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39 例接受伊马替尼治疗的激素难治性慢性移植物抗宿主病患者的 NIH 反应标准的长期结果和前瞻性验证。

Long-term outcome and prospective validation of NIH response criteria in 39 patients receiving imatinib for steroid-refractory chronic GVHD.

机构信息

Clinica di Ematologia, Università Politecnica delle Marche, Ancona, Italy;

出版信息

Blood. 2013 Dec 12;122(25):4111-8. doi: 10.1182/blood-2013-05-494278. Epub 2013 Oct 23.

DOI:10.1182/blood-2013-05-494278
PMID:24152907
Abstract

Forty adults aged 28 to 73 years were entered into a prospective trial of imatinib for the treatment of steroid-refractory chronic graft-versus-host disease (SR-cGVHD). After 6 months, intention-to-treat (ITT) analysis of 39 patients who received the drug, regardless of the duration of treatment, revealed 14 partial responses (PR), 4 minor responses (MR) with relevant steroid sparing (46%) according to Couriel criteria, and 20 ≥ PR (51.3%), as per the National Institutes of Health (NIH) criteria and NIH severity score changes. The best responses were seen in the lungs, gut, and skin (35%, 50%, and 32%, respectively). After a median follow-up of 40 months, 28 patients were alive, with a 3-year overall survival (OS) and event-free survival of 72% and 46%, respectively. The 3-year OS was 94% for patients responding at 6 months and 58% for nonresponders according to NIH response, suggesting that these criteria represent a reliable tool for predicting OS after second-line treatment. Monitoring of anti-platelet-derived growth factor receptor (PDGF-R) antibodies showed a significant decrease in PDGF-R stimulatory activity in 7 responders, whereas it remained high in 4 nonresponders. This study confirms the efficacy of imatinib against SR-cGVHD and suggests that the response at 6 months significantly predicts long-term survival.

摘要

40 名年龄在 28 岁至 73 岁的成年人参与了一项前瞻性伊马替尼治疗类固醇难治性慢性移植物抗宿主病(SR-cGVHD)的试验。6 个月后,对接受药物治疗的 39 名患者进行意向治疗(ITT)分析,无论治疗持续时间如何,根据 Couriel 标准,14 名患者有部分缓解(PR),4 名患者有相关类固醇节省的轻微缓解(MR)(46%),根据美国国立卫生研究院(NIH)标准和 NIH 严重程度评分变化,20 名患者有 ≥ PR(51.3%)。最佳反应发生在肺部、肠道和皮肤(分别为 35%、50%和 32%)。中位随访 40 个月后,28 名患者存活,3 年总生存率(OS)和无事件生存率分别为 72%和 46%。根据 NIH 反应,6 个月时应答患者的 3 年 OS 为 94%,无应答患者为 58%,表明这些标准是预测二线治疗后 OS 的可靠工具。监测抗血小板衍生生长因子受体(PDGF-R)抗体显示,7 名应答者的 PDGF-R 刺激活性显著下降,而 4 名无应答者的活性仍然很高。这项研究证实了伊马替尼治疗 SR-cGVHD 的疗效,并表明 6 个月时的反应显著预测长期生存。

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