de Lavallade Hugues, Apperley Jane F, Khorashad Jamshid S, Milojkovic Dragana, Reid Alistair G, Bua Marco, Szydlo Richard, Olavarria Eduardo, Kaeda Jaspal, Goldman John M, Marin David
Department of Haematology, Imperial College London, Du Cane Rd, London W12 0NN, United Kingdom.
J Clin Oncol. 2008 Jul 10;26(20):3358-63. doi: 10.1200/JCO.2007.15.8154. Epub 2008 Jun 2.
Imatinib is remarkably effective in treating newly diagnosed patients with chronic myeloid leukemia (CML) in chronic phase (CP). To date, most of the available data come from a single multicenter study in which some of the patients were censored for diverse reasons. Here, we report our experience in treating patients at a single institution in a setting where all events were recorded.
A total of 204 consecutive adult patients with newly diagnosed CML in CP received imatinib from June 2000 until August 2006. Response (hematologic, cytogenetic, and molecular), progression-free survival (PFS) and survival were evaluated.
At 5 years, cumulative incidences of complete cytogenetic response (CCyR) and major molecular response (MMR) were 82.7% and 50.1%, respectively. Estimated overall survival and PFS were 83.2% and 82.7%, respectively. By 5 years, 25% of patients had discontinued imatinib treatment because of an unsatisfactory response and/or toxicity. The 5-year probability of remaining in major cytogenetic response while still receiving imatinib was 62.7%. Patients achieving a CCyR at 1 year had a better PFS and overall survival than those failing to reach CCyR, but achieving a MMR conferred no further advantage. The identification of a kinase domain mutation was the only factor predicting for loss of CCyR.
Imatinib is highly effective in most patients with CML-CP; patients who respond are likely to live substantially longer than those treated with earlier therapies. Achieving CCyR correlated with PFS and overall survival, but achieving MMR had no further predictive value. However, approximately one third of patients still need better therapy.
伊马替尼在治疗新诊断的慢性期慢性髓性白血病(CML)患者方面疗效显著。迄今为止,大多数现有数据来自一项单一的多中心研究,其中一些患者因各种原因被 censored(此处可能有拼写错误,推测可能是“censored”,意为“审查、剔除”等,暂按此理解翻译)。在此,我们报告在单一机构治疗患者的经验,该机构记录了所有事件。
2000年6月至2006年8月,共有204例连续的新诊断慢性期CML成年患者接受伊马替尼治疗。评估了反应(血液学、细胞遗传学和分子学)、无进展生存期(PFS)和生存期。
5年时,完全细胞遗传学反应(CCyR)和主要分子反应(MMR)的累积发生率分别为82.7%和50.1%。估计总生存期和PFS分别为83.2%和82.7%。到5年时,25%的患者因反应不佳和/或毒性而停止伊马替尼治疗。仍接受伊马替尼治疗且维持主要细胞遗传学反应的5年概率为62.7%。1年时达到CCyR的患者比未达到CCyR的患者有更好的PFS和总生存期,但达到MMR并无进一步优势。激酶结构域突变的鉴定是预测CCyR丧失的唯一因素。
伊马替尼对大多数慢性期CML患者高度有效;有反应的患者可能比接受早期治疗的患者活得长得多。达到CCyR与PFS和总生存期相关,但达到MMR没有进一步的预测价值。然而,约三分之一的患者仍需要更好的治疗。