Department of Medicine V, University of Heidelberg, Heidelberg, Germany.
Blood. 2012 May 24;119(21):4851-9. doi: 10.1182/blood-2011-09-378505. Epub 2012 Apr 5.
The CLL3 trial was designed to study intensive treatment including autologous stem cell transplantation (autoSCT) as part of first-line therapy in patients with chronic lymphocytic leukemia (CLL). Here, we present the long-term outcome of the trial with particular focus on the impact of genomic risk factors, and we provide a retrospective comparison with patients from the fludarabine-cyclophosphamide-rituximab (FCR) arm of the German CLL Study Group (GCLLSG) CLL8 trial. After a median observation time of 8.7 years (0.3-12.3 years), median progression-free survival (PFS), time to retreatment, and overall survival (OS) of 169 evaluable patients, including 38 patients who did not proceed to autoSCT, was 5.7, 7.3, and 11.3 years, respectively. PFS and OS were significantly reduced in the presence of 17p- and of an unfavorable immunoglobulin heavy variable chain mutational status, but not of 11q-. Five-year nonrelapse mortality was 6.5%. When 110 CLL3 patients were compared with 126 matched patients from the FCR arm of the CLL8 trial, 4-year time to retreatment (75% vs 77%) and OS (86% vs 90%) was similar despite a significant benefit for autoSCT in terms of PFS. In summary, early treatment intensification including autoSCT can provide very effective disease control in poor-risk CLL, although its clinical benefit in the FCR era remains uncertain. The trial has been registered with www.clinicaltrials.gov as NCT00275015.
CLL3 试验旨在研究强化治疗,包括自体干细胞移植(autoSCT),作为慢性淋巴细胞白血病(CLL)患者一线治疗的一部分。在此,我们报告了该试验的长期结果,特别关注基因组风险因素的影响,并与德国 CLL 研究组(GCLLSG)CLL8 试验 FCR 臂的患者进行回顾性比较。在中位观察时间为 8.7 年(0.3-12.3 年)后,169 例可评估患者的中位无进展生存期(PFS)、复发时间和总生存期(OS)分别为 5.7、7.3 和 11.3 年。存在 17p-和不利的免疫球蛋白重链可变区突变状态时,PFS 和 OS 显著降低,但 11q-时则不然。5 年非复发死亡率为 6.5%。将 110 例 CLL3 患者与 CLL8 试验 FCR 臂的 126 例匹配患者进行比较,尽管 autoSCT 在 PFS 方面具有显著优势,但 4 年复发时间(75%比 77%)和 OS(86%比 90%)相似。总之,早期强化治疗包括 autoSCT 可以为高危 CLL 提供非常有效的疾病控制,尽管其在 FCR 时代的临床获益仍不确定。该试验已在 www.clinicaltrials.gov 上注册,编号为 NCT00275015。