The Significance of CD20 Intensity Variance in Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia.
Andreea Nicoleta SerbanicaDelia Codruta PopaConstantin CaruntuSergiu PascaCristian ScheauIonut Vlad SerbanicaRaluca SuciuValeria TicaElisa BusescuLuminita Nicoleta CimaCerasela JardanMihaela DragomirDaniel CoriuAndrei ColitaAnca ColitaPublished in: Journal of clinical medicine (2023)
B-cell precursor acute lyphoblastic leukemia (ALL) is a common pediatric malignancy and patients may have significant benefits from monoclonal antibodies therapy with increased survival rates. Positive CD20 expression is identified in about half of these patients and its presence may serve as a prognostic factor in disease evolution. We performed a retrospective study including 114 patients diagnosed with B-ALL and evaluated the expression of CD20 through flow cytometry at diagnosis and on day 15. Additional immunophenotypic analyses as well as cytogenetic and molecular genetic analyses were also performed. We observed an increase in the mean fluorescence intensity (MFI) of CD20 between diagnosis-1.9 (1.2-3.26) and day 15: 6.17 (2.14-27.4), ( p < 0.0001). Furthermore, we assessed that both diagnosis and day 15 CD20 MFI had an impact on RFS and OS, respectively, for cut-off values of >8.08 at diagnosis and >28.65 at day 15. In conclusion, CD20 expression appears to be a poor prognostic feature of B-ALL in pediatric patients. In this study, stratification of the outcome by the intensity of CD20 has implications concerning the allocation to rituximab-based chemotherapy and may offer new, potentially useful information for pediatric patients with B-ALL.
Keyphrases
- prognostic factors
- end stage renal disease
- ejection fraction
- newly diagnosed
- acute lymphoblastic leukemia
- poor prognosis
- chronic kidney disease
- machine learning
- nk cells
- stem cells
- healthcare
- acute myeloid leukemia
- flow cytometry
- patient reported outcomes
- deep learning
- long non coding rna
- young adults
- mesenchymal stem cells
- binding protein
- diffuse large b cell lymphoma
- genome wide
- quantum dots
- hepatitis b virus
- cell therapy
- respiratory failure
- free survival