首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Inolimomab in steroid-refractory acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: retrospective analysis and comparison with other interleukin-2 receptor antibodies.
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Inolimomab in steroid-refractory acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation: retrospective analysis and comparison with other interleukin-2 receptor antibodies.

机译:同种异体造血干细胞移植后类固醇难治性急性移植物抗宿主病中的inolimomab:回顾性分析并与其他IL-2受体抗体进行比较。

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BACKGROUND: The use of monoclonal antibodies against interleukin-2 receptor (IL-2R)-alpha chains could be an effective treatment of acute graft-versus-host disease (GvHD). Experimental model and clinical studies have reported various results. METHODS: Inolimomab is a murine anti-IL-2R. Eighty-five patients were evaluated retrospectively for the safety and efficacy of inolimomab given for the treatment of steroid-resistant acute GvHD (aGvHD) following allogeneic hematopoietic stem cell transplantation (HSCT). Diseases were immune deficiency, hematological malignancies, or solid tumors. Seventy-six percent of the patients received a myeloablative regimen. The source of HSCT was bone marrow for 45 patients, peripheral blood for 36 patients, and cord blood for 4 patients. Donors were 49 siblings and 36 unrelated. Acute GvHD was diagnosed within a median of 28 days after transplantation (grade II, 26 patients; grade III, 26 patients; grade IV, 33 patients). Inolimomab was administered in the event of steroid-resistant aGvHD with a median dose of 0.468 mg per kg (median period of treatment: 18 days). RESULTS: Twenty-five complete responses and 29 partial responses (total response rate: 63%) were observed with no side effects. There was no correlation between aGvHD grading and quality of response. Better responses were observed in cutaneous aGvHD. The overall survival probability was 26% (median follow-up: 20 months). Fifty-seven percent of patients died of toxicity related mortality, mostly aGvHD. Response to inolimomab seemed sustained (11% relapse in responders). CONCLUSION: Inolimomab is well-tolerated and effective for severe steroid-resistant aGvHD. The optimum regimen remains to be defined.
机译:背景:针对白介素2受体(IL-2R)-α链的单克隆抗体的使用可能是急性移植物抗宿主病(GvHD)的有效治疗方法。实验模型和临床研究报告了各种结果。方法:Inolimomab是一种鼠抗IL-2R。回顾性评估了85例异基因造血干细胞移植(HSCT)后用于治疗类固醇抵抗性急性GvHD(aGvHD)的inolimomab的安全性和有效性。疾病是免疫缺陷,血液系统恶性肿瘤或实体瘤。 76%的患者接受了清髓治疗。 HSCT的来源为45例骨髓,36例外周血和4例脐带血。捐助者是49个兄弟姐妹,36个无关。在移植后的中位数28天内诊断出急性GvHD(II级,26例患者; III级,26例患者; IV级,33例)。发生类固醇耐药性aGvHD时,应给予Inolimomab,中位剂量为每公斤0.468 mg(中位治疗期:18天)。结果:观察到25例完全缓解和29例部分缓解(总缓解率:63%),无副作用。 aGvHD分级与反应质量之间没有相关性。在皮肤aGvHD中观察到更好的反应。总生存概率为26%(中位随访时间:20个月)。 57%的患者死于与毒性相关的死亡率,其中大部分是aGvHD。对inolimomab的应答似乎持续(应答者复发11%)。结论:Inolimomab耐受性良好,对严重的类固醇耐药性aGvHD有效。最佳方案仍有待确定。

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