临床儿科杂志 ›› 2018, Vol. 36 ›› Issue (8): 590-.doi: 10.3969/j.issn.1000-3606.2018.08.006

• 综合报道 • 上一篇    下一篇

伴有 inv(16)/CBFβ-MYH11 阳性的儿童急性髓系 白血病临床特点及预后研究#br#

吴珺, 于水, 陆爱东, 左英熹, 贾月萍, 张乐萍
  

  1. 北京大学人民医院儿科(北京 100044)
  • 收稿日期:2018-08-15 出版日期:2018-08-15 发布日期:2018-08-15
  • 通讯作者: 张乐萍 E-mail:zhangleping@pkuph.edu.cn

Study of clinical characteristics and prognosis in pediatric inv(16)/CBFβ-MYH11-positive acute myeloid leukemia 

WU Jun, YU Shui, LU Aidong, ZUO Yingxi, JIA Yueping, ZHANG Leping   

  1. Department of Pediatrics, People’s Hospital, Peking University, Beijing 100044, China
  • Received:2018-08-15 Online:2018-08-15 Published:2018-08-15

摘要:  目的 分析伴inv(16)/CBFβ-MYH11阳性的儿童急性髓系白血病(AML)的临床特点、生物学特征及预后。 方法 回顾分析2008年12月至2017年9月初诊并治疗的30例inv(16)/CBFβ-MYH11阳性AML患儿的临床和生物学特征, 随访至2017年11月,观察患儿的生存状态和影响因素。结果 30例伴inv(16)/CBFβ-MYH11阳性的AML患儿中,首诊表 现为肝肿大19例、脾肿大18例、淋巴结肿大19例,初诊时外周血WBC≥50×109/L者19例。 5年无事件生存(EFS)率、总 生存(OS)率分别为(84.2±7.6)%、( 89.8±5.6)%。COX多因素回归分析显示,性别、发病时年龄、WBC、乳酸脱氢酶 水平、是否有髓外白血病、是否伴c-kit基因突变、染色体是否单独为inv(16)、初诊时CBFβ-MYH11定量是否大于中位数 水平、第一疗程是否完全缓解,对EFS、OS的影响均无统计学意义(P>0.05)。 将初诊时CBFβ-MYH11基因定量水平作为 基线,诱导缓解结束后的CBFβ-MYH11基因下降≥2 log者与<2 log者比较, 5年EFS、OS的差异均无统计学意义(P>0.05)。 3例患儿在巩固治疗期间监测CBFβ-MYH11融合基因进行性上升,调整治疗强度后未出现复发,至今均全部存活。结论  伴inv(16)/CBFβ-MYH11阳性AML患儿发病时肝、脾、淋巴结肿大多见,外周血WBC多明显升高,治疗疗效好,巩固治 疗阶段定期监测CBFβ-MYH11定量可指导治疗,具有重要作用。

Abstract: Objective To investigate clinical and biological characteristics and prognosis of pediatric inv(16)/CBFβMYH11-positive acute myeloid leukemia. Methods From December 2008 to September 2017, 30 patients diagnosed as inv(16)/ CBFβ-MYH11-positive acute myeloid leukemia were enrolled in this study and their clinical and biological features were retrospectively analyzed. Following-up of 30 patients were ended in November 2017, and the survival status was calculated by K-M curve and prognostic factors were analyzed by COX model. Results At preliminary diagnosis of the total 30 patients, 19 patients had hepatomegaly (63.3%), 18 cases had splenomegaly (60.0%), and 19 cases had lymphoadenopathy (63.3%). Patients at diagnosis with high leukocyte counts (≥50×109/L) accounted for 63.3%. In all patients, the 5-year anticipated EFS and OS were (84.2±7.6)% and(89.8±5.6)%, respectively. Cox multivariate regression analysis showed that gender, age at onset, leukocyte count, lactate dehydrogenase level, extramedullary leukemia, c-kit gene mutation, chromosome inv (16) alone, initial CBFβ-MYH11 quantification and the response to the first course of treatment did not statistically affect EFS and OS (P>0.05).  The level of CBFβ-MYH11 gene at diagnosis was used as the baseline to determine whether the level of gene after treatment had a more than 2 logarithmic (2-log) reduction. When patients with a more than 2-log reduction of CBFβ-MYH11 transcript levels (≥2-log) compared with other patients after a course of induction therapy, the differences of 5-year EFS and OS were not statistically significant (P>0.05). When periodically monitoring the CBFβ-MYH11 gene, three cases with progressively increasing CBFβ-MYH11 fusion gene during the consolidation therapy were identified, and no relapse was found after adjustment of treatment intensity. All of them survived so far. Conclusions In patients with inv(16)/CBFβ-MYH11-positive AML, hepatosplenomegaly, lymphadenopathy and high initial leukocyte counts are most common features, and the therapeutic effect is good. It is important to regularly monitor CBFβ-MYH11 quantitation in the consolidation therapy phase.