ETM Experimental and Therapeutic Medicine 1792-0981 1792-1015 D.A. Spandidos ETM-29-3-12800 10.3892/etm.2025.12800 Case report Successful treatment of a chronic myeloid leukemia patient with extreme thrombocytosis by a combination of imatinib and interferon‑α: A case report JiaMeng-Xiao 1 * DiDa-Lin 2 * LiuZhen-Zhen 1 WangHai-Ying 1 ChenLei 1 Department of Hematology, Affiliated Hospital of Shandong Second Medical University, Weifang, Shandong 261031, P.R. China Department of Immunology, Shandong Second Medical University, Weifang, Shandong 261053, P.R. China Correspondence to: Dr Lei Chen, Department of Hematology, Affiliated Hospital of Shandong Second Medical University, 2428 Yuhe Road, Weifang, Shandong 261031, P.R. China 350797107@qq.com huangxh2022@hebmu.edu.cn

*Contributed equally

 03 2025 16 01 2025 29 3 50 22 09 2024 02 01 2025 Copyright: © 2025 Jia et al. 2025 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

Chronic myeloid leukemia with extreme thrombocytosis (CML-T), defined by a platelet count >1,000x109/l is a rare leukemia subtype. The present case report described a 66-year-old female CML-T patient presenting with a platelet count of 3,798x109/l, but a consistently normal spleen size. Following treatment with imatinib combined with interferon-α, the patient achieved hematological remission within 2 months, with a platelet count reduction to 311x109/l and complete cytogenetic remission after 10 months. The patient experienced myocardial infarction and liver injury during treatment, which was managed with supportive care. The present case suggested that imatinib combined with interferon-α may be a safe and effective treatment option for patients with CML-T and extreme thrombocytosis and suboptimal response to imatinib monotherapy.

 chronic myeloid leukemia with thrombocytosis imatinib interferon-α thrombocytosis Funding: No funding was received. Introduction

Chronic myeloid leukemia (CML), a clonal myeloproliferative neoplasm arising from pluripotent hematopoietic stem cells, is characterized by the Philadelphia chromosome and the resulting BCR-ABL1 fusion gene (1,2). This genetic abnormality leads to the production of a constitutively active tyrosine kinase, which drives the pathogenesis of CML (3,4). While CML typically follows a predictable course through chronic, accelerated and blast crisis phases, its clinical presentation may be heterogeneous. A subset of patients with CML present with marked thrombocytosis and when the platelet count reaches or exceeds 1,000x109/l, the condition is defined as CML with thrombocytosis (CML-T). This marked thrombocytosis significantly increases the risk of thromboembolic events, making CML-T a clinically challenging subtype of CML (5-7). Distinguishing CML-T from other myeloproliferative neoplasms, particularly essential thrombocythemia (ET), which is also characterized by elevated platelet counts (≥450x109/l), is paramount for accurate diagnosis and treatment (8). Although early clinical presentations can be similar, the underlying genetic abnormalities and therapeutic approaches differ. Management of ET primarily focuses on symptom control with agents like aspirin, hydroxyurea, anagrelide, or interferon-α (IFN-α), but these treatments are generally not curative (9). By contrast, CML-T, like other forms of CML, relies on tyrosine kinase inhibitors (TKIs), such as imatinib, to target the BCR-ABL1 fusion protein and control disease progression (10). Combining imatinib with IFN-α has shown synergistic potential in CML, potentially leading to improved outcomes (11,12). However, there is no established standard of care for CML-T, especially in cases with extreme thrombocytosis, and the optimal treatment strategy remains to be defined and warrants further study. The present report described a patient with CML-T presenting with an exceptionally high platelet count of 3,798x109/l and the unusual finding of normal spleen size, posing a significant diagnostic challenge. The patient's successful treatment with imatinib and interferon-α, resulting in complete hematological and cytogenetic remission, highlights the potential of this combination therapy in managing this rare and complex clinical entity. The present case underscored the need for further research into the efficacy and safety of combination therapy in CML-T, particularly in cases with extreme thrombocytosis.

 Case presentation <sec> <title>Patient information

A 66-year-old female patient was admitted to Shandong Second Medical University (Weifang, China) in August 2023 with recurrent chest tightness and pain. The patient's medical history was notable for hypertension, diabetes mellitus and coronary artery disease for 20 years. The family history was noncontributory for thrombocytosis or other hematologic malignancies. The present case report was approved by the Medical Ethics Committee of the Affiliated Hospital of Shandong Second Medical University (approval no. wyfy-2024-qt-051; date of approval: September 18, 2024; Weifang, China).

