Highly Sensitive Circulating Tumor DNA Assay Aids Clinical Management of Radiographically Occult Isolated Peritoneal Metastases in Patients With GI Cancer

医学 神秘的 腺癌 癌症 内科学 疾病 原发性肿瘤 局限性疾病 胃肠病学 肿瘤科 外科 病理 转移 替代医学 前列腺癌
作者
Harshabad Singh,Samuel J. Klempner,Nelya Melnitchouk,Deepak P. Chander,O. George Negrea,Anuj K. Patel,Benjamin L. Schlechter,Douglas A. Rubinson,Brandon M. Huffman,Chetan Nambiar,Joshua Remland,Elizabeth Andrews,Michael Leahy,Lauren K. Brais,Peter C. Enzinger,Harvey J. Mamon,Marios Giannakis,Jeffrey A. Meyerhardt,Kimmie Ng,Kimberly Perez,Andrew J. Aguirre,Jeffrey W. Clark,James M. Cleary,Brian M. Wolpin
出处
期刊:JCO precision oncology [American Society of Clinical Oncology]
卷期号: (7)
标识
DOI:10.1200/po.22.00572
摘要

PURPOSE GI cancers commonly spread to the peritoneal cavity, particularly from primary adenocarcinomas of the stomach and appendix. Peritoneal metastases are difficult to visualize on cross-sectional imaging and cause substantial morbidity and mortality. The purpose of this study was to determine whether serial highly sensitive tumor-informed circulating tumor DNA (ctDNA) measurements could longitudinally track changes in disease burden and inform clinical care. METHODS This was a retrospective case series of patients with gastric or appendiceal adenocarcinoma and isolated peritoneal disease that was radiographically occult. Patients underwent quantitative tumor-informed ctDNA testing (Signatera) as part of routine clinical care. No interventions were prespecified based on ctDNA results. RESULTS Of 13 patients studied, the median age was 65 (range, 45-75) years, with 7 (54%) women, 5 (38%) patients with gastric, and 8 (62%) patients with appendiceal adenocarcinoma. Eight (62%) patients had detectable ctDNA at baseline measurement, with median value 0.13 MTM/mL (range, 0.06-11.68), and assay was technically unsuccessful in two cases with appendiceal cancer because of limited tumor tissue. Five (100%) patients with gastric cancer and 3 (50%) patients with appendiceal cancer had detectable ctDNA at baseline. Although baseline levels of ctDNA were low, longitudinal assessment tracked with changes in disease burden among patients undergoing chemotherapy for metastatic disease. In two patients undergoing surveillance after definitive surgical management of gastric adenocarcinoma, detection of ctDNA prompted diagnosis of isolated peritoneal disease. CONCLUSION Quantitative tumor-informed serial ctDNA testing aids clinical management of patients with isolated peritoneal disease. Low levels of baseline ctDNA suggest a role for highly sensitive ctDNA approaches over panel-based testing. Further exploration of this approach should be considered in patients with isolated peritoneal malignant disease.
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