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LRF CLL4试验中患者的长期预后:挽救治疗及生物学标志物对存活10年患者的影响。

The long-term outcome of patients in the LRF CLL4 trial: the effect of salvage treatment and biological markers in those surviving 10 years.

作者信息

Else Monica, Wade Rachel, Oscier David, Catovsky Daniel

机构信息

Division of Molecular Pathology, The Institute of Cancer Research, London, UK.

Clinical Trial Service Unit, Oxford, UK.

出版信息

Br J Haematol. 2016 Jan;172(2):228-37. doi: 10.1111/bjh.13824. Epub 2015 Oct 12.

Abstract

With 10+ years follow-up in the Leukaemia Research Fund (LRF) CLL4 trial, we report the effect of salvage therapy, and the clinical/biological features of the 10-year survivors treated for chronic lymphocytic leukaemia (CLL). Overall survival (OS) was similar in the three randomized arms. With fludarabine-plus-cyclophosphamide (FC), progression-free survival (PFS) was significantly longer (P < 0.0001), but OS after progression significantly shorter, than in the chlorambucil or fludarabine arms (P < 0.0001). 614/777 patients progressed; 524 received second-line and 260 third-line therapy, with significantly better complete remission (CR) rates compared to first-line in the chlorambucil arm (7% vs. 13% after second-, 18% after third-line), but worse in the FC arm (38% vs. 15% after both second and third-line). OS 10 years after progression was better after a second-line CR versus a partial response (36% vs. 16%) and better with FC-based second-line therapy (including rituximab in 20%) or a stem cell transplant (28%) versus all other treatments (10%, P < 0.0001). The 176 (24%) 10-year survivors tended to be aged <70 years, with a "good risk" prognostic profile, stage A-progressive, achieving at least one CR, with a first-line PFS >3 years and receiving ≤2 lines of treatment. In conclusion, clinical/biological features and salvage treatments both influence the long-term outcome. Second-line therapies that induce a CR can improve OS in CLL patients.

摘要

在白血病研究基金(LRF)的CLL4试验中进行了10多年的随访后,我们报告了挽救治疗的效果,以及接受慢性淋巴细胞白血病(CLL)治疗的10年幸存者的临床/生物学特征。三个随机分组的治疗组的总生存期(OS)相似。使用氟达拉滨加环磷酰胺(FC)方案时,无进展生存期(PFS)显著更长(P < 0.0001),但进展后的总生存期明显短于苯丁酸氮芥或氟达拉滨治疗组(P < 0.0001)。614/777例患者病情进展;524例接受二线治疗,260例接受三线治疗,与苯丁酸氮芥治疗组的一线治疗相比,完全缓解(CR)率显著提高(二线治疗后为7% vs. 13%,三线治疗后为18%),但FC治疗组情况较差(二线和三线治疗后均为38% vs. 15%)。进展后10年的总生存期在二线治疗达到CR后优于部分缓解(36% vs. 16%),基于FC的二线治疗(包括20%使用利妥昔单抗)或干细胞移植(28%)后的总生存期优于所有其他治疗(10%,P < 0.0001)。176例(24%)10年幸存者年龄往往小于70岁,具有“低危”预后特征,A期进展型,至少达到一次CR,一线PFS>3年且接受≤2线治疗。总之,临床/生物学特征和挽救治疗均影响长期预后。诱导CR的二线治疗可改善CLL患者的总生存期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d607/4832371/0998dae94dfd/BJH-172-228-g001.jpg

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