Hematology/Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Blood Adv. 2023 Sep 12;7(17):5189-5198. doi: 10.1182/bloodadvances.2023009853.
Graft-versus-host disease (GVHD) of the gastrointestinal (GI) tract is the main cause of nonrelapse mortality (NRM) after allogeneic hematopoietic cell transplantation. Ann Arbor (AA) scores derived from serum biomarkers at onset of GVHD quantify GI crypt damage; AA2/3 scores correlate with resistance to treatment and higher NRM. We conducted a multicenter, phase 2 study using natalizumab, a humanized monoclonal antibody that blocks T-cell trafficking to the GI tract through the α4 subunit of α4β7 integrin, combined with corticosteroids as primary treatment for patients with new onset AA2/3 GVHD. Seventy-five patients who were evaluable were enrolled and treated; 81% received natalizumab within 2 days of starting corticosteroids. Therapy was well tolerated with no treatment emergent adverse events in >10% of patients. Outcomes for patients treated with natalizumab plus corticosteroids were compared with 150 well-matched controls from the MAGIC database whose primary treatment was corticosteroids alone. There were no significant differences in overall or complete response between patients treated with natalizumab plus corticosteroids and those treated with corticosteroids alone (60% vs 58%; P = .67% and 48% vs 48%; P = 1.0, respectively) including relevant subgroups. There were also no significant differences in NRM or overall survival at 12 months in patients treated with natalizumab plus corticosteroids compared with controls treated with corticosteroids alone (38% vs 39%; P = .80% and 46% vs 54%; P = .48, respectively). In this multicenter biomarker-based phase 2 study, natalizumab combined with corticosteroids failed to improve outcome of patients with newly diagnosed high-risk GVHD. This trial was registered at www.clinicaltrials.gov as # NCT02133924.
移植物抗宿主病(GVHD)的胃肠道(GI)是异基因造血细胞移植后非复发死亡率(NRM)的主要原因。GVHD 发病时源于血清生物标志物的安阿伯(AA)评分量化了 GI 隐窝损伤;AA2/3 评分与治疗抵抗和更高的 NRM 相关。我们进行了一项多中心、2 期研究,使用那他珠单抗,一种通过α4β7 整合素的α4 亚基阻断 T 细胞向胃肠道转移的人源化单克隆抗体,联合皮质类固醇作为新发 AA2/3 GVHD 患者的主要治疗药物。有 75 名可评估的患者入组并接受治疗;81%的患者在开始使用皮质类固醇的 2 天内接受了那他珠单抗治疗。治疗耐受性良好,没有 10%以上的患者出现治疗后新发不良事件。接受那他珠单抗联合皮质类固醇治疗的患者的结局与 MAGIC 数据库中 150 名匹配良好的仅接受皮质类固醇治疗的对照组进行了比较。接受那他珠单抗联合皮质类固醇治疗的患者与单独接受皮质类固醇治疗的患者之间的总反应率或完全反应率没有显著差异(60% vs 58%;P=.67%和 48% vs 48%;P= 1.0,分别),包括相关亚组。在接受那他珠单抗联合皮质类固醇治疗的患者与单独接受皮质类固醇治疗的对照组之间,12 个月时的 NRM 或总生存率也没有显著差异(38% vs 39%;P=.80%和 46% vs 54%;P=.48,分别)。在这项多中心基于生物标志物的 2 期研究中,那他珠单抗联合皮质类固醇未能改善新发高危 GVHD 患者的结局。该试验在 www.clinicaltrials.gov 上注册,编号为#NCT02133924。