Adenovirus-mediated intralesional interferon-γ gene transfer induces tumor regressions in cutaneous lymphomas

被引:89
|
作者
Dummer, R
Hassel, JC
Fellenberg, F
Eichmüller, S
Maier, T
Slos, P
Acres, B
Bleuzen, P
Bataille, V
Squiban, P
Burg, G
Urosevic, M
机构
[1] Univ Zurich Hosp, Dept Dermatol, CH-8091 Zurich, Switzerland
[2] German Canc Res Ctr, Skin Canc Unit, Heidelberg, Germany
[3] Transgene SA, Strasbourg, France
基金
中国国家自然科学基金;
关键词
D O I
10.1182/blood-2004-01-0360
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary cutaneous lymphomas have been successfully treated with interferons (IFNs), counterbalancing the T-helper 2 (Th2)-skewing state. We undertook a phase 1, open-label, dose-escalating trial of repeated intratumoral administration of TG1042 in patients with advanced primary cutaneous T-cell lymphomas (CTCLs) and multilesional cutaneous B-cell lymphomas (CBCLs). TG1042 is a third-generation, non-replicating human adenovirus vector containing a human IFN-gamma cDNA insert. Nine patients (7 CTCL, 2 CBCL) were enrolled at the following TG1042 doses: 3 x 10(9), 3 x 10(10), and 3 x 10(11) total particles. Local clinical response was observed in 5 of 9 treated patients (3 patients with complete response [CR] and 2 patients with partial response [PR]). Out of these, 3 patients showed systemic CR with the clearance of other noninjected skin lesions. Clinical response lasted for a median of 3 months (range, 1-6 months). Adverse events were mostly of grades 1 and 2. Seven of 9 treated patients had a detectable TG1042- derived IFN-gamma message in injected lesions after the first treatment cycle. A TG 1042IFN-gamma message was also detectable after several treatment cycles. We demonstrate the induction of humoral immune response to lymphoma tumor-antigen se70-2 after treatment. Our study shows that intralesional injections of TG1042 are both safe and well tolerated. (C) 2004 by The American Society of Hematology.
引用
收藏
页码:1631 / 1638
页数:8
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