 Diagnosis

On presentation, the patient's platelet count was markedly elevated at 3,798x109/l (normal range:150-450x109/l). Peripheral blood smear analysis revealed 5% blasts. Bone marrow aspiration and biopsy were performed as part of the diagnostic workup. Peripheral blood and bone marrow aspirate smears were collected before treatment and stained with Wright-Giemsa stain for 1 min at room temperature, followed by staining with a buffer solution for ~15 min at room temperature. The slides were then examined microscopically at 1,000x magnification. The bone marrow biopsy sample was fixed in 4% neutral buffered formalin at room temperature for at least 6 h, underwent gradient ethanol dehydration, xylene clearing and paraffin embedding following standard protocols, was sectioned at 3 µm thickness and stained with hematoxylin and eosin at room temperature for 3 min each. Microscopic evaluation was performed at x40 and x400 magnification. Results showed hypercellularity with myeloid predominance, marked megakaryocytic hyperplasia and prominent platelet aggregation (Fig. 1), as well as a markedly cellular marrow with an increased myeloid-to-erythroid ratio and a significant increase in predominantly small megakaryocytes on biopsy (Fig. 2). The cytogenetic analysis identified the Philadelphia chromosome t (9;22) (q34;q11.2; Fig. 3). Reverse transcription-quantitative PCR (RT-qPCR) was performed to detect the BCR-ABL1 p210 transcript, with an expression level of 70.78% on the International Scale (IS) (Fig. 4). RNA was extracted from 1x106 cells using the Lab-Aid 896 Blood Total RNA Extraction Kit (Xiamen Zeesan Biotech Co., Ltd.). RNA purity and concentration were assessed using a Thermo Scientific NanoDrop 2000 Spectrophotometer (Thermo Fisher Scientific, Inc.). cDNA synthesis was performed, and qPCR was carried out using TaqMan Gene Expression Master Mix (Applied Biosystems; Thermo Fisher Scientific, Inc.) in a 20 µl reaction volume. The forward primer sequences for BCR-ABL1 p210 were 5'-TCCGCTGACCATCAACAAGGA-3' and 5'-TCCGCTGACCATCAATAAGGA-3', and the reverse primer sequence was 5'-CACTCAGACCCTGAGGCTCAA-3'. ABL1 served as the reference gene with the following primer sequences: Forward 5'-TGGAGATAACACTCTAAGCATAACTAAAGGT-3' and reverse 5'-GATGTAGTTGCTTGGGACCCA-3'. PCR cycling conditions were: 50˚C for 20 min, 95˚C for 10 min, followed by 40 cycles of 95˚C for 15 sec and 60˚C for 60 sec. Quantification was performed using the standard curve method. Experiments were performed with three biological replicates, each in triplicate (technical replicates). To exclude ET, targeted sequencing was performed to screen for mutations within CALR (exon 9), JAK2 (exons 12,14, and 16), MPL (exon 10), and CSF3R (exons 14 and 17), which represent the most frequent mutational hotspots in myeloproliferative neoplasms, and no mutations were detected in this analysis.

Echocardiography demonstrated left ventricular hypertrophy and a reduced left ejection fraction, with an LVEF of 55% (normal range, 50-70%) and an electrocardiogram showed ST-T segment changes and T-wave inversion. All cardiac enzymes were within normal limits except for an elevated NT-proBNP level of 2,914.34 pg/ml (normal <125 pg/ml). Chest and abdominal computed tomography scans showed no evidence of pulmonary embolism or hepatosplenomegaly. Liver and kidney function tests and lipid profile were within normal limits. Based on these findings, the patient was diagnosed with extreme CML-T complicated by acute myocardial infarction.

 Treatment and outcomes

At the initiation of treatment, the patient's platelet count was markedly elevated at 3,798x109/l, along with a white blood cell count of 38.75x109/l and a hemoglobin level of 117 g/l. Imatinib was initiated at 400 mg once daily. Imatinib therapy promptly normalized the leukocyte count; however, the reduction in platelet count was less pronounced. To mitigate the risk of thrombosis due to extreme thrombocytosis, the patient received seven sessions of therapeutic plateletpheresis. Despite these interventions, the platelet count remained at 1,356x109/l on day 10. After 10 days of imatinib monotherapy, the patient experienced episodes of chest tightness, shortness of breath and angina. Electrocardiography findings were consistent with acute subendocardial myocardial infarction. At the time of these cardiac events, the patient's platelet count was still markedly elevated at 1,356x109/l, suggesting a potential correlation between the extreme thrombocytosis and the myocardial infarction. Following treatment with aspirin, ticagrelor, isosorbide mononitrate and rosuvastatin, the patient's symptoms subsequently improved. Subsequent BCR-ABL1 kinase domain mutation analysis revealed no DNA or amino acid mutations, excluding imatinib resistance. Given the inadequate response of thrombocytosis to imatinib monotherapy, IFN-α was initiated on day 11 at a dose of 30 µg once daily via subcutaneous injection and this combination therapy led to a more rapid reduction in platelet count. After 20 days, the patient's clinical symptoms improved and discharge to home treatment followed. At discharge, the white blood cell count was 5.44 x109/l, hemoglobin was 106 g/l and platelet count was 752x109/l. which, although markedly reduced, remained above the threshold for complete remission. Notably, the patient experienced episodes of chest tightness, shortness of breath and angina during treatment. Electrocardiography findings were consistent with acute subendocardial myocardial infarction. These symptoms resolved following anticoagulant and antiplatelet therapy. The patient also experienced mild adverse events, including hypocalcemia, liver injury, fever and dizziness, all of which were managed with supportive care. Following discharge, the patient continued treatment with oral imatinib 400 mg once daily. The IFN-α regimen was adjusted to 30 µg twice weekly via subcutaneous injection. After one month of this adjusted combination therapy, a follow-up complete blood count revealed further hematologic improvement, with a white blood cell count of 5.21x109/l, hemoglobin of 112 g/l and platelet count of 311x109/l (Fig. 5). Complete hematological response (CHR) was confirmed by peripheral blood and bone marrow examination, with findings demonstrating normal white blood cell, platelet, and absolute neutrophil counts, absence of blasts and immature myeloid cells in peripheral blood, normocellular bone marrow with normal maturation, and <5% blasts. IFN-α was then discontinued and the patient continued on imatinib monotherapy 400 mg once daily. After 10 months, cytogenetic analysis showed no detectable Philadelphia chromosome, indicating complete cytogenetic remission (CCyR). Since diagnosis in August 2023, the patient has received seven BCR-ABL1 fusion gene transcript level assessments, demonstrating a progressive reduction in transcript levels. The most recent evaluation in June 2024 revealed a BCR-ABL1 transcript level of 0.14% IS, approaching major molecular remission (MMR), defined as a BCR-ABL1 transcript level less than 0.1%. It is worth noting that imaging studies consistently showed a normal spleen size throughout the treatment course.

