Multimodal detection in plasma of molecular residual disease (MRD) in locally advanced head and neck squamous cell carcinoma (LA-HNSCC).

person Enrique Sanz Garcia Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada info_outline Enrique Sanz Garcia, Jinfeng Zou, Lisa Avery, Anna Spreafico, John Waldron, David Paul Goldstein, Aaron Richard Hansen, John Cho, John R de Almeida, Andrew Hope, Ali Hosni, Ezra Hahn, Bayardo Perez-Ordonez, Zhen Zhao, Christopher Gareth Smith, Yangqiao Zheng, Nitzan Rosenfeld, Nittusha Singaravelan, Scott Victor Bratman, Lillian L. Siu

Authors person Enrique Sanz Garcia Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada info_outline Enrique Sanz Garcia, Jinfeng Zou, Lisa Avery, Anna Spreafico, John Waldron, David Paul Goldstein, Aaron Richard Hansen, John Cho, John R de Almeida, Andrew Hope, Ali Hosni, Ezra Hahn, Bayardo Perez-Ordonez, Zhen Zhao, Christopher Gareth Smith, Yangqiao Zheng, Nitzan Rosenfeld, Nittusha Singaravelan, Scott Victor Bratman, Lillian L. Siu Organizations Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada, Princess Margaret Cancer Centre, Toronto, ON, Canada, Department of Biostatistics, University Health Network, University of Toronto, Toronto, ON, Canada, Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada, Department of Radiation Oncology, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada, Department of Otolaryngology-Head & Neck Surgery, Princess Margaret Cancer Centre, Toronto, ON, Canada, Department of Radiation Oncology, Princess Margaret Cancer Centre, Toronto, ON, Canada, Department of Otolaryngology-Head & Neck Surgery/Surgical Oncology, Princess Margaret Cancer Centre, Toronto, ON, Canada, Department of Radiation Oncology - Princess Margaret Cancer Centre - University Heath Network, Toronto, ON, Canada, Department of Radiation Oncology - Princess Margaret - University Health Network, Toronto, ON, Canada, Laboratory Medicine Program, Princess Margaret Cancer Centre, Toronto, ON, Canada, Princess Margaret - University Health Network, Toronto, ON, Canada, Neogenomics Ltd, Babraham Research Park, Cambridge, United Kingdom, Princess Margaret Cancer Centre - University Health Network, Toronto, ON, Canada, NeoGenomics Ltd, Cambridge, United Kingdom, Cancer Genomics Program - Princess Margaret Cancer Centre, Toronto, ON, Canada Abstract Disclosures Research Funding Institutional Funding Princess Margaret Cancer Centre, BMO Chair of Precision Medicine Background: Despite intensive therapy, 30% of patients (pts) with LA-HNSCC relapse. Published data shows that MRD detection during follow up (FU) may predict relapse, e.g. human papillomavirus (HPV) DNA in p16+ pts post radiation (RT) or chemoradiation (CRT); or circulating tumor DNA (ctDNA) post surgery. MRD detection using multiple assays after definitive RT/CRT has not been reported. Methods: We enrolled pts with high risk LA-HNSCC (stage III HPV+, III-IVB HPV-) treated with curative intent: surgery ± adjuvant therapy, RT or CRT. Plasma was collected pre-treatment at baseline (B), at 4-6 weeks (FU1) and 8-12 weeks (FU2) post-treatment. RaDaR, a personalized liquid biopsy assay that targets patient specific somatic variants identified in whole exome sequencing (WES) from matched tumor tissue, was used to detect ctDNA, reported as estimated Variant Allele Fraction (eVAF). Cancer Personalized Profiling by deep sequencing (CAPP-seq) was used as a tumor naïve assay for ctDNA, reported as mean VAF. HPV sequencing (HPV-seq) in all and digital PCR (dPCR) in p16+ pts were used to detect HPV DNA. Relapse free survival (RFS) was estimated using Kaplan Meier and associations of ctDNA or HPV DNA with RFS using log-rank test. Assays were compared with Spearman correlation. Results: A total of 89 plasma samples from 35 pts were collected prospectively; 32 pts with at least a FU sample were evaluable: 26 had both. Median age was 63 years (34-71). Most pts were stage III HPV + (N = 16, 50%) and received CRT (N = 25, 78%). No pts had clinical or radiological residual disease at FU2. Median FU was 18.3 months (5.1-25.9), there were 7 clinical relapses. RaDar was applied in 17 pts with WES in matched tissue, including 6 with relapse. ctDNA at B was detected in 15/17 (88%). eVAF at B was not associated with RFS (p = 0.98). Two pts relapsed < 1 year after RT/CRT and had eVAF > 0.001% in FU2 sample; lead time to relapse was 100 and 245 days. FU1 sample of a pt who relapsed > 1 year post-CRT was close to the threshold for ctDNA+ with eVAF 0.0001%; lead time was 494 days. Three pts who received CRT relapsed > 500 days from FU2 sample (ctDNA-). CAPP-seq was applied to 29 pts; mean VAF correlated with eVAF at B (r = 0.75) but not at FU. ctDNA+ at FU using CAPP-seq was not associated with RFS (p = 0.25). HPV-seq was applied to 32 pts; specificity and sensitivity was 100% at B. Among p16+ pts with FU sample (N = 15), HPV DNA was detected in 4/4 with relapse and not in those without, predicting shorter RFS (p < 0.01). dPCR detected HPV DNA in 2/4 pts with relapse. HPV-seq and dPCR correlation was high at B (r = 0.99), lower at FU2 (r = 0.66). Conclusions: HPV DNA and ctDNA can be detected in LA-HNSCC before and after definitive therapy. RaDaR but not CAPP-seq may detect MRD in pts who relapse within 1 year after RT/CRT with a significant lead time. HPV-seq may be more sensitive than dPCR to detect HPV DNA in MRD. Validation in an interception study is planned (NCT04599309).

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