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Circulating tumor DNA in primary mediastinal large B-cell lymphoma versus classical Hodgkin lymphoma: a retrospective study.
Camus, Vincent; Viennot, Mathieu; Lévêque, Emilie; Viailly, Pierre-Julien; Tonnelet, David; Veresezan, Elena-Liana; Drieux, Fanny; Etancelin, Pascaline; Dubois, Sydney; Stamatoullas, Aspasia; Tilly, Hervé; Bohers, Elodie; Jardin, Fabrice.
Affiliation
  • Camus V; Department of Hematology, Centre Henri Becquerel, Rouen, France.
  • Viennot M; INSERM U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.
  • Lévêque E; INSERM U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.
  • Viailly PJ; Clinical Research Unit, Centre Henri Becquerel, Rouen, France.
  • Tonnelet D; INSERM U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.
  • Veresezan EL; Department of Nuclear Medicine and Radiology, Centre Henri Becquerel and QuantIF (Litis EA4108 - FR CNRS 3638), Rouen, France.
  • Drieux F; Department of Pathology, Centre Henri Becquerel, Rouen, France.
  • Etancelin P; Department of Pathology, Centre Henri Becquerel, Rouen, France.
  • Dubois S; Department of Genetic Oncology, Centre Henri Becquerel, Rouen, France.
  • Stamatoullas A; Department of Hematology, Centre Henri Becquerel, Rouen, France.
  • Tilly H; INSERM U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.
  • Bohers E; Department of Hematology, Centre Henri Becquerel, Rouen, France.
  • Jardin F; INSERM U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.
Leuk Lymphoma ; 63(4): 834-844, 2022 04.
Article de En | MEDLINE | ID: mdl-35075971
Few data exist concerning circulating tumor DNA (ctDNA) relevance in primary mediastinal B-cell lymphoma (PMBL). To explore this topic, we applied a 9-gene next-generation sequencing pipeline to samples from forty-four PMBL patients (median age 36.5 years). The primary endpoint was a similarity between paired biopsy/plasma mutational profiles. We detected at least one variant in 32 plasma samples (80%). The similarity between the biopsy and ctDNA genetic profiles for the 30 patients with paired mutated biopsy/plasma samples was greater than or equal to 80% in 19 patients (63.3%). We then compared PMBL ctDNA features with those of a cohort of Hodgkin lymphoma patients (n = 60). The top three mutated genes were SOCS1, TNFAIP3, and B2M in both lymphoma types. PMBL displayed more alterations in TNFAIP3 (71.9% vs. 46.3%, p = 0.029) and GNA13 (46.9% vs. 17.1%, p = 0.013) than cHL. Our 9-gene set may delineate tumor genotypes using ctDNA samples from both lymphoma types.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie de Hodgkin / Lymphome B / Lymphome B diffus à grandes cellules / ADN tumoral circulant / Tumeurs du médiastin Type d'étude: Diagnostic_studies / Observational_studies Limites: Adult / Humans Langue: En Journal: Leuk Lymphoma Sujet du journal: HEMATOLOGIA / NEOPLASIAS Année: 2022 Type de document: Article Pays d'affiliation: France Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladie de Hodgkin / Lymphome B / Lymphome B diffus à grandes cellules / ADN tumoral circulant / Tumeurs du médiastin Type d'étude: Diagnostic_studies / Observational_studies Limites: Adult / Humans Langue: En Journal: Leuk Lymphoma Sujet du journal: HEMATOLOGIA / NEOPLASIAS Année: 2022 Type de document: Article Pays d'affiliation: France Pays de publication: États-Unis d'Amérique