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Expression and Clinical Correlation of PD-1/PD-L1 and VE1(BRAFp.V600E) in Pediatric Langerhans Cell Histiocytosis.

Authors :
Tandon, Sneha
Weitzman, Sheila
Joyce, Brooklyn
Mcguire, Bryan
Stephens, Derek
Whitlock, James
Hawkins, Cynthia
Bo Yee Ngan
Abla, Oussama
Source :
Mediterranean Journal of Hematology & Infectious Diseases. 2023, Vol. 15 Issue 1, p1-9. 9p.
Publication Year :
2023

Abstract

Background And Objectives: Langerhans cell histiocytosis (LCH) is an inflammatory myeloid neoplasm with a wide spectrum of clinical presentations. Programmed Cell Death-1 (PD- 1) receptor and its ligand (PD-L1) are overexpressed in LCH, but their clinical significance is unknown. We performed a clinical correlation study of PD-1/PD-L1 and VE1(BRAFp.V600E) expression in 131 children with LCH. Methods: A total of 111 samples were tested for PD-1/PD-L1 and 109 for VE1(BRAFp.V600E) mutant protein by immunohistochemistry. Results: PD-1, PD-L1 and VE1(BRAFp.V600E) positivity was observed in 40.5%, 31.53% and 55%, respectively. PD-1/PD-L1 expression showed no significant effect on the rate of disease reactivations, early response to therapy or late sequelae. The 5-year EFS was not statistically different between patients with PD-1 positive compared to those with PD-1 negative tumours (47.7% vs.58.8%, p=0.17). Similar 5-year EFS rates were also seen in those who were PD-L1 positive compared to PD-L1 negative cases (50.5% vs.55.5%, p=0.61). VE1(BRAFp.V600E) positivity was associated with a significantly higher frequency of risk-organ involvement (p=0.0053), but no significant effect on early response to therapy or rates of reactivations or late sequelae. Conclusions: Our study showed no significant correlation between VE1(BRAFp.V600E) expression, PD-1 and PD-L1 and clinical outcome in pediatric LCH. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20353006
Volume :
15
Issue :
1
Database :
Academic Search Index
Journal :
Mediterranean Journal of Hematology & Infectious Diseases
Publication Type :
Academic Journal
Accession number :
174775392
Full Text :
https://doi.org/10.4084/MJHID.2023.035