Population-based prostate cancer screening using a prospective, blinded, paired screen-positive comparison of PSA and fast MRI: The IP1-PROSTAGRAM study.

Authors

null

David Eldred-Evans

Imperial Prostate, London, United Kingdom

David Eldred-Evans , Paula Burak , Martin John Connor , Emily Day , Martin Evans , Francesca Fiorentino , Martin Gammon , Feargus Hosking-Jervis , Natalia Klimowska- Nassar , William McGuire , Anwar R Padhani , Derek Price , Toby Prevost , Heminder Sokhi , Henry Tam , Mathias Winkler , Hashim Uddin Ahmed

Organizations

Imperial Prostate, London, United Kingdom, Imperial Clinical Trials Unit, London, United Kingdom, Imperial College London, London, United Kingdom, Imperial Clinical Trials Unit, Imperial College London, London, United Kingdom, Imperial Prostate, Imperial College London, London, United Kingdom, Paul Strickland Scanner Centre, Mount Vernon Cancer Centre, Middlesex, United Kingdom, Paul Strickland Scanner Centre, Mount Vernon Cancer Centre, London, United Kingdom, Department of Radiology, Imperial College Healthcare NHS Trust, London, United Kingdom, Imperial Urology, Charing Cross Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom

Research Funding

Other Foundation
Wellcome Trust, Other Foundation, The Urology Foundation

Background: The prostate-specific antigen (PSA) test can lead to under- and over-diagnosis of prostate cancer and has not been recommended for population screening. A fast MRI scan might overcome the limitations of PSA. IP1-PROSTAGRAM is the first study to evaluate the performance of a 15-minute non-contrast MRI for prostate cancer screening in comparison to PSA. Methods: IP1-PROSTAGRAM was a prospective, population-based, screen-positive paired-cohort study. Men aged 50-69 years in the UK were invited for prostate cancer screening through seven primary care practices or community-based recruitment. Participants underwent a PSA and MRI scan (T2-weighted and diffusion). MRI was scored using PIRADS version 2.0 without knowledge of PSA; screen-positive MRI (defined as either PIRADS score 3-5 or 4-5) were compared against a screen-positive PSA defined as ≥3ng/ml. If any test was screen-positive, a systematic 12-core biopsy was performed with MRI-ultrasound image-fusion targeted biopsy to MRI suspicious areas, as appropriate. Clinically-significant cancer was defined as any Gleason score ≥3+4. The primary outcome was the proportion of screen-positive MRI at different scores; important secondary outcomes were the number of clinically-significant and insignificant cancers detected. Results: 2034 men were invited to participate of whom 408 consented and 406 were screened by both PSA and MRI (10/Oct/2018-15/May/2019). The proportion with a screen-positive MRI (score 3-5) was higher than the proportion with a screen-positive PSA (17.7% [95%CI 14.3-21.8] vs. 9.9% [95%CI 7.3-13.2]; p < 0.001). A screen-positive MRI (score 4-5) was similar to a screen-positive PSA (10.6% [95%CI 7.9-14.0] vs. 9.9% [95%CI 7.3-13.2], p = 0.71). An MRI score 3-5 or 4-5 used to denote a screen-positive MRI, compared to PSA alone, detected 14, 11 and 7 clinically-significant cancers, respectively. There were 7, 5 and 6 clinically-insignificant cancers detected, respectively. No serious adverse events occurred. Conclusions: When screening the general population for prostate cancer, MRI using a score of 4-5 to define a screen-positive test, compared to PSA alone at ≥3ng/ml, could lead to more men diagnosed with clinically-significant cancer without increasing the number of men biopsied or diagnosed with clinically-insignificant cancer. Clinical trial information: NCT03702439.

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Discussion Session

Session Title

Genitourinary Cancer—Prostate, Testicular, and Penile

Track

Genitourinary Cancer—Prostate, Testicular, and Penile

Sub Track

Epidemiology/Outcomes

Clinical Trial Registration Number

NCT03702439

Citation

J Clin Oncol 38: 2020 (suppl; abstr 5513)

DOI

10.1200/JCO.2020.38.15_suppl.5513

Abstract #

5513

Poster Bd #

94

Abstract Disclosures

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