Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine

Abstract Objective Pediatric acute lymphoblastic leukemia (ALL) is the most prevalent type of cancer among children. This study was conducted to describe and correlate the clinical characteristics and outcomes of treatment of patients with pediatric ALL in the main referral hospital in Palestine. Re...

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Main Authors: Ramzi Shawahna, Sultan Mosleh, Yahya Odeh, Rami Halawa, Majd Al-Ghoul
Format: Article
Language:English
Published: BMC 2021-07-01
Series:BMC Research Notes
Subjects:
Online Access:https://doi.org/10.1186/s13104-021-05678-6
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spelling doaj-c56f88d3adb94184931e25469b31adf52021-07-11T11:34:46ZengBMCBMC Research Notes1756-05002021-07-011411810.1186/s13104-021-05678-6Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from PalestineRamzi Shawahna0Sultan Mosleh1Yahya Odeh2Rami Halawa3Majd Al-Ghoul4Department of Physiology, Pharmacology and Toxicology, Faculty of Medicine and Health Sciences, An-Najah National UniversityDepartment of Medicine, Faculty of Medicine and Health Sciences, An-Najah National UniversityAn-Najah National University Hospital, An-Najah National UniversityAn-Najah National University Hospital, An-Najah National UniversityAn-Najah National University Hospital, An-Najah National UniversityAbstract Objective Pediatric acute lymphoblastic leukemia (ALL) is the most prevalent type of cancer among children. This study was conducted to describe and correlate the clinical characteristics and outcomes of treatment of patients with pediatric ALL in the main referral hospital in Palestine. Results Complete data of 69 patients were included in this analysis. The majority (79.7%) of the patients had B-ALL phenotype. After induction chemotherapy, remission was experienced by the vast majority of the patients and 5 (7.2%) experienced relapses. Cytogenetics for patients with B-ALL phenotype indicated that 10 (18.2%) patients had t(12, 21) translocation, 5 (9.1%) had hyperdiploidy, 4 (7.3%) had t(1, 19) translocation, and 2 (3.6%) had t(9, 22) translocation. The initial white blood cells (p value < 0.001), absolute neutrophils (p value = 0.011), and hemoglobin (p value < 0.001) were significantly lower in patients with B-cell ALL. Platelet counts were significantly lower (p value = 0.012) in patients with splenomegaly and those with bleeding symptoms (p value = 0.008). Presence of palmar pollar was positively associated (p value = 0.035) with T-cell ALL. Presence of hepatomegaly was positively associated (p value < 0.001) with splenomegaly.https://doi.org/10.1186/s13104-021-05678-6Acute lymphoblastic leukemiaInduction chemotherapyTreatmentTranslocationPalestine
collection DOAJ
language English
format Article
sources DOAJ
author Ramzi Shawahna
Sultan Mosleh
Yahya Odeh
Rami Halawa
Majd Al-Ghoul
spellingShingle Ramzi Shawahna
Sultan Mosleh
Yahya Odeh
Rami Halawa
Majd Al-Ghoul
Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine
BMC Research Notes
Acute lymphoblastic leukemia
Induction chemotherapy
Treatment
Translocation
Palestine
author_facet Ramzi Shawahna
Sultan Mosleh
Yahya Odeh
Rami Halawa
Majd Al-Ghoul
author_sort Ramzi Shawahna
title Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine
title_short Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine
title_full Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine
title_fullStr Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine
title_full_unstemmed Clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from Palestine
title_sort clinical characteristics and outcomes of patients with pediatric acute lymphoblastic leukemia after induction of chemotherapy: a pilot descriptive correlational study from palestine
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2021-07-01
description Abstract Objective Pediatric acute lymphoblastic leukemia (ALL) is the most prevalent type of cancer among children. This study was conducted to describe and correlate the clinical characteristics and outcomes of treatment of patients with pediatric ALL in the main referral hospital in Palestine. Results Complete data of 69 patients were included in this analysis. The majority (79.7%) of the patients had B-ALL phenotype. After induction chemotherapy, remission was experienced by the vast majority of the patients and 5 (7.2%) experienced relapses. Cytogenetics for patients with B-ALL phenotype indicated that 10 (18.2%) patients had t(12, 21) translocation, 5 (9.1%) had hyperdiploidy, 4 (7.3%) had t(1, 19) translocation, and 2 (3.6%) had t(9, 22) translocation. The initial white blood cells (p value < 0.001), absolute neutrophils (p value = 0.011), and hemoglobin (p value < 0.001) were significantly lower in patients with B-cell ALL. Platelet counts were significantly lower (p value = 0.012) in patients with splenomegaly and those with bleeding symptoms (p value = 0.008). Presence of palmar pollar was positively associated (p value = 0.035) with T-cell ALL. Presence of hepatomegaly was positively associated (p value < 0.001) with splenomegaly.
topic Acute lymphoblastic leukemia
Induction chemotherapy
Treatment
Translocation
Palestine
url https://doi.org/10.1186/s13104-021-05678-6
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