 Follow-up and outcome

As of the most recent follow-up in September 2024, the patient remains on imatinib therapy and is stable, with no evidence of disease relapse. The patient's blood counts have remained within the normal range (Fig. 6).

 Discussion

CML-T is a rare subtype of CML, defined by platelet counts that typically reach or exceed 1,000x109/l. Although no standardized treatment for CML-T is currently available, previous studies have demonstrated a favorable response to imatinib therapy (10,13). Given the distinct therapeutic approaches required, differentiating CML-T from ET is crucial for treatment decision-making. The diagnosis of ET is primarily established by elevated platelet counts, increased bone marrow megakaryocytes and the presence of CALR, JAK2, MPL, or CSF3R mutations (14,15). By contrast, the presence of the Philadelphia chromosome or BCR-ABL rearrangement with isolated thrombocytosis should be diagnosed as CML, not ET, according to the World Health Organization diagnostic criteria (16). The patient presented with a platelet count of 3,798x109/l, significantly higher than previously reported levels. This highlighted the rarity of CML-T and the challenges associated with its diagnosis, suggesting a potential unique mechanism underlying thrombocytosis in this patient. Notably, despite the extreme thrombocytosis, the patient's spleen size remained normal, adding to the diagnostic complexity. Although splenomegaly is a typical feature in most patients with CML, this patient consistently lacked splenomegaly throughout the disease course. Previous literature has documented cases of CML with concomitant myelofibrosis or thrombocytosis without splenomegaly (17,18). Additionally, research suggests that ~40% of patients with CML are asymptomatic in the early stages of the disease, with diagnosis often relying solely on laboratory abnormalities. Furthermore, the clinical presentation of CML can vary across different geographical regions (19,20). These findings highlight that factors such as the stage of CML and individual patient variability can influence the presence or absence of splenomegaly. The diagnosis and assessment of CML necessitate a comprehensive evaluation incorporating a multi-faceted approach rather than relying solely on spleen size.

Significant thrombocytosis, a hallmark of CML-T, is associated with increased blood viscosity, promoting thrombosis and elevating the risk of thromboembolic events (21). The patient experienced recurrent angina during treatment, potentially attributable to thrombosis secondary to extreme thrombocytosis. The mechanisms underlying the profound thrombocytosis observed in CML-T remain incompletely understood. The patient's extreme thrombocytosis and high BCR-ABL1 p210 fusion gene expression level (IS: 70.78%) suggested a potential role for BCR-ABL1 overexpression, and previous research has demonstrated a correlation between the BCR-ABL1 fusion gene and elevated platelet counts in CML (22). However, the precise mechanisms by which BCR-ABL1 directly influences megakaryocyte differentiation and platelet production remain unclear and warrant further investigation. BCR-ABL1 overexpression is hypothesized to disrupt normal megakaryocyte development, leading to excessive platelet production. Imatinib, a targeted BCR-ABL1 tyrosine kinase inhibitor, restores megakaryocyte function and reduces platelet counts in CML (23,24). BCR-ABL1p210, the most prevalent variant in CML, is associated with thrombocytosis, disease progression and adverse prognosis, as well as response to IFN-α and imatinib therapy (25-32). Other BCR-ABL1 variants, such as p185, p190 and p230, have also been implicated in lymphoid progenitor cell transformation and thrombocytosis in CML. Furthermore, these variants also contribute to favorable outcomes, including complete remission and improved long-term survival, in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (33-40) (Table I). Furthermore, two major BCR-ABL1 mRNA transcript types exist, e14a2 and e13a2, with e14a2 associated with higher platelet counts and e13a2 with higher white blood cell counts (41). BCR-ABL1 transcript typing was not performed in this case and future research should explore the relationship between BCR-ABL1 transcript type and thrombocytosis in CML-T. Furthermore, the pathogenesis of thrombocytosis in CML-T may involve additional molecular mechanisms beyond BCR-ABL1. Mutations in genes such as MPL, THPO and JAK2, as well as dysregulated expression of thrombopoietin, IL-6 and other inflammatory mediators, have been implicated in driving platelet production in various thrombocytosis contexts, a finding that warrants further investigation (14,42-45).

Imatinib, the first-generation BCR-ABL1 TKI approved by the US Food and Drug Administration, significantly improves CML treatment by competitively binding to the BCR-ABL1 kinase domain, thereby inhibiting kinase activity, promoting apoptosis in leukemic cells and ultimately improving the prognosis of patients with CML (46,47). Previous reports suggest imatinib as a valuable treatment option for patients with CML presenting with the rare complication of thrombocytosis (48). Despite its efficacy in reducing platelet counts in CML, imatinib may increase bleeding risk potentially due to platelet apoptosis, aggregation inhibition, platelet derived growth factor receptor (PDGFR) downregulation and megakaryocyte apoptosis via PI3K/Akt pathway (49-51). Conversely, increased platelet activation after imatinib treatment in CML has also been reported (52). Close monitoring of platelet-related parameters during imatinib therapy is therefore warranted. Prolonged imatinib therapy may lead to drug resistance, potentially due to acquired BCR-ABL1 mutations, including point mutations, insertions and deletions, which compromise TKI therapy efficacy and potentially lead to treatment failure (53). While second- and third-generation TKIs show potential in overcoming resistance, they are associated with inherent cardiovascular risks, such as thrombotic vascular occlusion and heart failure. Consequently, caution is advised when prescribing these newer TKIs to patients with pre-existing cardiovascular conditions (3,54-58).

