Radical Prostatectomy With and Without Neoadjuvant Chemohormonal Pretreatment for High-Risk Localized Prostate Cancer: A Comparative Propensity Score Matched Analysis.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 15 05 2018
revised: 29 08 2018
accepted: 22 09 2018
pubmed: 6 11 2018
medline: 8 8 2019
entrez: 5 11 2018
Statut: ppublish

Résumé

To investigate the clinical outcomes in patients with high-risk prostate cancer (PCa) treated with neoadjuvant chemohormonal therapy (NCHT) before radical prostatectomy (RP). Our NCHT protocol involved complete androgen blockade followed by 6 cycles of docetaxel (30 mg/m In the NCHT group, 10.0% experienced pathologic complete response, 3.3% had positive surgical margins, and 13.3% developed severe complications (Clavien-Dindo grade III or higher) after RP. The median follow-up duration was 42.5 months, and the 5-year biochemical recurrence (BCR)-free survival was 60.1%. In multivariate analysis, pN+ was an independent prognostic factor for BCR (hazard ratio = 5.251, 95%CI 1.300-21.201; P = .020). In propensity score matching, the BCR rate in the NCHT group was significantly lower than that in the RP alone group (P = .021). In subgroup analyses, the BCR rate in patients with a single high-risk factor was significantly lower in the NCHT group than in the RP-alone group (P = .027). NCHT before RP can reduce the risk of BCR in patients with high-risk PCa, particularly if a single high-risk factor is present. However, the potential for perioperative complications should be considered.

Sections du résumé

BACKGROUND BACKGROUND
To investigate the clinical outcomes in patients with high-risk prostate cancer (PCa) treated with neoadjuvant chemohormonal therapy (NCHT) before radical prostatectomy (RP).
PATIENTS AND METHODS METHODS
Our NCHT protocol involved complete androgen blockade followed by 6 cycles of docetaxel (30 mg/m
RESULTS RESULTS
In the NCHT group, 10.0% experienced pathologic complete response, 3.3% had positive surgical margins, and 13.3% developed severe complications (Clavien-Dindo grade III or higher) after RP. The median follow-up duration was 42.5 months, and the 5-year biochemical recurrence (BCR)-free survival was 60.1%. In multivariate analysis, pN+ was an independent prognostic factor for BCR (hazard ratio = 5.251, 95%CI 1.300-21.201; P = .020). In propensity score matching, the BCR rate in the NCHT group was significantly lower than that in the RP alone group (P = .021). In subgroup analyses, the BCR rate in patients with a single high-risk factor was significantly lower in the NCHT group than in the RP-alone group (P = .027).
CONCLUSION CONCLUSIONS
NCHT before RP can reduce the risk of BCR in patients with high-risk PCa, particularly if a single high-risk factor is present. However, the potential for perioperative complications should be considered.

Identifiants

pubmed: 30391137
pii: S1558-7673(18)30393-8
doi: 10.1016/j.clgc.2018.09.019
pii:
doi:

Substances chimiques

Docetaxel 15H5577CQD
Estramustine 35LT29625A
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Comparative Study Journal Article

Langues

eng

Pagination

e113-e122

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Shintaro Narita (S)

Department of Urology, Akita University School of Medicine, Akita, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG). Electronic address: nari6202@gipc.akita-u.ac.jp.

Taketoshi Nara (T)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Sohei Kanda (S)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Kazuyuki Numakura (K)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Mitsuru Saito (M)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Takamitsu Inoue (T)

Department of Urology, Akita University School of Medicine, Akita, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Shigeru Satoh (S)

Department of Urology, Akita University School of Medicine, Akita, Japan.

Hiroshi Nanjo (H)

Department of Pathology, Akita University School of Medicine, Akita, Japan.

Norihiko Tsuchiya (N)

Department of Urology, Yamagata University School of Medicine, Yamagata, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Koji Mitsuzuka (K)

Department of Urology, Tohoku University School of Medicine, Sendai, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Takuya Koie (T)

Department of Urology, Hirosaki University School of Medicine, Hirosaki, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Sadafumi Kawamura (S)

Department of Urology, Miyagi Cancer Center, Natori, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Chikara Ohyama (C)

Department of Urology, Hirosaki University School of Medicine, Hirosaki, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Tatsuo Tochigi (T)

Department of Urology, Miyagi Cancer Center, Natori, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Yoichi Arai (Y)

Department of Urology, Tohoku University School of Medicine, Sendai, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

Tomonori Habuchi (T)

Department of Urology, Akita University School of Medicine, Akita, Japan; Michinoku Japan Urological Cancer Study Group (MJUCSG).

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Classifications MeSH