Phase II study of gemcitabine combined with oxaliplatin in relapsed or refractory paediatric solid malignancies: An innovative therapy for children with Cancer European Consortium Study

被引:37
作者
Geoerger, Birgit [1 ]
Chisholm, Julia [2 ]
Le Deley, Marie-Cecile
Gentet, Jean-Claude [3 ]
Zwaan, Christian Michel [4 ]
Dias, Nathalie
Jaspan, Timothy [5 ]
Mc Hugh, Kieran [2 ]
Couanet, Dominique
Hain, Sharon [6 ]
Devos, Annick [4 ]
Riccardi, Riccardo [7 ]
Cesare, Colosimo [7 ]
Boos, Joachim [8 ]
Frappaz, Didier [9 ]
Leblond, Pierre [10 ]
Aerts, Isabelle [11 ]
Vassal, Gilles
机构
[1] Univ Paris 11, Dept Pediat, Inst Gustave Roussy, F-94805 Villejuif, France
[2] Great Ormond St Hosp Sick Children, London WC1N 3JH, England
[3] Hop Enfants La Timone, F-13385 Marseille, France
[4] Sophia Childrens Univ Hosp, Erasmus MC Rotterdam, NL-3015 GJ Rotterdam, Netherlands
[5] Univ Nottingham Hosp, Nottingham NG7 2UH, England
[6] Univ Coll London Hosp, London NW1 2BU, England
[7] Univ Cattolica, I-00168 Rome, Italy
[8] Univ Klinikum Munster, Klin & Poliklin Kinderund Jugendmed Padiatr Hamat, D-48129 Munster, Germany
[9] Ctr Leon Berard, F-69373 Lyon, France
[10] Ctr Oscar Lambret, F-59020 Lille, France
[11] Univ Paris 05, Inst Curie, F-75248 Paris, France
关键词
Gemcitabine; Oxaliplatin; Phase II; Paediatric solid malignancies; METASTATIC PANCREATIC-CANCER; CELL LUNG-CANCER; PLUS OXALIPLATIN; COMBINATION; CHEMOTHERAPY; CARCINOMA; LEUKEMIA; TUMORS; GEMOX; PHARMACOKINETICS;
D O I
10.1016/j.ejca.2010.09.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: To assess objective response rates after 4 cycles of gemcitabine in combination with oxaliplatin in children and adolescents with relapsed or refractory solid tumours. Methods: This multicentre, non-randomised Phase II study included five strata: neuroblastoma, osteosarcoma, medulloblastoma and other CNS tumours strata with two-stage Simon designs and a miscellaneous, extra-cranial solid tumour stratum with descriptive design. Eligibility criteria included: age 6 months to 21 years; measurable, relapsed or refractory solid malignancy; no more than one previous salvage therapy. Gemcitabine was administered intravenously at 1000 mg/m(2) over 100 min followed by oxaliplatin at 100 mg/m(2) over 120 min on Day 1 of a 14-d cycle. Thmour response was assessed every 4 cycles according to WHO criteria. Results: Ninety-three out of 95 patients enrolled in 25 centres received treatment: 12 neuroblastoma; 12 osteosarcoma; 14 medulloblastoma; 13 other CNS tumours and 42 miscellaneous non-CNS solid tumours. Median age was 11.7 years (range, 1.3-20.8 years). Tumour control (CR + PR + SD) at 4 cycles was obtained in 30/93 evaluable patients (32.3%; 95% confidence interval (CI), 22.9-42.7%), including four PR: 1/12 patients with osteosarcoma, 1/12 with medulloblastoma, 1/12 with rhabdomyosarcoma and 1/4 with other sarcoma. Five out of 12 eligible patients with neuroblastoma experienced stable disease. During a total of 481 treatment cycles (median 4, range 1-24 per patient), the most common treatment-related toxicities were haematologic (leukopenia, neutropenia, thrombocytopenia) and neurological (dysesthesia, paresthesia). Concluding statement: The gemcitabine-oxaliplatin combination administered in a bi-weekly schedule has acceptable safety profile with limited activity in children with relapsed or refractory solid tumours. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:230 / 238
页数:9
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