机构:[1]Department of Hematology, Qilu Hospital, Shandong University, Jinan,Shandong, China[2]Institute of Hematology and Blood Diseases Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College,Tianjin, China[3]Fujian Provincial Key Laboratory of Hematology, Fujian Instituteof Hematology, Fujian Medical University Union Hospital, Fuzhou, Fujian,China[4]Jiangsu Institute of Hematology, Key Laboratory of Thrombosis andHemostasis of Ministry of Health, The First Affiliated Hospital of SoochowUniversity, Suzhou, Jiangsu, China[5]Department of Hematology, The FirstAffiliated Hospital, Zhejiang University College of Medicine, Hangzhou,Zhejiang, China[6]Department of Hematology, West China Hospital, SichuanUniversity, Chengdu, Sichuan, China四川大学华西医院[7]Department of Hematology, TongjiHospital, Tongji Medical College, Huazhong University of Science andTechnology, Wuhan, Hubei, China[8]Institute of Hematology, Union Hospital,Tongji Medical College, Huazhong University of Science and Technology,Wuhan, Hubei, China华中科技大学同济医学院附属协和医院[9]Institute of Hematology, Peking University People’sHospital, Beijing, China
An early molecular response is spectacularly predictive of outcome in chronic myeloid leukemia (CML) and early response landmarks may identify the high-risk patients likely to be benefit from an early therapy switch. In this study, we evaluated the most relevant cutoffs for early molecular response markers (BCR-ABL1 values at 3 months, log reduction and halving time between diagnosis and 3 months) in 476 first-line imatinib-treated Chinese patients with chronic phase CML. All outcomes were significantly superior for the 324 patients with 3-month BCR-ABL1 <= 10%, so did for the 270 patients with BCR-ABL1 >0.61 log reduction. BCR-ABL1 halving time <= 22 days was identified for patients with the most favorable outcome. Moreover, the prognosis was significantly poorest for patients with both halving time >44 days and BCR-ABL1 >10%. Importantly, multivariate regression analysis demonstrated that a BCR-ABL1 log reduction calculated at 3 months of 0.61 was the only variable that significantly predicted for OS. Our results highlight the importance of rapid initial decline of BCR-ABL1 in predicting satisfactory outcome. Our data support the evidence that monitoring BCR-ABL1 values at an early time point could contribute to accurately assess response and ultimately guide clinical decisions regarding the timing of therapeutic intervention.
基金:
Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81400118, 81470319, 91642110, 81370662, 91442126]
第一作者机构:[1]Department of Hematology, Qilu Hospital, Shandong University, Jinan,Shandong, China
通讯作者:
推荐引用方式(GB/T 7714):
Zhang Jingru,Wang Yingqiao,Wang Jianxiang,et al.Early BCR-ABL1 decline in imatinib-treated patients with chronic myeloid leukemia: results from a multicenter study of the Chinese CML alliance[J].BLOOD CANCER JOURNAL.2018,8:doi:10.1038/s41408-018-0093-4.
APA:
Zhang, Jingru,Wang, Yingqiao,Wang, Jianxiang,Hu, Jianda,Chen, Suning...&Hou, Ming.(2018).Early BCR-ABL1 decline in imatinib-treated patients with chronic myeloid leukemia: results from a multicenter study of the Chinese CML alliance.BLOOD CANCER JOURNAL,8,
MLA:
Zhang, Jingru,et al."Early BCR-ABL1 decline in imatinib-treated patients with chronic myeloid leukemia: results from a multicenter study of the Chinese CML alliance".BLOOD CANCER JOURNAL 8.(2018)