Treatment of oral mucositis after peripheral blood SCT with ATL-104 mouthwash: results from a randomized, double-blind, placebo-controlled trial

被引:8
|
作者
Hunter, A. [2 ]
Mahendra, P. [3 ]
Wilson, K. [4 ]
Fields, P. [5 ]
Cook, G. [6 ]
Peniket, A. [7 ]
Crawley, C. [1 ]
Hickling, R. [8 ]
Marcus, R. [1 ]
机构
[1] Addenbrookes Hosp, Dept Haematol, Cambridge CB2 2QQ, England
[2] Leicester Royal Infirm, Dept Haematol, Leicester, Leics, England
[3] Queen Elizabeth Hosp, Dept Haematol, Birmingham, W Midlands, England
[4] Univ Wales Coll Cardiff, Coll Med, Dept Haematol, Cardiff CF1 3NS, S Glam, Wales
[5] Guys Hosp, Dept Haematol, London SE1 9RT, England
[6] St James Univ Hosp, Dept Haematol, Leeds LS9 7TF, W Yorkshire, England
[7] John Radcliffe Hosp, Dept Haematol, Oxford OX3 9DU, England
[8] Alizyme Therapeut Ltd, Cambridge, England
关键词
mucositis; lectin; peripheral blood SCT; STEM-CELL TRANSPLANTATION; PHASEOLUS-VULGARIS LECTIN; INDUCED GROWTH; CHEMOTHERAPY; MALIGNANCIES; RADIOTHERAPY; SEVERITY;
D O I
10.1038/bmt.2008.363
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
ATL-104 is a potent mitogen for epithelial cells of the gastrointestinal tract. In animal models, ATL-104 aids regeneration of the gastrointestinal tract after treatment with chemotherapeutic agents. The effect of ATL-104 on mucositis in patients requiring high-dose melphalan or BEAM before peripheral blood SCT (PBSCT) was investigated in a randomized, placebo-controlled, double-blind, two-part study. Patients were randomized to ATL-104 (50, 100 or 150 mg) or placebo once daily for 3 days before chemotherapy and 3 days after PBSCT. Part one of the study was a dose-escalation design; part two was a parallel group design using all three ATL-104 doses. Patients were followed up for 28 days post-treatment. Severity of signs and symptoms were assessed and used to calculate scores for standard toxicity rating scales (WHO, Western Consortium for Cancer Nursing Research (WCCNR)). Sixty-three patients were treated. Treatment with ATL-104 substantially reduced the median duration of severe oral mucositis (WHO grade 3 or 4) compared with placebo (median duration: ATL-104 groups 2 or 3 days, placebo 10.5 days). The effect of ATL-104 on the incidence of severe oral mucositis was inconclusive. Similar results were obtained using the WCCNR Scale. Adverse events (AEs) were predominantly mild or moderate in intensity. Gastrointestinal AE were most common.
引用
收藏
页码:563 / 569
页数:7
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