ArticleFrontiers in medicine2026
Hand-foot skin reaction associated with vascular endothelial growth factor receptor tyrosine kinase inhibitors: a FAERS-based pharmacovigilance study.
Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Case Report: Lenvatinib-induced lichenoid drug reaction mimicking disseminated zoster in a patient with metastatic hepatocellular carcinoma.Frontiers in oncology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Hand-foot skin reaction (HFSR) is a prevalent and dose-limiting cutaneous toxicity associated with vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKIs), often compromising treatment continuity and efficacy. Methods: This pharmacovigilance study analyzed reports from the FDA Adverse Event Reporting System (FAERS) database (Q1 2004-Q2 2025). After standard data cleaning, disproportionality analyses using the ROR, PRR, MGPS, and BCPNN were performed to quantify signals for HFSR associated with 11 VEGFR-TKIs. Patient demographics, time-to-onset, and clinical outcomes were also assessed. Results: A total of 8,668 HFSR reports were analyzed. Eight VEGFR-TKIs generated positive HFSR signals across all four algorithms. Sorafenib and regorafenib showed greater disproportionality. The median time to HFSR onset was 16 days, with most drugs showing an early failure pattern. Subgroup analysis showed that female patients reported stronger signals and had a median onset time (14 days) earlier than male patients (17 days). Hospitalization was the most frequently reported serious outcome. Conclusion: This large-scale analysis confirmed a significant association between VEGFR-TKIs and HFSR, with significant differences in reported signal values between specific drugs. Proactive, individualized monitoring, particularly during the initial weeks of therapy, is crucial for managing this impactful toxicity.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.