Early Detection of Circulating Tumor DNA Postoperatively Enables Discovery of Resectable Metastatic Disease in a Patient with Colon Cancer

Abstract Currently, serum carcinoembryonic agent (CEA) along with contrast-enhanced imaging and colonoscopy are used for evaluation of recurrence of colorectal cancer. However, CEA is an unreliable and nonspecific biomarker that may fail to rise and signal relapse. Analysis of circulating tumor DNA...

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Veröffentlicht in:Case Reports in Oncology 2021-12, Vol.14 (3), p.1748-1753
Hauptverfasser: Weinberg, Benjamin A., Winslow, Emily R., Bayasi, Mohammed, Krainock, Michael R., Olshan, Perry M., Billings, Paul R., Aleshin, Alexey
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container_end_page 1753
container_issue 3
container_start_page 1748
container_title Case Reports in Oncology
container_volume 14
creator Weinberg, Benjamin A.
Winslow, Emily R.
Bayasi, Mohammed
Krainock, Michael R.
Olshan, Perry M.
Billings, Paul R.
Aleshin, Alexey
description Abstract Currently, serum carcinoembryonic agent (CEA) along with contrast-enhanced imaging and colonoscopy are used for evaluation of recurrence of colorectal cancer. However, CEA is an unreliable and nonspecific biomarker that may fail to rise and signal relapse. Analysis of circulating tumor DNA (ctDNA) in patients offers a minimally invasive method to assess risk of relapse several months ahead of conventional clinical means. Here, we report the case of a colon adenocarcinoma with postoperative liver metastasis diagnosed early by ctDNA measurement, using a personalized NGS-mPCR assay. While ctDNA levels continued to rise, CEA levels tested negative. Metastatic relapse to the liver was promptly confirmed by PET/CT scan. The patient underwent a successful metastasectomy with curative intent. Following surgery, the patient exhibited no evidence of disease and ctDNA levels remained negative. Our case report suggests that the early detection of postoperative molecular residual disease by means of ctDNA measurement can accurately predict mCRC relapse in cases where CEA levels fail to increase. Close monitoring of ctDNA levels during the postoperative period can allow for earlier intervention and more favorable outcomes in relapsing mCRC patients.
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However, CEA is an unreliable and nonspecific biomarker that may fail to rise and signal relapse. Analysis of circulating tumor DNA (ctDNA) in patients offers a minimally invasive method to assess risk of relapse several months ahead of conventional clinical means. Here, we report the case of a colon adenocarcinoma with postoperative liver metastasis diagnosed early by ctDNA measurement, using a personalized NGS-mPCR assay. While ctDNA levels continued to rise, CEA levels tested negative. Metastatic relapse to the liver was promptly confirmed by PET/CT scan. The patient underwent a successful metastasectomy with curative intent. Following surgery, the patient exhibited no evidence of disease and ctDNA levels remained negative. Our case report suggests that the early detection of postoperative molecular residual disease by means of ctDNA measurement can accurately predict mCRC relapse in cases where CEA levels fail to increase. 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subjects Abdomen
Biomarkers
Cancer cells
Cancer therapies
carcinoembryonic agent
Care and treatment
Case Report
Case reports
Case studies
circulating tumor dna
Colon cancer
Colorectal cancer
Complications and side effects
Diagnosis
DNA
DNA methylation
Genetic aspects
Health aspects
Identification and classification
Intestinal obstruction
liver metastasis
Medical imaging
Metastasis
metastatic colorectal cancer
Methods
Mutation
Patients
Postoperative care
Prognosis
Surgery
Surveillance
title Early Detection of Circulating Tumor DNA Postoperatively Enables Discovery of Resectable Metastatic Disease in a Patient with Colon Cancer
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