Phase II study of ET-743 in advanced soft tissue sarcomas: A European Organisation for the Research and Treatment of Cancer (EORTC) soft tissue and bone sarcoma group trial

被引:336
作者
Le Cesne, A
Blay, JY
Judson, I
Van Oosterom, A
Verweij, J
Radford, J
Lorigan, P
Rodenhuis, S
Ray-Coquard, I
Bonvalot, S
Collin, F
Jimeno, J
Di Paola, E
Van Glabbeke, M
Nielsen, OS
机构
[1] Inst Gustave Roussy, Dept Med, F-94805 Villejuif, France
[2] Ctr Leon Berard, F-69373 Lyon, France
[3] Ctr Leclerc, Dijon, France
[4] Royal Marsden Hosp, London SW3 6JJ, England
[5] Weston Pk Hosp, Sheffield, S Yorkshire, England
[6] Christie Hosp NHS Trust, Manchester M20 4BX, Lancs, England
[7] UZ Gasthuisberg, Louvain, Belgium
[8] Eortc Data Ctr, Brussels, Belgium
[9] Rotterdam Canc Inst, Rotterdam, Netherlands
[10] Antoni Van Leuuwenhoekhuis, Amsterdam, Netherlands
[11] Pharma Mar, Tres Cantos, Spain
[12] Aarhus Univ Hosp, DK-8000 Aarhus, Denmark
关键词
D O I
10.1200/JCO.2005.01.180
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose This nonrandomized multicenter phase II study was performed to evaluate the activity and safety of Ecteinascidin (ET-743) administered at a dose of 1.5 mg/m(2) as a 24-hour continuous infusion every 3 weeks in patients with pretreated advanced soft tissue sarcoma. Patients and Methods Patients with documented progressive advanced soft tissue sarcoma received ET-743 as second- or third-line chemotherapy. Antitumor activity was evaluated every 6 weeks until progression, excessive toxicity, or patient refusal. Results One hundred four patients from eight European institutions were included in the study (March 1999 to November 2000). A total of 410 cycles were administered in 99 assessable patients. Toxicity mainly involved reversible grade 3 to 4 asymptomatic elevation of transaminases in 40% of patients, and grade 3 to 4 neutropenia was observed in 52% of patients. There were eight partial responses (PR; objective regression rate, 8%), 45 no change (NC; > 6 months in 26% of patients), and 39 progressive disease. A progression arrest rate (PR + NC) of 56% was observed in leiomyosarcoma and 61% in synovialosarcoma. The median duration of the time to progression was 105 days, and the 6-month progression-free survival was 29%. The median duration of survival was 9.2 months. Conclusion ET-743 seems to be a promising active agent in advanced soft tissue sarcoma, with no cumulative toxicities. The 6-months progression-free survival observed in advanced soft tissue sarcoma compares favorably with those obtained with other active drugs tested in second-line chemotherapy in previous European Organisation for the Research and Treatment of Cancer trials. The median overall survival was unusually long in these heavily pretreated patients mainly due to the high number of patients who benefit from the drug in terms of tumor control. (C) 2005 by American Society of Clinical Oncology.
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页码:576 / 584
页数:9
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