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Salvage therapy with everolimus reduces the severity of treatment-refractory chronic GVHD without impairing disease control: A dual center retrospective analysis

机译:依维莫司的挽救疗法在不损害疾病控制的情况下降低了难治性慢性GVHD的严重程度:双中心回顾性分析

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Chronic GVHD (cGVHD) remains the most important cause of late non-relapse mortality post allogeneic hematopoietic SCT (HSCT). Although first-line treatment of cGVHD with steroids is well established, evidence for second-line treatment remains limited. Here, we report a dual center retrospective analysis of the off-label salvage treatment of steroid-refractory cGVHD with everolimus. Out of 80 patients with a median age of 50 (17-70) years, 14 (17%) suffered from mild, 39 (49%) from moderate and 27 (34%) from severe cGVHD. At the final analysis, median follow-up after introduction of everolimus was 724 (14-2205) days. Thirty-four patients (43%) required the addition of further immunosuppression during everolimus-based therapy. Global NIH Severity Score improved in 34 patients (43%), remained stable in 37 patients (46%) and worsened in 9 patients (11%). The total sum of Global NIH Severity Scores in all patients assessable was significantly reduced after treatment with everolimus (P<0.0001). Most frequent grade 3/4 toxicities included infections (n=30) and thrombocytopenia (n=15). There was a single case of relapse. Everolimus-based salvage treatment of refractory cGVHD results in significant improvement of the NIH Severity Score without impairing control of the malignant disease. Finally, these preliminary results demand further verification in prospective trials.
机译:慢性GVHD(cGVHD)仍然是同种异体造血SCT(HSCT)后晚期非复发死亡率的最重要原因。尽管使用类固醇对cGVHD进行一线治疗已经很成熟,但是二线治疗的证据仍然有限。在这里,我们报告了依维莫司对甾体难治性cGVHD的标签外打捞治疗的双重中心回顾性分析。在80位中位年龄为50(17-70)岁的患者中,有14位(17%)患有轻度cGVHD,39位(49%)为中度,而27位(34%)为重度cGVHD。归根结底,引入依维莫司后的中位随访时间为724(14-2205)天。 34名患者(43%)在依维莫司为基础的治疗期间需要进一步的免疫抑制。全球NIH严重度评分改善了34例(43%),保持稳定的37例(46%),恶化了9例(11%)。在接受依维莫司治疗后,所有可评估患者的全球NIH严重程度评分总和显着降低(P <0.0001)。最常见的3/4级毒性包括感染(n = 30)和血小板减少症(n = 15)。只有一例复发。基于依维莫司的难治性cGVHD抢救治疗可显着改善NIH严重度评分,而不会损害对恶性疾病的控制。最后,这些初步结果需要在前瞻性试验中进一步验证。

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