Department of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Hematology, Guangdong Second Provincial General Hospital, Guangzhou, China.
Front Immunol. 2024 Jul 3;15:1408211. doi: 10.3389/fimmu.2024.1408211. eCollection 2024.
Steroid-resistant (SR) lower gastrointestinal (LGI) tract graft-versus-host disease (GVHD) is the predominant cause of morbidity and mortality from GVHD after allogeneic hematopoietic stem cell transplantation (allo-HSCT). The role of vedolizumab in the treatment of SR-LGI acute GVHD (aGVHD) remains uncertain. We aimed to assess the efficacy and safety of vedolizumab combined with basiliximab as second-line therapy for SR-LGI-aGVHD.
This study aimed to explore the efficacy of vedolizumab combined with basiliximab for SR-LGI-aGVHD. The primary endpoint was the overall response (OR) on day 28. Secondary and safety endpoints included durable OR at day 56, overall survival (OS), chronic GVHD (cGVHD), non-relapse mortality (NRM), failure-free survival (FFS), and adverse events.
Twenty-eight patients with SR-LGI-aGVHD were included. The median time to start of combination therapy after SR-LGI-aGVHD diagnosis was 7 (range, 4-16) days. The overall response rate (ORR) at 28 days was 75.0% (95% CI: 54.8%-88.6%), and 18 achieved a complete response (CR) (64.3%, 95% CI: 44.1%-80.7%). The durable OR at day 56 was 64.3% (95% CI: 44.1%-80.7%). The 100-day, 6-month, and 12-month OS rates for the entire cohort of patients were 60.7% (95% CI: 45.1%-81.8%), 60.7% (95% CI: 45.1%-81.8%), and 47.6% (95% CI: 31.4%-72.1%), respectively. The median failure-free survival was 276 days; (95% CI: 50-not evaluable) 12-month NRM was 42.9% (95% CI: 24.1%-60.3%). The 1-year cumulative incidence of cGVHD was 35.7%. Within 180 days after study treatments, the most common grade 3 and 4 adverse events were infections. Nine (32.1%) patients developed cytomegalovirus (CMV) reactivation complicated with bacterial infections (25.0%, CMV infection; 7.1%, CMV viremia). Epstein-Barr virus (EBV) reactivation occurred in five patients (17.9%, 95% CI: 6.8%-37.6%). Only three patients (10.7%, 95% CI: 2.8%-29.4%) in our study developed pseudomembranous colitis.
Vedolizumab plus basiliximab demonstrated efficacy in severe SR-LGI-aGVHD and was well-tolerated. Vedolizumab plus basiliximab may be considered a potential treatment option for patients with LGI-aGVHD.
激素耐药(SR)下消化道(LGI)移植物抗宿主病(GVHD)是异基因造血干细胞移植(allo-HSCT)后 GVHD 发病和死亡的主要原因。维得利珠单抗在治疗 SR-LGI 急性 GVHD(aGVHD)中的作用仍不确定。我们旨在评估维得利珠单抗联合巴利昔单抗作为 SR-LGI-aGVHD 二线治疗的疗效和安全性。
本研究旨在探讨维得利珠单抗联合巴利昔单抗治疗 SR-LGI-aGVHD 的疗效。主要终点为第 28 天的总体缓解(OR)。次要终点和安全性终点包括第 56 天的持久 OR、总生存(OS)、慢性 GVHD(cGVHD)、非复发死亡率(NRM)、无失败生存(FFS)和不良事件。
共纳入 28 例 SR-LGI-aGVHD 患者。在诊断为 SR-LGI-aGVHD 后开始联合治疗的中位时间为 7(范围,4-16)天。第 28 天的总体缓解率(ORR)为 75.0%(95%CI:54.8%-88.6%),18 例患者达到完全缓解(CR)(64.3%,95%CI:44.1%-80.7%)。第 56 天的持久 OR 为 64.3%(95%CI:44.1%-80.7%)。整个患者队列的 100 天、6 个月和 12 个月 OS 率分别为 60.7%(95%CI:45.1%-81.8%)、60.7%(95%CI:45.1%-81.8%)和 47.6%(95%CI:31.4%-72.1%)。中位无失败生存为 276 天;(95%CI:50-不可评估)12 个月 NRM 为 42.9%(95%CI:24.1%-60.3%)。1 年累积 cGVHD 发生率为 35.7%。在研究治疗后 180 天内,最常见的 3 级和 4 级不良事件为感染。9 例(32.1%)患者发生巨细胞病毒(CMV)再激活合并细菌感染(25.0%,CMV 感染;7.1%,CMV 血症)。5 例(17.9%)患者发生 EBV 再激活(95%CI:6.8%-37.6%)。在我们的研究中,只有 3 例(10.7%)患者发生伪膜性结肠炎。
维得利珠单抗联合巴利昔单抗在严重的 SR-LGI-aGVHD 中显示出疗效,并具有良好的耐受性。维得利珠单抗联合巴利昔单抗可能是 LGI-aGVHD 患者的潜在治疗选择。