# Comparative Clinical Outcomes and Safety of Generic Versus Original Imatinib in the Treatment of Chronic Myeloid Leukemia: A Real-World Cohort Study from Thailand

**Authors:** Jirapath Tangkitchot, Adisak Tantiworawit, Piangrawee Niprapan, Nuttanun Wongsarikan, Sirichai Srichairatanakool, Teerachat Punnachet, Nonthakorn Hantrakun, Pokpong Piriyakhuntorn, Thanawat Rattanathammethee, Chatree Chai-Adisaksopha, Ekarat Rattarittamrong, Lalita Norasetthada, Sasinee Hantrakool

PMC · DOI: 10.3390/jcm14113695 · 2025-05-25

## TL;DR

This study compares the effectiveness and safety of generic and original imatinib for treating chronic myeloid leukemia in Thailand, finding similar early responses but worse long-term survival with the generic version.

## Contribution

The study provides real-world evidence on the comparative safety and outcomes of generic versus original imatinib in CML patients.

## Key findings

- No significant differences in early treatment responses between original and generic imatinib.
- Overall survival was significantly longer for patients receiving original imatinib.
- Event-free survival showed no significant difference between the two groups.

## Abstract

Background/Objectives: Imatinib, a first-generation tyrosine kinase inhibitor, is the standard treatment for chronic myeloid leukemia (CML). Although generic formulations have improved access, concerns regarding their efficacy and safety remain. This study aimed to compare the clinical outcomes and adverse events of original and generic imatinib in patients with CML in Thailand. Methods: We conducted a retrospective cohort study of patients with chronic-phase CML receiving frontline imatinib at Chiang Mai University Hospital between January 2012 and September 2022. Treatment responses, event-free survival (EFS), overall survival (OS), and adverse events were also analyzed. Results: Among the 71 patients, 46 (64.8%) received original imatinib, and 25 (35.2%) received generic imatinib. The median follow-up period was 80.3 months (IQR: 52.0–106.4). At 12 months, there were no significant differences in the cumulative complete cytogenetic response (73.3% vs. 70.8%, p = 0.825) or major molecular response (35.6% vs. 41.7%, p = 0.618). Although EFS was not significantly different between the groups, OS was significantly longer in patients receiving original imatinib (p < 0.001). Conclusions: Although early treatment responses and EFS were similar, generic imatinib was associated with an inferior OS. These findings highlight the need for close monitoring and further evaluation of long-term outcomes when using generic formulations.

## Linked entities

- **Chemicals:** imatinib (PubChem CID 5291)
- **Diseases:** chronic myeloid leukemia (MONDO:0011996)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}
- **Diseases:** CML (MESH:D015464)
- **Chemicals:** Imatinib (MESH:D000068877)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12155937/full.md

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Source: https://tomesphere.com/paper/PMC12155937