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Hematologic improvement after flavopiridol treatment of pentostatin and rituximab refractory hairy cell leukemia

机译:黄酮哌啶醇治疗喷司他丁和利妥昔单抗难治性毛细胞白血病后的血液学改善

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摘要

Initial therapy of hairy cell leukemia (HCL) with the purine analog pentostatin or cladribine achieves durable complete remission in 85-90% of patients. Most patients will achieve second remission when retreated with either drug, but complete remission is far less likely with subsequent courses [1]. Rituximab has activity in this setting, but response rates range from no more than 10 to 54%, emphasizing the need for novel therapies [2,3]. Promising responses after treatment with recombinant immunotoxins such as BL22 have recently been reported, but there are few other agents under active clinical investigation for this rare disease [4]. We report the case of a patient with longstanding HCL refractory to both pentostatin and rituximab who was successfully treated with the cyclin-dependent kinase inhibitor (CDKI) flavopiridol.
机译:嘌呤类似物喷司他丁或克拉屈滨对毛细胞白血病(HCL)的初始治疗可在85-90%的患者中实现持久的完全缓解。大多数患者在用任何一种药物治疗后都将获得第二次缓解,但是随后的疗程完全缓解的可能性要小得多[1]。利妥昔单抗在这种情况下具有活性,但应答率范围不超过10%至5​​4%,强调需要新型疗法[2,3]。最近已经报道了用重组免疫毒素(例如BL22)治疗后有希望的反应,但是对于这种罕见疾病,尚无其他药物在积极的临床研究中[4]。我们报告了一个患者,他司他汀和利妥昔单抗均对HCL具有长期耐药性,该患者已成功用细胞周期蛋白依赖性激酶抑制剂(CDKI)黄酮哌啶醇治疗。

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