Department of Haematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Sci Rep. 2020 Jul 29;10(1):12694. doi: 10.1038/s41598-020-69465-2.
Cold agglutinin disease (CAD) is a rare form of autoimmune haemolytic anaemia, and because of its rareness, there is no standard treatment for CAD patients. We retrospectively analysed the response to rituximab-containing therapy in CAD patients at our hospital. All patients received rituximab-containing therapy for at least 1 month. A total of 16 patients (11 males and 5 females) were included. The median age at the onset of the disease was 63.5 years (range 41-79). Most patients had manifestations including anaemia (81.3%) or cold-induced circulatory symptoms (75.0%). The median haemoglobin level was 72 g/L (range 29-101), and the median cold agglutinin titre was 1,024 (range 64-2,048). Thirteen of 16 patients (81%) responded to the therapy. Responders achieved a median increase in haemoglobin levels of 45 g/L. Grade 3-4 neutropenia occurred in 3 patients (19%), but only 1 (6%) of them experienced infection. Anaphylaxis related to rituximab occurred in 1 patient. During follow-up, five patients experienced relapse, and two patients died. The estimated median progression-free survival was 36 months, and median overall survival was not yet reached. In conclusion, A rituximab-based therapy in accordance with individual patient characteristics may be a reasonable choice for CAD patients.
冷凝集素病(CAD)是一种罕见的自身免疫性溶血性贫血,由于其罕见性,CAD 患者没有标准的治疗方法。我们回顾性分析了我院 CAD 患者接受含利妥昔单抗治疗的反应。所有患者均接受至少 1 个月的含利妥昔单抗治疗。共纳入 16 例患者(男 11 例,女 5 例)。发病时的中位年龄为 63.5 岁(范围 41-79)。大多数患者有贫血(81.3%)或冷诱导循环症状(75.0%)等表现。中位血红蛋白水平为 72g/L(范围 29-101),中位冷凝集素滴度为 1024(范围 64-2048)。16 例患者中有 13 例(81%)对治疗有反应。有反应者的血红蛋白水平中位数增加了 45g/L。3 例(19%)患者出现 3-4 级中性粒细胞减少症,但只有 1 例(6%)患者发生感染。1 例发生与利妥昔单抗相关的过敏反应。随访期间,5 例患者复发,2 例患者死亡。估计无进展生存的中位时间为 36 个月,中位总生存时间尚未达到。总之,根据患者个体特征,以利妥昔单抗为基础的治疗可能是 CAD 患者的合理选择。