JCHOR

The Journal of Current Hematology & Oncology Research regularly publishes internationally qualified research in hematology and oncology within the current scholarly knowledge.

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Original Article
Clinical features and management outcomes of hairy cell leukemia in routine clinical practice: a single center retrospective experience
Aims: In this study, we aimed to review the clinical and treatment characteristics of hairy cell leukemai (HCL) patients.
Methods: This is a single-center retrospective study conducted at University of Health Sciences, Adana City Hospital, Hematology department between January 2018 and August 2025. The data of 33 patients with the diagnosis of hairy cell leukemia from the database of hospital records were analysed.
Results: First line treatment was cladribine in 27 (81.8%) patients, rituximab-cladribin in 2 (6.1 %) patients, interferon in 1 (3 %) patient and splenectomy in 3 (9.1 %) patients. Thirty one (93.9 %) patients responded to treatment and only 2 (6.1 %) did not. The progression was observed in 8 (25.8 %) of 31 responding patients. The probablity of progression free survival (PFS) at 10 years was 33 %. When the data is analysed according to the age groups of <50 y, 50-60 y and >60 y, the probability of PFS was 42.9 %, 83.3 %, 31.3 %,respectively (p=0.096). Also patients were grouped according to the age <=60 y and >60 y; and the probability of PFS at 10 years were 40.8% v.s 31.3% (p=0.034). All patients were alive at the end of follow up period, so median OS was not reached.
Conclusion: Cladribin was verified to be an effective treatment modality in HCL with high response rate, but low PFS. And the differences in the PFS according to age groups should be reevalated in the era of rituximab-cladribine combination and novel agents.
Ethical Statement

<p>This study was approved by the Scientific Researches Ethics Committee of Adana City Training and Research Hospital (Date: 15.01.2026, Decision No: 983).</p>

Informed Consent

<p>This retrospective study used pre-existing anonymized patient data. No additional intervention was performed, and there was no direct patient contact. The study was approved by the Ethics Committee, and the requirement for written informed consent was waived by the ethics committee.</p>

Author Contributions

<p>Concept: ES; Design: ES; Control: ES, DD; Resources: NB; Materials: NB; Data Collection and/or Processing: ES, DD, BA, DYA, ZTK, &Ccedil;&Uuml;, NB; Analysis and/or Interpretation: ES; Literature Review: ES, DD, BA, DYA, ZTK, &Ccedil;&Uuml;, NB; Writing the Article: ES, DD; Critical Review: ES, DD, BA, DYA, ZTK, &Ccedil;&Uuml;, NB.</p>

Conflict of Interest

<p>The authors declare no conflicts of interest related to this study.</p>

Financial Disclosure

<p>The authors received no financial support for the conduct or publication of this research.</p>


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Volume 4, Issue 4, 2026
Page : 130-134
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