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利妥昔单抗联合喷司他丁或克拉屈滨:用于复发性毛细胞白血病的有效联合治疗方案。

Rituximab with pentostatin or cladribine: an effective combination treatment for hairy cell leukemia after disease recurrence.

机构信息

The Institute of Cancer Research and the Royal Marsden NHS Trust, Sutton, UK.

出版信息

Leuk Lymphoma. 2011 Jun;52 Suppl 2:75-8. doi: 10.3109/10428194.2011.568650. Epub 2011 Apr 19.

DOI:10.3109/10428194.2011.568650
PMID:21504288
Abstract

The purine analogs pentostatin and cladribine are effective treatments for hairy cell leukemia (HCL). However, alternative treatments are needed for patients with recurrent disease. We reviewed retrospectively data from 18 patients who were retreated with either pentostatin (n = 12) or cladribine (n = 6) in combination with rituximab, after 1-6 (median 2) previous treatments with either purine analog as a single agent. All 18 patients responded to therapy, with a complete response (CR) rate of 89%. This compared favorably with CR rates of 68% after second-line therapy and 47% after third-line therapy in 88 patients retreated one or more times with a purine analog alone. Toxicity with the combination treatment was minimal. At a median follow-up of 36 months (range 5-83 months) all 16 complete responders remained in CR, while one partial responder developed recurrent disease at 10 months. The estimated recurrence rate at 3 years was 7%. This compares with 21% after second-line therapy and 42% after third-line therapy in the 88 patients retreated with a purine analog alone. Furthermore, it was a marked improvement on the 55% recurrence at 3 years previously seen in these same 18 patients after their own first-line treatment with single-agent pentostatin or cladribine (p = 0.006). The combination of a purine analog with rituximab was safe and effective for patients with recurrent HCL. The results suggest an added benefit compared with single-agent purine analog therapy.

摘要

嘌呤类似物喷司他丁和克拉屈滨是治疗毛细胞白血病(HCL)的有效药物。然而,对于复发性疾病患者,需要替代治疗方法。我们回顾性分析了 18 例患者的数据,这些患者在接受 1-6 次(中位数 2 次)嘌呤类似物单药治疗后,分别接受喷司他丁(n=12)或克拉屈滨(n=6)联合利妥昔单抗治疗。18 例患者均对治疗有反应,完全缓解(CR)率为 89%。与 88 例单独使用嘌呤类似物接受二线或三线治疗的患者相比,二线治疗的 CR 率为 68%,三线治疗的 CR 率为 47%,这一结果具有优势。联合治疗的毒性较小。在中位数为 36 个月(范围 5-83 个月)的随访中,16 例完全缓解者均持续处于 CR 状态,而 1 例部分缓解者在 10 个月时出现疾病复发。3 年的复发率估计为 7%。与单独使用嘌呤类似物接受二线或三线治疗的患者相比,这一结果具有优势,后者的复发率分别为 21%和 42%。此外,与这 18 例患者首次接受单药喷司他丁或克拉屈滨治疗时 3 年的 55%复发率相比,这一结果也有显著改善(p=0.006)。嘌呤类似物联合利妥昔单抗治疗复发性 HCL 安全有效。结果表明,与单药嘌呤类似物治疗相比,联合治疗具有额外的益处。

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