Improved outcome in high-risk childhood acute lymphoblastic leukemia defined by prednisone-poor response treated with double Berlin-Frankfurt-Muenster protocol II

被引:61
作者
Aricò, M
Valsecchi, MG
Conter, V
Rizzari, C
Pession, A
Messina, C
Barisone, E
Poggi, V
De Rossi, G
Locatelli, F
Micalizzi, MC
Basso, G
Masera, G
机构
[1] Osped Bambini G Di Critina, Palermo, Italy
[2] Policlin San Matteo, IRCCS, I-27100 Pavia, Italy
[3] Univ Milan, Clin Pediat & Med Stat Sect, Milan, Italy
[4] Univ Bologna, Pediat Clin, I-40126 Bologna, Italy
[5] Univ Turin, Pediat Clin, I-10124 Turin, Italy
[6] Osped Pausilipon, Naples, Italy
[7] Osped Bambin Gesu Roma, IRCCS, Rome, Italy
[8] IRCCS, Genoa, Italy
关键词
D O I
10.1182/blood.V100.2.420
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
One hundred ninety-eight children and adolescents were entered in the Associazione Italiana di Ematologia ed Oncologia Pediatrica (AIEOP)-ALL95 study for high-risk acute lymphoblastic leukemia (ALL). Inclusion criteria were poor response to initial prednisone/intrathecal methotrexate (prednisone-poor response [Pi resistance to induction therapy, translocation t(9;22), infants with the t(4;11), or CD10(-) ALL. The event-free survival (EFS) rate at 4 years was 56.5% (SE, 3.9%) for the entire group. The overall EFS rate in the current study was significantly better (P =.002) than that obtained in a comparable group of patients treated in the early 1990s in the AIEOP-ALL91 study. In particular, patients with PPR had a 4-year EFS of 61.1% (SE, 4.4%) versus 42.8% (SE, 5.4%) in the ALL 91 study (P =.008). Among PPR patients, those who were PPR-only(60.11% that is, they achieved CR and were negative for t(9;22) and t(4;11) translocations-had the best outcomes with this intensive treatment, even when additional adverse features (hyperleukocytosis, T phenotype) were present (4-year EFS, 70.1%; SE, 4.7%.). We attribute this improvement to the replacement of 6 alternating blocks of non-crossresistant drugs with an 8-drug reinduction regimen (Berlin-Frankfurt-Muenster [BFM] protocol 11), repeated twice, in the context of a standard BFM-type intensive chemotherapy for high-risk ALL. This modified therapy may lead to high cure rates for patients defined as at high risk for Intrinsic resistance to corticosteroids only. (Blood. 2002;100:420-426). (C) 2002 by The American Society of Hematology.
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页码:420 / 426
页数:7
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