Detection of relevant pharmacogenetic information through exome sequencing in oncology

Author:

Verdez Simon12ORCID,Albuisson Juliette34,Duffourd Yannis12,Boidot Romain345,Reda Manon356,Thauvin-Robinet Christel247,Fumet Jean-David6,Ladoire Sylvain6,Nambot Sophie27,Callier Patrick12,Faivre Laurence247,Ghiringhelli François3456,Picard Nicolas8

Affiliation:

1. UMR1231 GAD, Inserm – Université Bourgogne-Franche Comté, Dijon, France

2. Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, 21000, France

3. Platform of Transfer in Cancer Biology, Georges François Leclerc Cancer Center – UNICANCER, Dijon, 21000, France

4. Genomic & Immunotherapy Medical Institute, Dijon, 21000, France

5. Department of Tumour Biology & Pathology, Georges François Leclerc Cancer Center – UNICANCER, Dijon, 21000, France

6. Department of Medical Oncology, Georges François Leclerc Cancer Center – UNICANCER, 1 rue Professeur Marion, Dijon, 21000, France

7. Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Centre de Génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, 21000, France

8. Inserm U1248, Service de Pharmacologie et Toxicologie, Université de Limoges, CHU de Limoges, Limoges, 87000, France

Abstract

Background: Germline sequencing of individual genomes can detect alleles responsible for adverse drug reactions (ADRs) in relation to chemotherapy, targeted agents, antiemetics or pain treatment. Materials & methods: To evaluate the interest of such pharmacogenetic information, the authors retrospectively analyzed genes known to have an impact on cancer therapy in a cohort of 445 solid cancers patients. Results: Six patients treated with 5-fluorouracil carrying one DPYD variant classified as 1A showed decreased drug mean clearance (p = 0.01). Regarding CYP2D6, all patients (n = 5) with predicted CYP2D6 poor or ultra-rapid metabolizer status experienced adverse drug reactions related to opioid therapy. Conclusion: Genomic germline sequencing performed for theragnostic issues in patients with a solid tumor, can provide relevant information about common pharmacogenetic alleles.

Publisher

Future Medicine Ltd

Subject

Pharmacology,Genetics,Molecular Medicine

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