Phase II study of high-dose cyclophosphamide in relapsing and/or resistant hepatoblastoma in children:: a study from the SIOPEL group

被引:12
作者
Cacciavillano, WD
Brugières, L
Childs, M
Shafford, E
Brock, P
Pritchard, J
Mailbach, R
Scopinaro, M
Perilongo, G
机构
[1] Inst Gustave Roussy, Dept Paediat Oncol, Villejuif, France
[2] Hosp Nacl Pediat, Serv Hematooncol, Buenos Aires, DF, Argentina
[3] Univ Leicester, UKCCSG Data Ctr, Leicester, Leics, England
[4] St Bartholomews Hosp, Paediat Oncol Unit, London, England
[5] Hosp Sick Children, London WC1N 3JH, England
[6] Royal Hosp Sick Children, Edinburgh EH9 1LF, Midlothian, Scotland
[7] Swiss Inst Appl Canc Res, Bern, Switzerland
[8] Univ Hosp, Div Paediat Haematol & Oncol, Padua, Italy
关键词
hepatoblastoma; cyclophosphamide; phase II study;
D O I
10.1016/j.ejca.2004.01.042
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The study sought to evaluate the response to cyclophosphamide (CPM) in hepatoblastoma (HB). Patients with a refractory or relapsing HB after first-line therapy as per SIOPEL 2 and 3 protocols were eligible. All patients were to receive two courses of CPM 2 g/m(2) on days I and 2 at 3-week intervals. Eighteen patients were included; 17 were evaluable for response. Prior treatment was cisplatinum alone (I patient) or cisplatinum-carboplatin-doxorubicin (17 patients). The disease status at the beginning of CPM was: progressive during first-line treatment (10 patients), persistent unresectable disease at the end of the protocol (2 patients), relapse (6 patients). Tumour response was partial response (I patient), stable disease (I patient), progressive disease (15 patients) and not evaluable in one. All patients died, 17 of progressive disease and one of surgery complications. The low response rate (1/17) led the SIOPEL group to conclude that single-agent CPM is not effective for the treatment of relapsing or refractory HB. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2274 / 2279
页数:6
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