International Multicenter Validation of an Intermediate Risk Subclassification of Prostate Cancer Managed with Radical Treatment without Hormone Therapy.


Journal

The Journal of urology
ISSN: 1527-3792
Titre abrégé: J Urol
Pays: United States
ID NLM: 0376374

Informations de publication

Date de publication:
02 2019
Historique:
pubmed: 29 8 2018
medline: 21 3 2019
entrez: 29 8 2018
Statut: ppublish

Résumé

The NCCN Guidelines® recently endorsed a subclassification of intermediate risk prostate cancer into favorable and unfavorable subgroups. However, this subclassification was developed in a treatment heterogeneous cohort. Thus, to our knowledge the natural history of androgen deprivation treatment naïve favorable and unfavorable intermediate risk prostate cancer cases remains unknown. Groups at 3 academic centers pooled data on patients with intermediate risk prostate cancer treated with radical monotherapy (dose escalated external beam radiotherapy, brachytherapy or radical prostatectomy) without combined androgen deprivation treatment. We used the cumulative incidence with competing risk analysis to estimate biochemical recurrence, distant metastasis and prostate cancer specific mortality. A total of 2,550 men at intermediate risk were included in study, of whom 1,063 and 1,487 were at favorable and unfavorable risk, respectively. Of the men 1,149 underwent radical prostatectomy, 1,143 underwent dose escalated external beam radiotherapy and 258 underwent brachytherapy. Median followup after the different treatments ranged from 60.4 to 107.4 months. The 10-year cumulative incidence of distant metastasis in the favorable vs unfavorable risk groups was 0.2% (95% CI 0.2-0.2) vs 11.6% (95% CI 7.7-15.5) for radical prostatectomy (p <0.001), 2.8% (95% CI 0.8-4.8) vs 13.5% (95% CI 9.6-17.4) for dose escalated external beam radiotherapy (p <0.001) and 3.5% (95% CI 0-7.4) vs 10.2% (95% CI 4.3-16.1) for brachytherapy (p = 0.063). The 10-year rate of prostate cancer specific mortality in the favorable vs unfavorable risk groups was 0% (95% CI 0-0) vs 3.7% (95% CI 1.7-5.7) for radical prostatectomy (p = 0.016), 0.5% (95% CI 0.5-0.5) vs 5.6% (95% CI 3.6-7.6) for dose escalated external beam radiotherapy (p = 0.015) and 0% (95% CI 0-0) vs 2.5% (95% CI 0.5-4.5) for brachytherapy (p = 0.028). This multicenter international effort independently validates the prognostic value of the intermediate risk prostate cancer subclassification in androgen deprivation treatment naïve cases across all radical treatment modalities. It is unlikely that treatment intensification would meaningfully improve oncologic outcomes in men at favorable intermediate risk.

Identifiants

pubmed: 30153435
pii: S0022-5347(18)43782-2
doi: 10.1016/j.juro.2018.08.044
doi:

Types de publication

Journal Article Multicenter Study Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

284-291

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Rachel Glicksman (R)

Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
Hospital Sirio-Libanes, São Paulo, Brazil.

Alexander Koven (A)

Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

Osvaldo Espin-Garcia (O)

Department of Biostatistics, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.

Elton T T Leite (ETT)

Hospital Sirio-Libanes, São Paulo, Brazil.

João L F Silva (JLF)

Hospital Sirio-Libanes, São Paulo, Brazil.

Rafael Gadia (R)

Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
Hospital Sirio-Libanes, São Paulo, Brazil.

Michael Nesbitt (M)

Division of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ontario, Canada.

Charles N Catton (CN)

Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.

Samuel Kaffenberger (S)

Department of Urology, University of Michigan, Ann Arbor, Michigan.

Simpa S Salami (SS)

Department of Urology, University of Michigan, Ann Arbor, Michigan.

Todd M Morgan (TM)

Department of Urology, University of Michigan, Ann Arbor, Michigan.

Jason W D Hearn (JWD)

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

Will C Jackson (WC)

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

Rohit Mehra (R)

Department of Pathology, University of Michigan, Ann Arbor, Michigan.

Peter Chung (P)

Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network, Toronto, Ontario, Canada.
Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.

Neil E Fleshner (NE)

Division of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ontario, Canada.

Zachary S Zumsteg (ZS)

Department of Radiation Oncology, Cedars-Sinai Medical Center, Los Angeles.

Robert T Dess (RT)

Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan.

Felix Y Feng (FY)

Department of Urology, University of California-San Francisco, San Francisco, California.

Antonio Finelli (A)

Division of Urology, Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ontario, Canada.

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