Evidence map›Paper›PMID 41691540›Full record

ArticleClinical and translational science2026

Concomitant Use of DPP-4 Inhibitors May Prevent the Development of Oxaliplatin-Induced Peripheral Neuropathy: A Retrospective Cohort Study.

Yusuke Koura, Keisuke Mine, Shunsuke Fujita, Takehiro Kawashiri, Yusuke Mori, Mami Ueda, Risa Kaneko, Takeshi Hirota, Mayako Uchida, Daisuke Kobayashi

Abstract read
In one paragraph

Article in Clinical and translational science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yusuke KouraDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Keisuke MineDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0009-0009-8409-7260
Shunsuke FujitaDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0009-0006-9526-5934
Takehiro KawashiriDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0000-0002-7708-2855
Yusuke MoriDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Mami UedaDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Risa KanekoDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Takeshi HirotaDepartment of Pharmacy, Kyushu University Hospital, Fukuoka, Japan.ORCID 0000-0002-4846-3421
Mayako UchidaDepartment of Pharmacy, Kyushu University Hospital, Fukuoka, Japan.ORCID 0000-0003-0507-7309
Daisuke KobayashiDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0000-0002-7312-9919

Funding

Japan Science and Technology AgencyJapan Society for the Promotion of ScienceSupport for Pioneering Research Initiated by the Next Generation
6 · The paper itself

Abstract

Oxaliplatin-induced peripheral neuropathy (OIPN) causes numbness and pain in the limbs, often leading to interruption of chemotherapy and representing a significant clinical problem. Previous basic studies have suggested that the dipeptidyl peptidase-4 (DPP-4) inhibitor alogliptin may prevent OIPN. To evaluate whether concomitant use of DPP-4 inhibitors could prevent the development of OIPN in clinical practice, we retrospectively analyzed data from 1180 patients who initiated oxaliplatin treatment at Kyushu University Hospital between January 1, 2009 and December 31, 2019. The primary endpoint was the occurrence of OIPN of any grade. Kaplan-Meier analysis with cumulative doses demonstrated a significantly lower incidence of OIPN in the DPP-4 inhibitor group (p = 0.0422). After propensity score matching to adjust for patient backgrounds, the protective association remained significant (p = 0.0389). Furthermore, Cox proportional hazards analysis incorporating gender, age, regimen, and concomitant DPP-4 inhibitor use as covariates confirmed that DPP-4 inhibitor use was an independent protective factor for OIPN (HR = 0.690; 95% CI, 0.490-0.972; p = 0.034). These findings suggest that concomitant use of DPP-4 inhibitors may moderate the development of OIPN in patients receiving oxaliplatin.

Indexed as

Antineoplastic AgentsDipeptidyl-Peptidase IV InhibitorsOxaliplatinPeripheral Nervous System DiseasesAgedFemaleHumansIncidenceKaplan-Meier EstimateMaleMiddle AgedPiperidinesRetrospective StudiesUracilalogliptinAntineoplastic AgentsDipeptidyl-Peptidase IV InhibitorsOxaliplatinPiperidinesUracildipeptidyl peptidase 4 inhibitorsoxaliplatinperipheral neuropathyretrospective study

Identifiers

PMID41691540
PMCPMC12906695

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Registered trials

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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.