Analysis of patients with supratentorial primitive neuro-ectodermal tumours entered into the SIOP/UKCCSG PNET 3 study

被引:76
作者
Pizer, BL [1 ]
Weston, CL [1 ]
Robinson, KJ [1 ]
Ellison, DW [1 ]
Ironside, J [1 ]
Saran, F [1 ]
Lashford, LS [1 ]
Tait, D [1 ]
Lucraft, H [1 ]
Walker, DA [1 ]
Bailey, CC [1 ]
Taylor, RE [1 ]
机构
[1] Alder Hey Childrens Hosp, Oncol Unit, Liverpool L12 2AP, Merseyside, England
关键词
children; cancer; brain tumour; primitive neuroectodermal tumour; PNET; pineal; supratentorial;
D O I
10.1016/j.ejca.2006.01.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The SIOP PNET 3 study was designed to determine whether 10 weeks of moderately intensive chemotherapy given after surgery and before radiotherapy (RT) would improve the outcome for patients with primitive neuroectodermal tumours (PNETs) compared with RT alone. Patients with a histological diagnosis of supratentorial. PNET (StPNET) and no radiological evidence of metastatic disease were initially eligible for randomisation to either chemotherapy followed by craniospinal RT 35 Gy in 21 fractions with a boost of 20 Gy in 12 fractions to the primary site, or RT alone. In respect of the increasing recognition that StPNET were high-risk tumours, randomisation for this group closed in November 1999. This analysis includes both randomised and non-randomised patients with StPNET entered into the study database. Sixty-eight patients aged 2.9-16.6 years (median 6.5 years) were included in the analysis (chemotherapy + RT: 44, RT alone: 24). Fifty-four patients (79%) had a non-pineal and 14 (21%) a pineal site. At a median follow-up of 7.4 years, for all patients overall survival (OS) at 3 and 5 years was 54.4% and 48.3%, respectively Event-free survival (EFS) at 3 and S years was 50.0% and 47.0%, respectively. There was no statistically significant difference in OS or EFS according to treatment received. OS (P = 0.05) and EFS (P = 0.03) were significantly better for patients with pineal primary sites. EFS for pineal tumours were 92.9% at 3 years and 71.4% at S years and for non-pineal primaries 40.7% at 3 years and 40.7% at 5 years. This study confirmed the relatively good survival for non-metastatic pineal PNETs but Poor survival of non-pineal StPNETs. There was no evidence that pre-radiation chemotherapy improved outlook. Future treatment programs should be directed at the particular natural history of these tumours, to further define prognostic factors and to explore further biological characteristics. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1120 / 1128
页数:9
相关论文
共 22 条
[1]  
ALBRIGHT AL, 1995, PEDIATR NEUROSURG, V22, P1
[2]  
BRUNO LA, 1981, PEDIATRIC ONCOLOGY, V1, P265
[3]   PROGNOSTIC FACTORS AND TREATMENT RESULTS FOR SUPRATENTORIAL PRIMITIVE NEUROECTODERMAL TUMORS IN CHILDREN USING RADIATION AND CHEMOTHERAPY - A CHILDRENS CANCER GROUP RANDOMIZED TRIAL [J].
COHEN, BH ;
ZELTZER, PM ;
BOYETT, JM ;
GEYER, JR ;
ALLEN, JC ;
FINLAY, JL ;
MCGUIRECULLEN, P ;
MILSTEIN, JM ;
RORKE, LB ;
STANLEY, P ;
STEHBENS, JA ;
SHURIN, SB ;
WISOFF, J ;
STEVENS, KR ;
ALBRIGHT, AL .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (07) :1687-1696
[4]  
COLLETT D, 1996, MODELLING SURVIVAL D
[5]   Supratentorial primitive neuroectodermal tumors in children [J].
Dirks, PB ;
Harris, L ;
Hoffman, HJ ;
Humphreys, RP ;
Drake, JM ;
Rutka, JT .
JOURNAL OF NEURO-ONCOLOGY, 1996, 29 (01) :75-84
[6]  
GAFFNEY CC, 1985, J NEURO-ONCOL, V3, P23
[7]   High-dose chemotherapy with autologous stem-cell rescue in children and adults with newly diagnosed pineoblastomas [J].
Gururangan, S ;
McLaughlin, C ;
Quinn, J ;
Rich, J ;
Reardon, D ;
Halperin, EC ;
Herndon, J ;
Fuchs, H ;
George, T ;
Provenzale, J ;
Watral, M ;
McLendon, RE ;
Friedman, A ;
Friedman, HS ;
Kurtzberg, J ;
Vredenbergh, J ;
Martin, PL .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (11) :2187-2191
[8]   Patterns of failure in supratentorial primitive neuroectodermal tumors treated in children's cancer group study 921, a phase III combined modality study [J].
Hong, TS ;
Mehta, MP ;
Boyett, TM ;
Donahue, B ;
Rorke, LB ;
Yao, MS ;
Zeltzer, PM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (01) :204-213
[9]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[10]  
Kleihues P., 2000, TUMOURS NERVOUS SYST