Evidence map›Paper›PMID 41790137›Full record

ArticleCancer chemotherapy and pharmacology2026

NFE2L2 rs35652124C>T polymorphism predicts Grade 4 neutropenia in esophageal cancer patients treated with docetaxel, cisplatin, and fluorouracil chemotherapy: results from exploratory and validation cohorts.

Hisanaga Nomura, Takaya Suzuki, Takashi Kojima, Kunihiko Itoh, Daiki Tsuji

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Article in Cancer chemotherapy and pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Hisanaga NomuraDepartment of Clinical Pharmacology and Therapeutics, Kyoto University Hospital, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto, Kyoto, 606-8507, Japan. hisanaga0726@kuhp.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0002-0744-7425
Takaya SuzukiDepartment of Clinical Pharmacology & Genetics, University of Shizuoka, Shizuoka, Shizuoka, Japan.
Takashi KojimaDepartment of Gastroenterology and Endoscopy, National Cancer Center Hospital East, Kashiwa, Chiba, Japan.ORCID http://orcid.org/0000-0002-2554-8334
Kunihiko ItohDepartment of Clinical Pharmacology & Genetics, University of Shizuoka, Shizuoka, Shizuoka, Japan.ORCID http://orcid.org/0000-0003-4436-0529
Daiki TsujiDepartment of Clinical Pharmaceutics, University of Shizuoka, Shizuoka, Shizuoka, Japan.ORCID http://orcid.org/0000-0001-8894-2841

Funding

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6 · The paper itself

Abstract

purposeChemotherapy-induced neutropenia is a serious adverse event. Combination chemotherapy with docetaxel, cisplatin, and 5-fluorouracil (DCF) is an effective neoadjuvant therapy for esophageal cancer, but it is associated with a high incidence of Grade 4 neutropenia. In previous study, we identified associations between genetic variants and severe neutropenia. The aim of this study was to explore genetic factors related to pharmacokinetics and endogenous antioxidant defense mechanisms that may be associated with the development of Grade 4 neutropenia in esophageal cancer patients treated with DCF chemotherapy using two independent cohorts.

methodsWe conducted a retrospective pharmacogenetic analysis using DNA samples from the National Cancer Center Biobank in Japan. Two independent cohorts of esophageal cancer patients treated with the DCF chemotherapy were analyzed: an exploratory cohort (n = 157) and a validation cohort (n = 121). Single nucleotide polymorphisms (SNPs) in genes related to docetaxel pharmacokinetics and the Keich-like ECH-associated protein 1-Nuclear factor erythroid2-related factor 2 (Keap1-Nrf2) antioxidant system were examined.

resultsA total 53 (33.8%) and 62 (51.2%) patients developed Grade 4 neutropenia in exploratory and validation cohort, respectively. Multivariate analysis revealed that age, Adenosine triphosphate-binding cassette (ABC) G2 rs2231137G > A and Nuclear factor, erythroid 2 like 2 (NFE2L2) rs35652124C > T were significant in exploratory cohort, while baseline absolute neutrophil count and NFE2L2 rs35652124C > T were significant in the validation cohort.

conclusionsNFE2L2 rs35652124C > T was identified as an independent predictive genetic factor for Grade 4 neutropenia in esophageal cancer patients treated with DCF chemotherapy.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsEsophageal NeoplasmsNeutropeniaNF-E2-Related Factor 2AgedCisplatinCohort StudiesDocetaxelFemaleFluorouracilHumansMaleMiddle AgedNeoadjuvant TherapyPolymorphism, Single NucleotideRetrospective StudiesCisplatinDocetaxelFluorouracilNFE2L2 protein, humanNF-E2-Related Factor 2DCF chemotherapyEsophageal cancerNFE2L2Variants

Identifiers

PMID41790137
PMCPMC12966213

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.