Your browser doesn't support javascript.
loading
Multi-institutional Analysis of Metastasis-directed Therapy with or Without Androgen Deprivation Therapy in Oligometastatic Castration-sensitive Prostate Cancer.
Deek, Matthew P; Sutera, Philip; Jing, Yuezhou; Gao, Robert; Rothman, Emily; Day, Heather; Chang, David; Dirix, Piet; Armstrong, Andrew J; Campbell, Bethany; Campos, Fernando Lopez; Berenguer, Miguel; Ramotar, Matthew; Conde-Moreno, Antonio; Berlin, Alejandro; Bosetti, Davide Giovanni; Corcoran, Niall; Koontz, Bridget; Mercier, Carole; Siva, Shankar; Pryor, David; Ost, Piet; Huynh, Mai Anh; Kroeze, Stephanie; Stish, Bradley; Kiess, Ana; Trock, Bruce; Tran, Phuoc T; Gillessen, Silke; Sweeney, Christopher.
Affiliation
  • Deek MP; Department of Radiation Oncology, Rutgers Cancer Institute of New Jersey Robert Wood Johnson Medical School, Rutgers University, New Brunswick, NJ, USA.
  • Sutera P; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Jing Y; The James Buchanan Brady Urological Institute of Department of Urology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Gao R; Department of Radiation Oncology, The Mayo Clinic, Rochester, MN, USA.
  • Rothman E; Department of Radiation Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
  • Day H; Department of Radiation Oncology, Australian Prostate Cancer Research Center, Queensland, Australia.
  • Chang D; Department of Radiation Oncology, Peter MacCallum Cancer Centre, Victoria, Australia.
  • Dirix P; Department of Radiation-Oncology, GasthuisZusters Antwerp (GZA) 'Sisters of the Hospital', Antwerp, Belgium.
  • Armstrong AJ; Department of Medicine, Division of Medical Oncology, Duke Cancer Institute Center for Prostate and Urologic Cancer, Duke University Medical Center, Durham, NC, USA.
  • Campbell B; Urology Unit, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Campos FL; Department of Radiation Oncology, Hospital Ramón y Cajal, Madrid, Spain.
  • Berenguer M; Radiation Oncology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
  • Ramotar M; Department of Radiation Oncology, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
  • Conde-Moreno A; Radiation Oncology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
  • Berlin A; Radiation Oncology Department, Hospital Universitario y Politécnico La Fe, Valencia, Spain.
  • Bosetti DG; Oncology Institute of Southern Switzerland, Ente Ospedaliero Cantonale (EOC), Bellinzona, Switzerland.
  • Corcoran N; Urology Unit, Royal Melbourne Hospital, Parkville, Victoria, Australia.
  • Koontz B; GenesisCare US, Fort Myers, FL, USA.
  • Mercier C; Department of Radiation-Oncology, GasthuisZusters Antwerp (GZA) 'Sisters of the Hospital', Antwerp, Belgium.
  • Siva S; Department of Radiation Oncology, Peter MacCallum Cancer Centre, Victoria, Australia.
  • Pryor D; Department of Radiation Oncology, Australian Prostate Cancer Research Center, Queensland, Australia.
  • Ost P; Department of Human Structure and Repair, Ghent University, Ghent, Belgium.
  • Huynh MA; Department of Radiation Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
  • Kroeze S; Department of Radiation Oncology, University Hospital Zurich, Zurich, Switzerland.
  • Stish B; Department of Radiation Oncology, The Mayo Clinic, Rochester, MN, USA.
  • Kiess A; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Trock B; The James Buchanan Brady Urological Institute of Department of Urology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
  • Tran PT; Department of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Gillessen S; Oncology Institute of Southern Switzerland, Ente Ospedaliero Cantonale (EOC), Bellinzona, Switzerland.
  • Sweeney C; South Australian Immunogenomics Cancer Institute, University of Adelaide, Adelaide, Australia. Electronic address: christopher.sweeney@adelaide.edu.au.
Eur Urol Oncol ; 2024 Apr 02.
Article in En | MEDLINE | ID: mdl-38570239
ABSTRACT

BACKGROUND:

Metastasis-directed therapy (MDT) is increasingly being used in oligometastatic castration-sensitive prostate cancer (omCSPC). However, it is currently unclear how to optimally integrate MDT with the standard of care of systemic hormonal therapy.

OBJECTIVE:

To report long-term outcomes of MDT alone versus MDT and a defined course of androgen deprivation therapy (ADT) in omCSPC. DESIGN, SETTING, AND

PARTICIPANTS:

Here, a multicenter, international retrospective cohort of omCSPC as defined by conventional imaging was reported. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

Biochemical progression-free survival (bPFS), distant progression-free survival (dPFS), and combined biochemical or distant progression-free survival (cPFS) were evaluated with Kaplan-Meier and multivariable Cox proportional hazard regression models. RESULTS AND

LIMITATIONS:

A total of 263 patients were included, 105 with MDT + ADT and 158 with MDT alone. The majority of patients had metachronous disease (90.5%). Five-year bPFS, dPFS, and cPFS were, respectively, 24%, 41%, and 19% in patients treated with MDT + ADT and 11% (hazard ratio [HR] 0.48, 95% confidence interval [CI] 0.36-0.64), 29% (HR 0.56, 95% CI 0.40-0.78), and 9% (HR 0.50, 95% CI 0.38-0.67) in patients treated with MDT alone. On a multivariable analysis adjusting for pretreatment variables, the use of ADT was associated with improved bPFS (HR 0.43, p < 0.001), dPFS (HR 0.45, p = 0.002), and cPFS (HR 0.44, p < 0.001).

CONCLUSIONS:

In this large multi-institutional report, the addition of concurrent ADT to MDT appears to improve time to prostate-specific antigen progression and distant recurrence, noting that about 10% patients had durable control with MDT alone. Ongoing phase 3 studies will help further define treatment options for omCSPC. PATIENT

SUMMARY:

Here, we report a large retrospective review evaluating the outcomes of metastasis-directed therapy with or without a limited course of androgen deprivation for patients with oligometastatic castration-sensitive prostate cancer. This international multi-institutional review demonstrates that the addition of androgen deprivation therapy to metastasis-directed therapy (MDT) improves progression-free survival. While a proportion of patients appear to have long-term disease control with MDT alone, further work in biomarker discovery is required to better identify which patients would be appropriate for de-escalated therapy.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur Urol Oncol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Eur Urol Oncol Year: 2024 Document type: Article