Improved outcome in childhood acute lymphoblastic leukemia despite reduced use of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90. German-Austrian-Swiss ALL-BFM Study Group - PubMed (original) (raw)
Clinical Trial
. 2000 Jun 1;95(11):3310-22.
A Reiter, W D Ludwig, J Harbott, M Zimmermann, W Hiddemann, C Niemeyer, G Henze, A Feldges, F Zintl, B Kornhuber, J Ritter, K Welte, H Gadner, H Riehm
Affiliations
- PMID: 10828010
Free article
Clinical Trial
Improved outcome in childhood acute lymphoblastic leukemia despite reduced use of anthracyclines and cranial radiotherapy: results of trial ALL-BFM 90. German-Austrian-Swiss ALL-BFM Study Group
M Schrappe et al. Blood. 2000.
Free article
Abstract
Trial ALL-BFM 90 was designed to improve outcome in patients with childhood acute lymphoblastic leukemia (ALL) by using a reduced treatment regimen. Patients were stratified into a standard-risk group (SRG), a medium-risk group (MRG), both defined by adequate early treatment response; and a high-risk group (HRG), defined by inadequate response to the cytoreductive prednisone prephase, induction failure, or Philadelphia-chromosome-positive ALL. Four treatment modifications were evaluated: dose intensification in induction by a more rapid drug sequence; administration of L-asparaginase during consolidation therapy in the MRG (randomized); enforced consolidation by rotational elements in the HRG; and reduction in the dose of anthracyclines and use of only 12-Gy preventive cranial radiotherapy in the MRG and HRG, with the aim of avoiding toxicity. Among all 2178 patients (</= 18 years of age), the 6-year event-free survival (EFS) rate (+/- SE) was 78% +/- 1%, with a median observation time of 4.8 years. EFS was 85% +/- 2% in the SRG (n = 636) and 82% +/- 1% in the MRG (n = 1299). L-asparaginase did not improve outcome in the MRG: the event-free interval was 83% +/- 2% with L-asparaginase (n = 528) and 81% +/- 2% without it (n = 557). Because there were more systemic relapses in the HRG (n = 243), EFS was 34% +/- 3%, an outcome inferior to that in the HRG in a previous trial, ALL-BFM 86, in which EFS was 47% +/- 5% (P =.04). The rates of isolated central nervous system relapse in the MRG and HRG were 0.8% and 1.6%, respectively; thus, the 12-Gy preventive cranial radiotherapy regimen apparently provided sufficient central nervous system prophylaxis. The overall improvement over the results in ALL-BFM 86 (6-year EFS, 72%; P =. 001) was based on fewer recurrences among patients in the MRG with B-cell-precursor ALL, indicating an advantage of more condensed induction therapy. In multivariate analysis, inadequate in vivo response emerged as the strongest adverse prognostic variable.
Similar articles
- [Concept and interim result of the ALL-BFM 90 therapy study in treatment of acute lymphoblastic leukemia in children and adolescents: the significance of initial therapy response in blood and bone marrow].
Schrappe M, Reiter A, Sauter S, Ludwig WD, Wörmann B, Harbott J, Bender-Götze C, Dörffel W, Dopfer R, Frey E, et al. Schrappe M, et al. Klin Padiatr. 1994 Jul-Aug;206(4):208-21. doi: 10.1055/s-2008-1046607. Klin Padiatr. 1994. PMID: 7526027 Clinical Trial. German. - Effective preventive central nervous system therapy with extended triple intrathecal therapy and the modified ALL-BFM 86 chemotherapy program in an enlarged non-high risk group of children and adolescents with non-B-cell acute lymphoblastic leukemia: the Israel National Study report.
Stark B, Sharon R, Rechavi G, Attias D, Ballin A, Cividalli G, Burstein Y, Sthoeger D, Abramov A, Zaizov R. Stark B, et al. Cancer. 2000 Jan 1;88(1):205-16. doi: 10.1002/(sici)1097-0142(20000101)88:1<205::aid-cncr28>3.0.co;2-7. Cancer. 2000. PMID: 10618625 Clinical Trial. - BFM-oriented treatment for children with acute lymphoblastic leukemia without cranial irradiation and treatment reduction for standard risk patients: results of DCLSG protocol ALL-8 (1991-1996).
Kamps WA, Bökkerink JP, Hakvoort-Cammel FG, Veerman AJ, Weening RS, van Wering ER, van Weerden JF, Hermans J, Slater R, van den Berg E, Kroes WG, van der Does-van den Berg A. Kamps WA, et al. Leukemia. 2002 Jun;16(6):1099-111. doi: 10.1038/sj.leu.2402489. Leukemia. 2002. PMID: 12040440 Clinical Trial. - Low relapse rate in children with acute lymphoblastic leukemia after risk-directed therapy.
Tzortzatou-Stathopoulou F, Papadopoulou AL, Moschovi M, Botsonis A, Tsangaris GT. Tzortzatou-Stathopoulou F, et al. J Pediatr Hematol Oncol. 2001 Dec;23(9):591-7. doi: 10.1097/00043426-200112000-00008. J Pediatr Hematol Oncol. 2001. PMID: 11902303 Review. - [Therapeutic strategies for childhood high-risk acute lymphoblastic leukemia].
Lu XT. Lu XT. Beijing Da Xue Xue Bao Yi Xue Ban. 2013 Apr 18;45(2):327-32. Beijing Da Xue Xue Bao Yi Xue Ban. 2013. PMID: 23591360 Review. Chinese.
Cited by
- Long-term outcomes of modified BFM-95 regimen in adults with newly diagnosed standard-risk acute lymphoblastic leukemia: a retrospective single-center study.
Li C, Cai X, Chen X, Liang Y, Xia Z, Wang H. Li C, et al. Int J Hematol. 2019 Oct;110(4):458-465. doi: 10.1007/s12185-019-02703-0. Epub 2019 Jul 18. Int J Hematol. 2019. PMID: 31321731 - Mesenchymal cells regulate the response of acute lymphoblastic leukemia cells to asparaginase.
Iwamoto S, Mihara K, Downing JR, Pui CH, Campana D. Iwamoto S, et al. J Clin Invest. 2007 Apr;117(4):1049-57. doi: 10.1172/JCI30235. Epub 2007 Mar 22. J Clin Invest. 2007. PMID: 17380207 Free PMC article. - Approaches to treatment for acute lymphoblastic leukemia in adolescents and young adults.
Mattison R, Stock W. Mattison R, et al. Curr Hematol Malig Rep. 2008 Jul;3(3):144-51. doi: 10.1007/s11899-008-0021-y. Curr Hematol Malig Rep. 2008. PMID: 20425459 Review. - High-risk childhood acute lymphoblastic leukemia.
Bhojwani D, Howard SC, Pui CH. Bhojwani D, et al. Clin Lymphoma Myeloma. 2009;9 Suppl 3(Suppl 3):S222-30. doi: 10.3816/CLM.2009.s.016. Clin Lymphoma Myeloma. 2009. PMID: 19778845 Free PMC article. Review. - Acute Lymphoblastic Leukemia Immunotherapy Treatment: Now, Next, and Beyond.
Aureli A, Marziani B, Venditti A, Sconocchia T, Sconocchia G. Aureli A, et al. Cancers (Basel). 2023 Jun 26;15(13):3346. doi: 10.3390/cancers15133346. Cancers (Basel). 2023. PMID: 37444456 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous