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在慢性期 CML 接受伊马替尼治疗 3 个月后早期分子反应失败的情况下,6 个月时的 BCR/ABL 水平可确定 CML 亚组的良好风险。

BCR/ABL level at 6 months identifies good risk CML subgroup after failing early molecular response at 3 months following imatinib therapy for CML in chronic phase.

机构信息

Department of Medical Oncology and Hematology, Princess Margaret Hospital, University Health Network, University of Toronto, Ontario, Canada.

出版信息

Am J Hematol. 2014 Jun;89(6):626-32. doi: 10.1002/ajh.23707. Epub 2014 Apr 10.

DOI:10.1002/ajh.23707
PMID:24619861
Abstract

It is unclear if patients with CML treated with imatinib who fail to achieve BCR/ABL transcript levels <10%(IS) at 3 months i.e. an early molecular response (EMR) have a better prognosis if they achieve a response by 6 months. We reviewed 320 patients with chronic myeloid leukemia (CML) in chronic phase receiving Imatinib therapy with 3 and 6 month BCR/ABL transcript levels available, and divided them into four groups. Group I (achieved an EMR at 3 months), Group II (did not achieve an EMR at 3 months, but achieved a transcript level of <1% at 6 months), Group III (did not achieve an EMR at 3 months, then at 6 months achieved a level between 1% and 10%) and Group IV (failed to achieve a response at 3 and 6 months). Compared to Group I, Group IV showed significantly worse freedom from treatment failure (FTF; 93.1% vs 69.0%, P < 0.001), progression free survival (97.7% vs 77.3%, P < 0.001) and overall survival (98.3% vs 78.9%, P < 0.001). While, group III showed inferior PFS (98.3% vs 90.4%, P = 0.013) and OS (97.7% vs 90.4%, P = 0.037), but no difference in FTF (93.1% vs 92.0%, P = 0.520). There were no significant differences between Groups I and II. A BCR/ABL transcript level at 6 months can identify a "good-risk" subgroup among patients who fail to achieve an EMR on Imatinib therapy for CML.

摘要

对于在 3 个月时未能达到 BCR/ABL 转录水平<10%(IS)即早期分子反应(EMR)的接受伊马替尼治疗的 CML 患者,如果在 6 个月时达到缓解,他们的预后是否更好尚不清楚。我们回顾了 320 例接受伊马替尼治疗的慢性期慢性髓性白血病(CML)患者的资料,这些患者在 3 个月和 6 个月时有 BCR/ABL 转录水平的记录,并将他们分为四组。第 I 组(在 3 个月时达到 EMR),第 II 组(在 3 个月时未达到 EMR,但在 6 个月时达到转录水平<1%),第 III 组(在 3 个月时未达到 EMR,然后在 6 个月时达到 1%至 10%之间的水平),第 IV 组(在 3 个月和 6 个月时未达到反应)。与第 I 组相比,第 IV 组的无治疗失败率(FTF;93.1%比 69.0%,P<0.001)、无进展生存率(97.7%比 77.3%,P<0.001)和总生存率(98.3%比 78.9%,P<0.001)显著更差。而第 III 组的 PFS(98.3%比 90.4%,P=0.013)和 OS(97.7%比 90.4%,P=0.037)较差,但 FTF 无差异(93.1%比 92.0%,P=0.520)。第 I 组和第 II 组之间没有显著差异。在伊马替尼治疗 CML 未能达到 EMR 的患者中,6 个月时的 BCR/ABL 转录水平可识别出“低危”亚组。

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