J 2019

Genetic Determinants of Ototoxicity During and After Childhood Cancer Treatment: Protocol for the PanCareLIFE Study

CLEMENS, Eva, Annelot J. M. MEIJER, Linda BROER, Thorsten LANGER, Anne-Lode L. F. VAN DER KOOI et. al.

Základní údaje

Originální název

Genetic Determinants of Ototoxicity During and After Childhood Cancer Treatment: Protocol for the PanCareLIFE Study

Autoři

CLEMENS, Eva (528 Nizozemské království, garant), Annelot J. M. MEIJER (528 Nizozemské království), Linda BROER (528 Nizozemské království), Thorsten LANGER (276 Německo), Anne-Lode L. F. VAN DER KOOI (528 Nizozemské království), Andre G. UITTERLINDEN (528 Nizozemské království), Andrica DE VRIES (528 Nizozemské království), Claudia E. KUEHNI (756 Švýcarsko), Maria L. GARRE (380 Itálie), Tomáš KEPÁK (203 Česká republika, domácí), Jarmila KRUSEOVA (203 Česká republika), Jeanette F. WINTHER (208 Dánsko), Leontien C. KREMER (528 Nizozemské království), Eline VAN DULMEN-DEN BROEDER (528 Nizozemské království), Wim J. E. TISSING (528 Nizozemské království), Catherine RECHNITZER (208 Dánsko), Line KENBORG (208 Dánsko), Henrik HASLE (208 Dánsko), Desiree GRABOW (276 Německo), Ross PARFITT (276 Německo), Harald BINDER (276 Německo), Bruce C. CARLETON (124 Kanada), Julianne BYRNE (372 Irsko), Peter KAATSCH (276 Německo), Antoinette Am ZEHNHOFF-DINNESEN (276 Německo), Oliver ZOLK (276 Německo) a Marry M. VAN DEN HEUVEL-EIBRINK (528 Nizozemské království)

Vydání

JMIR RESEARCH PROTOCOLS, TORONTO, JMIR PUBLICATIONS, INC, 2019, 1929-0748

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30204 Oncology

Stát vydavatele

Kanada

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Kód RIV

RIV/00216224:14110/19:00112793

Organizační jednotka

Lékařská fakulta

UT WoS

000462890300033

Klíčová slova anglicky

ototoxicity; hearing loss; childhood cancer survivors; cisplatin; genetics; GWAS; candidate genes; polymorphisms

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 27. 2. 2020 14:14, Mgr. Tereza Miškechová

Anotace

V originále

Background: Survival rates after childhood cancer now reach nearly 80% in developed countries. However, treatments that lead to survival and cure can cause serious adverse effects with lifelong negative impacts on survivor quality of life. Hearing impairment is a common adverse effect in children treated with cisplatin-based chemotherapy or cranial radiotherapy. Ototoxicity can extend from high-tone hearing impairment to involvement of speech frequencies. Hearing impairment can impede speech and language and neurocognitive development. Although treatment-related risk factors for hearing loss following childhood cancer treatment have been identified, the individual variability in toxicity of adverse effects after similar treatment between childhood cancer patients suggests a role for genetic susceptibility. Currently, 12 candidate gene approach studies have been performed to identify polymorphisms predisposing to platinum-induced ototoxicity in children being treated for cancer. However, results were inconsistent and most studies were underpowered and/or lacked replication. Objective: We describe the design of the PanCareLIFE consortium's work packages that address the genetic susceptibility of platinum-induced ototoxicity. Methods: As a part of the PanCareLIFE study within the framework of the PanCare consortium, we addressed genetic susceptibility of treatment-induced ototoxicity during and after childhood cancer treatment in a large European cohort by a candidate gene approach and a genome-wide association screening. Results: This study included 1124 survivors treated with cisplatin, carboplatin, or cranial radiotherapy for childhood cancer, resulting in the largest clinical European cohort assembled for this late effect to date. Within this large cohort we defined a group of 598 cisplatin-treated childhood cancer patients not confounded by cranial radiotherapy. The PanCareLIFE initiative provided, for the first time, a unique opportunity to confirm already identified determinants for hearing impairment during childhood cancer using a candidate gene approach and set up the first international genome-wide association study of cisplatin-induced direct ototoxicity in childhood cancer patients to identify novel allelic variants. Results will be validated in an independent replication cohort. Patient recruitment started in January 2015 and final inclusion was October 2017. We are currently performing the analyses and the first results are expected by the end of 2019 or the beginning of 2020. Conclusions: Genetic factors identified as part of this pan-European project, PanCareLIFE, may contribute to future risk prediction models that can be incorporated in future clinical trials of platinum-based therapies for cancer and may help with the development of prevention strategies.