Early Detection of Metastatic Relapse and Monitoring of Therapeutic Efficacy by Ultra-Deep Sequencing of Plasma Cell-Free DNA in Patients With Urothelial Bladder Carcinoma

Author:

Christensen Emil1,Birkenkamp-Demtröder Karin1,Sethi Himanshu2,Shchegrova Svetlana2,Salari Raheleh2,Nordentoft Iver1,Wu Hsin-Ta2,Knudsen Michael1,Lamy Philippe1,Lindskrog Sia Viborg1,Taber Ann1,Balcioglu Mustafa2,Vang Søren1,Assaf Zoe2,Sharma Shruti2,Tin Antony S.2,Srinivasan Ramya2,Hafez Dina2,Reinert Thomas1,Navarro Samantha2,Olson Alexander2,Ram Rosalyn2,Dashner Scott2,Rabinowitz Matthew2,Billings Paul2,Sigurjonsson Styrmir2,Andersen Claus Lindbjerg1,Swenerton Ryan2,Aleshin Alexey2,Zimmermann Bernhard2,Agerbæk Mads1,Lin Cheng-Ho Jimmy2,Jensen Jørgen Bjerggaard13,Dyrskjøt Lars13

Affiliation:

1. Aarhus University Hospital, Aarhus, Denmark

2. Natera, San Carlos, CA

3. Aarhus University, Aarhus, Denmark

Abstract

PURPOSE Novel sensitive methods for early detection of relapse and for monitoring therapeutic efficacy may have a huge impact on risk stratification, treatment, and ultimately outcome for patients with bladder cancer. We addressed the prognostic and predictive impact of ultra-deep sequencing of cell-free DNA in patients before and after cystectomy and during chemotherapy. PATIENTS AND METHODS We included 68 patients with localized advanced bladder cancer. Patient-specific somatic mutations, identified by whole-exome sequencing, were used to assess circulating tumor DNA (ctDNA) by ultra-deep sequencing (median, 105,000×) of plasma DNA. Plasma samples (n = 656) were procured at diagnosis, during chemotherapy, before cystectomy, and during surveillance. Expression profiling was performed for tumor subtype and immune signature analyses. RESULTS Presence of ctDNA was highly prognostic at diagnosis before chemotherapy (hazard ratio, 29.1; P = .001). After cystectomy, ctDNA analysis correctly identified all patients with metastatic relapse during disease monitoring (100% sensitivity, 98% specificity). A median lead time over radiographic imaging of 96 days was observed. In addition, for high-risk patients (ctDNA positive before or during treatment), the dynamics of ctDNA during chemotherapy was associated with disease recurrence ( P = .023), whereas pathologic downstaging was not. Analysis of tumor-centric biomarkers showed that mutational processes (signature 5) were associated with pathologic downstaging ( P = .024); however, no significant correlation for tumor subtypes, DNA damage response mutations, and other biomarkers was observed. Our results suggest that ctDNA analysis is better associated with treatment efficacy compared with other available methods. CONCLUSION ctDNA assessment for early risk stratification, therapy monitoring, and early relapse detection in bladder cancer is feasible and provides a basis for clinical studies that evaluate early therapeutic interventions.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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