Comparison of augmented Berlin-Frankfurt-Münster (BFM) and BFM 2000 treatment protocols in children diagnosed with high-risk acute lymphoblastic leukemia
Abstract
Objectives: The main purpose of this study is comparing the augmented Berlin-Frankfurt-Münster (BFM) and BFM 2000 treatment protocols applied to pediatric patients diagnosed with high-risk acute lymphoblastic leukemia (ALL) in our clinic in different years in terms of relapse incidence and survival rates.
Methods: When evaluated all patients considering the Children's Oncology Group (COG) criteria, 53 of our patients who were in the medium or high risk group according to the BFM 2000 protocol and were in the high risk group received treatment with Augmented BFM protocol and 17 of them received the BFM 2000 protocol. Age, gender, bone pathology, physical examination, hepatomegaly, splenomegaly, lymphadenopathy, presence of bleeding, hemogram values, immunophenotype, 8th, 14th and 33rd day treatment response, presence of translocation, central nervous system (CNS), extramedullary involvement, risk group, presence of relapse, time to relapse, follow-up period and hospital stay until maintenance treatment were examined.
Results: Event-Free Survival (EFS) and Overall Survival (OS) values of patients were 83.6% and 90.1%, respectively. While EFS was 89.4% and OS was 90.6% in the group receiving the Augmented BFM treatment protocol, EFS was calculated as 71.7% and OS was 88.2% in those receiving the BFM-2000 treatment protocol. Accordingly, when the EFS values of those who received the Augmented BFM treatment protocol were compared with those who received BFM-2000, statistically significant values were found (P<0.01).
Conclusions: It was observed that the augmented BFM treatment protocol was more protective against relapses and shortened the duration of hospitalization compared to the BFM 2000 treatment protocol.
Keywords
References
- 1. Ağaoğlu L. Neoplastik hastalıklar. Pediatri. Cilt 2, 4. Baskı. İstanbul: Nobel Tıp Kitabevleri; 2010: pp.1359-1373.
- 2. Soycan YL. Akut Lenfoblastik Lösemi; Tanı, Klinik in Pediyatrik Hematoloji. 1. Baskı. İstanbul: İstanbul Medikal Yayıncılık; 2011: pp.597-611.
- 3. Miranda-Filho A, Piñeros M, Ferlay J, Soerjomataram I, Monnereau A, Bray F. Epidemiological patterns of leukaemia in 184 countries: a population-based study. Lancet Haematol. 2018;5(1):e14-e24. doi: 10.1016/S2352-3026(17)30232-6.
- 4. Hayashi H, Makimoto A, Yuza Y. Treatment of Pediatric Acute Lymphoblastic Leukemia: A Historical Perspective. Cancers (Basel). 2024;16(4):723. doi: 10.3390/cancers16040723.
- 5. Allemani C, Matsuda T, Di Carlo V, et al. Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries. Lancet. 2018;391(10125):1023-1075. doi: 10.1016/S0140-6736(17)33326-3.
- 6. Salzer WL, Devidas M, Carroll WL, et al. Long-term results of the pediatric oncology group studies for childhood acute lymphoblastic leukemia 1984-2001: a report from the children's oncology group. Leukemia. 2010;24(2):355-370. doi: 10.1038/leu.2009.261.
- 7. Hunger SP. Development and refinement of augmented treatment regimens for pediatric high-risk acute lymphoblastic leukemia. Am Soc Clin Oncol Educ Book. 2012:611-615. doi: 10.14694/EdBook_AM.2012.32.180.
- 8. Seibel NL. Acute lymphoblastic leukemia: an historical perspective. Hematology Am Soc Hematol Educ Program. 2008:365. doi: 10.1182/asheducation-2008.1.365.
Details
Primary Language
English
Subjects
Pediatric Hematology and Oncology
Journal Section
Research Article
Authors
Samet Özer
*
0000-0003-0880-7215
Türkiye
Zeynep Karakaş
0000-0002-8835-3235
Türkiye
Ayşegül Ünüvar
0000-0002-4730-7697
Türkiye
Ömer Devecioğlu
0000-0001-6378-0516
Türkiye
Early Pub Date
August 6, 2024
Publication Date
September 4, 2024
Submission Date
July 5, 2024
Acceptance Date
August 4, 2024
Published in Issue
Year 2024 Volume: 10 Number: 5