IFN-α demonstrates myelosuppressive activity, inhibiting the uncontrolled clonal proliferation of hematopoietic cells in MPNs, including CML and ET. Before the advent of TKIs, IFN-α was the standard first-line treatment for CML, particularly in patients ineligible for allogeneic hematopoietic stem cell transplantation (59-61). Additionally, IFN-α significantly reduces platelet counts in ET and other MPNs with thrombocytosis, probably through megakaryocyte normalization (62-64). Furthermore, its immunomodulatory effects enhance natural killer cell activity, leading to the destruction of CML cells (65). While imatinib has largely superseded IFN-α in CML treatment, it remains a valuable therapeutic option for patients intolerant to imatinib (66). Moreover, IFN-α can promote monocyte differentiation into anti-tumor dendritic cells and activate CD8+ T cells, thus bolstering anti-tumor immunity in CML (67).

Combined IFN-α and imatinib therapy shows additive effects in chronic-phase CML, improving hematological responses, extending event-free survival and enhancing MMR rates (11,12,68). In the present case, initial imatinib monotherapy effectively controlled leukocyte counts but failed to adequately address persistently elevated platelet levels, thereby increasing the risk of thromboembolic events, as evidenced by recurrent angina. Therefore, IFN-α was added to the treatment regimen to further manage platelet counts and mitigate thrombotic risk. Although this combined therapy may offer benefits for patients with CML, particularly those with extreme thrombocytosis, including enhanced platelet reduction and the possibility of complete remission, as observed in this patient, it is crucial to acknowledge the increased risk of adverse events such as myelosuppression, hepatotoxicity and flu-like symptoms (69-72). This patient experienced neutropenia and liver injury during combined therapy, which were successfully managed with symptomatic treatment. Therefore, implementing IFN-α alongside imatinib necessitates carefully considering the risk-benefit profile and close clinical monitoring.

In conclusion, the present case report highlighted the successful treatment of a patient with CML-T and severe thrombocytosis using combined IFN-α and imatinib therapy, emphasizing the challenges in diagnosing and managing this rare condition. While imatinib monotherapy initially failed to control platelet counts adequately, the addition of IFN-α led to complete hematologic and cytogenetic remission, suggesting this combination may be a promising strategy for similar cases. However, as this is a single-center report with a limited sample size, larger prospective studies, ideally multicenter, randomized controlled trials, are crucial to validate these findings and establish optimal treatment regimens. Further research should investigate the long-term efficacy and safety of the combination therapy, refine patient selection criteria and explore alternative therapeutic approaches like novel TKIs. Additionally, elucidating the molecular mechanisms driving severe thrombocytosis in CML-T, including the role of BCR-ABL1 mutations, remains essential for developing targeted therapeutic interventions.

 Acknowledgements

Not applicable.

 Availability of data and materials

The data generated in the present study may be requested from the corresponding author.

 Authors' contributions

MXJ was the primary investigator, leading the study design, data analysis and manuscript drafting. DLD conducted the literature review, revised the manuscript, prepared the figures and confirmed the authenticity of the raw data. ZZL contributed to data collection and experimental procedures. HYW independently verified the authenticity of all data cited in the manuscript, reviewed the manuscript and confirmed the treatment course. LC reviewed and edited the manuscript for final submission. DLD and HYW confirm the authenticity of all the raw data. All authors read and approved the final manuscript.

 Ethics approval and consent to participate

The present case report was approved by the Medical Ethics Committee of the Affiliated Hospital of Shandong Second Medical University (grant no. wyfy-2024-qt-051; date of approval: September 18, 2024; Weifang, China).

 Patient consent for publication

Written informed consent was obtained from the patient's family for the publication of this report and the accompanying images.

 Competing interests

The authors declare that they have no competing interests.

