Circulating Tumor DNA Predicts Early Recurrence Following Locoregional Therapy for Oligometastatic Colorectal Cancer

Author:

O’Donnell Conor D. J.1ORCID,Naleid Nikolas2,Siripoon Teerada13ORCID,Zablonski Kevin G.2ORCID,Storandt Michael H.1ORCID,Selfridge Jennifer E.4,Hallemeier Christopher L.5,Conces Madison L.4,Jethwa Krishan R.5,Bajor David L.4,Thiels Cornelius A.6,Warner Susanne G.6,Starlinger Patrick P.6ORCID,Atwell Thomas D.7,Mitchell Jessica L.8ORCID,Mahipal Amit4ORCID,Jin Zhaohui8ORCID

Affiliation:

1. Mayo Clinic School of Graduate Education, Mayo Clinic College of Medicine, Mayo Building, Rochester, MN 55905, USA

2. Department of Medicine, University Hospitals of Cleveland, Lakeside Building, 11100 Euclid Avenue, Cleveland, OH 44016, USA

3. Division of Medical Oncology, Department of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand

4. University Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland, OH 44106, USA

5. Department of Radiation Oncology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA

6. Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, Mayo Clinic College of Medicine, Rochester, MN 55905, USA

7. Department of Radiology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA

8. Division of Medical Oncology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA

Abstract

(1) Background: Local therapies offer a potentially curative approach for patients with oligometastatic colorectal cancer (CRC). An evidence-based consensus recommendation for systemic therapy following definitive locoregional therapy is lacking. Tumor-informed circulating tumor DNA (ctDNA) might provide information to help guide management in this setting. (2) Methods: A multi-institutional retrospective study was conducted, including patients with CRC that underwent curative-intent locoregional therapy to an isolated site of metastatic disease, followed by tumor-informed ctDNA assessment. The Kaplan–Meier method and log-rank tests were used to compare disease-free survival based on ctDNA results. ctDNA test performance was compared to carcinoembryonic antigen (CEA) test results using McNemar’s test. (3) Results: Our study cohort consisted of 87 patients treated with locoregional interventions who underwent ctDNA testing. The initial ctDNA test post-intervention was positive in 28 patients and negative in 59 patients. The median follow-up time was 14.0 months. Detectable ctDNA post-intervention was significantly associated with early disease recurrence, with a median disease-free survival (DFS) of 6.63 months compared to 21.30 months in ctDNA-negative patients (p < 0.001). ctDNA detected a numerically higher proportion of recurrences than CEA (p < 0.097). Post-intervention systemic therapy was not associated with improved DFS (p = 0.745). (4) Conclusions: ctDNA results are prognostically important in oligometastatic CRC, and further prospective studies are urgently needed to define its role in guiding clinical decisions.

Publisher

MDPI AG

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