Wu Sijing, Yang Shijia, Zhu Li, Wang Ying, Zhang Yicheng, Zhou Jianfeng, Li Dengju
Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Am J Med Sci. 2016 May;351(5):473-9. doi: 10.1016/j.amjms.2016.02.034. Epub 2016 Mar 2.
Initial induction chemotherapy is critical for patients with newly diagnosed de novo acute myeloid leukemia (AML). The aim of the present study was to analyze the factors affecting the outcome of patients with AML who failed to initial chemotherapy.
We retrospectively analyzed clinical data of 311 adults with de novo AML.
Compared with 179 patients showing complete remission (CR), 132 patients who failed to achieve CR were older with poorer prognostic stratification, higher proportion of FLT3-ITD mutations, higher expression rates of CD9, lower expression rates of cMPO and CD64 and poorer overall survival (OS). The 2-year OS rate of the non-CR groups was inferior to that of the CR groups (28.3% versus 53.3%, P < 0.001). However, there was no dramatic difference in 2-year OS rate between initial and reinduction chemotherapy if patients achieved a same remission status. The 2-year OS rate significantly improved following allogeneic hematopoietic cell transplant in patients who failed to initial treatment. The survival of patients with similar remission status was affected by FLT3-ITD mutation instead of CD9(+) expression.
Initial induction failure or poorer prognostic stratification seriously affected the survival of patients with de novo AML. The allogeneic hematopoietic cell transplant is an alternative strategy to improve the survival of patients resistant to initial treatment.
初始诱导化疗对新诊断的原发性急性髓系白血病(AML)患者至关重要。本研究旨在分析影响AML患者初始化疗失败结局的因素。
我们回顾性分析了311例成人原发性AML患者的临床资料。
与179例达到完全缓解(CR)的患者相比,132例未达到CR的患者年龄更大,预后分层更差,FLT3-ITD突变比例更高,CD9表达率更高,cMPO和CD64表达率更低,总生存期(OS)更差。非CR组的2年OS率低于CR组(28.3%对53.3%,P<0.001)。然而,如果患者达到相同的缓解状态,初始化疗和再诱导化疗的2年OS率没有显著差异。初始治疗失败的患者在接受异基因造血细胞移植后,2年OS率显著提高。具有相似缓解状态的患者的生存受FLT3-ITD突变而非CD9(+)表达的影响。
初始诱导失败或预后分层较差严重影响原发性AML患者的生存。异基因造血细胞移植是提高初始治疗耐药患者生存率的一种替代策略。