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利妥昔单抗治疗类固醇难治性慢性移植物抗宿主病。

Rituximab for steroid-refractory chronic graft-versus-host disease.

作者信息

Cutler Corey, Miklos David, Kim Haesook T, Treister Nathaniel, Woo Sook-Bin, Bienfang Don, Klickstein Lloyd B, Levin Jesse, Miller Katherine, Reynolds Carol, Macdonell Rebecca, Pasek Mildred, Lee Stephanie J, Ho Vincent, Soiffer Robert, Antin Joseph H, Ritz Jerome, Alyea Edwin

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Blood. 2006 Jul 15;108(2):756-62. doi: 10.1182/blood-2006-01-0233. Epub 2006 Mar 21.

Abstract

B cells may be implicated in the pathophysiology of chronic graft-versus-host disease (GVHD), as evidenced by antibody production against sex-mismatched, Y chromosome-encoded minor HLA antigens in association with chronic GVHD. We therefore designed a phase 1/2 study of anti-B-cell therapy with rituximab in steroid-refractory chronic GVHD. Twenty-one patients were treated with 38 cycles of rituximab. Rituximab was tolerated well, and toxicity was limited to infectious events. The clinical response rate was 70%, including 2 patients with complete responses. Responses were limited to patients with cutaneous and musculoskeletal manifestations of chronic GVHD and were durable through 1 year after therapy. The median dose of prednisone among treated subjects fell from 40 mg/day to 10 mg/day, 1 year after rituximab therapy (P < .001). A chronic GVHD symptom score improved in the majority of treated patients. Antibody titers against Y chromosome-encoded minor HLA antigens fell and remained low, whereas titers against infectious antigens (EBV, tetanus) remained stable or rose during the treatment period. We conclude that specific anti-B-cell therapy with rituximab may be beneficial for patients with steroidrefractory chronic GVHD. This trial was registered at www.clinicaltrials.gov as #NCT00136396.

摘要

B细胞可能参与了慢性移植物抗宿主病(GVHD)的病理生理过程,这一点可由与慢性GVHD相关的针对性别不匹配的、Y染色体编码的次要HLA抗原的抗体产生来证明。因此,我们设计了一项关于利妥昔单抗抗B细胞疗法治疗类固醇难治性慢性GVHD的1/2期研究。21例患者接受了38个周期的利妥昔单抗治疗。利妥昔单抗耐受性良好,毒性仅限于感染事件。临床缓解率为70%,包括2例完全缓解患者。缓解仅限于有慢性GVHD皮肤和肌肉骨骼表现的患者,且在治疗后1年内持续存在。利妥昔单抗治疗1年后,治疗对象中泼尼松的中位剂量从40毫克/天降至10毫克/天(P < .001)。大多数接受治疗的患者慢性GVHD症状评分有所改善。针对Y染色体编码的次要HLA抗原的抗体滴度下降并维持在低水平,而针对感染性抗原(EBV、破伤风)的滴度在治疗期间保持稳定或上升。我们得出结论,利妥昔单抗特异性抗B细胞疗法可能对类固醇难治性慢性GVHD患者有益。该试验已在www.clinicaltrials.gov上注册,编号为#NCT00136396。

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