 References JabbourEKantarjianHChronic myeloid leukemia: 2020 update on diagnosis, therapy and monitoringAm J Hematol9569170920203223975810.1002/ajh.25792 RinaldiIWinstonKChronic myeloid leukemia, from pathophysiology to treatment-free remission: A narrative literature reviewJ Blood Med1426127720233705102510.2147/JBM.S382090 OsmanAEGDeiningerMWChronic myeloid leukemia: Modern therapies, current challenges and future directionsBlood Rev4910082520213377384610.1016/j.blre.2021.100825 ArberDAOraziAHasserjianRPBorowitzMJCalvoKRKvasnickaHMWangSABaggABarbuiTBranfordSInternational consensus classification of myeloid neoplasms and acute leukemias: Integrating morphologic, clinical and genomic dataBlood1401200122820223576789710.1182/blood.2022015850 ThakralBSalujaKMalhotraPSharmaRRMarwahaNVarmaSTherapeutic plateletpheresis in a case of symptomatic thrombocytosis in chronic myeloid leukemiaTher Apher Dial849749920041566355010.1111/j.1774-9987.2004.00187.x EbrahemRAhmedBKadhemSTruongQChronic myeloid leukemia: A case of extreme thrombocytosis causing syncope and myocardial infarctionCureus8e47620162700415310.7759/cureus.476 TurakhiaSKMurugesanGCottaCVTheilKSThrombocytosis and STAT5 activation in chronic myelogenous leukaemia are not associated with JAK2 V617F or calreticulin mutationsJ Clin Pathol6971371920162675483010.1136/jclinpath-2015-203498 Chiatamone RanieriSArleoMATrasartiSBizzoniLCarmosinoIDe LucaMLMohamedSMariggiòEScalzulliERosatiSClinical and prognostic features of essential thrombocythemia: Comparison of 2001 WHO Versus 2008/2016 WHO criteria in a large single-center cohortClin Lymphoma Myeloma Leuk21e328e33320213334272810.1016/j.clml.2020.11.003 HaznedarogluICThe therapeutic goals of essential thrombocythemia under the clouds of over-treatment and under-treatmentExpert Opin Pharmacother141431143620132364722510.1517/14656566.2013.799140 VermaSPSubbiahAJacobSEBasuDChronic myeloid leukaemia with extreme thrombocytosisBMJ Case Rep2015bcr201420456420152629056210.1136/bcr-2014-204564 TalpazMInterferon-alfa-based treatment of chronic myeloid leukemia and implications of signal transduction inhibitionSemin Hematol38 (Suppl 8)S22S2720011152659810.1016/s0037-1963(01)90114-3 PalandriFCastagnettiFIacobucciIMartinelliGAmabileMGugliottaGPoerioATestoniNBrecciaMBocchiaMThe response to imatinib and interferon-alpha is more rapid than the response to imatinib alone: A retrospective analysis of 495 Philadelphia-positive chronic myeloid leukemia patients in early chronic phaseHaematologica951415141920102030513910.3324/haematol.2009.021246 LiuZFanHLiYLiuCAnalysis of clinical characteristics and efficacy of chronic myeloid leukemia onset with extreme thrombocytosis in the era of tyrosine kinase inhibitorsOnco Targets Ther103515352020172876136010.2147/OTT.S142587 TefferiABarbuiTPolycythemia vera and essential thrombocythemia: 2021 update on diagnosis, risk-stratification and managementAm J Hematol951599161320203297493910.1002/ajh.26008 JangMAChoiCWRecent insights regarding the molecular basis of myeloproliferative neoplasmsKorean J Intern Med3511120203177860610.3904/kjim.2019.317 ByunYJParkBBLeeESChoiKSLeeDSA case of chronic myeloid leukemia with features of essential thrombocythemia in peripheral blood and bone marrowBlood Res4912712920142502501510.5045/br.2014.49.2.127 HirumaKSaitohHSomeyaKKashimuraMHematologic abnormalities in a patient with chronic myelogenous leukemia with advanced myelofibrosis were improved by G-CSFRinsho Ketsueki3513514119947511182(In Japanese) ShahNPFront-line treatment options for chronic-phase chronic myeloid leukemiaJ Clin Oncol3622022420182920655410.1200/JCO.2017.75.4663 GranatowiczAPiatekCIMoschianoEEl-HemaidiIArmitageJDAkhtariMAn overview and update of chronic myeloid leukemia for primary care physiciansKorean J Fam Med3619720220152643580810.4082/kjfm.2015.36.5.197 RajabtoWAngkasaYKAsymptomatic chronic-phase chronic myeloid leukemia BCR-ABL. (+) without splenomegaly: A case reportNiger J Clin Pract2537337520223529506310.4103/njcp.njcp_1401_21 GalvezCSteinBLThrombocytosis and thrombosis: Is there really a correlation?Curr Hematol Malig Rep1526126720203239976510.1007/s11899-020-00588-z ZhengYWenJLiJPediatric chronic myeloid leukemia presenting with extreme thrombocytosis and acute upper gastrointestinal hemorrhage: A case reportJ Pediatr Hematol Oncol43e1049e105120213405404610.1097/MPH.0000000000002216 TurroniSTolomeoMMamoneGPicarielloGGiacominiEBrigidiPRobertiMGrimaudoSPipitoneRMDi CristinaARecanatiniMA natural-like synthetic small molecule impairs bcr-abl signaling cascades and induces megakaryocyte differentiation in erythroleukemia cellsPLoS One8e5765020132346089010.1371/journal.pone.0057650 ThieleJKvasnickaHMVarusEOlligESchmitt-GraeffAStaibPGriesshammerMMegakaryocyte features and bcr/abl translocation in chronic myeloid leukemia following imatinib mesylate (STI571) therapy-a fluorescence in-situ hybridization studyLeuk Lymphoma451627163120041537021610.1080/10428190410001683732 ten BoschGJKesslerJHBlomJJoostenAMGambacorti-PasseriniCMeliefCJLeeksmaOCBCR-ABL oncoprotein is expressed by platelets from CML patients and associated with a special pattern of CrkL phosphorylationBr J Haematol103110911151998988632810.1046/j.1365-2141.1998.01115.x BennourAOuahchiIAchourBZaierMYoussefYBKhelifASaadASennanHAnalysis of the clinico-hematological relevance of the breakpoint location within M-BCR in chronic myeloid leukemiaMed Oncol3034820132326958310.1007/s12032-012-0348-z Arana-TrejoRMRuíz SánchezRIgnacio-IbarraGBáez de la FuenteEGarcesOGómez MoralesECastro GranadosMOvilla MartínezRRubio-BorjaMESolís AnayaLBCR/ABL p210, p190 and p230 fusion genes in 250 Mexican patients with chronic myeloid leukaemia (CML)Clin Lab Haematol2414515020021206727710.1046/j.1365-2257.2002.00413.x PolampalliSChoughuleANegiNShindeSBaisaneCAmrePSubramanianPGGujralSPrabhashKParikhPAnalysis and comparison of clinicohematological parameters and molecular and cytogenetic response of two Bcr/Abl fusion transcriptsGenet Mol Res71138114920081904849210.4238/vol7-4gmr485 Al-AchkarWMoassassFYoussefNWafaACorrelation of p210 BCR-ABL transcript variants with clinical, parameters and disease outcome in 45 chronic myeloid leukemia patientsJ BUON21444449201627273956 PaneFMostardaISelleriCSalzanoRRaiolaAMLucianoLSaglioGRotoliBSalvatoreFBCR/ABL mRNA and the P210(BCR/ABL) protein are downmodulated by interferon-alpha in chronic myeloid leukemia patientsBlood9422002207199910498589 JunmeiZFengkuanYYongpingSBaijunFYuzhangLLinaLQinglanZCoexistence of P190 and P210 BCR/ABL transcripts in chronic myeloid leukemia blast crisis resistant to imatinibSpringerplus417020152589741410.1186/s40064-015-0930-x ZhangXSunHSuYYiHLong-term molecular remission after treatment with imatinib in a chronic myeloid leukemia patient with extreme thrombocytosis harboring rare e14a3 (b3a3) BCR::ABL1 transcript: A case reportCurr Oncol298171817920223635470510.3390/curroncol29110645 PuilLLiuJXGishGMbamaluGBowtellDPelicciPGArlinghausRPawsonTBcr-Abl oncoproteins bind directly to activators of the Ras signalling pathwayEMBO J137647731994811229210.1002/j.1460-2075.1994.tb06319.x LiuRYFanCGarciaRJoveRZuckermanKSConstitutive activation of the JAK2/STAT5 signal transduction pathway correlates with growth factor independence of megakaryocytic leukemic cell linesBlood9323692379199910090948 VermaDKantarjianHMJonesDLuthraRBorthakurGVerstovsekSRiosMBCortesJChronic myeloid leukemia (CML) with P190 BCR-ABL: Analysis of characteristics, outcomes and prognostic significanceBlood1142232223520091953165710.1182/blood-2009-02-204693 MeloJVBCR-ABL gene variantsBaillieres Clin Haematol102032221997937666010.1016/s0950-3536(97)80003-0 BalatzenkoGGuenovaMStoimenovAJotovGToshkovSPhiladelphia