Department of Research and Innovation, Haugesund Hospital, Haugesund, Norway.
Department of Pathology, Oslo University Hospital, Oslo, Norway.
Blood. 2017 Jul 27;130(4):537-541. doi: 10.1182/blood-2017-04-778175. Epub 2017 May 22.
Primary chronic cold agglutinin disease (CAD) is a well-defined clinicopathologic entity in which a bone marrow clonal B-cell lymphoproliferation results in autoimmune hemolytic anemia and cold-induced circulatory symptoms. Rituximab monotherapy and fludarabine-rituximab in combination are documented treatment options. In a prospective, nonrandomized multicenter trial, 45 eligible patients received rituximab 375 mg/m day 1 and bendamustine 90 mg/m days 1 and 2 for 4 cycles at a 28-day interval. Thirty-two patients (71%) responded; 18 (40%) achieved complete response (CR) and 14 (31%) partial response (PR). Among 14 patients previously treated with rituximab or fludarabine-rituximab, 7 (50%) responded to bendamustine-rituximab (3 CR and 4 PR). Hemoglobin levels increased by a median of 4.4 g/dL in the complete responders, 3.9 g/dL in those achieving PR, and 3.7 g/dL in the whole cohort. The 10th percentile of response duration was not reached after 32 months. Grade 3-4 neutropenia occurred in 15 patients (33%), but only 5 (11%) experienced infection with or without neutropenia. Thirteen patients (29%) had their dose of bendamustine reduced. In conclusion, bendamustine-rituximab combination therapy is highly efficient, sufficiently safe, and may be considered in first line for patients with CAD requiring therapy. The trial was registered at www.clinicaltrials.gov as #NCT02689986.
原发性慢性冷凝集素病(CAD)是一种明确的临床病理实体,其骨髓克隆 B 细胞淋巴增生导致自身免疫性溶血性贫血和冷诱导的循环症状。利妥昔单抗单药治疗和氟达拉滨-利妥昔单抗联合治疗已被证实为有效治疗方案。在一项前瞻性、非随机、多中心试验中,45 名符合条件的患者接受了利妥昔单抗 375mg/m2,第 1 天,苯达莫司汀 90mg/m2,第 1 和第 2 天,每 28 天为 1 个周期,共 4 个周期。32 名患者(71%)有反应;18 名(40%)患者达到完全缓解(CR),14 名(31%)患者达到部分缓解(PR)。在 14 名先前接受过利妥昔单抗或氟达拉滨-利妥昔单抗治疗的患者中,7 名(50%)对苯达莫司汀-利妥昔单抗有反应(3 名 CR 和 4 名 PR)。完全缓解者血红蛋白水平平均升高 4.4g/dL,部分缓解者升高 3.9g/dL,整个队列升高 3.7g/dL。32 个月后,未达到反应持续时间的第 10 百分位数。15 名患者(33%)出现 3-4 级中性粒细胞减少,但仅有 5 名(11%)发生中性粒细胞减少伴或不伴感染。13 名患者(29%)减少了苯达莫司汀的剂量。总之,苯达莫司汀-利妥昔单抗联合治疗高效、安全性足够,对于需要治疗的 CAD 患者,可考虑作为一线治疗方案。该试验在 www.clinicaltrials.gov 上注册,编号为 #NCT02689986。