Humanized anti-interleukin-6 receptor antibody treatment of multicentric Castleman disease

被引:584
作者
Nishimoto, N
Kanakura, Y
Aozasa, K
Johkoh, T
Nakamura, M
Nakano, S
Nakano, N
Ikeda, Y
Sasaki, T
Nishioka, K
Hara, M
Taguchi, H
Kimura, Y
Kato, Y
Asaoku, H
Kumagai, S
Kodama, F
Nakahara, H
Hagihara, K
Yoshizaki, K
Kishimoto, T
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Lab Immune Regulat, Osaka 5650871, Japan
[2] Kyowakai Hosp, Osaka, Japan
[3] Kyushu Univ, Fukuoka 812, Japan
[4] Keio Univ, Tokyo, Japan
[5] Tohoku Univ, Sendai, Miyagi 980, Japan
[6] Tokyo Med & Dent Univ, Tokyo, Japan
[7] Ehime Prefectural Cent Hosp, Matsuyama, Ehime, Japan
[8] Kochi Med Sch, Kochi, Japan
[9] Tokyo Med Univ, Tokyo, Japan
[10] Aichi Med Univ, Aichi, Japan
[11] Hiroshima Red Cross Hosp, Hiroshima, Japan
[12] Atom Bomb Survivors Hosp, Hiroshima, Japan
[13] Kobe Univ, Kobe, Hyogo, Japan
[14] Kanagawa Canc Ctr, Kanagawa, Japan
关键词
D O I
10.1182/blood-2004-12-4602
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multicentric Castleman disease (MCD) is an atypical lymphoproliferative disorder characterized by systemic lymphadenopathy and constitutional inflammatory symptoms. Dysregulated overproduction of interleukin-6 is responsible for the clinical abnormalities. This multicenter prospective study was undertaken to evaluate the safety and efficacy of a humanized antihuman interleukin-6 (IL-6) receptor monoclonal antibody (MRA) in patients with MCD. We report here results of the first 60 weeks of the study enrolling 28 patients. The initial dosing period consisted of 8 infusions of 8 mg/kg MRA administered biweekly. Adjustments in the dose and treatment interval were allowed for each patient in an extension phase after 16 weeks. Within 16 weeks, treatment with MRA consistently alleviated lymphadenopathy and all the inflammatory parameters. Hemoglobin, albumin, and total cholesterol levels, high-density lipoprotein cholesterol values, and body mass index all increased significantly. In addition, fatigue diminished. Chronic inflammatory symptoms were successfully managed over 60 weeks. In 8 (28.6%) patients, the MRA dose was decreased or the treatment interval was extended without exacerbation. Eleven (73.3%) of 15 patients who had received oral corticosteroids before study entry were able to do well on a reduced corticosteroid dose. Most adverse events were mild to moderate in severity. MRA was tolerated well and significantly alleviated chronic inflammatory symptoms and wasting in patients with MCD.
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收藏
页码:2627 / 2632
页数:6
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