Detection of circulating tumor DNA with ultradeep sequencing of plasma cell‐free DNA for monitoring minimal residual disease and early detection of recurrence in early‐stage lung cancer

Author:

Tan Aaron C.12ORCID,Lai Gillianne G. Y.12,Saw Stephanie P. L.12,Chua Kevin L. M.23,Takano Angela4,Ong Boon‐Hean25,Koh Tina P. T.12,Jain Amit12,Tan Wan Ling12,Ng Quan Sing12,Kanesvaran Ravindran12,Rajasekaran Tanujaa12,Kalashnikova Ekaterina6,Renner Derrick6ORCID,Sudhaman Sumedha6,Malhotra Meenakshi6,Sethi Himanshu6,Liu Minetta C.6,Aleshin Alexey6,Lim Wan‐Teck127,Tan Eng‐Huat12,Skanderup Anders J.8,Ang Mei‐Kim12,Tan Daniel S. W.128

Affiliation:

1. Division of Medical Oncology National Cancer Centre Singapore Singapore Singapore

2. Duke‐NUS Medical School National University of Singapore Singapore Singapore

3. Division of Radiation Oncology National Cancer Centre Singapore Singapore Singapore

4. Division of Pathology Singapore General Hospital Singapore Singapore

5. Department of Cardiothoracic Surgery National Heart Centre Singapore Singapore Singapore

6. Natera, Inc San Carlos California USA

7. Institute of Molecular and Cell Biology Singapore Singapore

8. Genome Institute of Singapore Singapore Singapore

Abstract

AbstractBackgroundIn early‐stage non–small cell lung cancer (NSCLC), recurrence is frequently observed. Circulating tumor DNA (ctDNA) has emerged as a noninvasive tool to risk stratify patients for recurrence after curative intent therapy. This study aimed to risk stratify patients with early‐stage NSCLC via a personalized, tumor‐informed multiplex polymerase chain reaction (mPCR) next‐generation sequencing assay.MethodsThis retrospective cohort study included patients with stage I–III NSCLC. Recruited patients received standard‐of‐care management (surgical resection with or without adjuvant chemotherapy, followed by surveillance). Whole‐exome sequencing of NSCLC resected tissue and matched germline DNA was used to design patient‐specific mPCR assays (Signatera, Natera, Inc) to track up to 16 single‐nucleotide variants in plasma samples.ResultsThe overall cohort with analyzed plasma samples consisted of 57 patients. Stage distribution was 68% for stage I and 16% each for stages II and III. Presurgery (i.e., at baseline), ctDNA was detected in 15 of 57 patients (26%). ctDNA detection presurgery was significantly associated with shorter recurrence‐free survival (RFS; hazard ratio [HR], 3.54; 95% confidence interval [CI], 1.00–12.62; p = .009). In the postsurgery setting, ctDNA was detected in seven patients, of whom 100% experienced radiological recurrence. ctDNA positivity preceded radiological findings by a median lead time of 2.8 months (range, 0–12.9 months). Longitudinally, ctDNA detection at any time point was associated with shorter RFS (HR, 16.1; 95% CI, 1.63–158.9; p < .0001).ConclusionsctDNA detection before surgical resection was strongly associated with a high risk of relapse in early‐stage NSCLC in a large unique Asian cohort. Prospective studies are needed to assess the clinical utility of ctDNA status in this setting.

Publisher

Wiley

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