28 years of high-dose therapy and SCT for neuroblastoma in Europe:: lessons from more than 4000 procedures

被引:68
作者
Ladenstein, R. [1 ,2 ]
Poetschger, U. [1 ]
Hartman, O. [3 ]
Pearson, A. D. J. [4 ]
Klingebiel, T. [5 ]
Castel, V. [6 ]
Yaniv, I. [7 ]
Demirer, T. [8 ]
Dini, G. [9 ]
机构
[1] St Anna Kinderkerbsforsch, Childrens Canc Res Inst, Integrated Res & Projects, Unit Studies & Stat, A-1090 Vienna, Austria
[2] St Anna Childrens Hosp, Vienna, Austria
[3] Inst Gustave Roussy, Villejuif, France
[4] Royal Marsden Hosp, Inst Canc Res, Surrey, England
[5] Klinikum Univ Frankfurt, Klin Kinderheilkunde & Jugendmed, Frankfurt, Germany
[6] Hosp Univ Infantil La Fe, Valencia, Spain
[7] Schneider Childrens Med Ctr Israel, Petah Tiqwa, Israel
[8] Ankara Univ, Fac Med, TR-06100 Ankara, Turkey
[9] Ist Giannina Gaslini, I-16148 Genoa, Italy
关键词
neuroblastoma; high-dose treatment; stem cells; EBMT;
D O I
10.1038/bmt.2008.69
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Between 1978 and 2006, the European Group for Blood and Marrow Transplantation registered 4098 high-dose therapy (HDT) procedures followed by stem cell rescue (SCR) (3974 autologous/124 allogeneic) in patients with neuroblastoma. The 5-year rates for overall (OS) and event-free survival are 37 and 32%, respectively. The median age at diagnosis is 3.9 years (0.3-62 years) with 76 patients older than 18 years. Patients above 10 years carry a 2.5-fold higher risk. Younger patients cure significantly (< 0.001) better with OS rates of 40 and 30% for age groups 2-4 years and 4-10 years, respectively. Their risks are about twofold higher than that of patients below 2 years with OS rates of 60%. The better the quality of remission status before HDT/SCT the better are the observed OS rates: 43% in CR1 (1199 patients) and 42% for CR2 (140 patients), and 36% for those in very good partial or partial remission (1413 patients) and 21% for those with sensitive relapse (134 patients). Patients reported with stable disease in first remission still had an OS rate of 30%. Multivariate analysis shows significantly better OS in the age group of less than 2 years (< 0.0001), as well as a better quality of remission status before HDT/SCT (P < 0.0001), with the use of peripheral stem cells (P = 0.014), autologous SCT (P = 0.031) and busulphan/melphalan HDT (P < 0.001). Busulphan/melphalan HDT/SCT in first remission achieves an OS of 48%, while it is only 35% with other regimens (P < 0.001), including melphalan alone, other melphalan-containing regimens, a variety of other drugs given as a single HDT as well as the addition of TBI or sequential HDT/SCT procedures. Further progress in the field may only be expected from large-scale international randomized trials.
引用
收藏
页码:S118 / S127
页数:10
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