PHASE I/II STUDY OF I-131 METAIODOBENZYLGUANIDINE IN CHEMORESISTANT NEUROBLASTOMA - A UNITED-KINGDOM CHILDRENS CANCER STUDY-GROUP INVESTIGATION

被引:122
作者
LASHFORD, LS
LEWIS, IJ
FIELDING, SL
FLOWER, MA
MELLER, S
KEMSHEAD, JT
ACKERY, D
机构
[1] ST JAMES UNIV HOSP,DEPT PAEDIAT ONCOL,BECKETT ST,LEEDS LS9 7TF,W YORKSHIRE,ENGLAND
[2] IMPERIAL CANC RES FUND,LEEDS,ENGLAND
[3] ROYAL MARSDEN HOSP,LONDON,ENGLAND
[4] SOUTHAMPTON GEN HOSP,SOUTHAMPTON SO9 4XY,HANTS,ENGLAND
[5] FRENCHAY HOSP,IMPERIAL CANC RES FUND,PAEDIAT & NEUROONCOL LAB,BRISTOL BS16 1LE,AVON,ENGLAND
[6] UNIV LEICESTER,UNITED KINGDOM CHILDRENS CANC STUDY GRP,NEW AGENTS GRP,LEICESTER LE1 7RH,ENGLAND
关键词
D O I
10.1200/JCO.1992.10.12.1889
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The goal of this study was to evaluate the toxicity of iodine 131 metaiodobenzylguanidine (mIBG) in metastatic neuroblastoma. Patients and Methods: A multicenter phase I study of 131I mIBG has been undertaken by the United Kingdom Children's Cancer Study Group (UKCCSG) in children with advanced chemoresistant neuroblastoma. Activity prescription was based on a prescribed whole-body radiation dose, which was established for individual patients by performing an initial tracer investigation with 75 MBq of 131I mIBG. An activity was derived from this pharmacokinetic study that would deliver an initial whole-body-absorbed radiation dose of 1 Gy. Subsequent dose escalations were based on observed toxicity. Results: Twenty-five patients, aged 1 to 10 years, were treated with prescribed whole-body dose levels of 1.0 Gy (n = 2), 2.0 Gy (n = 13), and 2.5 Gy (n = 10). This necessitated administration of 2.4 to 12.1 GBq of activity. Hematologic, hepatic, kidney, and adrenal toxicity were observed, with bone marrow suppression being the principal dose-limiting toxicity. Bone marrow toxicity increased with prescribed whole-body-absorbed radiation dose, with 80% of patients developing grade 3 or 4 thrombocytopenia at a prescribed whole-body radiation dose of 2.5 Gy. Objective evidence of tumor response was seen in soft tissue (primary or nodal disease), bone, and bone marrow, with an overall response rate of 33% (partial response, n = 8; static disease, n = 9; progressive disease, n = 7). Conclusions: This study has established an effective method of activity prescription that predicts subsequent toxicity, with the maximally tolerated dose being sufficient activity to deliver a whole-body-absorbed radiation dose of 2.5 Gy. The objective response rate is comparable to other single agents in chemoresistant neuroblastoma and suggests that 131I mIBG may be a useful method for targeting radiotherapy in metastatic neuroblastoma.
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收藏
页码:1889 / 1896
页数:8
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