The Significance of CD20 Intensity Variance in Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia

Author:

Serbanica Andreea Nicoleta12,Popa Delia Codruta34,Caruntu Constantin56ORCID,Pasca Sergiu7,Scheau Cristian5ORCID,Serbanica Ionut Vlad1,Suciu Raluca4ORCID,Tica Valeria4,Busescu Elisa2,Cima Luminita Nicoleta89,Jardan Cerasela14,Dragomir Mihaela4,Coriu Daniel410,Colita Andrei1011,Colita Anca12ORCID

Affiliation:

1. Department of Pediatrics, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania

2. Department of Pediatric Hematology and Stem Cell Transplantation, Fundeni Clinical Institute, 022328 Bucharest, Romania

3. Department of Biochemistry, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania

4. Department of Hematology, Fundeni Clinical Institute, 022328 Bucharest, Romania

5. Department of Physiology, The “Carol Davila” University of Medicine and Pharmacy, 050474 Bucharest, Romania

6. Department of Dermatology, ‘Prof. N.C. Paulescu’ National Institute of Diabetes, Nutrition and Metabolic Diseases, 011233 Bucharest, Romania

7. Department of Hematology, Iuliu Haţieganu University of Medicine and Pharmacy, 400347 Cluj-Napoca, Romania

8. Department of Endocrinology and Diabetes, Nutrition and Metabolic Diseases—“Elias” Emergency University Hospital, 011461 Bucharest, Romania

9. Department of Endocrinology, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania

10. Department of Hematology, Carol Davila University of Medicine and Pharmacy, 420003 Bucharest, Romania

11. Department of Hematology, Coltea Hospital, 420003 Bucharest, Romania

Abstract

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.

Publisher

MDPI AG

Subject

General Medicine

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