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CASE REPORT article

Front. Med.

Sec. Hematology

Volume 12 - 2025 | doi: 10.3389/fmed.2025.1515002

Molecular Response of a Patient With e19a2-Positive Chronic Myeloid Leukemia to Flumatinib: A Case Report and Literature Review

Provisionally accepted
Yaqing Feng Yaqing Feng 1*Lidong Zhang Lidong Zhang 1Jinying Gong Jinying Gong 2Xi Liu Xi Liu 1Caiqin Mu Caiqin Mu 1Jun Qiao Jun Qiao 1Haitao Meng Haitao Meng 1Yanfang Zhang Yanfang Zhang 1Hongjin Wang Hongjin Wang 1
  • 1 The Third People’s Hospital of Datong, Datong, China
  • 2 Tianjin Union Precision Medical Diagnostics Co. Ltd, Tianjin , China;, tianjing, China

The final, formatted version of the article will be published soon.

    Objective: Chronic myeloid leukemia (CML) is a malignancy driven by the BCR::ABL1fusion gene, with the e19a2 transcript being a rare variant, accounting for 0.4% of CML cases. Patients with the e19a2 transcript often show poor response to first-line treatment with imatinib, and no standard therapy has been established for this subtype.We report a case of a 28-year-old female with e19a2-positive CML. The patient exhibited poor response and tolerance to dasatinib. After 6 months, she achieved partial cytogenetic response (PCyR) but developed grade 3 pleural effusion. Following treatment discontinuation and prednisone therapy, the patient continued dasatinib (80 mg/d). At 12 months, the patient achieved complete cytogenetic response (CCyR), but BCR::ABL1 levels remained suboptimal, with recurrent pleural effusion. The patient was then switched to flumatinib (600 mg/d), achieving major molecular response (MMR) at 6 months and deep complete molecular response (MR4.5) at 24 months, with good tolerance.Conclusions: Flumatinib demonstrated excellent deep molecular response and good tolerability in e19a2-positive CML patients, suggesting that it may be one of the preferred treatment options for such patients.

    Keywords: Chronic myeloid leukemia, e19a2 transcript, Second-generation tyrosine kinase inhibitor, Flumatinib, molecular response

    Received: 22 Oct 2024; Accepted: 11 Feb 2025.

    Copyright: © 2025 Feng, Zhang, Gong, Liu, Mu, Qiao, Meng, Zhang and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Yaqing Feng, The Third People’s Hospital of Datong, Datong, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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