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The role of rituximab in combination with pentostatin or cladribine for the treatment of recurrent/refractory hairy cell leukemia

机译:利妥昔单抗联合喷司他丁或克拉屈滨在治疗复发/难治性毛细胞白血病中的作用

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摘要

BACKGROUND: The purine analogs pentostatin and cladribine have revolutionized the treatment of hairy cell leukemia (HCL) with overall responses in greater than 85% of patients and a median progression-free survival of up to 15 years. They continue to be effective at second- and even third-line therapy; however, alternative treatments are needed for patients who are or have become refractory to these agents or whose remissions are shorter with each course of therapy. METHODS: The authors conducted a retrospective review of 8 patients who received pentostatin or cladribine combined concurrently (n = 6 patients) or sequentially (n = 2 patients) with rituximab at second-line therapy (n = 3 patients) and at subsequent lines of therapy (n = 5 patients). Results from a previously reported database of 219 patients with HCL (73 patients who received second-line therapy and 20 patients who received third-line therapy) were used as a historic control group against which to measure benefit. RESULTS: All 8 patients responded to therapy, with 7 complete responses (CRs) (87.5%) and minimal toxicity. All patients who had CRs were negative for minimal residual disease (MRD). At a median follow-up of 29 months (range, 5-39 months) 1 patient developed recurrent disease, and the estimated 2-year recurrence rate was 20% (0% after second-line therapy and 25% after subsequent lines of therapy). In the historic control group, the CR rates were 70% after second-line therapy and 45% after third-line therapy, and the recurrence rates at 2 years were 15% and 33%, respectively. CONCLUSIONS: The combination of purine analogs with rituximab was safe and effective for patients with recurrent and/or refractory HCL, and the current results suggested an added benefit compared with standard treatment.
机译:背景:嘌呤类似物喷司他丁和克拉屈滨已经彻底改变了毛细胞白血病(HCL)的治疗方法,超过85%的患者总体反应良好,中位无进展生存期长达15年。它们在二线甚至三线治疗中仍然有效;但是,对于这些药物难治性或已变得难治或在每个疗程中缓解时间较短的患者,需要其他治疗方法。方法:作者回顾性回顾了8例在二线治疗(n = 3例)和随后的治疗中同时接受喷喷抑素或克拉屈滨联合(n = 6例)或顺序(n = 2例)联合利妥昔单抗治疗的患者。治疗(n = 5例)。先前报道的219例HCL患者的结果(73例接受二线治疗的患者和20例接受三线治疗的患者)的结果用作衡量获益的历史对照组。结果:全部8例患者对治疗均有效,其中7例完全缓解(CR)(87.5%),且毒性极小。所有患有CR的患者的最小残留疾病(MRD)均为阴性。在中位随访期29个月(5-39个月)中,有1名患者复发疾病,估计的2年复发率为20%(二线治疗后为0%,后续治疗后为25%) )。在历史对照组中,二线治疗后的CR率为70%,三线治疗后的CR为45%,两年后的复发率分别为15%和33%。结论:嘌呤类似物与利妥昔单抗联合治疗对复发和/或难治性HCL患者安全有效,目前的结果表明与标准治疗相比,其获益更大。

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