Tumour growth rates of prostate cancer during active surveillance: is there a difference between MRI-visible low and intermediate-risk disease?

Author:

Giganti Francesco12ORCID,Allen Clare1,Stavrinides Vasilis23,Stabile Armando24,Haider Aiman5,Freeman Alex5,Pashayan Nora6,Punwani Shonit17,Emberton Mark3,Moore Caroline M23,Kirkham Alex1

Affiliation:

1. Department of Radiology, University College London Hospital NHS Foundation Trust, London, UK

2. Division of Surgery & Interventional Science, University College London, London, UK

3. Department of Urology, University College London Hospital NHS Foundation Trust, London, UK

4. Department of Urology and Division of Experimental Oncology, Vita-Salute San Raffaele University, Milan, Italy

5. Department of Pathology, University College London Hospital NHS Foundation Trust, London, UK

6. Department of Applied Health Research, University College London, London, UK

7. Centre for Medical Imaging, University College London, London, UK

Abstract

Objectives: The aim of this study was to evaluate the changes in lesion volume on serial multiparametric magnetic resonance (mpMRI) during active surveillance for prostate cancer. Methods: A total of 160 patients with a targeted biopsy-confirmed visible lesion on mpMRI, stratified by low- and intermediate-risk disease (Gleason Grade Group 1 vs Gleason Grade Group 2), were analysed. The % change per year was calculated using the formula: [(final volume/initial volume) exp (1/interval between scans in years)]-1. Results: There was no significant difference in the annual median percentage change between Gleason Grade Group 1 (18%) and Gleason Grade Group 2 (23%) disease (p = 0.16), and between ≤ 10% (23%) and > 10% (22%) of Gleason pattern 4 (p = 0.78). Assuming a spherical lesion, these changes corresponded to annual increases in mean tumour diameter of 6% and 7% for Gleason Grade Group 1 and Gleason Grade Group 2 respectively, which may be less than the interscan variability of serial mpMRI. Conclusion: In an active surveillance cohort, we did not see a significant difference in the annual growth rate of Gleason Grade Group 1 and 2 tumours. Advances in knowledge: In patients on active surveillance, the measured growth rates for visible tumours in Gleason Grade Groups 1 and 2 were similar. The annual growth rate was small in most cases and this may have implications for the MRI follow-up interval in active surveillance.

Publisher

British Institute of Radiology

Subject

Radiology, Nuclear Medicine and imaging,General Medicine

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