chromosome-positive chronic myeloid leukemia with p190(BCR-ABL) rearrangement, overexpression of the EVI1 gene and extreme thrombocytosis: A case reportCancer Genet Cytogenet181757720081826206110.1016/j.cancergencyto.2007.11.009 Adnan-AwadSKimDHohtariHJavarappaKKBrandstoetterTMayerIPotdarSHeckmanCAKytöläSPorkkaKCharacterization of p190-Bcr-Abl chronic myeloid leukemia reveals specific signaling pathways and therapeutic targetsLeukemia351964197520213316894910.1038/s41375-020-01082-4 GleissnerBGökbugetNBartramCRJanssenBRiederHJanssenJWFonatschCHeyllAVoliotisDBeckJLeading prognostic relevance of the BCR-ABL translocation in adult acute B-lineage lymphoblastic leukemia: A prospective study of the German Multicenter Trial Group and confirmed polymerase chain reaction analysisBlood991536154320021186126510.1182/blood.v99.5.1536 QiuLLLuYJJingYYuLLiuDHWangLLComparison of clinical outcomes between P190 and P210 trans-cripts in adult Ph chromosome positive acute lymphoblastic leukemia in the new Era of TKIZhongguo Shi Yan Xue Ye Xue Za Zhi2436937420162715099410.7534/j.issn.1009-2137.2016.02.012(In Chinese) VasconcelosAPAzevedoIFMeloFCBCNevesWBAzevedoACACMeloRAMBCR-ABL1 transcript types showed distinct laboratory characteristics in patients with chronic myeloid leukemiaGenet Mol Res1620172843755210.4238/gmr16029541 GuglielmelliPCalabresiLThe MPL mutationInt Rev Cell Mol Biol36516317820213475624310.1016/bs.ircmb.2021.09.003 StockklausnerCDuffertCMCarioHKnöflerRStreifWKulozikAETHROMKID-Plus Studiengruppe der Gesellschaft für Thrombose-und Hämostaseforschung (GTH) and of Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH)Thrombocytosis in children and adolescents-classification, diagnostic approach and clinical managementAnn Hematol1001647166520213371286610.1007/s00277-021-04485-0 RottenstreichABusselJBTreatment of immune thrombocytopenia during pregnancy with thrombopoietin receptor agonistsBr J Haematol20387288520233783025110.1111/bjh.19161 RubensteinAIPiersonSKShyamsundarSBustamanteMSGonzalezMVMilllerIDBrandstadterJDMumauMDFajgenbaumDCImmune-mediated thrombocytopenia and IL-6-mediated thrombocytosis observed inidiopathic multicentric Castleman diseaseBr J Haematol20492193020243816872710.1111/bjh.19279 WolfeHRReinLAMThe evolving landscape of frontline therapy in chronic phase chronic myeloid leukemia (CML)Curr Hematol Malig Rep1644845420213466187410.1007/s11899-021-00655-z FlynnJPGerrietsVImatinib. In: StatPearls. StatPearls Publishing, Treasure Island, FL, 2025. GaoLRenMQTianZGPengZYShiGYuanZManagement of chronic myeloid leukemia presenting with isolated thrombocytosis and complex Philadelphia chromosome: A case reportMedicine (Baltimore)100e2713420213447716210.1097/MD.0000000000027134 RepsoldLPoolRKarodiaMTintingerGBeckerPJoubertAMApoptotic profiling of chronic myeloid leukaemia patients' platelets ex vivo before and after treatment with ImatinibCell Biochem Funct3956257020213356980810.1002/cbf.3625 SenerYOkayMAydinSBuyukasikYAkbiyikFDikmenZGTKI-related platelet dysfunction does not correlate with bleeding in patients with chronic phase-chronic myeloid leukemia with complete hematological responseClin Appl Thromb Hemost25107602961985840920193121888310.1177/1076029619858409 ShuLLJiangQLMengFYYangMMolecular mechanism of imatinib-induced thrombocytopenia in treatment of patients with CMLZhongguo Shi Yan Xue Ye Xue Za Zhi1913141318201122040995(In Chinese) RepsoldLPoolRKarodiaMTintingerGJoubertAMEx vivo platelet morphology assessment of chronic myeloid leukemia patients before and after Imatinib treatmentMicrosc Res Tech852222223320223517493310.1002/jemt.24079 AkramAMIqbalZAkhtarTKhalidaAMSabarMFQaziMHAzizeZSajidNAleemARasoolhMPresence of novel compound BCR-ABL mutations in late chronic and advanced phase imatinib sensitive CML patients indicates their possible role in CML progressionCancer Biol Ther1821422120172827807810.1080/15384047.2017.1294289 Al-AliHKHeinrichMCLangeTKrahlRMuellerMMüllerCNiederwieserDDrukerBJDeiningerMWHigh incidence of BCR-ABL kinase domain mutations and absence of mutations of the PDGFR and KIT activation loops in CML patients with secondary resistance to imatinibHematol J5556020041474543110.1038/sj.thj.6200319 TanakaRKimuraSAbl tyrosine kinase inhibitors for overriding Bcr-Abl/T315I: From the second to third generationExpert Rev Anticancer Ther81387139820081875969110.1586/14737140.8.9.1387 DhillonSOlverembatinib: First approvalDrugs8246947520223519587610.1007/s40265-022-01680-9 BinzaidAABaqalOJSoheibMNahedhMASamarkandiHHAljurfMCardiovascular toxicity associated with tyrosine kinase inhibitor therapy in chronic myeloid leukemiaGulf J Oncolog17984202135152199 CaocciGMulasOAnnunziataMLucianoLAbruzzeseEBonifacioMOrlandiEMAlbanoFGalimbertiSIurloALong-term mortality rate for cardiovascular disease in 656 chronic myeloid leukaemia patients treated with second- and third-generation tyrosine kinase inhibitorsInt J Cardiol30116316620203171185110.1016/j.ijcard.2019.10.036 RobakTUse of interferon in the treatment of chronic myeloproliferative disordersActa Haematol Pol23 (2 Suppl 1)S30S3719921488870(In Polish) TalpazMMercerJHehlmannRThe interferon-alpha revival in CMLAnn Hematol94 (Suppl 2)S195S20720152581408610.1007/s00277-015-2326-y KujawskiLATalpazMThe role of interferon-alpha in the treatment of chronic myeloid leukemiaCytokine Growth Factor Rev1845947120071770398610.1016/j.cytogfr.2007.06.015 SeewannHLInterferon therapy in essential thrombocythemiaWien Med Wochenschr14342042419938273365(In German) KoikeGOtsukaTShibuyaTNihoYThrombocytosis in chronic myelogenous leukemia (CML) controlled by interferon alpha (IFN-alpha)Rinsho Ketsueki3040040319892769964(In Japanese) ThieleJZirbesTKvasnickaHMNiederleNDammaschJSchmidtMWindeckerRLederLDDiehlVFischerRInterferon therapy, but not busulfan restores normal-sized megakaryopoiesis in CML-a comparative histo- and immunomorphometric studyAnal Cell Pathol11314219968844103 KongJQinYZZhaoXSHouYLiuKYHuangXJJiangHProfiles of NK cell subsets are associated with successful tyrosine kinase inhibitor discontinuation in chronic myeloid leukemia and changes following interferon treatmentAnn Hematol1002557256620213427852410.1007/s00277-021-04606-9 RüdigerHandreasHMicheleBEuropean LeukemiaNetChronic myeloid leukaemiaLancet37034235020071766288310.1016/S0140-6736(07)61165-9 GabrieleLBorghiPRozeraCSestili PandreottiMGuariniAMontefuscoEFoàRBelardelliFIFN-alpha promotes the rapid differentiation of monocytes from patients with chronic myeloid leukemia into activated dendritic cells tuned to undergo full maturation after LPS treatmentBlood10398098720041452578110.1182/blood-2003-03-0981 SimonssonBGedde-DahlTMarkevärnBRemesKStentoftJAlmqvistABjöremanMFlogegårdMKoskenvesaPLindblomACombination of pegylated IFN-α2b with imatinib increases molecular response rates in patients with low- or intermediate-risk chronic myeloid leukemiaBlood1183228323520112168537410.1182/blood-2011-02-336685 McGlavePMamusSVilenBDewaldGEffect of recombinant gamma interferon on chronic myelogenous leukemia bone marrow progenitorsExp Hematol1533133519873106077 FoonKASherwinSAAbramsPGStevensonHCHolmesPMaluishAEOldhamRKHerbermanRBA phase I trial of recombinant gamma interferon in patients with cancerCancer Immunol Immunother201931971985393381810.1007/BF00205575 DouXLWangSSFangJLYuLRenXHuangXJJiangQHepatic adverse events associated with tyrosine kinase inhibitors in patients with chronic myeloid leukemiaZhonghua Nei Ke Za Zhi5764965520183018044910.3760/cma.j.issn.0578-1426.2018.09.006(In Chinese) O'BrienSKantarjianHTalpazMPractical guidelines for the management of chronic myelogenous leukemia with interferon alphaLeuk Lymphoma232472521996903110510.3109/10428199609054827

