BLINATUMOMAB FOR FIRST RELAPSE OF PEDIATRIC B-CELL PRECURSOR ACUTE LYMPHOBLASTIC LEUKEMIA: A SINGLE-CENTER AMBISPECTIVE COHORT STUDY FROM CARTAGENA, COLOMBIA
Author(s)
Angel Castro, MD, Pediatric Oncologist1, Angel Andrade, MD Student1, Daniela Camacho Pérez, MD Student1, Maripaz Bermudez, MD Student1, Juan Martínez de Avila, MD Student1, Nelson R. Alvis Zakzuk, Jr., MBA2, Nelson José Alvis Zakzuk, MSc3, Josefina Zakzuk, PhD4;
1University of Cartagena, Paediatrics, Cartagena, Colombia, 2ALZAK Foundation, Cartagena, Colombia, 3Universidad de la Costa, Barranquilla, Colombia, 4University of Cartagena, Institute for Immunological Research, Cartagena, Colombia
1University of Cartagena, Paediatrics, Cartagena, Colombia, 2ALZAK Foundation, Cartagena, Colombia, 3Universidad de la Costa, Barranquilla, Colombia, 4University of Cartagena, Institute for Immunological Research, Cartagena, Colombia
OBJECTIVES: B-cell precursor acute lymphoblastic leukemia (ALL) is the most common childhood cancer. In Colombia, ALL accounts for 35.5% of new pediatric cancer cases and contributes to approximately one in three deaths from malignant neoplasms in individuals <18 years. Although therapeutic advances have improved survival, major challenges persist in middle-income settings, and evidence on blinatumomab in Latin American pediatric populations remains limited. We aimed to characterize the experience with blinatumomab for first relapse of pediatric B-cell precursor ALL in an oncology service of a high complexity hospital in Cartagena, Colombia.
METHODS: We conducted an ambispective observational cohort study (2015-2025) including 31 patients aged 1-18 years with first relapse of ALL. Patients were grouped according to relapse treatment: blinatumomab (n=14) or systemic chemotherapy (n=17). Outcomes included overall survival, second relapse, access to hematopoietic stem cell transplantation, and adverse events. Comparisons were performed using contingency tables and Fisher’s exact test.
RESULTS: Patients receiving blinatumomab had a mean age of 8.21 years (SD 4.9) and 21.4% were female, while those receiving chemotherapy had a mean age of 10.0 years (SD 4.8) and 35.0% were female. Blinatumomab was associated with higher overall survival (71.4% vs. 17.6%; p=0.003) and greater access to transplantation (92.8% vs. 58.8%; p<0.001), along with lower second relapse rates (n=1, 7% vs n=8, 47%). Adverse events occurred in 5 out of 14 blinatumomab-treated patients, all grade I. In the chemotherapy group, 2 adverse events were recorded (one grade I and one grade IV), both leading to treatment discontinuation.
CONCLUSIONS: In this single-center cohort of pediatric patients with first relapse of ALL, blinatumomab was associated with improved survival and higher access to transplantation compared with systemic chemotherapy, with predominantly mild adverse events.
METHODS: We conducted an ambispective observational cohort study (2015-2025) including 31 patients aged 1-18 years with first relapse of ALL. Patients were grouped according to relapse treatment: blinatumomab (n=14) or systemic chemotherapy (n=17). Outcomes included overall survival, second relapse, access to hematopoietic stem cell transplantation, and adverse events. Comparisons were performed using contingency tables and Fisher’s exact test.
RESULTS: Patients receiving blinatumomab had a mean age of 8.21 years (SD 4.9) and 21.4% were female, while those receiving chemotherapy had a mean age of 10.0 years (SD 4.8) and 35.0% were female. Blinatumomab was associated with higher overall survival (71.4% vs. 17.6%; p=0.003) and greater access to transplantation (92.8% vs. 58.8%; p<0.001), along with lower second relapse rates (n=1, 7% vs n=8, 47%). Adverse events occurred in 5 out of 14 blinatumomab-treated patients, all grade I. In the chemotherapy group, 2 adverse events were recorded (one grade I and one grade IV), both leading to treatment discontinuation.
CONCLUSIONS: In this single-center cohort of pediatric patients with first relapse of ALL, blinatumomab was associated with improved survival and higher access to transplantation compared with systemic chemotherapy, with predominantly mild adverse events.
Conference/Value in Health Info
2026-05, ISPOR 2026, Philadelphia, PA, USA
Value in Health, Volume 29, Issue S6
Code
CO103
Topic
Clinical Outcomes
Topic Subcategory
Performance-based Outcomes
Disease
SDC: Oncology, SDC: Pediatrics