Which protocol for prostate biopsies in patients with a positive MRI? Interest of systematic biopsies by sectors.


Journal

Prostate cancer and prostatic diseases
ISSN: 1476-5608
Titre abrégé: Prostate Cancer Prostatic Dis
Pays: England
ID NLM: 9815755

Informations de publication

Date de publication:
19 Dec 2023
Historique:
received: 27 07 2023
accepted: 24 11 2023
revised: 16 11 2023
medline: 20 12 2023
pubmed: 20 12 2023
entrez: 19 12 2023
Statut: aheadofprint

Résumé

Current prostate biopsy (PBx) protocol for prostate cancer (PCa) diagnosis is to perform systematic biopsies (SBx) combined with targeted biopsies (TBx) in case of positive MRI (i.e. PI-RADS ≥ 3). To assess the utility of performing SBx in combination with TBx, we determined the added value of SBx brought to the diagnosis of PCa according to their sextant location and MRI target characteristics. In our local prospectively collected database, we conducted a single-center retrospective study including all patients with a suspicion of PCa, who underwent transrectal ultrasound-guided (TRUS) prostate biopsies (PBx) with a prior MRI and a single lesion classified as PI-RADS ≥ 3. We have characterized the SBx according to their location on MRI: same sextant (S-SBx), adjacent sextant (A-SBx), ipsilateral side (I-SBx) and contralateral side (C-SBx). The added value of SBx and TBx was defined as any upgrading to significant PCa (csPCa) (ISUP ≥2). 371 patients were included in the study. The added value of SBx was 10% overall. Regarding the lesion location and the SBx sextant, the added value of SBx was: 5.1% for S-SBx, 5.4% for A-SBx, 4.9% for I-SBx and 1.9% for C-SBx. The overall added value of SBx was 6.8% for PI-RADS 3 lesions, 14% for PI-RADS 4 lesions and 6.7% for PI-RADS 5 lesions (p = 0.063). The added value of SBx for contralateral side was 1.9% (2/103), 3.1% (5/163) and 0% (0/105) for PI-RADS 3, PI-RADS 4 and PI-RADS 5 lesions, respectively (p = 0,4). The added value of SBx was lower when the number of TBx was higher (OR 0.57; CI 95% 0.37-0.85; p = 0.007). Our results suggest that the utility of performing SBx in the contralateral lobe toward the MRI lesion was very low, supporting that they might be avoided.

Sections du résumé

BACKGROUND BACKGROUND
Current prostate biopsy (PBx) protocol for prostate cancer (PCa) diagnosis is to perform systematic biopsies (SBx) combined with targeted biopsies (TBx) in case of positive MRI (i.e. PI-RADS ≥ 3). To assess the utility of performing SBx in combination with TBx, we determined the added value of SBx brought to the diagnosis of PCa according to their sextant location and MRI target characteristics.
METHODS METHODS
In our local prospectively collected database, we conducted a single-center retrospective study including all patients with a suspicion of PCa, who underwent transrectal ultrasound-guided (TRUS) prostate biopsies (PBx) with a prior MRI and a single lesion classified as PI-RADS ≥ 3. We have characterized the SBx according to their location on MRI: same sextant (S-SBx), adjacent sextant (A-SBx), ipsilateral side (I-SBx) and contralateral side (C-SBx). The added value of SBx and TBx was defined as any upgrading to significant PCa (csPCa) (ISUP ≥2).
RESULTS RESULTS
371 patients were included in the study. The added value of SBx was 10% overall. Regarding the lesion location and the SBx sextant, the added value of SBx was: 5.1% for S-SBx, 5.4% for A-SBx, 4.9% for I-SBx and 1.9% for C-SBx. The overall added value of SBx was 6.8% for PI-RADS 3 lesions, 14% for PI-RADS 4 lesions and 6.7% for PI-RADS 5 lesions (p = 0.063). The added value of SBx for contralateral side was 1.9% (2/103), 3.1% (5/163) and 0% (0/105) for PI-RADS 3, PI-RADS 4 and PI-RADS 5 lesions, respectively (p = 0,4). The added value of SBx was lower when the number of TBx was higher (OR 0.57; CI 95% 0.37-0.85; p = 0.007).
CONCLUSIONS CONCLUSIONS
Our results suggest that the utility of performing SBx in the contralateral lobe toward the MRI lesion was very low, supporting that they might be avoided.

Identifiants

pubmed: 38114598
doi: 10.1038/s41391-023-00770-3
pii: 10.1038/s41391-023-00770-3
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

A Zambon (A)

Urology Department, Brest University Hospital, Brest, France. audrey.zambon@gmail.com.

T-A Nguyen (TA)

Urology Department, Brest University Hospital, Brest, France.
LaTIM-UMR 1101, INSERM, EFS, Université de Bretagne Occidentale, Brest, France.

A Fourcade (A)

Urology Department, Brest University Hospital, Brest, France.

T Segalen (T)

Urology Department, Brest University Hospital, Brest, France.

K Saout (K)

Urology Department, Brest University Hospital, Brest, France.

C Deruelle (C)

Urology Department, Brest University Hospital, Brest, France.

V Joulin (V)

Urology Department, Brest University Hospital, Brest, France.

V Tissot (V)

Radiology Department, Brest University Hospital, Brest, France.

L Doucet (L)

Pathology Department, Brest University Hospital, Brest, France.

G Fournier (G)

Urology Department, Brest University Hospital, Brest, France.
LaTIM-UMR 1101, INSERM, EFS, Université de Bretagne Occidentale, Brest, France.
CeRePP, Paris, France.

A Valeri (A)

Urology Department, Brest University Hospital, Brest, France.
LaTIM-UMR 1101, INSERM, EFS, Université de Bretagne Occidentale, Brest, France.
CeRePP, Paris, France.

Classifications MeSH