van Groningen Lenneke F J, Liefferink Aleida M, de Haan Anton F J, Schaap Nicolaas P M, Donnelly J Peter, Blijlevens Nicole M A, van der Velden Walter J F M
Department of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands; Radboud Institute of Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
Department of Hematology, Radboud University Medical Center, Nijmegen, the Netherlands.
Biol Blood Marrow Transplant. 2016 Jan;22(1):179-82. doi: 10.1016/j.bbmt.2015.08.039. Epub 2015 Sep 18.
Steroid-refractory acute graft-versus-host disease (aGVHD) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT). A protocol on the management of aGVHD was introduced in our center that incorporated a prospective study on combination therapy with inolimomab (anti-IL-2Rα) and etanercept (anti-tumor necrosis factor-α) for steroid-refractory aGVHD. We evaluated the efficacy and safety in 21 consecutively treated patients. The patients had developed refractory aGVHD after SCT (n = 16) or donor lymphocyte infusion (n = 5), and aGVHD was classified as severe in all patients, mostly due to gastrointestinal involvement stages 2 to 4. No drug-related side effects were observed apart from the infections expected to occur in these severely immunocompromised patients. Overall response at day 28 of second-line therapy was 48% (10/21), with 6 and 4 patients achieving a complete and partial response, respectively. Eventually, 19 patients died (90%), with early mortality (<6 months) predominantly resulting from refractory aGVHD and secondary infections and late mortality resulting from relapse of the underlying disease. With a median follow-up of 55 days, the estimated rates of 6-month and 2-year overall survival were dismal, 29% and 10%, respectively. In conclusion, the combination of inolimomab and etanercept for steroid-refractory aGVHD failed to improve the dismal prognosis of severe steroid-refractory aGVHD.
类固醇难治性急性移植物抗宿主病(aGVHD)仍然是异基因干细胞移植(SCT)后发病和死亡的重要原因。我们中心引入了一项aGVHD管理方案,其中纳入了一项关于英夫利昔单抗(抗IL-2Rα)和依那西普(抗肿瘤坏死因子-α)联合治疗类固醇难治性aGVHD的前瞻性研究。我们评估了21例连续接受治疗患者的疗效和安全性。这些患者在SCT后(n = 16)或供体淋巴细胞输注后(n = 5)发生了难治性aGVHD,所有患者的aGVHD均被分类为重度,主要是由于胃肠道2至4期受累。除了这些严重免疫功能低下患者预期会发生的感染外,未观察到与药物相关的副作用。二线治疗第28天的总体缓解率为48%(10/21),分别有6例和4例患者达到完全缓解和部分缓解。最终,19例患者死亡(90%),早期死亡(<6个月)主要由难治性aGVHD和继发感染导致,晚期死亡由基础疾病复发导致。中位随访55天,6个月和2年的总生存率估计令人沮丧,分别为29%和10%。总之,英夫利昔单抗和依那西普联合治疗类固醇难治性aGVHD未能改善严重类固醇难治性aGVHD的不良预后。