Genetic variation of cisplatin-induced ototoxicity in non-cranial-irradiated pediatric patients using a candidate gene approach: The International PanCareLIFE Study

PanCareLIFE Consortium, Eva Clemens*, Linda Broer, Thorsten Langer, Andre G. Uitterlinden, Andrica C. H. de Vries, Martine van Grotel, Saskia F. M. Pluijm, Harald Binder, Julianne Byrne, Eline van Dulmen-den Broeder, Marco Crocco, Desiree Grabow, Peter Kaatsch, Melanie Kaiser, Line Kenborg, Jeanette F. Winther, Catherine Rechnitzer, Henrik Hasle, Tomas KepakAnne-Lotte F. van der Kooi, Leontien C. Kremer, Jarmila Kruseova, Claudia E. Kuehni, Heleen van der Pal, Ross Parfitt, Dirk Deuster, Peter Matulat, Claudia Spix, Amelie Tillmanns, Wim J. E. Tissing, Lara Maier, Antoinette Zehnhoff-Dinnesen, Oliver Zolk, Marry M. van den Heuvel-eibrink

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

9 Citations (Scopus)

Abstract

Ototoxicity is a common side effect of platinum treatment and manifests as irreversible, high-frequency sensorineural hearing loss. Genetic association studies have suggested a role for SNPs in genes related to the disposition of cisplatin or deafness. In this study, 429 pediatric patients that were treated with cisplatin were genotyped for 10 candidate SNPs. Logistic regression analyses revealed that younger age at treatment (≤5 years vs >15 years: OR: 9.1; 95% CI: 3.8–21.5; P = 5.6 × 10−7) and higher cumulative dose of cisplatin (>450 vs ≤300 mg/m2: OR: 2.4; 95% CI: 1.3–4.6; P = 0.007) confer a significant risk of ototoxicity. Of the SNPs investigated, none of them were significantly associated with an increase of ototoxicity. In the meta-analysis, ACYP2 rs1872328 (OR: 3.94; 95% CI: 1.04–14.03; P = 0.04) and SLC22A2 rs316019 (OR: 1.46; 95% CI: 1.07–2.00; P = 0.02) were associated with ototoxicity. In order to increase the understanding of the association between SNPs and ototoxicity, we propose a polygenic model, which takes into account multiple interacting genes of the cisplatin pathway that together confer an increased risk of ototoxicity.

Original languageEnglish
Pages (from-to)294-305
Number of pages12
JournalPharmacogenomics journal
Volume20
Issue number2
DOIs
Publication statusPublished - Apr-2020

Keywords

  • INDUCED HEARING-LOSS
  • CHILDHOOD-CANCER
  • PLATINUM CHEMOTHERAPY
  • CHILDREN
  • VARIANTS
  • ACYP2
  • TPMT
  • COMT
  • REPLICATION
  • SURVIVORS

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