ctDNA-Guided Immunotherapy following Radical Cystectomy for Muscle-Invasive Bladder Cancer: Results from the TOMBOLA Trial

L Dyrskjøt*, K Birkenkamp-Demtröder, I Nordentoft, T Strandgaard, S V Lindskrog, R V Milling, S K Körner, S B Brandt, M Knudsen, T G Andreasen, C F Hansen, P Lamy, G Lam, L H Dohn, K Fabrin, A Carus, A C Petersen, U N Joensen, H Pappot, P S HoltN V Jensen, M Agerbæk, J B Jensen

*Corresponding author af dette arbejde

Abstract

BACKGROUND: Standard treatment of localized muscle-invasive bladder cancer (MIBC) is neoadjuvant chemotherapy (NAC) followed by radical cystectomy (RC), but ∼50% of patients relapse within 2 years. Adjuvant immunotherapy is currently administered based on pathology and clinical assessment in high-risk patients only, potentially resulting in under- and overtreatment.

PATIENTS AND METHODS: TOMBOLA is a Danish, multicenter, open-label, single-arm phase II trial evaluating serial circulating tumor DNA (ctDNA) testing to guide postoperative immunotherapy. Low- and high-risk patients with MIBC (cT2-4aN0-1M0) treated with NAC and RC were monitored postoperatively with tumor-informed ctDNA assays. ctDNA-positive (ctDNA+) patients initiated atezolizumab for up to 1 year, irrespective of imaging; ctDNA-negative (ctDNA-) patients received immunotherapy only upon radiographic detection of metastases. The primary endpoint was molecular and radiographic complete response. Key secondary endpoints included recurrence-free survival and overall survival.

RESULTS: In total 192 patients were enrolled, and among 178 evaluable patients in the intention-to-treat population (median follow-up 34 months), 104 (58%) were ctDNA+ within 2 years after RC, 63% within 4 months. The median lead-time from ctDNA detection to imaging-confirmed recurrence was 90 days (range -61 to 961). Of the ctDNA+ patients, 84 completed atezolizumab and had scanning and ctDNA analyses available for primary endpoint assessment. 60% (50/84) of patients achieved the primary endpoint of complete response. One-year recurrence-free survival was 97% in ctDNA- patients and 76% in ctDNA+ patients. Prespecified biomarker analyses showed that ctDNA status and levels, risk stratification, and immune-related gene-expression signatures were associated with both recurrence-risk and response to immunotherapy. Treatment was well tolerated with no new safety concerns.

CONCLUSIONS: Tumor-informed ctDNA testing after NAC and RC predicts recurrence risk and enables personalized postoperative management in MIBC. TOMBOLA demonstrates that ctDNA+, low-risk patients may benefit from early immunotherapy, while ctDNA- high-risk patients may safely avoid adjuvant treatment without compromising outcomes.

CLINICAL TRIAL REGISTRATION NUMBER: NCT04138628.

OriginalsprogEngelsk
TidsskriftAnnals of Oncology
ISSN0923-7534
DOI
StatusE-pub ahead of print - 14 jan. 2026

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