The GoTEBORG prostate cancer screening 2 trial: a prospective, randomised, population-based prostate cancer screening trial with prostate-specific antigen testing followed by magnetic resonance imaging of the prostate

被引:31
作者
Kohestani, Kimia [1 ,2 ]
Mansson, Marianne [1 ]
Godtman, Rebecka Arnsrud [1 ,2 ]
Stranne, Johan [1 ,2 ]
Wallstrom, Jonas [3 ,4 ]
Carlsson, Sigrid [1 ,5 ]
Hellstrom, Mikael [3 ,4 ]
Hugosson, Jonas [1 ,2 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Clin Sci, Dept Urol, Bruna Straket 11B, S-41345 Gothenburg, Sweden
[2] Sahlgrens Univ Hosp, Dept Urol, Reg Vastra Gotaland, Gothenburg, Sweden
[3] Univ Gothenburg, Sahlgrenska Acad, Inst Clin Sci, Dept Radiol, Gothenburg, Sweden
[4] Sahlgrens Univ Hosp, Dept Radiol, Reg Vastra Gotaland, Gothenburg, Sweden
[5] Mem Sloan Kettering Canc Ctr, Dept Surg Urol Serv & Epidemiol, 1275 York Ave, New York, NY 10021 USA
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
Mass testing; screening; prostate cancer; prostate-specific antigen; MRI; study protocol; RADICAL PROSTATECTOMY; OVERDETECTION; OVERTREATMENT; MORTALITY; SERUM;
D O I
10.1080/21681805.2021.1881612
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective To describe the study design of the GoTEBORG prostate cancer screening (PC) 2 (Goteborg-2), a prospective, randomised, population-based trial of PC screening. This trial evaluates whether prostate-specific antigen (PSA) testing followed by 3 Tesla prostate magnetic resonance imaging (MRI) and targeted biopsy can reduce overdiagnosis, while maintaining the detection of clinically significant cancer, compared to PSA-screening and systematic biopsy. Materials and methods A random sample of men 50-60 years in the Goteborg area, Sweden, identified from the Total Population Register, were randomised to either a screening or control group (CG). Participants in the screening group (SG) were further randomised into one of three arms: (1) PSA-test; if PSA >= 3 ng/mL, then MRI and systematic biopsy, plus targeted biopsy to suspicious lesions as per Prostate Imaging - Reporting and Data System, version 2 (PI-RADSv2) 3-5; (2) PSA-test; if PSA >= 3 ng/mL, then MRI, and targeted biopsy only if PI-RADSv2 3-5; (3) identical to Arm 2, except lower PSA-cut-off >= 1.8 ng/mL. The primary outcome is the detection rate of clinically insignificant PC (defined as Gleason Score 3 + 3 [Grade Group 1]) comparing all men with PSA >= 3 ng/mL in Arm 1 vs. Arm 2 + 3. Results Randomisation and enrolment started in September 2015. Accrual has hitherto resulted in 38,770 men randomised to the SG. The participation rate is 50%. Invitation to the first screening round was completed in June 2020. Conclusions The Goteborg-2 trial will provide new knowledge about the performance of prostate MRI in a screening setting.
引用
收藏
页码:116 / 124
页数:9
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