Evidence map›Paper›PMID 41021349›Full record

Observational studyClinical and translational science2025

Effectiveness of Statins for Oxaliplatin-Induced Peripheral Neuropathy: A Multicenter Retrospective Observational Study.

Kenshi Takechi, Takehiro Kawashiri, Keisuke Mine, Soichiro Ushio, Hirofumi Hamano, Noriko Hida, Kenji Momo, Masanobu Uchiyama, Mami Uchida, Mamoru Tanaka and 16 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Observational
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

26 authors.

Kenshi TakechiDepartment of Drug Information Analysis, College of Pharmaceutical Sciences, Matsuyama University, Matsuyama, Japan.ORCID 0000-0002-9376-2703
Takehiro KawashiriDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.ORCID 0000-0002-7708-2855
Keisuke MineDepartment of Clinical Pharmacy and Pharmaceutical Care, Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
Soichiro UshioDepartment of Emergency and Disaster Medical Pharmacy, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.ORCID 0000-0003-4365-7857
Hirofumi HamanoDepartment of Pharmacy, Okayama University Hospital, Okayama, Japan.ORCID 0000-0002-2231-0179
Noriko HidaDepartment of Clinical Research and Development, Graduate School of Pharmacy, SHOWA Medical University, Shinagawa-ku, Japan.ORCID 0000-0002-7481-597X
Kenji MomoDepartment of Hospital Pharmaceutics, Graduate School of Pharmacy, SHOWA Medical University, Shinagawa-ku, Japan.
Masanobu UchiyamaDepartment of Oncology and Infectious Disease Pharmacy, Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Mami UchidaDepartment of Pharmacy, Fukuoka University Hospital, Fukuoka, Japan.ORCID 0000-0002-4997-0302
Mamoru TanakaDivision of Pharmacy, Ehime University Hospital, Toon, Japan.
Noriaki HidakaDivision of Pharmacy, Ehime University Hospital, Toon, Japan.
Hideki YasuiCenter for Clinical Research, Hamamatsu University Hospital, Hamamatsu, Japan.
Masahiro UedaFaculty of Pharmaceutical Sciences, Setsunan University, Osaka, Japan.ORCID 0000-0002-5761-3698
Ryohei FujiiDepartment of Pharmacy, Kansai Medical University Hospital, Osaka, Japan.ORCID 0009-0003-7004-9889
Misaki HashimotoDepartment of Pharmacy, Kansai Medical University Hospital, Osaka, Japan.ORCID 0009-0006-0319-5466
Yasutaka SakamotoDepartment of Pharmacy, Yokohama City University Hospital, Yokohama, Japan.ORCID 0000-0002-8150-1231
Kana UyamaDepartment of Pharmacy, Yokohama City University Hospital, Yokohama, Japan.
Takahiro NiimuraDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.ORCID 0000-0003-2033-4246
Yuki HanaiDepartment of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Toho University, Funabashi, Japan.ORCID 0000-0002-4606-7150
Ayaka TsuboyaDepartment of Pharmacy, Kawasaki Municipal Tama Hospital, Kawasaki, Japan.ORCID 0000-0002-3388-7336
Keisuke SuzukiInnovation Center for Translational Research, National Center for Geriatrics and Gerontology, Obu, Japan.ORCID 0000-0001-5790-1289
Naoya KamiyamaAsahikawa Medical University Hospital, Asahikawa, Japan.ORCID 0000-0003-0433-1344
Hiromi HagiwaraNagoya City University Hospital, Nagoya, Japan.ORCID 0000-0003-0855-0210
Naoto OkadaPharmacy Department, Yamaguchi University Hospital, Yamaguchi, Japan.
Yoshito ZamamiDepartment of Pharmacy, Okayama University Hospital, Okayama, Japan.
Keisuke IshizawaDepartment of Clinical Pharmacology and Therapeutics, University of Tokushima Graduate School of Biomedical Sciences, Tokushima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapy-induced peripheral neuropathy, including oxaliplatin-induced peripheral neuropathy (OIPN), can have a negative impact on patient quality of life for months or even years after discontinuation of chemotherapy. Statins are commonly used for lowering cholesterol; however, evidence indicates that statins have multiple pleiotropic effects. Although statins are anticipated to exert neuroprotective actions against OIPN, no large-scale investigations have been conducted in real-world clinical settings. Our investigation aimed to determine if statins protected against OIPN. This multicentre retrospective study enrolled Japanese patients with cancer, including those with colorectal cancer (CRC), who received oxaliplatin-containing chemotherapy between April 2009 and December 2019. Propensity score matching between groups was performed to assess the relationship between the occurrence of OIPN and statin use. Among the examined 2657 patients receiving oxaliplatin, 24.7% had Grade ≥ 2 OIPN. There was no significant difference in the incidence of OIPN between the statin and non-statin groups, even after propensity score matching. However, among the matched patients with CRC (n = 510), statin use was associated with a significantly lower incidence of Grade ≥ 2 OIPN than no statin use (19.8% vs. 28.3%, respectively; p = 0.029). Our findings indicate that statins may protect against OIPN in patients with CRC.

Indexed as

Colorectal NeoplasmsHydroxymethylglutaryl-CoA Reductase InhibitorsOxaliplatinPeripheral Nervous System DiseasesAgedAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansIncidenceJapanMaleMiddle AgedPropensity ScoreQuality of LifeRetrospective StudiesAntineoplastic AgentsHydroxymethylglutaryl-CoA Reductase InhibitorsOxaliplatincancercolorectal canceroxaliplatinperipheral neuropathystatins

Identifiers

PMID41021349
PMCPMC12478450

What OpenQuestion holds

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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.