Outcomes and prognostic factors in intermediate-risk prostate cancer: multi-institutional analysis of the Spanish RECAP database.


Journal

Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
ISSN: 1699-3055
Titre abrégé: Clin Transl Oncol
Pays: Italy
ID NLM: 101247119

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 03 10 2018
accepted: 24 11 2018
pubmed: 12 12 2018
medline: 18 12 2019
entrez: 12 12 2018
Statut: ppublish

Résumé

To retrospectively assess outcomes and to identify prognostic factors in patients diagnosed with intermediate-risk (IR) prostate cancer (PCa) treated with primary external beam radiotherapy (EBRT). Data were obtained from the multi-institutional Spanish RECAP database, a population-based prostate cancer registry in Spain. All IR patients (NCCN criteria) who underwent primary EBRT were included. The following variables were assessed: age; prostate-specific antigen (PSA); Gleason score; clinical T stage; percentage of positive biopsy cores (PPBC); androgen deprivation therapy (ADT); and radiotherapy dose. The patients were stratified into one of three risk subcategories: (1) favourable IR (FIR; GS 6, ≤ T2b or GS 3 + 4, ≤ T1c), (2) marginal IR (MIR; GS 3 + 4, T2a-b), and (3) unfavourable IR (UIR; GS 4 + 3 or T2c). Biochemical relapse-free survival (BRFS), disease-free survival (DFS), cancer-specific survival (CSS), and overall survival (OS) were assessed. A total of 1754 patients from the RECAP database were included and stratified by risk group: FIR, n = 781 (44.5%); MIR, n = 252 (14.4%); and UIR, n = 721 (41.1%). Mean age was 71 years (range 47-86). Mean PSA was 10.4 ng/ml (range 6-20). The median radiotherapy dose was 74 Gy, with mean doses of 72.5 Gy (FIR), 73.4 Gy (MIR), and 72.8 Gy (UIR). Most patients (88%) received ADT for a median of 7.1 months. By risk group (FIR, MIR, UIR), ADT rates were, respectively, 88.9, 86.5, and 86.9%. Only patients with ≥ 24 months of follow-up post-EBRT were included in the survival analysis (n = 1294). At a median follow-up of 52 months (range 24-173), respective 5- and 10-year outcomes were: OS 93.6% and 79%; BRFS 88.9% and 71.4%; DFS 96.1% and 89%; CSS 98.9% and 94.6%. Complication rates (≥ grade 3) were: acute genitourinary (GU) 2%; late GU 1%; acute gastrointestinal (GI) 2%; late GI 1%. There was no significant association between risk group and BRFS or OS. However, patients with favourable-risk disease had significantly better 5- and 10-year DFS than patients with UIR: 98.7% vs. 92.4% and 92% vs. 85.8% (p = 0.0005). CSS was significantly higher (p = 0.0057) in the FIR group at 5 (99.7% vs. 97.3%) and 10 years (96.1% vs. 93.4%). On the multivariate analyses, the following were significant predictors of survival: ADT (BRFS and DFS); dose ≥ 74 Gy (BRFS); age (OS). This is the first nationwide study in Spain to report long-term outcomes of patients with intermediate-risk PCa treated with EBRT. Survival outcomes were good, with a low incidence of both acute and late toxicity. Patients with unfavourable risk characteristics had significantly lower 5- and 10-year disease-free survival rates. ADT and radiotherapy dose ≥ 74 Gy were both significant predictors of treatment outcomes.

Identifiants

pubmed: 30536208
doi: 10.1007/s12094-018-02000-y
pii: 10.1007/s12094-018-02000-y
doi:

Substances chimiques

Androgen Antagonists 0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

900-909

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Auteurs

A Hervás (A)

Department of Radiation Oncology, Hospital Ramón y Cajal, Madrid, Spain. hervasmoron@gmail.com.

J Pastor (J)

Department of Radiation Oncology, Hospital General de Valencia, Valencia, Spain.

C González (C)

Department of Radiation Oncology, Hospital Gregorio Marañón, Madrid, Spain.

J Jové (J)

Department of Radiation Oncology, Hospital Germans Trias i Pujol, Barcelona, Spain.

A Gómez (A)

Department of Radiation Oncology, Hospital Clínico Universitario, Santiago de Compostela, Spain.

M Casaña (M)

Department of Radiation Oncology, Instituto Valenciano de Oncologia, Valencia, Spain.

E Villafranca (E)

Department of Radiation Oncology, Hospital Clínico Universitario, Pamplona, Spain.

J L Mengual (JL)

Department of Radiation Oncology, Instituto Valenciano de Oncologia, Valencia, Spain.

V Muñoz (V)

Department of Radiation Oncology, Hospital do Mixoeiro, Vigo, Spain.

I Henriquez (I)

Department of Radiation Oncology, Hospital Universitario Sant Joan, Reus, Spain.

J Muñoz (J)

Department of Radiation Oncology, Hospital Infanta Cristina, Badajoz, Spain.

E Collado (E)

Department of Radiation Oncology, Hospital Uiversitario La Fe, Valencia, Spain.

J Clemente (J)

Department of Radiation Oncology, Instituto Valenciano de Oncologia, Alcoy, Spain.

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