DAB389IL2 (ONTAK®) fusion protein therapy of chronic lymphocytic leukaemia

被引:16
作者
Frankel, AE [1 ]
Fleming, DR
Powell, BL
Gartenhaus, R
机构
[1] Wake Forest Univ, Sch Med, Winston Salem, NC 27109 USA
[2] Med Ctr Vincennes, Vincennes, IN USA
[3] Northwestern Univ, Sch Med, Chicago, IL 60611 USA
关键词
chronic lymphocytic leukaemia; diphtheria fusion protein; interleukin-2; receptor;
D O I
10.1517/14712598.3.1.179
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Despite multiple new therapeutic options for patients with chronic lymphocytic leukaemia (CLL), the prognosis of patients with relapsed disease is poor. After first-line therapy with fludarabine, alkylating agents, rituximab or combinations of these agents, most patients relapse within a few years. While second-line therapy with alemtuzumab, or other combinations of the above agents, have produced remissions, most of these are partial responses lasting months rather than years. Patients commonly die from progressive disease or infections related to the underlying disease or treatment. The authors sought to develop a novel therapeutic with the capacity to kill chemotherapy-resistant CLL cells and with reduced toxicities to normal tissues. Based on the presence of high affinity interleukin-2 receptor (IL-2R) on CLL cells, therapy of relapsed CLL patients with a diphtheria fusion protein targeting IL-2R - DAB(389)IL2 (ONTAK((R)), Seragen, Inc., Hopkinton, MA, USA) - was tested in a pilot Phase II study. Biological activity and a partial remission were observed with modest drug-related side effects. Based on these encouraging findings, alternative schedules and combinations with agents that may enhance CLL cell expression of IL-2R are being tested. Hopefully, the use of these targeted therapeutic approaches will provide additional therapeutic options with fewer side effects for this common and incurable condition.
引用
收藏
页码:179 / 186
页数:8
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