Improved outcome with pulses of vincristine and corticosteroids in continuation therapy of children with average risk acute lymphoblastic leukemia (ALL) and lymphoblastic non-Hodgkin lymphoma (NHL): report of the EORTC randomized phase 3 trial 58951

被引:53
作者
De Moerloose, Barbara [1 ]
Suciu, Stefan [2 ]
Bertrand, Yves [3 ]
Mazingue, Francoise [4 ]
Robert, Alain [5 ]
Uyttebroeck, Anne [6 ]
Yakouben, Karima [7 ]
Ferster, Alice [8 ]
Margueritte, Genevieve [9 ]
Lutz, Patrick [10 ]
Munzer, Martine [11 ]
Sirvent, Nicolas [12 ]
Norton, Lucilia [13 ]
Boutard, Patrick [14 ]
Plantaz, Dominique [15 ]
Millot, Frederic [16 ]
Philippet, Pierre [17 ]
Baila, Liliana [2 ]
Benoit, Yves [1 ]
Otten, Jacques [18 ]
机构
[1] Ghent Univ Hosp, Dept Pediat Hematol Oncol, B-9000 Ghent, Belgium
[2] EORTC Headquarters, Brussels, Belgium
[3] Debrousse Hosp, Dept Immunohematopediat, Lyon, France
[4] CHR, Dept Pediat Hematol Oncol, Lille, France
[5] Childrens Hosp, Dept Hematol, Toulouse, France
[6] Univ Hosp Gasthuisberg, Dept Pediat, B-3000 Leuven, Belgium
[7] Hop Robert Debre, Dept Hematoimmunol, F-75019 Paris, France
[8] HUDE, Dept Hematooncol, Brussels, Belgium
[9] A Villeneuve Hosp, Dept Hematooncol, Montpellier, France
[10] Dept Hematol, Strasbourg, France
[11] Amer Hosp, Dept Hematol, Reims, France
[12] CHU, Dept Pediat Hematol Oncol, Nice, France
[13] Escolar San Joao Hosp, Dept Pediat, Oporto, Portugal
[14] CHRU, Dept Hematol, Caen, France
[15] CHR La Tronche, Dept Pediat, Grenoble, France
[16] J Bernard Hosp, Dept Hematol, Poitiers, France
[17] CHC Esperance, Dept Pediat, Montegnee, Belgium
[18] Univ Hosp, Dept Pediat, Brussels, Belgium
关键词
DEXAMETHASONE; PREDNISONE; CHEMOTHERAPY;
D O I
10.1182/blood-2009-10-247965
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The European Organisation for Research and Treatment of Cancer 58951 trial for children with acute lymphoblastic leukemia (ALL) or non-Hodgkin lymphoma (NHL) addressed 3 randomized questions, including the evaluation of dexamethasone (DEX) versus prednisolone (PRED) in induction and, for average-risk patients, the evaluation of vincristine and corticosteroid pulses during continuation therapy. The corticosteroid used in the pulses was that assigned at induction. Overall, 411 patients were randomly assigned: 202 initially randomly assigned to PRED (60 mg/m(2)/d), 201 to DEX (6 mg/m(2)/d), and 8 nonrandomly assigned to PRED. At a median follow-up of 6.3 years, there were 19 versus 34 events for pulses versus no pulses; 6-year disease-free survival (DFS) rate was 90.6% (standard error [SE], 2.1%) and 82.8% (SE, 2.8%), respectively (hazard ratio [HR] = 0.54; 95% confidence interval, 0.31-0.94; P = .027). The effect of pulses was similar in the PRED (HR = 0.56) and DEX groups (HR = 0.59) but more pronounced in girls (HR = 0.24) than in boys (HR = 0.71). Grade 3 to 4 hepatic toxicity was 30% versus 40% in pulses versus no pulses group and grade 2 to 3 osteonecrosis was 4.4% versus 2%. For average-risk patients treated according to Berlin-Frankfurt-Muenster-based protocols, pulses should become a standard component of therapy. This trial was registered at www.clinicaltrials.gov as #NCT00003728. (Blood. 2010; 116(1): 36-44)
引用
收藏
页码:36 / 44
页数:9
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