Exploring novel genomic biomarkers for response and survival after neoadjuvant chemotherapy and radical cystectomy of muscle-invasive bladder cancer.

BACKGROUND

Neoadjuvant cisplatin-based combination chemotherapy (NAC) is standard perioperative treatment of patients with muscle-invasive urothelial bladder cancer (MIBC); however, about half of the patients experience recurrence of the disease. Biomarkers for response and survival represent an unmet medical need. We used tumor specimens from transurethral resections of the bladder to explore genomic alterations and their association with response and survival in MIBC patients treated by NAC and radical cystectomy.

PATIENTS AND

METHODS

A pan cancer panel with single-nucleotide polymorphism backbone-based sequencing approach with coverage of the most commonly perturbed cancer genes and low-pass whole genome sequencing was applied for genomic characterization of 110 clinical routine patients treated with NAC before radical cystectomy. Pathological response rates, recurrence-free and overall survival were assessed.

RESULTS

Amplifications of genes on chromosome 6p22.3, particularly of the E2F3 and SOX4 gene loci, were associated with improved response and survival to NAC. Patients harboring these alterations had a high pathological treatment response rate and all remained recurrence-free during a median follow-up of 5 years. Conversely, patients with FGFR3 mutations demonstrated impaired response and survival, whereas CDKN1A mutations appeared not related to treatment response but may serve as a biomarker for poor prognosis.

CONCLUSIONS

We found the panel-based sequencing approach feasible for exploring genomic alterations associated with clinical benefits of NAC and radical cystectomy. Amplifications of genes on chromosome 6p22.3 and FGFR3 and CDKN1A mutations hold promise as biomarkers associated with response and survival to NAC.