CLIN CANCER RES:依鲁替尼联合利妥昔单抗治疗高风险慢性淋巴细胞性白血病

2017-05-05 MedSci MedSci原创

依鲁替尼是治疗慢性淋巴细胞性白血病(CLL),包括伴del17p或TP53突变的高风险患者的有效药物,安全性较高。依鲁替尼被广泛用于对CLL患者,尤其是伴17p缺失突变患者的治疗。但是依鲁替尼与其他药物联合使用尚存在争议。

依鲁替尼是治疗慢性淋巴细胞性白血病(CLL),包括伴del17p或TP53突变的高风险患者的有效药物,安全性较高。依鲁替尼被广泛用于对CLL患者,尤其是伴17p缺失突变患者的治疗。但是依鲁替尼与其他药物联合使用尚存在争议。

CLIN CANCER RES近期报道了一篇文章,报道了依鲁替尼联合利妥昔单抗(IR方案)治疗40例高风险CLL患者的长期随访结果。平均随访时间47个月,患者平均年龄65岁,21例患者存在17p缺失。平均治疗时间为41个月,平均治疗周期数为42。总反应率达到95%,9例患者达到完全缓解。21例患者未持续进行治疗,其中10例由于疾病进展,9例由于其他原因,2例由于干细胞移植,其余19例患者持续进行依鲁替尼治疗。所有患者平均无进展生存期为45个月,del17p亚组患者无进展生存期显着缩短,为32.3个月。14例患者死亡,其中5例死于疾病进展,5例死于感染,4例死于其他原因。

文章最后认为,IR联合治疗方案对高风险CLL患者有持续性的缓解作用,在该临床随机试验中探索了加用利妥昔单抗可能的临床获益。

原始出处:
Preetesh Jain,Michael J.Keating,et al.Long-term Follow-up of Treatment with Ibrutinib and Rituximab in Patients with High-Risk Chronic Lymphocytic Leukemia.CLIN CANCER RES.May 2017 doi:10.1158/1078-0432.CCR-16-1948

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    2017-05-07 卡圣

    学习了,谢谢

    0

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