Jain Ankur, Jain Aditi, Chaudhry Sumita, Gupta D K
Department of Haematology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, 110029 India.
Department of Medicine, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, 110029 India.
Indian J Hematol Blood Transfus. 2025 Jan;41(1):144-150. doi: 10.1007/s12288-024-01780-4. Epub 2024 Apr 19.
Warm autoimmune hemolytic anaemia (wAIHA) is a chronic condition. Despite the high initial responses seen with the first two treatment lines (corticosteroids and rituximab), relapses are frequent. Anecdotal data suggests the efficacy of bortezomib in relapsed/refractory (RR) wAIHA. This case series aimed to evaluate bortezomib as a third-line therapy in wAIHA in terms of efficacy, safety, and prospects of achieving treatment-free remission (TFR). Five adult patients ≥ 18 years of age with RR wAIHA after corticosteroids and rituximab were included over 1.5 years. Patients were treated uniformly with Vd (4 weeks = 1 cycle), bortezomib (1.3 mg/m subcutaneous/week), and dexamethasone (40 mg/week). Patients were assessed for response, side effects, and TFR following bortezomib discontinuation. The median age was 40 years (range, 17-55), and 60% were females. The overall response rate was 100%. The median time to partial response (PR) was 1 month (range, 0.5-4). With ongoing treatment, three patients achieved a complete response (CR). The median time to best response (PR- 40%, CR- 60%) was 4 months (range, 1-19.5). After a median follow-up of 21 months following bortezomib discontinuation, TFR rates were 60%, 40%, and 20% at 6 months, 1 year, and 2 years, respectively. Non-severe treatment-related thrombocytopenia was seen in 1/5 of patients. For patients with RR wAIHA, Vd represents a safe and highly effective third-line therapy with durable responses and high TFR rates.
温抗体型自身免疫性溶血性贫血(wAIHA)是一种慢性病。尽管在前两线治疗(皮质类固醇和利妥昔单抗)中最初反应率较高,但复发很常见。轶事数据表明硼替佐米对复发/难治性(RR)wAIHA有效。本病例系列旨在评估硼替佐米作为wAIHA三线治疗在疗效、安全性及实现无治疗缓解(TFR)前景方面的情况。在1.5年期间纳入了5例年龄≥18岁、经皮质类固醇和利妥昔单抗治疗后为RR wAIHA的成年患者。患者均接受Vd方案(4周 = 1个周期)治疗,即硼替佐米(1.3 mg/m²皮下注射/周)和地塞米松(40 mg/周)。在停用硼替佐米后评估患者的反应、副作用及TFR情况。中位年龄为40岁(范围17 - 55岁),60%为女性。总体缓解率为100%。部分缓解(PR)的中位时间为1个月(范围0.5 - 4个月)。随着治疗的进行,3例患者达到完全缓解(CR)。最佳反应(PR - 40%,CR - 60%)的中位时间为4个月(范围1 - 19.5个月)。在停用硼替佐米后中位随访21个月时,6个月、1年和2年的TFR率分别为60%、40%和20%。1/5的患者出现非严重的治疗相关血小板减少。对于RR wAIHA患者,Vd方案是一种安全且高效的三线治疗,缓解持久且TFR率高。