Peripheral blood and bone marrow smears. (A) Bone marrow aspirate before treatment: Hypercellular bone marrow with prominent granulocytic hyperplasia. Blasts and various stages of granulocytic maturation are observed. Eosinophils and basophils are readily identifiable. Megakaryocytes are significantly increased, with a predominance of small megakaryocytes. Platelets are seen in aggregates and sheets. (B) Peripheral blood smear before treatment: Leukocytosis is evident. Blasts and various stages of granulocytic maturation are observed. Eosinophils and basophils are readily identifiable. Platelet clumping is frequently observed. (C) Bone marrow aspirate after treatment: Cellular bone marrow with normal myeloid-to-erythroid ratios. Myelocytes and later stages of granulocytic maturation are observed. Megakaryocytes appear normal and platelets are dispersed with occasional small clusters. (D) Peripheral blood smear after treatment: White blood cell count is normal. Mature granulocytes, lymphocytes and monocytes are observed. Platelets are dispersed with occasional small clusters. (Magnification, x1,000, Wright-Giemsa stain).

Bone marrow biopsy. (A) The bone marrow is markedly cellular with an increased myeloid-to-erythroid ratio. Myeloid cells are present at various stages of maturation, with a slight increase in immature forms. Eosinophils are readily observed. Erythroid precursors are predominantly late erythroblasts (magnification, x40; H&E stain). (B) Megakaryocytes are significantly increased, predominantly small megakaryocytes with fewer nuclear lobes. Scattered lymphocytes and plasma cells are observed (magnification, x400; H&E stain). H&E, hematoxylin and eosin.

