Long-Term Outcomes of Whole Gland Salvage Cryotherapy for Locally Recurrent Prostate Cancer following Radiation Therapy: A Combined Analysis of Two Centers.


Journal

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

Informations de publication

Date de publication:
09 2021
Historique:
pubmed: 29 4 2021
medline: 31 8 2021
entrez: 28 4 2021
Statut: ppublish

Résumé

Radiation refractory prostate cancer (RRPCa) is common and salvage cryotherapy for RRPCa is emerging as a viable local treatment option. However, there is a paucity of long-term data. The purpose of this study is to determine long-term outcomes following salvage cryotherapy for RRPca. Patients undergoing salvage cryotherapy for biopsy-proven, localized RRPCa from 1992 through 2004 were prospectively accrued at two centers. Preoperative characteristics, perioperative morbidity and postoperative data were reviewed from our database. The primary outcomes were overall survival (OS) and disease-specific survival (DSS). The secondary outcomes were freedom from castration-resistant prostate cancer (CRPC) and freedom from androgen deprivation therapy (ADT). A total of 268 patients were identified with a median followup of 10.3 years. A total of 223 complication events were recorded; of them, 168 were Clavien I-II events and 55 Clavien III events. At 10 years, 69% had freedom from ADT and 76% had freedom from CRPC. The 10-year DSS rate was 81%, and the 10-year OS rate was 77%. A pre-salvage prostate specific antigen level of >10 ng/ml was associated with an increased risk of developing CRPC and initiation of ADT but was not associated with DSS or OS. The use of neoadjuvant ADT was associated with improved OS and DSS but did not affect freedom from CRPC or adjuvant ADT. Salvage cryotherapy for RRPCa provides excellent long-term freedom from ADT, CRPC and DSS with acceptable morbidity. OS at 10 years was 77%. Prospective trials are required for validation.

Identifiants

pubmed: 33908799
doi: 10.1097/JU.0000000000001831
doi:

Substances chimiques

Androgen Antagonists 0
KLK3 protein, human EC 3.4.21.-
Kallikreins EC 3.4.21.-
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Multicenter Study Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

646-654

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

Commentaires et corrections

Type : CommentIn

Auteurs

Joseph L Chin (JL)

Department of Urology, University of Western Ontario, London Health Sciences Centre, London, Ontario, Canada.

Arnon Lavi (A)

Department of Urology, University of Western Ontario, London Health Sciences Centre, London, Ontario, Canada.

Michael J Metcalfe (MJ)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Khuram Siddiqui (K)

Department of Urology, University of Western Ontario, London Health Sciences Centre, London, Ontario, Canada.

Malcolm Dewar (M)

Department of Urology, University of Western Ontario, London Health Sciences Centre, London, Ontario, Canada.

Firas G Petros (FG)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Roger Li (R)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Graciela M Nogueras González (GM)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Xuemei Wang (X)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Shiva M Nair (SM)

Department of Urology, University of Western Ontario, London Health Sciences Centre, London, Ontario, Canada.

John F Ward (JF)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Louis Pisters (L)

Department of Urology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Classifications MeSH