MP12-02 PROSPECTIVE EVALUATION OF CIRCULATING TUMOR DNA (ctdna) IN DETECTING EARLY PROGRESSION ON IMMUNE CHECKPOINT INHIBITORS IN PATIENTS WITH ADVANCED GENITOURINARY CANCERS

The Journal of Urology(2022)

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You have accessJournal of UrologyCME1 May 2022MP12-02 PROSPECTIVE EVALUATION OF CIRCULATING TUMOR DNA (ctDNA) IN DETECTING EARLY PROGRESSION ON IMMUNE CHECKPOINT INHIBITORS IN PATIENTS WITH ADVANCED GENITOURINARY CANCERS Albert Jang, Ellen Jaeger, Grant Rauterkus, Alex Liberman, Isabelle Sussman, Malcolm Light, Minqi Huang, Charlotte Manogue, Sydney Caputo, Patrick Miller, Brian Lewis, Jodi Layton, Oliver Sartor, Earle Burgess, Tiffany Farmer, Hayley Widden, Carrie Flippen, Alexey Aleshin, Claud Grigg, and Pedro Barata Albert JangAlbert Jang More articles by this author , Ellen JaegerEllen Jaeger More articles by this author , Grant RauterkusGrant Rauterkus More articles by this author , Alex LibermanAlex Liberman More articles by this author , Isabelle SussmanIsabelle Sussman More articles by this author , Malcolm LightMalcolm Light More articles by this author , Minqi HuangMinqi Huang More articles by this author , Charlotte ManogueCharlotte Manogue More articles by this author , Sydney CaputoSydney Caputo More articles by this author , Patrick MillerPatrick Miller More articles by this author , Brian LewisBrian Lewis More articles by this author , Jodi LaytonJodi Layton More articles by this author , Oliver SartorOliver Sartor More articles by this author , Earle BurgessEarle Burgess More articles by this author , Tiffany FarmerTiffany Farmer More articles by this author , Hayley WiddenHayley Widden More articles by this author , Carrie FlippenCarrie Flippen More articles by this author , Alexey AleshinAlexey Aleshin More articles by this author , Claud GriggClaud Grigg More articles by this author , and Pedro BarataPedro Barata More articles by this author View All Author Informationhttps://doi.org/10.1097/JU.0000000000002534.02AboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract INTRODUCTION AND OBJECTIVE: Immune checkpoint inhibitors (ICI) are approved for the treatment of advanced genitourinary (GU) malignancies. Tumor response to ICI is largely based on conventional scans with known limitations. Signatera is a commercially available personalized and tumor-informed mPCR NGS-based circulating tumor DNA (ctDNA) test (Natera Inc., Austin, TX) that is optimized to monitor tumor status in patient’s blood sample. In this pilot study, we investigate the serial ctDNA detection rate and the concordance of serial ctDNA changes with radiographic response rate of advanced GU patients undergoing ICI treatment. We hypothesize that serial ctDNA testing can accurately predict tumor response to immunotherapy compared with conventional scans. METHODS: We prospectively enrolled consecutive advanced GU cancer patients treated with an ICI-based regimen or monotherapy for at least 12 weeks, without evidence of disease progression, available ctDNA test result(s) and CT scans. To monitor ctDNA, patient blood was collected at the time of study entry and every 6-8 weeks until progressive disease occurred and/or until 2 years. Overall response rate (ORR) was assessed. We present the preliminary results after a median follow up of 7.5 months. RESULTS: Twelve patients [median age 68 (49-81), 75% renal cell, 17% urothelial cancer and 8% prostate cancer] had at least one ctDNA test result at the time of data cut-off. Tumors were more frequently PD-L1 negative (90%), one patient had microsatellite instability with a median tumor mutational burden of 6 (range 3-25) mut/Mb. Patients were on ICI [25% monotherapy, 33% ICI/ICI, 42% ICI/other) for a median of 6.5 months prior to first ctDNA test. Patients had a median number of 5 (range 1-6) ctDNA tests. The table summarizes the ctDNA and overall response rate of the study cohort. Detection rate was 50% and in all cases except one, ctDNA changes were concordant with ORR. One patient had progressive disease in scans with an initial decline in ctDNA, that later increased. At time of data cut-off, 50% discontinued ICI due to disease progression (33%), no evidence of disease (17%) or adverse reactions (8%). CONCLUSIONS: In this pilot study, ctDNA was frequently detected in advanced GU tumors and serial changes in ctDNA were concordant with staging scans to monitor disease response to ICIs. Source of Funding: This study was supported by Natera, Inc © 2022 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetails Volume 207Issue Supplement 5May 2022Page: e165 Advertisement Copyright & Permissions© 2022 by American Urological Association Education and Research, Inc.MetricsAuthor Information Albert Jang More articles by this author Ellen Jaeger More articles by this author Grant Rauterkus More articles by this author Alex Liberman More articles by this author Isabelle Sussman More articles by this author Malcolm Light More articles by this author Minqi Huang More articles by this author Charlotte Manogue More articles by this author Sydney Caputo More articles by this author Patrick Miller More articles by this author Brian Lewis More articles by this author Jodi Layton More articles by this author Oliver Sartor More articles by this author Earle Burgess More articles by this author Tiffany Farmer More articles by this author Hayley Widden More articles by this author Carrie Flippen More articles by this author Alexey Aleshin More articles by this author Claud Grigg More articles by this author Pedro Barata More articles by this author Expand All Advertisement PDF DownloadLoading ...
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