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Pediatric Lymphoma in Jordan: A Retrospective Single-Center Study of Clinical Presentation, Treatment, and Outcomes
Mousa A Qatawneh1, Moath Altarawneh1, Ayman Alhwayan1
1Pediatric Hematology-Oncology, Royal Medical Services, Queen Rania Children's Hospital, Amman, JOR.
Insights
Pediatric lymphoma in Jordan often presents at advanced stages, especially non-Hodgkin lymphoma (NHL), leading to higher mortality. Early diagnosis and biomarker use are crucial for improving outcomes in childhood lymphoma.
Area of Science:
- Pediatric oncology
- Hematology
- Cancer epidemiology
Background:
- Pediatric lymphoma (Hodgkin and non-Hodgkin) is a major childhood cancer.
- Limited data exists on pediatric lymphoma in Middle Eastern populations.
- This study addresses this gap by analyzing cases from Jordan.
Purpose of the Study:
- To characterize clinical features, biomarkers, treatments, and outcomes of pediatric Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL) in Jordan.
- To identify factors associated with treatment response and survival.
- To inform strategies for improved pediatric lymphoma care in the region.
Main Methods:
- Retrospective analysis of 49 pediatric lymphoma patients (0-16 years) diagnosed between 2015-2024 in Jordan.
- Data collection included demographics, clinical presentation, laboratory markers (CRP, LDH), treatment, and outcomes.
- Statistical analysis involved chi-square/Fisher's exact tests, Mann-Whitney U tests, and Kaplan-Meier survival curves.
Main Results:
- A high proportion (77.5%) of patients were diagnosed at advanced stages.
- Non-Hodgkin lymphoma (NHL) cases frequently involved aggressive subtypes and showed higher CRP and LDH levels compared to Hodgkin lymphoma (HL).
- Complete remission was achieved in 50% of treatment-evaluable patients; mortality (26.5%) and relapse (15%) occurred primarily in advanced NHL.
Conclusions:
- Pediatric lymphoma in Jordan is frequently diagnosed late, particularly NHL, which is linked to increased mortality.
- There is an urgent need for earlier diagnosis and targeted therapies.
- Biomarkers like lactate dehydrogenase (LDH) and C-reactive protein (CRP) can aid risk assessment and improve patient outcomes.
Background:
Pediatric lymphoma, encompassing Hodgkin lymphoma (HL) and non-Hodgkin lymphoma (NHL), represents a significant cause of childhood cancer morbidity with limited data available from Middle Eastern settings. This study aims to characterize the clinical presentations, biomarker profiles, treatment patterns, and outcomes of pediatric HL and NHL at a tertiary care center in Jordan.
Methods:
This retrospective study included children aged 0-16 years diagnosed with HL or NHL at Queen Rania Children's Hospital in Jordan from 2015 to 2024. Data were collected on demographics, clinical presentation, laboratory markers, treatment regimens, and outcomes. Categorical data were analyzed using chi-square or Fisher's exact tests, continuous variables using Mann-Whitney U tests, and Event-Free Survival (EFS) was assessed using Kaplan-Meier curves.
Results:
A total of 49 patients' data were analyzed. The findings indicate a high rate of late-stage diagnosis among pediatric lymphoma patients in Jordan, with 38 (77.5%) presenting at advanced stages. Most NHL cases involved aggressive subtypes, including Burkitt and T-lymphoblastic lymphoma. Compared with HL patients, those with NHL exhibited significantly higher median C-reactive protein (CRP; 78.5 mg/L vs. 12.0 mg/L, P = 0.027) and lactate dehydrogenase (LDH; 553 U/L vs. 355 U/L, P = 0.012), indicating greater systemic inflammation and tumor burden in NHL. Among 40 (81.6%) treatment-evaluable patients, chemotherapy achieved a 20 (50%) complete remission rate. Mortality occurred exclusively among NHL patients 13 (26.5%), primarily those with advanced or extranodal disease. Relapse was observed in six (15%) of patients, with a median time to relapse of 37.5 months.
Conclusions:
Pediatric lymphoma in Jordan is most often diagnosed at an advanced stage, particularly NHL. Advanced NHL is associated with increased mortality. Early diagnosis, targeted therapy implementation, and incorporation of biomarkers such as LDH and CRP are urgently needed to improve risk assessment and patient outcomes.
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