McGill University Health Centre, 1001 Decarie Blvd, Room D02.7722, Montreal, Quebec, H4A 3J1, Canada.
Curr Treat Options Oncol. 2018 Mar 8;19(3):15. doi: 10.1007/s11864-018-0532-2.
Strict criteria for when to stop tyrosine kinase inhibitor (TKI) therapy in clinical practice are not easily defined without an agreement on what probability of achieving a treatment-free remission (TFR) constitutes a medically acceptable standard and consideration of the potential medical risks of continued TKI therapy and/or patient preferences. Patients in sustained deep molecular response (DMR) have no significant chronic myelogenous leukemia-related risk of progression and death, and thus, safety is of paramount importance. Patients with prior history of advanced disease, additional chromosomal abnormalities (ACA), atypical transcripts, TKI resistance, high Sokal score, or who cannot be relied upon to come for regular molecular monitoring should generally be excluded from TKI cessation in clinical practice. Similarly, stopping TKIs should not be attempted without the availability of standardized BCR-ABL1 testing with a sensitivity of at least MR4.5 and a turnaround time of less than 4 weeks. Prior TKI therapy of 5 years and stable MR4.0 of 2 years or more constitutes reasonable minimal criteria for stopping TKIs with approximately a 50% chance of success. The risk of morbidity with continued TKI therapy and patient preferences need to be considered to determine to what extent these minimal criteria should be exceeded and at what threshold to re-initiate therapy whether on the loss of major molecular response or at a lower molecular endpoint.
在临床实践中,没有关于达到无治疗缓解 (TFR) 的概率构成可接受的医学标准的共识,也没有考虑继续 TKI 治疗和/或患者偏好的潜在医疗风险,因此,很难轻易确定停止酪氨酸激酶抑制剂 (TKI) 治疗的严格标准。持续深度分子反应 (DMR) 的患者没有显著的慢性粒细胞白血病进展和死亡风险,因此,安全性至关重要。有既往晚期疾病史、额外染色体异常 (ACA)、非典型转录本、TKI 耐药、高 Sokal 评分或不能定期进行分子监测的患者,一般应排除在临床实践中的 TKI 停药之外。同样,如果没有标准化的 BCR-ABL1 检测,检测灵敏度至少为 MR4.5,周转时间少于 4 周,就不应尝试停止 TKI。TKI 治疗 5 年且 MR4.0 稳定 2 年或更长时间,是停止 TKI 的合理最低标准,成功率约为 50%。需要考虑继续 TKI 治疗的发病率风险和患者偏好,以确定应在多大程度上超过这些最低标准,并在何种阈值下重新开始治疗,无论是在主要分子反应丧失时,还是在较低的分子终点时。