Related Experiment Video
Updated: Dec 30, 2025

Expression of Exogenous Cytokine in Patient-derived Xenografts via Injection with a Cytokine-transduced Stromal Cell Line
Published on: May 10, 2017
Cyclooxygenase-2 expression as a prognostic factor in pediatric classical Hodgkin lymphoma
Y Elborai1, A Elgammal2, A Salama3
1Pediatric Oncology Department, National Cancer Institute (NCI), Cairo University, Fom El-khalig Square Kasr El-Aini St., Cairo, 11796, Egypt. yasser.elborai@cu.edu.eg.
Cyclooxygenase-2 (COX-2) expression in pediatric classical Hodgkin lymphoma (CHL) did not independently predict outcomes. However, COX-2 positivity was linked to poorer survival in high-risk patients, suggesting a complex prognostic role.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Cyclooxygenase-2 (COX-2) is implicated in tumor development, angiogenesis, and proliferation.
- Elevated COX-2 expression is observed in many cancers and often correlates with a poor prognosis.
- The prognostic significance of COX-2 in pediatric classical Hodgkin lymphoma (CHL) remains to be fully elucidated.
Purpose of the Study:
- To investigate the prognostic value of COX-2 expression in Reed-Sternberg (RS) cells of pediatric classical Hodgkin lymphoma (CHL) patients.
- To correlate COX-2 immunostaining with clinical variables and patient outcomes.
Main Methods:
- Retrospective analysis of 127 pediatric CHL patients treated between January 2005 and June 2013.
- Immunohistochemical assessment of COX-2 expression in RS cells.
- Correlation of COX-2 status with overall survival (OS) and progression-free survival (PFS) using univariate and multivariate analyses.
Main Results:
- COX-2 was expressed in 38.6% of RS cells.
- No significant association was found between COX-2 positivity and overall 5-year OS or PFS in the entire cohort.
- However, COX-2 positivity was associated with significantly lower 5-year OS in high-risk patients and lower 5-year PFS in patients with B symptoms or bulky disease.
- Radiotherapy improved survival in both COX-2 positive and negative groups, with a numerically greater benefit in the COX-2 positive group.
Conclusions:
- COX-2 expression in pediatric CHL shows a trend towards being a poor prognostic factor but does not offer independent prognostic information.
- Further large-scale studies are warranted to confirm COX-2's prognostic role and explore its potential as a therapeutic target in CHL.
Related Concept Videos
Positive Regulator Molecules
Differentiation of Common Myeloid Progenitor Cells