Cytogenetic analysis. (A) Pre-treatment karyotype showing the typical Ph+ translocation t(9;22) (q34.1;q11.2), with red arrows indicating chromosomes 9 and 22 involved in the translocation. (B) Post-treatment karyotype, no Philadelphia chromosome detected, achieving complete cytogenetic response, with red arrows indicating the normal chromosomes 9 and 22.

BCR-ABL1 fusion gene transcript level (IS%) trend. The patient received 7 BCR-ABL1 fusion gene transcript level tests, with an initial value of 70.78%. The transcript level gradually decreased with treatment, reaching 0.14% in June 2024, approaching the MMR criteria (IS% ≤0.1%). MMR, major molecular response; IS, International Scale.

Changes of white blood cell and platelet count during the treatment. (A) Platelet count gradually decreased following imatinib therapy (blue arrow indicates the start of imatinib monotherapy), with plateletpheresis (red arrows indicate the time points of plateletpheresis) performed on days 2, 4, 7, 9, 12, 15 and 20. The addition of interferon-α (green arrow indicates the start of combined imatinib and interferon-α therapy) on day 11 further accelerated the decline. By day 30, platelet count had significantly decreased but remained elevated. (B) White blood cell count, initially elevated, rapidly decreased after imatinib therapy and remained within the normal range throughout treatment.

Clinical timeline. The patient received 10 days of imatinib monotherapy, followed by 20 days combined with daily IFN-α (QD) until symptom resolution and discharge. After discharge, treatment continued with imatinib combined with twice-weekly IFN-α (BIW) for one month, achieving a CHR. IFN-α was then discontinued and imatinib monotherapy was continued for 8 months, resulting in a CCyR. The final BCR-ABL1 level reached 0.14%, approaching MMR and the patient remains under follow-up. CHR, complete hematological response; CCyR, complete cytogenetic response; MMR, major molecular response; SD, stable disease.

Roles of different BCR-ABL variants in leukemia.

First author, year Cancer type BCR-ABL variants Clinical significance (Refs.)
Ten Bosch et al, 1998 CML BCR-ABLp210 Promotes thrombopoiesis through CrkL phosphorylation (25)
Bennour et al, 2013 CML BCR-ABLp210 Correlated with platelet counts in patients with CML (26)
Arana-Trejo et al, 2002 CML BCR-ABLp210/p 190/p230 Associated with platelet counts, splenomegaly and chromosomal abnormalities (27)
Polampalli et al, 2008 CML BCR-ABLp210 Associated with myeloid blast crisis in patients with CML (28)
Al-Achkar et al, 2016 CML BCR-ABLp210 Associated with prognosis in patients with CML (29)
Pane et al, 1999 CML BCR/ABLp 210 Affecting the responsiveness of patients with CML to IFN-α (30)
Zhao et al, 2015 CML BCR/ABLp 190/p210 Participation in imatinib resistance through ABL kinase domain mutations (31)
Zhang et al, 2022 CML BCR-ABLp210 Associated with thrombocytosis in patients with CML (32)
Puil et al, 1994 CML BCR-ABLp185/p 210 Participates in the occurrence of CML through Ras signaling pathway (33)
Liu et al, 1999 CML BCR-ABLp185 Activates megakaryocytes through JAK2/STAT5 signaling (34)
Verma et al, 2009 CML BCR-ABLp190 Induce rapid transformation of lymphoid progenitor cells and poor prognosis (35)
Melo et al, 1997 CML BCR-ABLp230 Associated with thrombocytosis in patients with CML (36)
Balatzenko et al, 2008 CML BCR-ABLp190 Associated with extreme thrombocytosis in patients with CML (37)
Adnan-Awad et al, 2008 CML BCR-ABLp190/210 Upregulating interferon receptor expression through Src signaling (38)
Gleissner et al, 2002 Ph(+) ALL BCR-ABLp210 Associated with long-term survival of patient (39)
Qiu et al, 2016 Ph(+) ALL BCR-ABLp190/p 210 Associated with CR and long-term survival of patient (40)

BCR, B cell receptor; ABL, Abelson murine leukemia viral oncogene homolog; CML, chronic myeloid leukaemia; ALL, acute lymphoblastic leukaemia; Ph, Philadelphia chromosome; IFN, interferon; CR, complete remission.