Division of Hematology and Internal Medicine, Department of Clinical and Biological Sciences of the University of Turin, San Luigi Gonzaga University Hospital, Turin, Italy.
J Natl Compr Canc Netw. 2012 Jan;10(1):121-9. doi: 10.6004/jnccn.2012.0011.
In patients with chronic myelogenous leukemia (CML) treated at diagnosis with the standard therapy consisting of imatinib, 400 mg once daily, the failure to achieve a complete cytogenetic response (CCyR) within 12 months from the start of therapy has been shown to be associated with an increased risk of progression and an overall inferior survival. Experts of the European LeukemiaNet and NCCN have indicated what degrees of hematologic, cytogenetic, and molecular responses should be expected at definite time points for patients with CML to have the highest probability of experiencing the final optimal response, defined as the achievement of at least a complete hematologic response with a minor cytogenetic response after 3 months; at least a partial cytogenetic response after 6 months; at least a CCyR after 12 months; and a major molecular response after 18 months of therapy. The last opportunity for a CCyR has been established at 18 months. Because the residual probability of attaining a CCyR is reduced for patients who do not experience a complete hematologic response by 3 months, any cytogenetic response by 6 months, or a major cytogenetic response by 12 months, these conditions are considered treatment failures. At this point, a change in therapy is highly recommended, such as second-line treatment with the second-generation tyrosine kinase inhibitors nilotinib or dasatinib and, in specific situations, a stem cell transplant. The loss of any grade of previously achieved cytogenetic response at any time point is also considered an imatinib failure demanding a change of therapy. Finally, intermediate gradations of response exist between optimal response and failure in which, although not totally compromised, the possibilities of achieving an optimal response later are decreased. The best therapeutic strategies to be followed in these intermediate situations, called suboptimal responses, have not been clearly established and are still under clinical investigation, but for the moment, a change of therapy is not required.
在接受标准治疗(伊马替尼,每日一次,400mg)治疗的慢性髓性白血病(CML)患者中,治疗开始后 12 个月内未达到完全细胞遗传学缓解(CCyR),已被证明与进展风险增加和整体生存质量下降相关。欧洲白血病网和 NCCN 的专家指出,在 CML 患者的特定时间点,应该期望达到何种程度的血液学、细胞遗传学和分子反应,才能使最终获得最佳反应的可能性最大,该反应定义为在 3 个月后至少达到完全血液学反应和轻微细胞遗传学反应;在 6 个月后至少达到部分细胞遗传学缓解;在 12 个月后至少达到 CCyR;以及在治疗 18 个月后达到主要分子反应。最后一次达到 CCyR 的机会是在 18 个月。由于在 3 个月时未达到完全血液学缓解、6 个月时未达到任何细胞遗传学反应或 12 个月时未达到主要细胞遗传学反应的患者,获得 CCyR 的残余可能性降低,因此这些情况被认为是治疗失败。此时强烈推荐改变治疗方法,例如使用第二代酪氨酸激酶抑制剂尼罗替尼或达沙替尼进行二线治疗,在特定情况下进行干细胞移植。在任何时间点失去以前达到的任何级别的细胞遗传学反应也被认为是伊马替尼治疗失败,需要改变治疗方法。最后,在最佳反应和失败之间存在中间反应梯度,尽管没有完全受到影响,但以后获得最佳反应的可能性降低。在这些中间情况下,称为次优反应,尚未明确确定最佳治疗策略,仍在临床研究中,但目前不需要改变治疗方法。