Abstract

BackgroundImatinib is the gold standard for the treatment of all phases of Philadelphia positive Chronic Myeloid Leukemia (CML). During treatment, patients may develop cytopenia. We aimed to study the baseline characteristics and factors associated with cytopenia at a Nairobi Hospital.MethodsThis was a retrospective case-control study of patients aged ≥18 years on follow-up at the Glivec International Patient Access Program (GIPAP) clinic from 2007 to 2015. The cases consisted of CML patients on imatinib who developed cytopenia. The controls were CML patients on imatinib who did not develop cytopenia. Baseline socio – demographic, clinical, hematologic, and molecular data were retrieved from patients’ files. Chi square or fishers’ exact tests were used to analyze for differences between cytopenia and no cytopenia. Binary logistic regressions were employed to identify relationships. Univariate and multivariate analyses were done to identify independent predictors of cytopenia. Odds ratios (OR) were presented including the 95% confidence intervals and respective p values.ResultsA total of 201 patients were studied consisting of ninety-four (94) patients with cytopenia and 107 with no cytopenia. Among the entire population, males were 52, and 42% were aged 36–50 years. Sex, age, marital status, occupation and education level were similar between the cytopenia and no cytopenia groups.Among the 201 patients, 70% had symptoms for > 12 months before diagnosis, 78.6% had B symptoms at baseline, 80% had a moderate splenomegaly at baseline.Among patients with cytopenia, 40 and 37.4% developed cytopenia within 3 months and 3–6 months respectively after imatinib initiation. Baseline neutrophilia, neutropenia, anaemia, thrombocytosis, thrombocytopenia was found in 68, 11, 11, 23.5 and 11% respectively. Baseline hemoglobin, neutrophil and platelet level were significantly different between the cytopenia and the no cytopenia group. On univariable analysis, baseline anemia with hb < 7.9 g/dL (p = 0.002), neutropenia (p = 0.001), neutrophilia > 100,000/mm3 (p = 0.002) and thrombocytopenia (p = 0.001) increased the odds of developing cytopenia. On multivariable analysis, baseline anaemia (p value < 0.002), neutropenia (p value < 0.001), thrombocytopenia (p value, < 0.001) and thrombocytosis (p value, 0.033) increased the odds of developing cytopenia.ConclusionOdds of cytopenia were higher in presence of baseline cytopenia and thrombocytosis. Clinicians should have a high index of suspicion for these patients.

Highlights

  • Chronic Myeloid Leukemia (CML) is a Philadelphia/BCR-ABL1-positive chronic neoplastic disease with an increase in blood granulocytes and bone marrow myeloid precursors, bone marrow hypercellularity composed of mature granulocytes and their precursors

  • The fusion protein resulting from this translocation, the BCR-ABL1, is a tyrosine kinase which acts independently of any stimulation and results in the development of CML [3]

  • We aimed to study the sociodemographic as well as the clinical and laboratory characteristics associated with increased odds of development of cytopenia among CML patients on imatinib at the Glivec Inter‐ national Patient Access Program (GIPAP) clinic

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Summary

Introduction

CML is a Philadelphia/BCR-ABL1-positive chronic neoplastic disease with an increase in blood granulocytes and bone marrow myeloid precursors, bone marrow hypercellularity composed of mature granulocytes and their precursors. The fusion protein resulting from this translocation, the BCR-ABL1, is a tyrosine kinase which acts independently of any stimulation and results in the development of CML [3]. Tyrosine kinase inhibitors (TKI) block this kinase and in turn block signaling pathways involved in myeloid proliferation while stimulating apoptosis and cellular adhesion [4, 5]. The disease is common in the elderly and in men in the developed world [6]. Imatinib is the gold standard for the treatment of all phases of Philadelphia positive Chronic Myeloid Leukemia (CML). We aimed to study the baseline characteristics and factors associated with cytopenia at a Nairobi Hospital

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