Use of prostate systematic and targeted biopsy on the basis of multiparametric MRI in biopsy-naive patients (MRI-FIRST): a prospective, multicentre, paired diagnostic study

被引:829
作者
Rouviere, Olivier [1 ,7 ]
Puech, Philippe [10 ,11 ]
Renard-Penna, Raphaele [12 ]
Claudon, Michel [13 ,14 ]
Roy, Catherine [15 ]
Mege-Lechevallier, Florence [2 ]
Decaussin-Petrucci, Myriam [2 ,8 ]
Dubreuil-Chambardel, Marine [1 ]
Magaud, Laurent [5 ,16 ]
Remontet, Laurent [6 ,9 ,17 ]
Ruffion, Alain [4 ,18 ]
Colombel, Marc [3 ,7 ]
Crouzet, Sebastien [3 ,7 ]
Schott, Anne-Marie [5 ,16 ]
Lemaitre, Laurent [10 ,11 ]
Rabilloud, Muriel [6 ,9 ,17 ]
Grenier, Nicolas [19 ]
机构
[1] Hosp Civils Lyon, Serv Imagerie Urinaire & Vasc, Lyon, France
[2] Hosp Civils Lyon, Serv Anat Pathol, Lyon, France
[3] Hosp Civils Lyon, Serv Urol, Lyon, France
[4] Hosp Civils Lyon, Serv Urol, Hop Edouard Herriot, Lyon, France
[5] Hosp Civils Lyon, Ctr Hosp Lyon Sud, Pole Sante Publ, Lyon, France
[6] Hosp Civils Lyon, Serv Biostat & Bioinformat, Lyon, France
[7] Univ Lyon, Univ Lyon 1, Fac Med Lyon Est, Lyon, France
[8] Univ Lyon, Univ Lyon 1, Fac Med Lyon Sud, Lyon, France
[9] Univ Lyon, Univ Lyon 1, Lyon, France
[10] Univ Lille, INSERM, CHU Lille, Serv Radiol, Lille, France
[11] ONCO THAI Image Assisted Laser Therapy Oncol, U1189, Lille, France
[12] Sorbonne Univ, GRC UPMC 5 Oncotype URO, Hop Tenon & Pitie Salpetriere, AP HP,Serv Radiol, Paris, France
[13] Univ Lorraine, IADI, INSERM, Nancy, France
[14] CHRU Nancy, Serv Radiol, Nancy, France
[15] CHU Strasbourg, Nouvel Hop Civil, Strasbourg, France
[16] Univ Lyon, Hlth Serv & Performance Res, EA 7425 HESPER, Lyon, France
[17] CNRS, UMR 5558, Lab Biometrie & Biol Evolut, Equipe Biostat Sante, Villeurbanne, France
[18] Univ Lyon 1, Ctr Leon Berard, Ctr Rech Cancerol Lyon, INSERM 1052 CNRS 5286, Lyon, France
[19] Univ Bordeaux, CHU Bordeaux, Serv Imagerie Diagnost & Intervent Adulte, Bordeaux, France
关键词
TRANSRECTAL ULTRASOUND FUSION; MAGNETIC-RESONANCE; CANCER DETECTION; ACCURACY; VALUES; MEN;
D O I
10.1016/S1470-2045(18)30569-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Whether multiparametric MRI improves the detection of clinically significant prostate cancer and avoids the need for systematic biopsy in biopsy-naive patients remains controversial. We aimed to investigate whether using this approach before biopsy would improve detection of clinically significant prostate cancer in biopsy-naive patients. Methods In this prospective, multicentre, paired diagnostic study, done at 16 centres in France, we enrolled patients aged 18-75 years with prostate-specific antigen concentrations of 20 ng/mL or less, and with stage T2c or lower prostate cancer. Eligible patients had been referred for prostate multiparametric MRI before a first set of prostate biopsies, with a planned interval of less than 3 months between MRI and biopsies. An operator masked to multiparametric MRI results did a systematic biopsy by obtaining 12 systematic cores and up to two cores targeting hypoechoic lesions. In the same patient, another operator targeted up to two lesions seen on MRI with a Liked score of 3 or higher (three cores per lesion) using targeted biopsy based on multiparametric MRI findings. Patients with negative multiparametric MRI (Likert score <= 2) had systematic biopsy only. The primary outcome was the detection of clinically significant prostate cancer of International Society of Urological Pathology grade group 2 or higher (csPCa-A), analysed in all patients who received both systematic and targeted biopsies and whose results from both were available for pathological central review, including patients who had protocol deviations. This study is registered with ClinicalTrials.gov, number NCT02485379, and is closed to new participants. Findings Between July 15, 2015, and Aug 11, 2016, we enrolled 275 patients. 24 (9%) were excluded from the analysis. 53 (21%) of 251 analysed patients had negative (Likert <= 2) multiparametric MRI. csPCa-A was detected in 94 (37%) of 251 patients. 13 (14%) of these 94 patients were diagnosed by systematic biopsy only, 19 (20%) by targeted biopsy only, and 62 (66%) by both techniques. Detection of csPCa-A by systematic biopsy (29.9%, 95% CI 24.3-36.0) and targeted biopsy (32.3%, 26.5-38.4) did not differ significantly (p=0.38). csPCa-A would have been missed in 5.2% (95% CI 2.8-8.7) of patients had systematic biopsy not been done, and in 7.6% (4.6-11.6) of patients had targeted biopsy not been done. Four grade 3 post-biopsy adverse events were reported (3 cases of prostatitis, and 1 case of urinary retention with haematuria). Interpretation There was no difference between systematic biopsy and targeted biopsy in the detection of ISUP grade group 2 or higher prostate cancer; however, this detection was improved by combining both techniques and both techniques showed substantial added value. Thus, obtaining a multiparametric MRI before biopsy in biopsy-naive patients can improve the detection of clinically significant prostate cancer but does not seem to avoid the need for systematic biopsy. Copyright (C) 2018 Elsevier Ltd. All rights reserved
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收藏
页码:100 / 109
页数:10
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