Prostate biopsy and prostate cancer management in patients with haemophilia: The experience of French Haemophilia Treatment Centres.


Journal

Haemophilia : the official journal of the World Federation of Hemophilia
ISSN: 1365-2516
Titre abrégé: Haemophilia
Pays: England
ID NLM: 9442916

Informations de publication

Date de publication:
May 2022
Historique:
revised: 18 01 2022
received: 03 11 2021
accepted: 26 01 2022
pubmed: 25 2 2022
medline: 14 5 2022
entrez: 24 2 2022
Statut: ppublish

Résumé

Data are limited on prostate cancer (PC) management in patients with haemophilia (PWH). To describe PC screening and diagnosis, treatment modalities and bleeding complications in a group of unselected PWH followed at French Haemophilia Treatment Centres (HTCs) PATIENTS AND METHODS: PC screening, management and bleeding complications were retrospectively investigated at 14 French HTCs between 2003 and 2018. Among> 1549 > 50-year-old PWHs, 73 (4.7%) underwent PC screening (median age 71.1 years; 67/6 HA/HB, 17/56 severe-moderate/mild). At diagnosis, haematuria was infrequent. Prophylaxis was administered during 76/86 (88%) prostate biopsies (PB) (n = 67 clotting factor concentrates, CFC; n = 9 desmopressin; n = 17 associated with tranexamic acid, TA). Bleeding (11/86, 12.8%) occurred mainly post-prophylaxis (median delay: 7 days): haematuria (9/11, 81.8%), and rectal bleeding (2/11, 18.2%) including one major (1.2%). PC was confirmed in 50/86 PB and in two prostatectomy specimens (total n = 50 patients, n = 6 with only active surveillance). Surgery (n = 28/44 patients) was managed with CFC. Fifteen patients had radiotherapy/brachytherapy, 10 had hormone therapy; CFC-based prophylaxis was only prescribed for brachytherapy (n = 2). Major bleedings occurred in 3/28 (10.7%) and 2/15 (13.3%) patients who underwent surgery and radio/brachytherapy, respectively. No bleeding risk factor was found. Our data indicate that PB requires prophylaxis for atleast 7 days, using CFC, desmopressin or TA in function of haemophilia severity. PC surgery should be considered at high bleeding risk. Long-term post-procedural CFC or oral TA could be discussed. Radiotherapy/brachytherapy also should be managed with prophylaxis (CFC or TA).

Sections du résumé

BACKGROUND BACKGROUND
Data are limited on prostate cancer (PC) management in patients with haemophilia (PWH).
AIM OBJECTIVE
To describe PC screening and diagnosis, treatment modalities and bleeding complications in a group of unselected PWH followed at French Haemophilia Treatment Centres (HTCs) PATIENTS AND METHODS: PC screening, management and bleeding complications were retrospectively investigated at 14 French HTCs between 2003 and 2018.
RESULTS RESULTS
Among> 1549 > 50-year-old PWHs, 73 (4.7%) underwent PC screening (median age 71.1 years; 67/6 HA/HB, 17/56 severe-moderate/mild). At diagnosis, haematuria was infrequent. Prophylaxis was administered during 76/86 (88%) prostate biopsies (PB) (n = 67 clotting factor concentrates, CFC; n = 9 desmopressin; n = 17 associated with tranexamic acid, TA). Bleeding (11/86, 12.8%) occurred mainly post-prophylaxis (median delay: 7 days): haematuria (9/11, 81.8%), and rectal bleeding (2/11, 18.2%) including one major (1.2%). PC was confirmed in 50/86 PB and in two prostatectomy specimens (total n = 50 patients, n = 6 with only active surveillance). Surgery (n = 28/44 patients) was managed with CFC. Fifteen patients had radiotherapy/brachytherapy, 10 had hormone therapy; CFC-based prophylaxis was only prescribed for brachytherapy (n = 2). Major bleedings occurred in 3/28 (10.7%) and 2/15 (13.3%) patients who underwent surgery and radio/brachytherapy, respectively. No bleeding risk factor was found.
CONCLUSION CONCLUSIONS
Our data indicate that PB requires prophylaxis for atleast 7 days, using CFC, desmopressin or TA in function of haemophilia severity. PC surgery should be considered at high bleeding risk. Long-term post-procedural CFC or oral TA could be discussed. Radiotherapy/brachytherapy also should be managed with prophylaxis (CFC or TA).

Identifiants

pubmed: 35201650
doi: 10.1111/hae.14507
doi:

Substances chimiques

Deamino Arginine Vasopressin ENR1LLB0FP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

437-444

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 John Wiley & Sons Ltd.

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Auteurs

Philippe Gautier (P)

Haemophilia Treatment Centre, Associated National Reference Willebrand Centre, University hospital, Caen, France.

Benoit Guillet (B)

Haemophilia Treatment Centre, University hospital, Rennes, France.

Marianne Sigaud (M)

Associated National Reference Haemophilia Treatment Centre, University hospital, Nantes, France.

Ségolène Claeyssens (S)

Haemophilia Treatment Centre, University hospital, Toulouse, France.

Fabienne Genre Volot (FG)

Haemophilia Treatment Centre, University hospital, Dijon, France.

Pierre Chamouni (P)

Haemophilia Treatment Centre, University hospital, Rouen, France.

Anne Lienahrt (A)

Reference Haemophilia Treatment Centre, University hospital, Lyon, France.

Birgit Frotscher (B)

Haemophilia Treatment Centre, University hospital, Nancy, France.

Alexandra Fournel (A)

Haemophilia Treatment Centre, University hospital, Besançon, France.

Sabine Castet (S)

Haemophilia Treatment Centre, University hospital, Bordeaux, France.

Catherine Poumayou (C)

Haemophilia Treatment Centre, La Timone Hospital APHM, Aix Marseille University, Marseille, France.

Valérie Gay (V)

hospital, Haemophilia Treatment Centre, Chambery, France.

Rodolphe Thuret (R)

Department of urologic surgery, University hospital, Montpellier, France.

Bénédicte Wibaut (B)

Haemophilia Treatment Centre, National Reference Willebrand Centre, University hospital, Lille, France.

Christine Biron-Andreani (C)

Haemophilia Treatment Centre, University hospital, Montpellier, France.

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