Evidence map›Paper›PMID 35105321›Full record

ArticleBMC cancer2022

Baseline blood count levels increase odds of cytopenia among CML patients in Kenya: a case control study.

Angela McLigeyo, Jamilla Rajab, Peter Oyiro, Mohammed Ezzi, Yatich Bett, Matilda Ong'ondi, Andrew Odhiambo, Sitna Mwanzi, Nicholas Othieno-Abinya

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Angela McLigeyoDepartment of Internal Medicine and therapeutics, Kenyatta University, Nairobi, Kenya. awinoligeyo@gmail.com.
Jamilla RajabDepartment of Human Pathology, School of Medicine, Unit of Hematology and Blood Transfusion, University of Nairobi, Nairobi, Kenya.
Peter OyiroHemato - Oncology Unit, Kenyatta National Hospital, Nairobi, Kenya.
Mohammed EzziDepartment of Human Pathology, School of Medicine, Unit of Hematology and Blood Transfusion, University of Nairobi, Nairobi, Kenya.
Yatich BettMoi Teaching and Referral Hospital, Eldoret, Kenya.
Matilda Ong'ondiHemato - Oncology Unit, Kenyatta National Hospital, Nairobi, Kenya.
Andrew OdhiamboDepartment of Clinical Medicine and Therapeutics, University of Nairobi, Nairobi, Kenya.
Sitna MwanziAga Khan University Hospital, Nairobi, Kenya.
Nicholas Othieno-AbinyaDepartment of Clinical Medicine and Therapeutics, University of Nairobi, Nairobi, Kenya.
University of Nairobi · KEKenyatta National Hospital · KEAga Khan University Hospital Nairobi · KEKenyatta University · KEMoi University · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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/mm

conclusionOdds of cytopenia were higher in presence of baseline cytopenia and thrombocytosis. Clinicians should have a high index of suspicion for these patients.

Indexed as

AdolescentAdultAgedAnemiaAntineoplastic AgentsFemaleHumansImatinib MesylateKenyaLeukemia, Myelogenous, Chronic, BCR-ABL PositiveLogistic ModelsMaleMiddle AgedMultivariate AnalysisNeutropeniaRetrospective StudiesAntineoplastic AgentsImatinib MesylateBCR-ABLCMLCytopeniaImatinibPhiladelphiaTyrosine Kinase

Identifiers

PMID35105321
PMCPMC8805406
OpenAlexW4220978571

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.