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| Natura: | Artículo Open Access |
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Wiley
2025
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| Accesso online: | https://onlinelibrary.wiley.com/doi/10.1002/pbc.32024 |
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| author | Hallie Coltin Ofélie Trudeau‐Ferrin Sébastien Perreault Lucie Lafay‐Cousin Derek S. Tsang Samuele Renzi Valérie Larouche Craig Erker Juliette Hukin Randy Barber Paul C. Nathan Annie Huang Eric Bouffet Vijay Ramaswamy |
| author_facet | Hallie Coltin Ofélie Trudeau‐Ferrin Sébastien Perreault Lucie Lafay‐Cousin Derek S. Tsang Samuele Renzi Valérie Larouche Craig Erker Juliette Hukin Randy Barber Paul C. Nathan Annie Huang Eric Bouffet Vijay Ramaswamy Hallie Coltin Ofélie Trudeau‐Ferrin Sébastien Perreault Lucie Lafay‐Cousin Derek S. Tsang Samuele Renzi Valérie Larouche Craig Erker Juliette Hukin Randy Barber Paul C. Nathan Annie Huang Eric Bouffet Vijay Ramaswamy |
| collection | Wiley Open Access |
| contents | Severe Hearing Loss in Children With Central Nervous System Tumors: A Population‐Based Cancer in Young People in Canada (CYP‐C) Report Hallie Coltin Ofélie Trudeau‐Ferrin Sébastien Perreault Lucie Lafay‐Cousin Derek S. Tsang Samuele Renzi Valérie Larouche Craig Erker Juliette Hukin Randy Barber Paul C. Nathan Annie Huang Eric Bouffet Vijay Ramaswamy Pediatric Blood & Cancer ABSTRACTPurposeChildren with central nervous system (CNS) tumors are prone to treatment‐related hearing loss (HL) and subsequent functional impairment. This study reports a dedicated population‐based analysis of CNS tumor‐specific rates and predictors of early severe HL.MethodsA cohort study of children ≤15 years diagnosed with CNS tumors between 2001 and 2019 through the Cancer in Young People in Canada (CYP‐C) program. The primary outcome was Grade 3 and 4 severe HL within 5 years following diagnosis.ResultsAmong 3201 children with CNS tumors, 5.1% experienced early severe HL. Children with medulloblastoma (N = 570) and ATRT/other embryonal tumors (N = 269) had higher rates of early HL (16.1%, 15.2%, respectively). Cisplatin was administered to 80.1% of children with embryonal tumors, and 67.3% received radiotherapy. In children with medulloblastoma, age less than 6 years at diagnosis (OR 2.4, 1.5–3.8; vs. ≥6 years), radiation (OR 3.5, 1.6–7.6), and cisplatin (OR 20.4, 1.3–329.7) predicted early severe HL. Younger age at diagnosis doubled the probability of early severe HL (10.6% in <6 years vs. 4.8% in ≥6 years), while radiation exposure tripled the probability across age groups (29.8% and 10.6% if <6 years; 15.3% and 4.8% in ≥6 years). In children with ATRT/other embryonal tumors, cisplatin (OR 31.6, 1.9–521.9) was the sole predictor of early severe HL.ConclusionsHigh rates of early HL were observed in children with embryonal tumors. Younger children who received radiotherapy had higher probabilities of early HL, suggesting an additive interaction between age and radiation. Standardized otoprotection and research on cisplatin avoidance and therapy de‐escalation in young children with embryonal tumors are urgently needed. 10.1002/pbc.32024 http://creativecommons.org/licenses/by-nc/4.0/ |
| doi_str_mv | 10.1002/pbc.32024 |
| format | Artículo Open Access |
| id | wiley_oa_10_1002_pbc_32024 |
| institution | Wiley Open Access |
| license_str_mv | http://creativecommons.org/licenses/by-nc/4.0/ |
| publishDate | 2025 |
| publisher | Wiley |
| record_format | wiley_oa |
| spellingShingle | Severe Hearing Loss in Children With Central Nervous System Tumors: A Population‐Based Cancer in Young People in Canada (CYP‐C) Report Hallie Coltin Ofélie Trudeau‐Ferrin Sébastien Perreault Lucie Lafay‐Cousin Derek S. Tsang Samuele Renzi Valérie Larouche Craig Erker Juliette Hukin Randy Barber Paul C. Nathan Annie Huang Eric Bouffet Vijay Ramaswamy Pediatric Blood & Cancer Severe Hearing Loss in Children With Central Nervous System Tumors: A Population‐Based Cancer in Young People in Canada (CYP‐C) Report Hallie Coltin Ofélie Trudeau‐Ferrin Sébastien Perreault Lucie Lafay‐Cousin Derek S. Tsang Samuele Renzi Valérie Larouche Craig Erker Juliette Hukin Randy Barber Paul C. Nathan Annie Huang Eric Bouffet Vijay Ramaswamy Pediatric Blood & Cancer ABSTRACTPurposeChildren with central nervous system (CNS) tumors are prone to treatment‐related hearing loss (HL) and subsequent functional impairment. This study reports a dedicated population‐based analysis of CNS tumor‐specific rates and predictors of early severe HL.MethodsA cohort study of children ≤15 years diagnosed with CNS tumors between 2001 and 2019 through the Cancer in Young People in Canada (CYP‐C) program. The primary outcome was Grade 3 and 4 severe HL within 5 years following diagnosis.ResultsAmong 3201 children with CNS tumors, 5.1% experienced early severe HL. Children with medulloblastoma (N = 570) and ATRT/other embryonal tumors (N = 269) had higher rates of early HL (16.1%, 15.2%, respectively). Cisplatin was administered to 80.1% of children with embryonal tumors, and 67.3% received radiotherapy. In children with medulloblastoma, age less than 6 years at diagnosis (OR 2.4, 1.5–3.8; vs. ≥6 years), radiation (OR 3.5, 1.6–7.6), and cisplatin (OR 20.4, 1.3–329.7) predicted early severe HL. Younger age at diagnosis doubled the probability of early severe HL (10.6% in <6 years vs. 4.8% in ≥6 years), while radiation exposure tripled the probability across age groups (29.8% and 10.6% if <6 years; 15.3% and 4.8% in ≥6 years). In children with ATRT/other embryonal tumors, cisplatin (OR 31.6, 1.9–521.9) was the sole predictor of early severe HL.ConclusionsHigh rates of early HL were observed in children with embryonal tumors. Younger children who received radiotherapy had higher probabilities of early HL, suggesting an additive interaction between age and radiation. Standardized otoprotection and research on cisplatin avoidance and therapy de‐escalation in young children with embryonal tumors are urgently needed. 10.1002/pbc.32024 http://creativecommons.org/licenses/by-nc/4.0/ |
| title | Severe Hearing Loss in Children With Central Nervous System Tumors: A Population‐Based Cancer in Young People in Canada (CYP‐C) Report |
| topic | Pediatric Blood & Cancer |
| url | https://onlinelibrary.wiley.com/doi/10.1002/pbc.32024 |