Genetic determinants of chemotherapy-induced oral mucositis in children with solid malignancies

Abstract Background Oral mucositis is a clinically significant, potentially severe side effect of systemic chemotherapy in children with cancer. Understanding genetic predisposition to this side effect may assist in development of stratified prophylactic and treatment strategies. However, existing literature primarily focuses on children with haematological malignancies. Methods We performed a candidate gene study of 101 children with solid tumours enrolled in the MARVEL-PIC study at the Royal Children’s Hospital, Melbourne. Clinical data were extracted from the electronic medical record, with NCI-CTCAE v6.0 grade ≥2 oral mucositis defined as the primary outcome. Genetic variants previously associated with oral mucositis were analysed under an additive genetic model to identify significant associations. Exploratory gene-drug interactions were identified based on chemotherapy exposure. Results 29 patients (28.7%) developed grade ≥2 oral mucositis. MTHFR A1298C (rs1801131) was associated with lower odds of grade ≥2 oral mucositis, lower peak mucositis grade, and lower odds of opioid use for oral mucositis. 25 exploratory gene-drug interaction signals were identified, including miR-1206 rs2114358 with methotrexate exposure and ABCB1 rs1045642 with anthracycline exposure. Conclusions MTHFR A1298C (rs1801131) demonstrated a protective effect against chemotherapy-induced oral mucositis in our cohort of children with solid tumours. Larger, ancestry-informed studies are required to validate our findings.

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Journal
Pharmacogenomics
Published
2026-11-09
DOI
https://doi.org/10.1080/14622416.2026.2753056
Primary Topic
Oral health in cancer treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Genetic determinants of chemotherapy-induced oral mucositis in children with solid malignancies

Fernando Jaime Rossello, Andreas Halman, Michael See, Anneke C Grobler et al.
2 links
Pharmacogenomics
Oral health in cancer treatment
article

Genetic determinants of chemotherapy-induced oral mucositis in children with solid malignancies

Fernando Jaime Rossello, Andreas Halman, Michael See, Anneke C Grobler, Rachel K. Conyers, Claire Moore, Sean William David Carter, Aniket Chawla
article en

Abstract

Abstract Background Oral mucositis is a clinically significant, potentially severe side effect of systemic chemotherapy in children with cancer. Understanding genetic predisposition to this side effect may assist in development of stratified prophylactic and treatment strategies. However, existing literature primarily focuses on children with haematological malignancies. Methods We performed a candidate gene study of 101 children with solid tumours enrolled in the MARVEL-PIC study at the Royal Children’s Hospital, Melbourne. Clinical data were extracted from the electronic medical record, with NCI-CTCAE v6.0 grade ≥2 oral mucositis defined as the primary outcome. Genetic variants previously associated with oral mucositis were analysed under an additive genetic model to identify significant associations. Exploratory gene-drug interactions were identified based on chemotherapy exposure. Results 29 patients (28.7%) developed grade ≥2 oral mucositis. MTHFR A1298C (rs1801131) was associated with lower odds of grade ≥2 oral mucositis, lower peak mucositis grade, and lower odds of opioid use for oral mucositis. 25 exploratory gene-drug interaction signals were identified, including miR-1206 rs2114358 with methotrexate exposure and ABCB1 rs1045642 with anthracycline exposure. Conclusions MTHFR A1298C (rs1801131) demonstrated a protective effect against chemotherapy-induced oral mucositis in our cohort of children with solid tumours. Larger, ancestry-informed studies are required to validate our findings.

Pharmacogenomics
Royal Children's Hospital (AU), The University of Melbourne (AU), Murdoch Children's Research Institute (AU), Monash University (AU), Western Sydney University (AU)
Novo Nordisk
Good health and well-being
Oral health in cancer treatment
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