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Article Dans Une Revue JCO precision oncology Année : 2023

Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With Glioma

Duy Thanh Tran
Clovis Adam
  • Fonction : Auteur
Michèle Bernier
  • Fonction : Auteur
Dominique Cazals-Hatem
  • Fonction : Auteur
Karima Mokhtari
  • Fonction : Auteur
Bertrand Mathon
  • Fonction : Auteur
Laurent Capelle
  • Fonction : Auteur

Résumé

PURPOSE The Lynch syndrome (LS)-glioma association is poorly documented. As for mismatch repair deficiency (MMRd) in glioma, a hallmark of LS-associated tumors, there are only limited data available. We determined MMRd and LS prevalence in a large series of unselected gliomas, and explored the associated characteristics. Both have major implications in terms of treatment, screening, and prevention. METHODS Somatic next-generation sequencing was performed on 1,225 treatment-naive adult gliomas referred between 2017 and June 2022. For gliomas with ≥1 MMR pathogenic variant (PV), MMR immunohistochemistry (IHC) was done. Gliomas with ≥1 PV and protein expression loss were considered MMRd. Eligible patients had germline testing. To further explore MMRd specifically in glioblastomas, isocitrate dehydrogenase (IDH)-wild type (wt), we performed IHC, and complementary sequencing when indicated, in a series of tumors diagnosed over the 2007-2021 period. RESULTS Nine gliomas were MMRd (9/1,225; 0.73%). Age at glioma diagnosis was <50 years for all but one case. Eight were glioblastomas, IDH-wt, and one was an astrocytoma, IDH-mutant. ATRX (n = 5) and TP53 (n = 8) PV were common. There was no TERT promoter PV or EGFR amplification. LS prevalence was 5/1,225 (0.41%). One 77-year-old patient was a known LS case. Four cases had a novel LS diagnosis, with germline PV in MSH2 (n = 3) and MLH1 (n = 1). One additional patient had PMS2-associated constitutional mismatch repair deficiency. Germline testing was negative in three MSH6-deficient tumors. In the second series of glioblastomas, IDH-wt, MMRd prevalence was 12.5% in the <40-year age group, 2.6% in the 40-49 year age group, and 1.6% the ≥50 year age group. CONCLUSION Screening for MMRd and LS should be systematic in glioblastomas, IDH-wt, diagnosed under age 50 years.
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Dates et versions

hal-04115776 , version 1 (02-06-2023)

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Patrick R Benusiglio, Fikret Elder, Mehdi Touat, Alexandre Perrier, Marc Sanson, et al.. Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With Glioma. JCO precision oncology, 2023, 7, ⟨10.1200/PO.22.00525⟩. ⟨hal-04115776⟩
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