Centre Henri Becquerel, Rouen, France.
Leuk Lymphoma. 2012 May;53(5):820-9. doi: 10.3109/10428194.2011.631636. Epub 2011 Dec 13.
The increase of fludarabine-resistant chronic lymphocytic leukemia (CLL) presents a new treatment challenge. The aim of this review is to evaluate the efficacy and safety of rituximab for patients with fludarabine-refractory CLL. Medline, Embase, The Cochrane Library and selected conference proceedings were searched. Seventeen relevant publications reporting stratified data were identified. Treatments included: rituximab in combination with etanercept, alemtuzumab, bendamustine or methylprednisolone alone, with fludarabine and cyclophosphamide (FCR), with oxaliplatin as well as fludarabine and cytarabine, with cyclophosphamide as well as fludarabine and alemtuzumab (CFAR), and with cytarabine, cisplatinum and dexamethasone (DHAP). One study evaluated rituximab with granulocyte-macrophage colony-stimulating factor in combination with alternating cyclophosphamide, liposomal daunorubicin, vincristine, dexamethasone and methotrexate plus Ara-C. One study evaluated rituximab as monotherapy. Of the nine studies considering overall response, eight reported rates above 50% (four reported rates above 75%). Median overall survival was 37 months for FCR, 11 months for CFAR, 20 months for rituximab with methylprednisolone, 30 months for rituximab with alemtuzumab and 44 months for an FCR/CFAR mixed treatment. The identified studies indicate that regimens containing rituximab may be highly efficacious in the fludarabine-refractory CLL setting. Nevertheless, further research is needed to facilitate the choice of treatment for the clinician.
氟达拉滨耐药性慢性淋巴细胞白血病(CLL)的增加带来了新的治疗挑战。本综述旨在评估利妥昔单抗对氟达拉滨难治性 CLL 患者的疗效和安全性。检索了 Medline、Embase、The Cochrane Library 和选定的会议记录。确定了 17 篇报告分层数据的相关出版物。治疗包括:利妥昔单抗联合依那西普、阿仑单抗、苯达莫司汀或单独甲基强的松龙,联合氟达拉滨和环磷酰胺(FCR),联合奥沙利铂以及氟达拉滨和阿糖胞苷,联合环磷酰胺以及氟达拉滨和阿仑单抗(CFAR),以及联合阿糖胞苷、顺铂和地塞米松(DHAP)。一项研究评估了利妥昔单抗联合粒细胞-巨噬细胞集落刺激因子与交替环磷酰胺、脂质体柔红霉素、长春新碱、地塞米松和甲氨蝶呤加阿糖胞苷联合使用。一项研究评估了利妥昔单抗单药治疗。在考虑总体反应的九项研究中,八项报告的反应率超过 50%(四项报告的反应率超过 75%)。FCR 的中位总生存期为 37 个月,CFAR 为 11 个月,利妥昔单抗联合甲基强的松龙为 20 个月,利妥昔单抗联合阿仑单抗为 30 个月,FCR/CFAR 混合治疗为 44 个月。确定的研究表明,含利妥昔单抗的方案在氟达拉滨难治性 CLL 中可能具有高度疗效。然而,需要进一步的研究来为临床医生提供治疗选择。