Ductal Carcinoma of the Prostate: An Uncommon Entity With Atypical Behaviour.


Journal

Clinical oncology (Royal College of Radiologists (Great Britain))
ISSN: 1433-2981
Titre abrégé: Clin Oncol (R Coll Radiol)
Pays: England
ID NLM: 9002902

Informations de publication

Date de publication:
02 2019
Historique:
received: 11 04 2018
revised: 03 10 2018
accepted: 10 10 2018
pubmed: 26 11 2018
medline: 8 2 2020
entrez: 26 11 2018
Statut: ppublish

Résumé

Ductal adenocarcinoma is a rare variant of prostate cancer, and as such clinical outcomes and best management are not well defined. This series demonstrates the atypical presentation and unusual clinical behaviour of ductal adenocarcinoma and proposes management guidelines to assist clinicians. A retrospective review of pure (nine patients) and mixed (18 patients) ductal adenocarcinoma of the prostate referred to the Departments of Radiation Oncology of the Sydney Cancer Centre, Royal Prince Alfred Hospital and Northern Sydney Cancer Centre, Royal North Shore Hospital, between 2000 and 2015. Twenty-seven patients were treated with definitive radiotherapy, nine patients (33%) with pure ductal and 18 (67%) with mixed ductal-acinar adenocarcinoma. The median follow-up was 38 months. Four patients (15%) failed locally, all of whom received less than 80 Gy, or no brachytherapy boost. Five patients (19%) failed distantly, four with biopsy-proven lung metastases. All distant failures occurred with a prostate-specific antigen (PSA) < 3 ng/ml. This series shows the atypical clinical presentation of this entity, as well as its propensity to metastasise to unusual sites. Relapse may occur at low absolute PSA values and is often asymptomatic. Ductal cancer should not simply be regarded as a high Gleason grade cancer. We propose management guidelines, including regular computed tomography examinations (rather than relying solely on PSA levels) as part of the follow-up for patients with any component of ductal adenocarcinoma.

Identifiants

pubmed: 30471806
pii: S0936-6555(18)30493-X
doi: 10.1016/j.clon.2018.10.011
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108-114

Informations de copyright

Crown Copyright © 2018. Published by Elsevier Ltd. All rights reserved.

Auteurs

S Bergamin (S)

Northern Sydney Cancer Centre, Radiation Oncology Unit, Royal North Shore Hospital, St Leonards, Sydney, NSW, Australia. Electronic address: skbergamin@gmail.com.

T Eade (T)

Northern Sydney Cancer Centre, Radiation Oncology Unit, Royal North Shore Hospital, St Leonards, Sydney, NSW, Australia; Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia.

A Kneebone (A)

Northern Sydney Cancer Centre, Radiation Oncology Unit, Royal North Shore Hospital, St Leonards, Sydney, NSW, Australia; Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia.

J G Kench (JG)

Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia; Department of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Camperdown, Sydney, NSW, Australia.

P Sved (P)

Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia; Department of Urology, Royal Prince Alfred Hospital, Camperdown, Sydney, NSW, Australia.

J-F Biset (JF)

5 Rue Contre-Amiral Joseph du Bouzet, Noumea, New Caledonia; Université Paris Descartes, Paris, France.

G Hruby (G)

Northern Sydney Cancer Centre, Radiation Oncology Unit, Royal North Shore Hospital, St Leonards, Sydney, NSW, Australia; Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia.

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Classifications MeSH