Department of Hematology, the First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, 300 Guangzhou Road, Nanjing 210029, China.
Med Oncol. 2012 Sep;29(3):2102-10. doi: 10.1007/s12032-011-0054-2. Epub 2011 Sep 1.
To determine whether prognostic factors remain relevant to chronic lymphocytic leukemia (CLL) patients treated with fludarabine and cyclophosphamide (FC), we prospectively evaluated 86 Chinese CLL patients who received FC in first-line therapy. Twenty-four patients (27.9%) achieved complete remission (CR), and overall response rate was 75.6%. With a median follow-up of 41 months, the median progression-free survival (PFS) was 36.0 months and median overall survival (OS) has not been reached. The strong correlations of lower CR rate with advanced Binet stage, unmutated IGHV, cytogenetic abnormalities of del(17p13) or del(11q23), and p53 mutations were observed by univariable analyses. Stepwise logistic regression identified that unmutated IGHV and p53 abnormality (p53 deletion or mutation) were associated with a decreased odds of achieving CR. The less cycles of treatment, not achieving CR, advanced Binet stage, and p53 abnormality significantly correlated with a shortened PFS. Furthermore, in a multivariate analysis, p53 abnormality and advanced Binet stage were identified as being significant risk factors for early relapse. Not achieving CR, advanced Binet stage, ZAP-70-positive, and p53 abnormality were the adverse factors in determining OS. Only p53 aberration was independently associated with significantly shorter OS by a multivariate analysis. These results suggest that patients with p53 abnormality should be considered for alternative therapies.
为了确定预后因素是否与接受氟达拉滨和环磷酰胺(FC)治疗的慢性淋巴细胞白血病(CLL)患者仍然相关,我们前瞻性评估了 86 例接受 FC 一线治疗的中国 CLL 患者。24 例(27.9%)达到完全缓解(CR),总缓解率为 75.6%。中位随访 41 个月,中位无进展生存期(PFS)为 36.0 个月,中位总生存期(OS)尚未达到。单变量分析显示,较低的 CR 率与较晚期的 Binet 分期、未突变的 IGHV、del(17p13)或 del(11q23)的细胞遗传学异常以及 p53 突变具有强相关性。逐步逻辑回归分析确定,未突变的 IGHV 和 p53 异常(p53 缺失或突变)与降低 CR 几率相关。治疗周期较少、未达到 CR、较晚期的 Binet 分期和 p53 异常与 PFS 缩短显著相关。此外,在多变量分析中,p53 异常和较晚期的 Binet 分期被确定为早期复发的显著危险因素。未达到 CR、较晚期的 Binet 分期、ZAP-70 阳性和 p53 异常是确定 OS 的不利因素。仅 p53 异常通过多变量分析与明显较短的 OS 相关。这些结果表明,p53 异常的患者应考虑替代疗法。