Journal article

Progressive or relapsed Burkitt lymphoma or leukemia in children and adolescents after BFM-type first-line therapy


Authors listWoessmann, Wilhelm; Zimmermann, Martin; Meinhardt, Andrea; Mueller, Stephanie; Hauch, Holger; Knoerr, Fabian; Oschlies, Ilske; Klapper, Wolfram; Niggli, Felix; Kabickova, Edita; Attarbaschi, Andishe; Reiter, Alfred; Burkhardt, Birgit

Publication year2020

Pages1124-1132

JournalBlood

Volume number135

Issue number14

ISSN0006-4971

eISSN1528-0020

Open access statusBronze

DOI Linkhttps://doi.org/10.1182/blood.2019003591

PublisherAmerican Society of Hematology (ASH Publications)


Abstract
Children with refractory or relapsed Burkitt lymphoma (BL) or Burkitt leukemia (B-AL) have a poor chance to survive. We describe characteristics, outcome, reinduction, and transplantation approaches and evaluate risk factors among children with progression of a BUB-AL included in Non-Hodgkin's Lymphoma-Berlin-Frankfurt-Miinster studies between 1986 and 2016. Treatment recommendation was reinduction including rituximab from the early 2000s followed by blood stem cell transplantation. The 3-year survival of the 157 children was 18.5 +/- 3%. Survival significantly improved from 11 +/- 3% before to 27 +/- 5% after 2000 (P < .001), allowing for risk factor analyses among the latter 75 patients. Survival of 14 patients with relapse after initial therapy for low-risk disease (R1/R2) was 50 +/- 13% compared with 21 +/- 5% for 61 patients progressing after R3/R4 therapy (P< .02). A total of 25 of 28 patients with progression during first-line therapy, 31 of 32 with progression during reinduction, 15 of 16 not reaching a complete remission (CR) before transplantation, 9 of 10 treated with rituximab front-line, and all 13 patients not receiving rituximab during reinduction died. Forty-six patients received stem cell transplantation (20 autologous, 26 allogeneic). Survival after a regimen combining rituximab with continuous-infusion chemotherapy followed by allogeneic transplantation was 67 +/- 12% compared with 18 +/- 5% for all other regimen and transplantations (P = .003). Patients with relapsed BL/B-AL have a poor chance to survive after current effective frontline therapies. Progression during initial or reinduction chemotherapy and initial high-risk disease are risk factors in relapse. Time-condensed continuous-infusion reinduction followed by stem cell transplantation forms the basis for testing new drugs.



Citation Styles

Harvard Citation styleWoessmann, W., Zimmermann, M., Meinhardt, A., Mueller, S., Hauch, H., Knoerr, F., et al. (2020) Progressive or relapsed Burkitt lymphoma or leukemia in children and adolescents after BFM-type first-line therapy, Blood, 135(14), pp. 1124-1132. https://doi.org/10.1182/blood.2019003591

APA Citation styleWoessmann, W., Zimmermann, M., Meinhardt, A., Mueller, S., Hauch, H., Knoerr, F., Oschlies, I., Klapper, W., Niggli, F., Kabickova, E., Attarbaschi, A., Reiter, A., & Burkhardt, B. (2020). Progressive or relapsed Burkitt lymphoma or leukemia in children and adolescents after BFM-type first-line therapy. Blood. 135(14), 1124-1132. https://doi.org/10.1182/blood.2019003591



Keywords


ACUTE-LYMPHOBLASTIC-LEUKEMIAB-CELL NEOPLASMSNON-HODGKIN-LYMPHOMARITUXIMAB

Last updated on 2025-10-06 at 11:10