TY - JOUR
T1 - 28 years of high-dose therapy and SCT for neuroblastoma in Europe
T2 - Lessons from more than 4000 procedures
AU - Ladenstein, R.
AU - Pötschger, U.
AU - Hartman, O.
AU - Pearson, A. D.J.
AU - Klingebiel, T.
AU - Castel, V.
AU - Yaniv, I.
AU - Demirer, T.
AU - Dini, G.
N1 - Funding Information:
1St Anna Kinderspital, Kinderspitalgasse, Vienna, Austria; 2Unit for Studies and Statistics of Integrated Research and Projects, Children’s Cancer Research Institute—St Anna Kinderkrebsforschung, Kinderspitalgasse, Vienna, Austria; 3Institut Gustave Roussy, Rue Camille Desmoulins, Villejuif, France; 4Royal Marsden Hospital, The Institute of Cancer Research, Sutton, Surrey, UK; 5Klinikum der Johann-Wolfgang Goethe Universitaet, Klinik für Kinderheilkunde und Jugendmedizin, Frankfurt am Main, Germany; 6Hospital Universitario Infantil La Fe, Oncologia Pediatrica, Avenida de Campanar, Valencia, Spain; 7Schneider Children’s Medical Center of Israel, Petach-Tikva, Israel; 8Ankara University Faculty of Medicine, Cebeci Campus Dirimevi, Ankara, Turkey and 9Istituto Giannina Gaslini, Largo G Gaslini, Genova, Italy
PY - 2008/6
Y1 - 2008/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=45749085798&partnerID=8YFLogxK
U2 - 10.1038/bmt.2008.69
DO - 10.1038/bmt.2008.69
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:45749085798
SN - 0268-3369
VL - 41
SP - S118-S127
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - SUPPL. 2
ER -