05-001: Treatment of Acute Lymphoblastic Leukemia in Children
3상
완료
NCT00400946
| 대상 질환 | Drug/Agent Toxicity by Tissue/Organ, Leukemia |
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| 임상 단계 | 3상 |
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| 스폰서 | Dana-Farber Cancer Institute |
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| 상태 | 완료 |
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| 참여자 수 | 800 명 |
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| 중재(약물) | asparaginase, cyclophosphamide, cytarabine, dexamethasone, dexrazoxane hydrochloride |
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| 시작일 | 2005년 4월 |
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| 완료일 | 2014년 8월 |
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| 결과 공개일 | 2017년 6월 14일 |
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요약
RATIONALE: L-asparaginase is an important component of treatment for childhood acute lymphoblastic leukemia, but is also associated with notable side-effects, including hypersensitivity, pancreatitis, and thrombosis. We have previously reported that patients with acute lymphoblastic leukemia in whom asparaginase treatment was discontinued because of intolerable side-effects had survival outcomes that were inferior to those who received all or nearly all of their intended doses. Two bacterial sources of asparaginase exist: Escherichia coli (E coli) and Erwinia chrysanthemia (Erwinia). Generally, the E coli-derived enzyme has been used as front-line therapy and the Erwinia-derived preparation has been reserved for patients who develop hypersensitivity reactions. Pegylated E coli asparaginase (PEG-asparaginase) has a longer half-life and is potentially less immunogenic than native E coli L-asparaginase, and has been used as the initial asparaginase preparation in some pediatric acute lymphoblastic leukemia treatment regimens. PURPOSE: Although the pharmacokinetics of each of these asparaginase preparations: intravenous PEG-asparaginase (IV-PEG) and intramuscular native E coli L-aspara
Asparaginase-Related Toxicity Rate
30-week post-induction asparaginase treatment period · percentage of participants
| Intramuscular Native E Coli L-asparaginase (IM-EC) | 26 percentage of participants |
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| Intravenous PEG-asparaginase (IV-PEG) | 28 percentage of participants |
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