Division of Hematology, Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan.
Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Clin Lymphoma Myeloma Leuk. 2018 May;18(5):353-360.e1. doi: 10.1016/j.clml.2018.03.004. Epub 2018 Mar 15.
We previously reported an interim analysis of the DADI (dasatinib discontinuation) trial. The results showed that 48% of patients with chronic myeloid leukemia in the chronic phase who maintained a deep molecular response (DMR) for ≥ 1 year could discontinue second- or subsequent-line dasatinib treatment safely at a median follow-up of 20 months. However, the results from longer follow-up periods would be much more useful from a clinical perspective.
The DADI trial was a prospective, multicenter trial conducted in Japan. After confirming a stable DMR for ≥ 1 year, dasatinib treatment subsequent to imatinib or nilotinib was discontinued. After discontinuation, the loss of DMR (even of 1 point) was defined as stringent molecular relapse, thereby triggering therapy resumption. The predictive factors of treatment-free remission (TFR) were analyzed.
The median follow-up period was 44.0 months (interquartile range, 40.5-48.0 months). The estimated overall TFR rate at 36 months was 44.4% (95% confidence interval, 32.0%-56.2%). Only 2 patients developed a molecular relapse after the 1-year cutoff point. The presence of imatinib resistance was a significant risk factor for molecular relapse. Moreover, high natural killer cell and low γδ T-cell and CD4 regulatory T-cell (CD25CD127) counts before discontinuation correlated significantly with successful therapy discontinuation.
These findings suggest that discontinuation of second- or subsequent-line dasatinib after a sustained DMR of ≥ 1 year is feasible, especially for patients with no history of imatinib resistance. In addition, the natural killer cell count was associated with the TFR.
我们之前报告了 DADI(达沙替尼停药)试验的中期分析结果。结果显示,在慢性期接受过 2 线或后续线达沙替尼治疗的慢性髓性白血病患者中,有 48%的患者在中位随访 20 个月时达到深度分子缓解(DMR)且持续时间≥1 年,可安全停药。然而,从临床角度来看,更长时间的随访结果将更加有用。
DADI 试验是一项在日本进行的前瞻性、多中心试验。在确认 DMR 稳定持续≥1 年后,停止伊马替尼或尼洛替尼后续的达沙替尼治疗。停药后,DMR 的丧失(甚至丢失 1 分)被定义为严格的分子复发,从而触发治疗的恢复。分析了无治疗缓解(TFR)的预测因素。
中位随访时间为 44.0 个月(四分位间距,40.5-48.0 个月)。36 个月时的总 TFR 率估计为 44.4%(95%置信区间,32.0%-56.2%)。只有 2 例患者在 1 年截止点后发生分子复发。伊马替尼耐药的存在是分子复发的显著危险因素。此外,停药前自然杀伤细胞和γδ T 细胞及 CD4 调节性 T 细胞(CD25CD127)计数高与成功停药显著相关。
这些发现表明,在持续 1 年以上的 DMR 后,停止二线或后续线达沙替尼治疗是可行的,尤其是对无伊马替尼耐药史的患者。此外,自然杀伤细胞计数与 TFR 相关。