Department of Haematology, Imperial College London, Hammersmith Hospital, London, United Kingdom.
Blood. 2012 Feb 23;119(8):1838-43. doi: 10.1182/blood-2011-10-383000. Epub 2011 Dec 14.
Second-generation tyrosine kinase inhibitors (2G-TKIs) are effective at inducing complete cytogenetic responses (CCyRs) in approximately half of chronic myeloid leukemia patients treated while still in the chronic phase and after failing imatinib. It is less clear whether these responses are durable. In the present study, we report the clinical outcome of 119 patients who received a 2G-TKI as second-line treatment while still in the chronic phase. In an intention-to-treat analysis, the 4-year probabilities of overall and event-free survival were 81.9% and 35.3%, respectively. Sixty-two patients discontinued the initial 2G-TKI because of resistance or intolerance. To further explore the durability of cytogenetic responses, irrespective of the need for a third-line TKI, we used the concept of "current CCyR-survival" (c-CCyRS). The c-CCyRS at 4 years was 54.4%. After introduction of a 2G-TKI, 77 patients had a 3-month BCR-ABL1/ABL1 transcript ratio of ≤ 10% and had significantly superior overall survival (91.3% vs 72.1%, P = .02), event-free survival (49.3% vs 13.0%, P < .001), and c-CCyRS (67.2% vs 11.2%, P = .0001) compared with the 33 patients with ratios > 10%. The 3-month molecular response was the only independent predictor for overall survival. Using an intention-to-treat analysis, we have shown that the responses to second-line therapies are durable. Patients destined to fare poorly can be identified early during therapy.
第二代酪氨酸激酶抑制剂 (2G-TKIs) 在慢性髓性白血病患者慢性期和伊马替尼治疗失败后,能有效诱导约半数患者出现完全细胞遗传学反应 (CCyR)。但这些反应的持久性尚不清楚。本研究报告了 119 例患者在慢性期接受 2G-TKI 二线治疗的临床结果。意向治疗分析中,总生存和无事件生存的 4 年概率分别为 81.9%和 35.3%。62 例患者因耐药或不耐受而停止初始 2G-TKI。为了进一步探讨细胞遗传学反应的持久性,我们不顾及是否需要三线 TKI,使用了“当前 CCyR 生存”(c-CCyRS)的概念。4 年时的 c-CCyRS 为 54.4%。在引入 2G-TKI 后,77 例患者的 BCR-ABL1/ABL1 转录比值在 3 个月时≤10%,总生存显著改善(91.3% vs. 72.1%,P =.02)、无事件生存(49.3% vs. 13.0%,P <.001)和 c-CCyRS(67.2% vs. 11.2%,P =.0001)均优于比值>10%的 33 例患者。3 个月时的分子反应是总生存的唯一独立预测因素。采用意向治疗分析,我们发现二线治疗的反应是持久的。在治疗早期就能识别出预后不良的患者。