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Highly Sensitive Circulating Tumor DNA Assay Aids Clinical Management of Radiographically Occult Isolated Peritoneal Metastases in Patients With GI Cancer.
Singh, Harshabad; Klempner, Samuel J; Melnitchouk, Nelya; Chander, Deepak P; Negrea, Ovidiu George; Patel, Anuj K; Schlechter, Benjamin L; Rubinson, Douglas A; Huffman, Brandon M; Nambiar, Chetan; Remland, Joshua; Andrews, Elizabeth; Leahy, Megan E; Brais, Lauren K; Enzinger, Peter C; Mamon, Harvey J; Giannakis, Marios; Meyerhardt, Jeffrey A; Ng, Kimmie; Perez, Kimberly J; Aguirre, Andrew J; Clark, Jeffrey W; Cleary, James M; Wolpin, Brian M.
Afiliação
  • Singh H; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Klempner SJ; Department of Medicine, Brigham and Women's Hospital, Boston, MA.
  • Melnitchouk N; Harvard Medical School, Boston, MA.
  • Chander DP; Harvard Medical School, Boston, MA.
  • Negrea OG; Massachusetts General Hospital Cancer Center, Boston, MA.
  • Patel AK; Harvard Medical School, Boston, MA.
  • Schlechter BL; Department of Surgery, Brigham and Women's Hospital, Boston, MA.
  • Rubinson DA; Dana-Farber Cancer Institute at South Shore Hospital, Weymouth, MA.
  • Huffman BM; Memorial Health University Medical Center, Savannah, GA.
  • Nambiar C; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Remland J; Department of Medicine, Brigham and Women's Hospital, Boston, MA.
  • Andrews E; Harvard Medical School, Boston, MA.
  • Leahy ME; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Brais LK; Department of Medicine, Brigham and Women's Hospital, Boston, MA.
  • Enzinger PC; Harvard Medical School, Boston, MA.
  • Mamon HJ; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Giannakis M; Department of Medicine, Brigham and Women's Hospital, Boston, MA.
  • Meyerhardt JA; Harvard Medical School, Boston, MA.
  • Ng K; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Perez KJ; Department of Medicine, Brigham and Women's Hospital, Boston, MA.
  • Aguirre AJ; Harvard Medical School, Boston, MA.
  • Clark JW; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Cleary JM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Wolpin BM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
JCO Precis Oncol ; 7: e2200572, 2023 06.
Article em En | MEDLINE | ID: mdl-37343200
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Apêndice / Neoplasias Peritoneais / Neoplasias Gástricas / Adenocarcinoma / DNA Tumoral Circulante Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Apêndice / Neoplasias Peritoneais / Neoplasias Gástricas / Adenocarcinoma / DNA Tumoral Circulante Tipo de estudo: Diagnostic_studies / Observational_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: JCO Precis Oncol Ano de publicação: 2023 Tipo de documento: Article