Department of Medicine, Haugesund Hospital, Haugesund, Norway.
Br J Haematol. 2011 May;153(3):309-17. doi: 10.1111/j.1365-2141.2011.08643.x. Epub 2011 Mar 8.
Primary chronic cold agglutinin disease (CAD) is a clonal lymphoproliferative disorder accounting for 13-15% of autoimmune haemolytic anaemias. Significant advances have been made in treatment, which was largely unsuccessful until recently. The essential clinical, immunological and pathological features are reviewed, focusing on their relevance for therapy. Non-pharmacological management still seems sufficient in some patients. With the recent improvements, however, drug therapy seems indicated more often than previously thought. Corticosteroids should not be used to treat CAD. Half of the patients respond to rituximab monotherapy; median response duration is 11 months. Fludarabine-rituximab combination therapy is very effective, resulting in 75% response rate, complete remissions in about 20%, and more than 66 months estimated response duration. Toxicity is a concern, and benefits should be carefully weighed against risks. An individualized approach is discussed regarding the choice of fludarabine-rituximab combination versus rituximab monotherapy. Patients requiring treatment should be considered for prospective trials.
原发性慢性冷凝集素病(CAD)是一种克隆性淋巴增生性疾病,占自身免疫性溶血性贫血的 13-15%。在治疗方面取得了重大进展,直到最近,治疗效果还不是很理想。本文回顾了其主要的临床、免疫和病理特征,重点关注它们对治疗的意义。在一些患者中,非药物治疗似乎仍然足够。然而,随着最近的治疗进展,药物治疗似乎比以前认为的更常见。CAD 不应使用皮质类固醇治疗。利妥昔单抗单药治疗有一半的患者有反应;中位反应持续时间为 11 个月。氟达拉滨-利妥昔单抗联合治疗非常有效,反应率为 75%,完全缓解率约为 20%,估计反应持续时间超过 66 个月。毒性是一个问题,应仔细权衡利弊。对于氟达拉滨-利妥昔单抗联合治疗与利妥昔单抗单药治疗的选择,讨论了个体化的方法。需要治疗的患者应考虑前瞻性试验。