National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland, USA.
Department of Clinical Haematology and Bone Marrow Transplantation, Peter MacCallum Cancer Centre/The Royal Melbourne Hospital, Melbourne, Victoria, Australia.
Br J Haematol. 2024 Sep;205(3):1170-1179. doi: 10.1111/bjh.19648. Epub 2024 Jul 17.
Uncertainty remains regarding the safety and tolerability of immunosuppressive therapy (IST) with anti-thymocyte globulin (ATG) and cyclosporine (CSA) in older patients. We retrospectively analysed two prospective clinical trials of IST in treatment-naïve severe aplastic anaemia (SAA) to assess safety in older compared to younger patients. Patients ≥18 years of age who had received IST with ATG and CSA +/- eltrombopag (EPAG) were included. Pre-treatment baseline characteristics and co-morbidities were assessed as predictors of therapy-related complications in younger (<60 years) versus older (≥60 years) patients. Out of 245 eligible patients, 54 were older and 191 were younger. Older patients had a similar frequency of SAEs, ICU admissions and hospital length of stay compared to younger patients. Older patients had a higher frequency of cardiac events related to IST, but none resulted in death. Older patients had worse long-term overall survival, and more relapse and clonal evolution post-IST. However, older patients who responded to IST had a similar survival at a median follow-up to younger patients. Disease-related factors and limited therapeutic options in refractory disease likely contribute to poorer outcomes in older patients, not complications of upfront IST. Therefore, IST should be considered first-line therapy for most older SAA patients.
在老年患者中使用抗胸腺细胞球蛋白(ATG)和环孢素(CSA)的免疫抑制治疗(IST)的安全性和耐受性仍存在不确定性。我们回顾性分析了两项治疗初治重型再生障碍性贫血(SAA)的 IST 前瞻性临床试验,以评估老年患者与年轻患者相比的安全性。纳入接受 ATG 和 CSA +/- 艾曲泊帕(EPAG)的 IST 治疗且年龄≥18 岁的患者。评估治疗相关并发症的预测因素为年龄<60 岁与≥60 岁患者的治疗前基线特征和合并症。在 245 名符合条件的患者中,54 名年龄较大,191 名年龄较小。与年轻患者相比,老年患者的严重不良事件(SAE)、入住 ICU 和住院时间相似。老年患者 IST 相关心脏事件的发生率较高,但均未导致死亡。老年患者的长期总体生存率较差,IST 后复发和克隆进化的发生率更高。然而,在中位随访时,对 IST 有反应的老年患者的生存与年轻患者相似。疾病相关因素和难治性疾病中有限的治疗选择可能导致老年患者预后较差,而不是 IST 治疗的并发症。因此,IST 应被视为大多数老年 SAA 患者的一线治疗方法。