Genetic Variants Influence the Severity of Oral Mucositis in Pediatric Osteosarcoma Patients

被引:0
作者
Zieger, Renata de Almeida [1 ]
Botton, Mariana Rodrigues [2 ]
Curra, Marina [1 ,3 ]
Gabriel, Amanda de Farias [1 ]
Thieme, Stefanie [1 ]
Jardim, Luisa Comerlato [1 ]
Martins, Marco Antonio Trevizani [1 ,4 ]
Matte, Ursula da Silveira [2 ,5 ]
Brunetto, Andre Tesainer [6 ]
Gregianin, Lauro Jose [6 ,7 ]
Roesler, Rafael [8 ]
Sonis, Stephen T. [9 ,10 ]
Siebert, Marina [11 ]
Martins, Manoela Domingues [1 ,4 ,11 ]
机构
[1] Univ Fed Rio Grande do Sul, Sch Dent, Dept Oral Pathol, Porto Alegre, RS, Brazil
[2] Hosp Clin Porto Alegre HCPA UFRGS, Transplant Immunol & Personalized Med Unit, Porto Alegre, Brazil
[3] Univ Caxias Do Sul UCS, Dept Oral Pathol, Porto Alegre, Brazil
[4] Hosp Clin Porto Alegre HCPA UFRGS, Dept Oral Med, Porto Alegre, Brazil
[5] Hosp Clin Porto Alegre HCPA, Med Genet Serv, Porto Alegre, Brazil
[6] Childhood Canc Inst, Porto Alegre, Brazil
[7] Hosp Clin Porto Alegre HCPA, Dept Radiol, Porto Alegre, Brazil
[8] Univ Fed Rio Grande do Sul, Porto Alegre Clin Hosp, Expt Res Ctr, Canc & Neurobiol Lab, Porto Alegre, RS, Brazil
[9] Brigham & Womens Hosp, Div Oral Med, Boston, MA USA
[10] Dana Farber Canc Inst, Boston, MA USA
[11] Hosp Clin Porto Alegre HCPA UFRGS, Expt Res Ctr, Unit Res Lab, Porto Alegre, Brazil
关键词
chemotherapy; genetic variants; oral mucositis; osteosarcoma; pediatric patients; pharmacogenetics; pharmacogenomic; HIGH-DOSE METHOTREXATE; ACUTE LYMPHOBLASTIC-LEUKEMIA; METHYLENETETRAHYDROFOLATE REDUCTASE C677T; INDUCED TOXICITY; ABCC2; POLYMORPHISMS; CHILDREN; MTHFR; CHEMOTHERAPY; IMPACT; ASSOCIATION;
D O I
10.1111/odi.15217
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BackgroundThe variability in patients' risk of oral mucositis (OM) has been, in part, attributed to differences in host genomics. The aim better define the role of genomics as an OM risk by investigating the association between genetic variants and the presence and severity of OM in pediatric patients with osteosarcoma (OS) undergoing chemotherapy (CT).MethodsA longitudinal observational retrospective study was conducted. Severity of OM was assessed daily using World Health Organization (WHO) criteria. Blood samples were collected, and DNA was extracted. 54 coding regions were analyzed for 17 candidate genes using next-generation sequencing.ResultsA total of 164 CT cycles were evaluated in 14 pediatric patients being treated for OS with HDMTX (66.9%) and doxorubicin + cisplatin (34.1%). OM was diagnosed in 129 cycles (78.7%). Whereas the presence of OM was associated with ABCA3 (rs13332514) in HDMTX cycles, OM severity was associated with ABCC2 (rs2273697) in multivariate analysis. In doxorubicin + cisplatin, genetic variants of ABC family genes (ABCC2 and ABCC6) were associated with OM in multivariate analysis.ConclusionOral mucositis risk and severity in a pediatric population being treated for OS with HDMTX, doxorubicin, and cisplatin were associated with genes in the ABC family (ABCA3, ABCC2, and ABCC6 genes).
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页数:11
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