Department of Internal Medicine, Seoul National University Hospital, 28 Yongon-dong, Jongno-gu, Seoul 110-744, Republic of Korea.
Ann Hematol. 2010 Jul;89(7):725-31. doi: 10.1007/s00277-010-0910-8. Epub 2010 Feb 24.
The aim of this phase IV study was to (1) to define efficacy of escalating dose imatinib in chronic myeloid leukemia (CML) patients showing suboptimal response to standard dose imatinib and (2) to find markers that predict the response to escalating doses of imatinib. CML patients in chronic phase (CP) who failed to achieve optimal response with 400 mg/day imatinib or patients in accelerated phase (AP) or blast crisis (BC) who failed to achieve complete hematologic response after 3 months of 400-600 mg/day imatinib were enrolled. CP patients received 600 mg/day, while AP/BC patients received 600-800 mg/day imatinib. Patients received imatinib for at least 12 months or until the disease progression or intolerable toxicity. Along with cytogenetic response (CyR), molecular response was assessed with BCR-ABL/ABL ratio. Baseline BCR-ABL gene mutation test was performed. Seventy-one patients (median age, 49.0 years, M:F = 50:21) received escalated dose imatinib. Grade 3 edema in two patients was the only nonhematologic toxicities more than grade 2. For evaluable patients, 30.8% of patients achieved CCyR at 6 months, and median time to treatment failure (TTFx) was 18.0 months. TTFx was longer in patients who achieved greater than 50% reduction in BCR-ABL/ABL within 6 months (early molecular responder (EMR)) compared with those who did not (non-EMR; p < 0.001). Of 31 patients who had mutational status data, three had mutation. All mutants failed to achieve CCyR. In conclusion, escalated dose imatinib shows considerable efficacy with tolerable toxicity in CML patients showing suboptimal response to standard dose imatinib. EMR is an early predictive marker for positive imatinib response.
(1) 确定在对标准剂量伊马替尼反应不佳的慢性髓性白血病 (CML) 患者中逐步增加伊马替尼剂量的疗效,以及 (2) 寻找预测伊马替尼逐步增加剂量反应的标志物。入组的 CML 慢性期 (CP) 患者在接受 400mg/天伊马替尼治疗后未达到最佳反应,或加速期 (AP) 或急变期 (BC) 患者在接受 400-600mg/天伊马替尼治疗 3 个月后未达到完全血液学反应。CP 患者接受 600mg/天治疗,AP/BC 患者接受 600-800mg/天伊马替尼治疗。患者接受伊马替尼治疗至少 12 个月或直至疾病进展或无法耐受毒性。除细胞遗传学反应 (CyR) 外,还通过 BCR-ABL/ABL 比值评估分子反应。进行了基线 BCR-ABL 基因突变检测。71 例患者(中位年龄 49.0 岁,M:F=50:21)接受了逐步增加剂量的伊马替尼治疗。两名患者出现 3 级水肿,为唯一大于 2 级的非血液学毒性。对于可评估的患者,6 个月时 30.8%的患者达到 CCyR,治疗失败时间(TTFx)的中位数为 18.0 个月。在 6 个月内 BCR-ABL/ABL 降低超过 50%的患者(早期分子反应者(EMR))与未达到的患者(非 EMR)相比,TTFx 更长(p<0.001)。在有突变状态数据的 31 名患者中,有 3 名发生突变。所有突变体均未达到 CCyR。总之,在对标准剂量伊马替尼反应不佳的 CML 患者中,逐步增加伊马替尼剂量显示出相当的疗效,且毒性可耐受。EMR 是伊马替尼阳性反应的早期预测标志物。