Evidence map›Paper›PMID 41322851›Full record

ArticleCureus2025

Exploratory Investigation of Predictive Factors for Reducing Adverse Effects in CapeOX Therapy for Colorectal Cancer Patients.

Makoto Kishimoto, Masayoshi Koinuma, Jin Tokunaga

Abstract read
In one paragraph

Article in Cureus, 2025. 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

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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

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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

3 authors.

Makoto KishimotoFirst Department of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Kyushu University of Medical Science, Nobeoka, JPN.
Masayoshi KoinumaFaculty of Pharmaceutical Sciences, Teikyo Heisei University, Tokyo, JPN.
Jin TokunagaFirst Department of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Kyushu University of Medical Science, Nobeoka, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOxaliplatin infusion plus oral capecitabine (CapeOX) is the standard chemotherapy regimen for colorectal cancer. It is commonly employed as adjuvant therapy and as first-line treatment for advanced disease. However, adverse effects, such as peripheral neuropathy, hand-foot syndrome, and gastrointestinal symptoms, may lead to dose reduction or discontinuation. Identifying reliable predictors of these adverse effects would support prophylactic strategies and enable safer, more personalized treatment.

methodsWe retrospectively analyzed 108 colorectal cancer patients who received CapeOX between September 2020 and October 2023. Adverse events after the first cycle were evaluated using Common Terminology Criteria for Adverse Events (CTCAE) v5.0 and categorized into Grade 0 and Grade ≥ 1 groups. Associations between pre-treatment blood test values (including aspartate aminotransferase (AST), alanine aminotransferase (ALT), red blood cells, monocytes, and basophils) and inflammatory or nutritional indices (including prognostic nutrition index (PNI), systemic inflammatory response index (SIRI), neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR)) were examined for adverse events. Variables demonstrating significant associations in univariate analysis were included in a multivariate logistic regression model. Receiver operating characteristic analysis was performed to determine optimal cut-off values of predictive markers.

resultsAST ≤ 22.0 IU/L was identified as a significant predictor of peripheral neuropathy. Nausea was significantly associated with a basophil count ≥ 0.28 × 10²/μL and occasional alcohol intake; anorexia with a basophil count ≥ 0.29 × 10²/μL and PLR ≤ 152.69; and diarrhea with a SIRI ≤ 0.37. These markers enabled effective risk stratification of adverse drug reactions in patients undergoing CapeOX.

conclusionsCertain adverse effects of CapeOX may be predicted using routine pre-treatment laboratory data. These findings could facilitate early identification of high-risk patients and enable personalized preventive interventions.

Indexed as

adverse effectcapeox therapycolorectal cancercut-off valueinflammatory markerpredictor

Identifiers

PMID41322851
PMCPMC12662650

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