Wu Yue, Sun Guangyu, Tang Baolin, Song Kaidi, Cheng Yaxin, Tu Meijuan, Zhu Xiaoyu
Department of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China; Anhui Provincial Key Laboratory of Blood Research and Applications, Hefei, China; Blood and Cell Therapy Institute, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Department of Hematology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Transplant Cell Ther. 2024 Sep;30(9):916.e1-916.e12. doi: 10.1016/j.jtct.2024.06.026. Epub 2024 Jul 4.
Steroid-refractory (SR) acute graft-versus-host disease (aGVHD) is a major cause of mortality after allogeneic hematopoietic stem cell transplantation. We aimed to evaluate the effectiveness and safety of ruxolitinib plus basiliximab for treating SR-aGVHD after unrelated cord blood transplantation (UCBT). Among the 1154 patients with hematological malignancies who underwent UCBT between February 2014 and May 2022, 198 patients with grade II to IV SR-aGVHD were enrolled, 112 of whom were treated with basiliximab alone (basiliximab group) and 86 of whom received basiliximab plus ruxolitinib (combined therapy group). The combined therapy group demonstrated a significantly higher complete response rate (CRR) on day 28 (36.0%) than did the basiliximab group (12.5%, P < .001). SR-aGVHD patients were further stratified into standard-risk and high-risk groups using the refined Minnesota aGVHD risk score. For standard-risk patients, combined therapy significantly improved the CRR (51.1% versus 13.6%, P < .001) and 3-year overall survival (74.5% versus 52.4%, P = .033). However, high-risk patients did not exhibit the same benefits. Compared with basiliximab monotherapy, ruxolitinib plus basiliximab therapy was an effective therapy for patients with standard-risk SR-aGVHD following UCBT. The effectiveness of combined therapy in high-risk patients was not apparent, indicating the need for other treatments.
类固醇难治性(SR)急性移植物抗宿主病(aGVHD)是异基因造血干细胞移植后死亡的主要原因。我们旨在评估芦可替尼联合巴利昔单抗治疗无关脐血移植(UCBT)后SR-aGVHD的有效性和安全性。在2014年2月至2022年5月期间接受UCBT的1154例血液系统恶性肿瘤患者中,198例II至IV级SR-aGVHD患者入组,其中112例仅接受巴利昔单抗治疗(巴利昔单抗组),86例接受巴利昔单抗联合芦可替尼治疗(联合治疗组)。联合治疗组在第28天的完全缓解率(CRR)显著高于巴利昔单抗组(36.0%对12.5%,P<0.001)。使用改良的明尼苏达aGVHD风险评分将SR-aGVHD患者进一步分为标准风险组和高风险组。对于标准风险患者,联合治疗显著提高了CRR(51.1%对13.6%,P<0.001)和3年总生存率(74.5%对52.4%,P = 0.033)。然而,高风险患者并未表现出同样的益处。与巴利昔单抗单药治疗相比,芦可替尼联合巴利昔单抗治疗对UCBT后标准风险SR-aGVHD患者是一种有效的治疗方法。联合治疗在高风险患者中的有效性不明显,表明需要其他治疗方法。