Hematology Branch, NHLBI, NIH, Bethesda, MD, USA.
Haematologica. 2013 Aug;98(8):1259-63. doi: 10.3324/haematol.2012.080929. Epub 2013 May 28.
Rituximab is an effective treatment for autoimmune cytopenias associated with chronic lymphocytic leukemia. Despite the incorporation of rituximab into fludarabine-based chemotherapy regimens, the incidence of autoimmune cytopenias has remained high. Inadequate rituximab exposure due to rapid antibody clearance may be a contributing factor. To test this hypothesis, we measured serum rituximab levels in patients treated with fludarabine and rituximab (375 mg/m(2)). All patients had undetectable rituximab trough levels by the end of cycle 1, and one-third had undetectable levels already on Day 6 of cycle 1. Although rituximab trough levels increased progressively with each cycle, only by cycle 4 did the median trough level exceed 10 ug/mL. The median half-life of rituximab during cycle 1 was 27 hours, compared to 199 hours during cycle 4 (P<0.0001). There was a significant inverse correlation between the rituximab half-life in cycle 1 and the degree of tumor burden (P=0.02). Two patients who were identified as having subclinical autoimmune hemolysis prior to therapy were given additional doses of rituximab during the initial cycles of therapy and did not develop clinically significant hemolysis. One patient who developed clinically significant hemolysis during therapy was given additional rituximab doses during cycles 3-5 and was able to successfully complete his treatment. In conclusion, rituximab is cleared so rapidly during the initial cycles of therapy for chronic lymphocytic leukemia that most patients have only transient serum levels. More frequent dosing of rituximab may be required to prevent autoimmune complications in at-risk patients (clinicaltrials.gov identifier:00001586).
利妥昔单抗是治疗与慢性淋巴细胞白血病相关的自身免疫性血细胞减少症的有效药物。尽管在氟达拉滨为基础的化疗方案中加入了利妥昔单抗,但自身免疫性血细胞减少症的发生率仍然很高。由于抗体快速清除,导致利妥昔单抗的暴露不足,这可能是一个促成因素。为了验证这一假说,我们检测了接受氟达拉滨和利妥昔单抗(375mg/m2)治疗的患者的血清利妥昔单抗水平。所有患者在第 1 周期结束时均检测不到利妥昔单抗的谷浓度,有三分之一的患者在第 1 周期第 6 天已经检测不到利妥昔单抗的浓度。虽然利妥昔单抗的谷浓度随着每个周期的进行而逐渐增加,但只有在第 4 周期时,中位数才超过 10ug/ml。第 1 周期的利妥昔单抗半衰期中位数为 27 小时,而第 4 周期为 199 小时(P<0.0001)。第 1 周期的利妥昔单抗半衰期与肿瘤负担程度呈显著负相关(P=0.02)。在治疗前被确定为存在亚临床自身免疫性溶血性贫血的 2 例患者在初始治疗周期中接受了额外剂量的利妥昔单抗治疗,且未发生临床显著的溶血。1 例在治疗期间发生临床显著溶血的患者在第 3-5 周期接受了额外剂量的利妥昔单抗治疗,成功完成了治疗。总之,在慢性淋巴细胞白血病的初始治疗周期中,利妥昔单抗清除得如此之快,以至于大多数患者只有短暂的血清水平。可能需要更频繁地给予利妥昔单抗剂量,以防止高危患者发生自身免疫性并发症(临床试验注册号:00001586)。