Assessing the utility of a cell-free tumor (ct)DNA assay (MSK-ACCESS) in patients (pts) with node-positive (N+) muscle-invasive bladder cancer (MIBC) undergoing neoadjuvant chemotherapy (NAC).

Authors

null

Andrew B Katims

Memorial Sloan Kettering Cancer Center, New York, NY

Andrew B Katims , Andrew T Lenis , Ronak H. Shah , Carissa E Chu , Neha Ratna , Ashley M Regazzi , Eugene J. Pietzak , David H Aggen , Samuel A Funt , Min Yuen Teo , Jonathan E. Rosenberg , Dean F. Bajorin , Timothy F. Donahue , Bernard H. Bochner , Michael F. Berger , David B. Solit , Gopa Iyer

Organizations

Memorial Sloan Kettering Cancer Center, New York, NY

Research Funding

No funding received
None.

Background: Circulating ctDNA is associated with disease progression, worse overall survival, and recurrence in pts with bladder cancer. This study correlated targeted exome ctDNA sequencing with pathologic response to NAC and metastatic recurrence in pts with N+ MIBC undergoing radical cystectomy (RC). Methods: We prospectively identified pts with cT2-3N1-2M0 bladder cancer who underwent NAC prior to RC. Node positivity was determined radiographically and/or by node biopsy. Plasma samples were collected pre-NAC, mid-treatment, after NAC completion, and 3 months after RC. Samples were analyzed using MSK-ACCESS, an ultrasensitive ctDNA platform designed to identify somatic mutations in 129 cancer associated genes. Primary bladder tumors were sequenced using targeted exome sequencing. Results: Samples (31) from 9 pts (6 men) were analyzed. Median age was 63 years (IQR 58-69). NAC regimens included gemcitabine and cisplatin alone (78%) or with paclitaxel (22%). Seven (78%) pts had >1 detectable mutation pre-NAC. The most altered genes detected in both tissue and ctDNA included: TERT (88% vs 28%), TP53 (76% vs 40%), ARID1A (43% vs 17%), RB1 (43% vs 15%), KDM6A (43% vs 15%), and ATM (17% vs 17%). Four (45%) pts had complete response (ypT0N0), 1 (11%) had a partial response (ypT1N0), and 4 (33.3%) were non-responders (ypT2N0-3). All non-responders had disease recurrence after RC (median 3 months, range 2-11 months). Of 7 pts with on-treatment MSK-ACCESS, 2 (29%) had detectable ctDNA (1 ypT2N0, 1 ypT0N0). The pt with a PR had detectable ctDNA post-NAC with 1 mutation identified that was not detected at 3 months. All pts with >ypT2N0 had detectable ctDNA post-NAC. Pts with recurrence/non-responders had a significantly higher mutation count 3 months after RC compared to responders, with a median of 7 vs. 0 mutations, respectively. Two pts with CR had detectable ctDNA at 3 months post-RC but have not recurred (Table). Conclusions: Clearance of ctDNA post-NAC correlated with pathologic complete response. Approximately 70% of pts had ctDNA clearance on NAC. All pts with residual disease at RC had detectable ctDNA post-NAC.

N+ disease correlated with persistent ctDNA detected at 3 months post-RC.

Clinical stageRC StagePre-Tx mut #On-Tx mut #Post-TX mut #3-month mut #RecurrenceTime to recurrence or last visit disease-free (months)
T2N1T0N03000No11
T2N2T0N032NA0No8
T2N1T0N00001No4
T2N1T0N00001No4
T2N2T1N05NA10No9
T1N1T3N31NA311Yes2
T2N2T2N33058Yes3
T2N2T2N01222No5
T3N2T3N250NA6Yes11

MSK-ACCESS mutation calls at multiple treatment timepoints. RC= radical cystectomy; NAC = neoadjuvant chemotherapy; Tx = treatment; mut = mutation. NA = Missed.

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2023 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session B: Prostate Cancer and Urothelial Carcinoma

Track

Urothelial Carcinoma,Prostate Cancer - Advanced

Sub Track

Translational Research, Tumor Biology, Biomarkers, and Pathology

Citation

J Clin Oncol 41, 2023 (suppl 6; abstr 544)

DOI

10.1200/JCO.2023.41.6_suppl.544

Abstract #

544

Poster Bd #

M7

Abstract Disclosures