The role of salvage lymph node dissection in nonmetastatic castration-resistant prostate cancer: A single center experience.

Androgen-deprivation therapy Castration-resistant prostate cancer Lymph nodes Salvage lymph node dissection Survival outcomes

Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
02 2020
Historique:
received: 24 05 2019
revised: 21 07 2019
accepted: 22 09 2019
pubmed: 28 10 2019
medline: 15 4 2021
entrez: 27 10 2019
Statut: ppublish

Résumé

To evaluate oncologic outcomes of patients with nonmetastatic, castration-resistant prostate cancer treated with salvage lymph node dissection (sLND) or androgen-deprivation therapy (ADT) for lymph nodes (LN)-only recurrence. Retrospective analysis of 23 (51.1%) patients who underwent sLND and 22 (48.9%) men who received ADT for LN-only recurrence. Biochemical recurrence (BCR) was defined as prostate-specific antigen (PSA) >0.2 ng/ml with an increased trend and radiological recurrence (RAR) was defined as a positive imaging study after sLND or ADT. Second line systemic therapies (SST) were defined as any systemic therapy administered for progression. Predictors of BCR, RAR, and SST were assessed with Cox regression analyses. Mean PSA reduction was significantly higher after sLND than ADT (62.8% vs. 17.7%; P = 0.04). Clinical outcomes were not statistically different between the 2 groups. However, there was a trend toward a longer time to BCR (13.3 vs. 6 months; P = 0.2) and RAR (21.1 vs. 14.2 months, P = 0.09) in sLND patients than ADT. Median time to SST was longer in the sLND group than ADT (P = 0.04). Univariable Cox regression analyses showed that PSA doubling time and pT stage were associated with RAR and SST (all P < 0.05). In patients with nonmetastatic, castration-resistant prostate cancer, sLND resulted in greater PSA decrease than ADT. We noted a nonstatistically significant trend toward longer time to BCR and longer time to RAR for patients treated with sLND than ADT. Additionally, sLND may increase time to SST as compared to ADT.

Identifiants

pubmed: 31653561
pii: S1078-1439(19)30367-9
doi: 10.1016/j.urolonc.2019.09.016
pii:
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

38.e9-38.e16

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Luca Boeri (L)

Department of Urology, Mayo Clinic, Rochester, MN; Department of Urology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy. Electronic address: dr.lucaboeri@gmail.com.

Vidit Sharma (V)

Department of Urology, Mayo Clinic, Rochester, MN.

Avinash Nehra (A)

Department of Urology, Mayo Clinic, Rochester, MN.

Eugene Kwon (E)

Department of Urology, Mayo Clinic, Rochester, MN.

R Jeffrey Karnes (RJ)

Department of Urology, Mayo Clinic, Rochester, MN.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH