# Safety Profile and Tumor Response of EGFR-TKIs in Clinical Practice: A Real-World Study in Thailand

**Authors:** Pattama Jainan, Chayanat Pongsathabordee, Kamala Sadabpod, Titima Junkrut, Thanakorn Jerasirichot, Oran Phetchuensakun, Taniya Paiboonvong, Saranporn Srithonrat

PMC · DOI: 10.3390/jcm15062437 · Journal of Clinical Medicine · 2026-03-23

## TL;DR

This study examines the safety and effectiveness of EGFR-TKIs in Thai patients with lung cancer, finding that most side effects are mild and early-onset, with pruritus linked to better treatment response.

## Contribution

The study identifies pruritus as a potential clinical indicator of treatment response to EGFR-TKIs in real-world Thai NSCLC patients.

## Key findings

- Cutaneous reactions like rash and xerosis were the most common adverse events, mostly mild to moderate.
- Pruritus was independently associated with objective tumor response in multivariable analysis.
- Most adverse events occurred within the first month of treatment initiation.

## Abstract

Background: Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are the first-line treatment for patients with non-small cell lung cancer (NSCLC) harboring EGFR mutations. Although EGFR-TKIs can cause various adverse events (AEs), their profiles have not been fully elucidated in Thai patients. This study aimed to determine the incidence, characteristics, severity, and duration of the first AEs and to evaluate their association with tumor response in patients with NSCLC receiving EGFR-TKIs. Method: This retrospective cohort study was conducted at a super-tertiary care hospital in Thailand. Patients with NSCLC who received EGFR-TKIs between August 2021 and July 2024 were included. Descriptive statistics were used to summarize safety profiles and tumor response. The association between AEs and objective response was assessed using logistic regression. Results: A total of 187 patients were included in this study. Overall, 177 AEs were observed in patients receiving erlotinib, osimertinib, or gefitinib. The most common cutaneous AEs were rash (30.7%), xerosis (24.1%), and acneiform rash (19.3%), while diarrhea (20.3%) was the most frequent gastrointestinal toxicity. Most AEs were grade 1–2 and occurred within 1 month after treatment initiation. In multivariable logistic regression analysis, pruritus (OR 8.26, 95% CI: 1.00–67.75, p = 0.049) and treatment line (OR 0.27, 95% CI: 0.10–0.68, p = 0.006) were independently associated with objective response. Conclusion: Most of the AEs occurred early during EGFR-TKI therapy, with cutaneous reactions being the most common and generally mild to moderate. Pruritus and treatment line were independently associated with objective response, suggesting that pruritus may serve as a potential clinical indicator of treatment response and highlighting the importance of monitoring of the EGFR-TKI-related AEs during therapy.

## Linked entities

- **Proteins:** EGFR (epidermal growth factor receptor)
- **Chemicals:** erlotinib (PubChem CID 176870), osimertinib (PubChem CID 71496458), gefitinib (PubChem CID 123631)
- **Diseases:** non-small cell lung cancer (MONDO:0005233), NSCLC (MONDO:0005233)

## Full-text entities

- **Genes:** EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** diarrhea (MESH:D003967), cutaneous reactions (MESH:D017445), Tumor (MESH:D009369), gastrointestinal toxicity (MESH:D005767), cutaneous AEs (MESH:D002318), NSCLC (MESH:D002289), acneiform rash (MESH:D005076), Pruritus (MESH:D011537)
- **Chemicals:** erlotinib (MESH:D000069347), osimertinib (MESH:C000596361), gefitinib (MESH:D000077156)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028144/full.md

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Source: https://tomesphere.com/paper/PMC13028144