinear, with a longer effective castration period being helpful for men receiving 6 mo of ADT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article