Correlation of Likert scores III–V with increasingly worse pathology in radical prostatectomy specimens significant only for men aged <60 or PSAD >0.15, with age <60 as good as PSAD <0.15 at discriminating lower risk in Likert III

Author:

Ord Jonathan J1ORCID,Crockett Matthew1,Green Jes1,Bell Lawrence TO1,Hicks Victoria2,Crawford-Smith Hugh1,Morss Amanda1,Poulton Lucinda1,Pellisery Bilgy1,Hayes Mark2,Ludeman Linmarie1,Beasley Matthew1,Fulmali Rahul1,Anniss Mark1,Barnes Elizabeth1,Foy Christopher3,Nayar Richard C2,McMeekin Faith1,Gilbert Hugh1,Okeke Aloysius1,Akhtar Mehmood2,Patel Biral1,Eaton Jonathan1

Affiliation:

1. Gloucestershire Hospitals NHS Foundation Trust, UK

2. Wye Valley NHS Trust, UK

3. Gloucestershire Research Support Service, UK

Abstract

Objectives: This study aimed to compare Likert scores with radical prostatectomy specimens. Methods: This study examined 443 men with validated pre-biopsy magnetic resonance imaging results and used cross-tabulation and chi-square significance testing with National Comprehensive Cancer Network risk categories. Results: The mean prostate-specific antigen (PSA) was 10, and the mean age was 64 years. Comparing Likert III to Likert V and Likert IV to Likert V, both (each p=0.02) were significantly associated with higher prostate cancer risk groups, but Likert III versus Likert IV was not ( p=0.1). Within the subgroup PSA density (PSAD) <0.15 ( n=140), the correlation of Likert score and final pathological risk group was lost ( p=0.5), but it was not lost within the subgroup PSAD >0.15 ( n=281; p=0.045 III vs. IV only and p=0.055 overall). Within the subgroup age <60 ( n=104), the correlation of Likert score and final pathological risk group was significant ( p=0.006 for III vs. IV and p=0.04 overall), whereas within the subgroup age >60 ( n=339) this significant difference was lost ( p=0.34). Further subgroup analysis within Likert III ( n=86) found that men <60 ( n=22) had neither high-grade (G3 or G4 or G5) nor very high-risk disease. There were only two high-risk cases, both of which were G2T3a (2/22; 10%). In men with Likert III and PSAD <0.15 ( n=31), there were seven high-risk and two very high-risk cases (9/31; 25%). This difference was not significant ( p=0.31) Conclusion: With these two findings, we recommend that men <60 with Likert III can be counselled like men with Likert III and PSAD <0.15, that they are unlikely to have unfavourable or high-risk disease and that they may wish to avoid biopsy or treatment. Level of evidence: Level 1b.

Publisher

SAGE Publications

Subject

Urology,Surgery

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