Department of Leukemia, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.
Blood. 2011 Feb 10;117(6):1822-7. doi: 10.1182/blood-2010-07-293977. Epub 2010 Oct 28.
We assessed the predictive factors for outcome and response in 123 patients with chronic myeloid leukemia in chronic phase treated with second-generation tyrosine kinase inhibitors (TKIs) after imatinib failure. Better event-free survival rates with second-generation TKI therapy were associated with a previous cytogenetic response to imatinib (P < .001) and a performance status of 0 (P = .001). Patients with 0, 1, or 2 adverse factors had 2-year event-free survival rates of 78%, 49%, and 20% (P < .001), respectively; 2-year overall survival rates of 95%, 85%, and 40%, (P = .002), respectively; and a 12-month probability of achieving a major cytogenetic response of 64%, 36%, and 20% (P = .007), respectively. In conclusion, patients with poor performance status and no previous cytogenetic response to imatinib therapy have a low likelihood of responding to second-generation TKI with poor event-free survival and therefore should be offered additional treatment options. This scoring system could serve to advise patients of their prognosis and treatment options, as well as to evaluate the benefit of newer alternate options.
我们评估了 123 例慢性髓性白血病慢性期患者在伊马替尼治疗失败后接受第二代酪氨酸激酶抑制剂(TKI)治疗的结局和反应的预测因素。第二代 TKI 治疗具有更好的无事件生存(EFS)率,与伊马替尼的先前细胞遗传学反应(P <.001)和表现状态为 0(P =.001)有关。无不良因素、有 1 个或 2 个不良因素的患者,2 年 EFS 率分别为 78%、49%和 20%(P <.001);2 年总生存率分别为 95%、85%和 40%(P =.002);12 个月时获得主要细胞遗传学反应的概率分别为 64%、36%和 20%(P =.007)。总之,表现状态差且对伊马替尼治疗无先前细胞遗传学反应的患者对第二代 TKI 反应的可能性较低,EFS 不良,因此应提供其他治疗选择。该评分系统可用于告知患者预后和治疗选择,并评估新的替代方案的获益。