2024-03-19T07:42:00Zhttp://repisalud.isciii.es/oai/requestoai:repisalud.isciii.es:20.500.12105/74342022-11-08T09:38:24Zcom_20.500.12105_2174com_20.500.12105_2051com_20.500.12105_2173col_20.500.12105_2175
Repisalud
author
Sereno, María
author
Gutiérrez-Gutiérrez, Gerardo
author
Rubio, Juan Moreno
author
Apellániz-Ruiz, María
author
Sánchez-Barroso, Lara
author
Casado, Enrique
author
Falagan, Sandra
author
López-Gómez, Miriam
author
Merino, María
author
Gómez-Raposo, César
author
Rodriguez-Salas, Nuria
author
Tébar, Francisco Zambrana
author
Rodriguez Antona, Cristina
funder
Ministerio de Economía y Competitividad (España)
funder
Instituto de Salud Carlos III
2019-04-04T08:50:41Z
2019-04-04T08:50:41Z
2017-01-19
BMC Cancer. 2017;17(1):63.
1471-2407
http://hdl.handle.net/20.500.12105/7434
28103821
10.1186/s12885-016-3031-5
1471-2407
BMC cancer
BACKGROUND: Oxaliplatin is a chemotherapy agent active against digestive tumors. Peripheral neuropathy is one of the most important dose-limiting toxicity of this drug. It occurs in around 60-80% of the patients, and 15% of them develop severe neuropathy. The pathophysiology of oxaliplatin neurotoxicity remains unclear. SCN9A is a gene codifying for a subtype sodium channel (type IX, subunit α) and mutations in this gene are involved in neuropathic perception. In this study we investigated whether SCN9A genetic variants were associated with risk of neurotoxicity in patients diagnosed of cancer on treatment with oxaliplatin. METHODS: Blood samples from 94 patients diagnosed of digestive cancer that had received oxaliplatin in adjuvant or metastatic setting were obtained from three hospitals in Madrid. These patients were classified into two groups: "cases" developed oxaliplatin-induced grade 3-4 neuropathy (n = 48), and "controls" (n = 46) had no neuropathy or grade 1. The neuropathy was evaluated by an expert neurologist and included a clinical examination and classification according to validated neurological scales: National Cancer Institute Common Toxicity Criteria (NCI-CTC), Oxaliplatin-Specific Neurotoxicity Scale (OSNS) and Total Neuropathy score (TNS). Genotyping was performed for 3 SCN9A missense polymorphisms: rs6746030 (R1150W), rs74401238 (R1110Q) and rs41268673 (P610T), and associations between genotypes and neuropathy were evaluated. RESULTS: We found that SCN9A rs6746030 was associated with protection for severe neuropathy (OR = 0.39, 95% CI = 0.16-0.96; p = 0.041). Multivariate analysis adjusting for diabetes provided similar results (p = 0.036). No significant differences in neuropathy risk were detected for rs74401238 and rs41268673. CONCLUSION: SCN9A rs6746030 was associated with protection for severe oxaliplatin-induced peripheral neuropathy. The validation of this exploratory study is ongoing in an independent series.
eng
Calcium channel
Oxaliplatin neuropathy
SCN9A
Genetic polymorphisms of SCN9A are associated with oxaliplatin-induced neuropathy
journal article
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URL
https://repisalud.isciii.es/bitstream/20.500.12105/7434/1/Geneticpolymorphismsof_2017.pdf
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https://repisalud.isciii.es/bitstream/20.500.12105/7434/3/Geneticpolymorphismsof_2017.pdf.txt
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