Urinary bladder recurrences following ureteroscopic biopsies of upper tract urothelial cancers: a multi-centre observational study with genomic assessment for clonality

Author:

Anbarasan Thineskrishna1,Nissar Sheikh2,Turbitt Julie3,Walls Kathryn4,McLuckie Sarah5,Clark Caroline3,Bourdon Jean-Christophe6,Tracey Joel3,Bray Susan67,Shamsuddin Atlaf8,Alcorn Jason9,Jain Sunjay10,Hislop Robert11,Biyani Chandra Shekhar9,Nabi Ghulam5

Affiliation:

1. College of Medicine and Veterinary Medicine, The University of Edinburgh, Edinburgh, UK

2. Department of Urology, Pilgrim Hospital, United Lincolnshire NHS Trust, England, UK

3. Department of Medical Genetics, Aberdeen Royal Infirmary, Aberdeen, UK

4. Tayside Centre for Genomic Analysis, University of Dundee, Ninewells Hospital, Dundee, UK

5. Academic Urology Unit, Division of Imaging Sciences and Technology, University of Dundee, Ninewells Hospital, Dundee, UK

6. Division of Cellular Medicine, University of Dundee, Ninewells Hospital, Dundee, UK

7. Tayside Biorepository (TBR), Ninewells Hospital, Dundee, UK

8. Department of Urology, Charing Cross Hospital, Imperial College Healthcare NHS Trust, London, UK

9. Department of Urology, Mid Yorkshire Hospitals NHS Trust, Wakefield, UK

10. Pyrah Department of Urology, Leeds Teaching hospitals, NHS Trust, Leeds, UK

11. Department of Pathology, Ninewells Hospital, Dundee, UK

Abstract

Background and aims Urinary bladder recurrences (UBRs) after radical nephroureterectomy (RNUx) are a known challenge in patients with upper-tract urothelial cancers (UTUCs). We aim to assess factors associated with UBR and clonal-relatedness with resected UTUC. Methods Patients who underwent RNUx for UTUC between 1998 and 2015 in five institutions were identified. Clonal relatedness between primary UTUC and subsequent UBR in a sub-cohort was assessed using next-generation sequencing. A Kaplan–Meier curve was used to assess differences in UBR between two groups (with or without ureteroscopic biopsy). Results Of 267 patients with complete records, 73 (27.3%) had UBR during follow-up. The five-year UBR-free survival in all patients was 64.7%. The five-year UBR-free-survival was inferior in patients who underwent URS biopsy compared with patients who did not undergo ureteroscopic biopsy (49.9% vs 76.4%, p < 0.001). History of bladder tumour (HR, 95% CI; 2.94, 1.73–5.00, p < 0.001), ureteroscopic biopsy (HR, 95% CI; 2.21, 1.38–3.53, p = 0.001) and preoperative urine cytology ≥C3 (HR, 95% CI; 2.06, 1.24–3.40, p = 0.005) were independently associated with UBR. Patients with ureteroscopic biopsy (n = 3/5) showed identical mutational changes for common genes ( TP53 and FGFR3) between primary UTUC and subsequent UBR. Conclusions Ureteroscopic biopsy of UTUC is a significant risk factor for UBR. Qualitative clonality assessment showed identical mutational signatures between primary UTUC and UBR.

Publisher

SAGE Publications

Subject

General Medicine

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