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Tailoring biopsy strategy in the MRI-fusion prostate biopsy era: systematic, targeted or neither?
Jäderling, Fredrik; Bergman, Martin; Engel, Jan Chandra; Mortezavi, Ashkan; Picker, Wolfgang; Haug, Erik Skaaheim; Eklund, Martin; Nordström, Tobias.
Afiliación
  • Jäderling F; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. fredrik.jaderling@ki.se.
  • Bergman M; Department of Radiology, Capio S:T Görans Hospital, Stockholm, Sweden. fredrik.jaderling@ki.se.
  • Engel JC; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, S-171 77, Sweden.
  • Mortezavi A; Department of Surgery, Capio S:T Görans Hospital, Stockholm, Sweden.
  • Picker W; Department of Clinical Sciences at Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.
  • Haug ES; Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, S-171 77, Sweden.
  • Eklund M; Department of Urology, University Hospital Zurich, Zurich, Switzerland.
  • Nordström T; Department of Urology, Karolinska University Hospital Solna, Stockholm, Sweden.
BMC Urol ; 24(1): 168, 2024 Aug 07.
Article en En | MEDLINE | ID: mdl-39112967
ABSTRACT

BACKGROUND:

Magnetic  resonance imaging (MRI) followed by targeted biopsy (TBx) is utilized for prostate cancer (PCa) detection. However, the value of adding systematic biopsies (SBx) to targeted biopsy procedures (combined biopsy; CBx) in men with suspicious MRI findings has not been determined.

METHODS:

We analysed biopsy outcomes in 429 men with MRI lesions in the prospective multicenter STHLM3MRI pilot study, planned for prostate biopsy. Participants underwent 1.5T biparametric MRI without contrast enhancement, reported according to the PI-RADS v2, and with TBx plus SBx if the MRI lesion score was ≥ 3. The endpoints were clinically nonsignificant (nsPCa) and clinically significant PCa (csPCa), defined as ISUP grade groups 1 and ≥ 2, respectively.

RESULTS:

The median age was 65 years (59-70), and the median PSA 6.0 ng/ml (4.1-9.0). The detection rates of csPCa when using TBx or SBx combined were 18%, 46%, and 85% in men with PIRADS scores of 3 (n = 195), 4 (n = 121), and 5 (n = 113), respectively. This combined strategy detected csPCa in more men than TBx alone (43.6% vs 39.2%, p < 0.02), with similar detection of nsPCa (19.3% vs 17.7%, p = 0.2). In men with equivocal lesions (PI-RADS 3), the detection rates for csPCa were similar for the combined strategy and for TBx alone (17.9% and 15.4%, p = 0.06). However, there was an increase in the detection of nsPCa when using the combined strategy (21.0% vs 15.4%, p < 0.02). Men with equivocal lesions and a PSA density < 0.1 ng/ml2 or a Stockholm 3 test < 0.11 had a low risk of harboring csPCa.

CONCLUSIONS:

Supplementing targeted with systematic biopsies enhances clinically significant cancer detection. However, in men with equivocal lesions, this combination has potential for detecting nonsignificant disease. A subgroup of men with equivocal MRI findings may be identified as having a low risk for significant cancer and spared unnecessary biopsies.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Imagen por Resonancia Magnética / Biopsia Guiada por Imagen Idioma: En Revista: BMC Urol Asunto de la revista: UROLOGIA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Imagen por Resonancia Magnética / Biopsia Guiada por Imagen Idioma: En Revista: BMC Urol Asunto de la revista: UROLOGIA Año: 2024 Tipo del documento: Article