Department of Leukemia, MD Anderson Cancer Center, The University of Texas, Houston, TX 77030, USA.
Leukemia. 2013 Apr;27(4):907-13. doi: 10.1038/leu.2012.305. Epub 2012 Nov 6.
The purpose was to assess predictive factors for outcome in patients with chronic myeloid leukemia (CML) in chronic phase (CML-CP) treated with nilotinib after imatinib failure. Imatinib-resistant and -intolerant patients with CML-CP (n=321) were treated with nilotinib 400 mg twice daily. Of 19 baseline patient and disease characteristics and two response end points analyzed, 10 independent prognostic factors were associated with progression-free survival (PFS). In the multivariate analysis, major cytogenetic response (MCyR) within 12 months, baseline hemoglobin ≥ 120 g/l, baseline basophils <4%, and absence of baseline mutations with low sensitivity to nilotinib were associated with PFS. A prognostic score was created to stratify patients into five groups (best group: 0 of 3 unfavorable risk factors and MCyR by 12 months; worst group: 3 of 3 unfavorable risk factors and no MCyR by 12 months). Estimated 24-month PFS rates were 90%, 79%, 67% and 37% for patients with prognostic scores of 0, 1, 2 and 3, respectively, (no patients with score of 4). Even in the presence of poor disease characteristics, nilotinib provided significant clinical benefit in patients with imatinib-resistant or -intolerant CML. This system may yield insight on the prognosis of patients.
目的是评估慢性髓性白血病(CML)慢性期(CML-CP)患者在伊马替尼治疗失败后接受尼洛替尼治疗的结局预测因素。对 321 例 CML-CP 伊马替尼耐药和不耐受的患者给予尼洛替尼 400mg,每日 2 次。在分析的 19 项基线患者和疾病特征及 2 项反应终点中,有 10 个独立的预后因素与无进展生存(PFS)相关。多变量分析显示,12 个月内获得主要细胞遗传学缓解(MCyR)、基线血红蛋白≥120g/l、基线嗜碱性粒细胞<4%以及基线无对尼洛替尼低敏感性的突变与 PFS 相关。创建了一个预后评分系统,将患者分为五组(最佳组:0 个不利风险因素和 12 个月时 MCyR;最差组:3 个不利风险因素和 12 个月时无 MCyR)。具有预后评分为 0、1、2 和 3 的患者 24 个月的 PFS 率分别为 90%、79%、67%和 37%(无评分 4 的患者)。即使存在疾病特征不良,尼洛替尼在伊马替尼耐药或不耐受的 CML 患者中也提供了显著的临床获益。该系统可能对患者的预后提供深入了解。