Analysis of Circulating Tumor DNA to Predict Risk of Recurrence in Patients With Esophageal and Gastric Cancers

Author:

Huffman Brandon M.1ORCID,Aushev Vasily N.2ORCID,Budde Griffin L.2,Chao Joseph3ORCID,Dayyani Farshid4ORCID,Hanna Diana5,Botta Gregory P.6ORCID,Catenacci Daniel V.T.7ORCID,Maron Steven B.8ORCID,Krinshpun Shifra2,Sharma Shruti2,George Giby V.2,Malhotra Meenakshi2ORCID,Jurdi Adham2,Moshkevich Solomon2,Aleshin Alexey2ORCID,Kasi Pashtoon M.9ORCID,Klempner Samuel J.1ORCID

Affiliation:

1. Department of Medicine, Division of Hematology-Oncology, Massachusetts General Hospital Cancer Center, Boston, MA

2. Natera, Inc, Austin, TX

3. City of Hope Comprehensive Cancer Center, Duarte, CA

4. University of California Irvine Chao Family Comprehensive Cancer Center, Orange, CA

5. Keck Hospital of USC, Los Angeles, CA

6. UCSD Moores Cancer Center, La Jolla, CA

7. University of Chicago, Chicago, IL

8. Memorial Sloan Kettering Cancer Center, New York City, NY

9. Weill Cornell Medicine, Englander Institute of Precision Medicine, New York Presbyterian Hospital, New York, NY

Abstract

PURPOSE Circulating tumor DNA (ctDNA) analyses allow for postoperative risk stratification in patients with curatively treated colon and breast cancers. Use of ctDNA in esophagogastric cancers (EGC) is less characterized and could identify high-risk patients who have been treated with curative intent. METHODS In this retrospective analysis of real-world data, ctDNA levels were analyzed in the preoperative, postoperative, and surveillance settings in patients with EGC using a personalized multiplex polymerase chain reaction–based next-generation sequencing assay. Plasma samples (n = 943) from 295 patients at > 70 institutions were collected before surgery, postoperatively, and/or serially during routine clinical follow-up from September 19, 2019, to February 21, 2022. ctDNA detection was annotated to clinicopathologic features and recurrence-free survival. RESULTS A total of 295 patients with EGC were analyzed, and 212 patients with stages I-III disease were further explored. Pretreatment ctDNA was detected in 96% (23/24) of patients with preoperative time points. Postoperative ctDNA was detected in 23.5% (16/68) of patients with stage I-III EGC within 16 weeks (molecular residual disease window) after surgery without receiving systemic therapy. ctDNA detection at any time point after surgery (hazard ratio [HR], 23.6; 95% CI, 10.2 to 66.0; P < .0001), within the molecular residual disease window (HR, 10.7; 95% CI, 4.3 to 29.3; P < .0001), and during the surveillance period (HR, 17.7; 95% CI, 7.3 to 50.7; P < .0001) was associated with shorter recurrence-free survival. In multivariable analysis, ctDNA status and clinical stage of disease were independently associated with outcomes. CONCLUSION Using real-world data, we demonstrate that postoperative tumor-informed ctDNA detection in EGC is feasible and allows for enhanced patient risk stratification and prognostication during curative-intent therapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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