Department of Hematology, Children's Hospital of Soochow University, Suzhou, Jiangsu, China.
Eur Rev Med Pharmacol Sci. 2018 Sep;22(18):6020-6029. doi: 10.26355/eurrev_201809_15938.
In this study, we retrospectively evaluated the therapeutic efficacy of China Children Leukemia Group-ALL2008 (CCLG-ALL 2008) protocol in pediatric patients with mixed-lineage leukaemia (MLL) gene rearrangement of acute lymphoblastic leukemia (ALL) to identify the prognostic factors.
Six hundred and thirty-four patients with ALL were enrolled in this study between June 2008 and Dec 2014. High-risk group (HR) consisted of 217 cases, of which 28 cases were MLL related positive (first group), 22 cases were BCR/ABL positive (second group), and 167 cases were negative with MLL related or BCR/ABL (third group). The therapeutic efficacy was evaluated at the time points of day 8 (TP1), day 15 (TP2), day 33 (TP3) and 12th week (TP4) with the protocol, respectively. Overall-survival (OS) and relapse-free-survival (RFS) and treatment-related mortality (TRD) were analyzed as well.
The first group accounted for 4.4% of all patients. Compared with the second and third group, the first group had more cases younger than 2 years, with initial leukocytes ≥50×109/L, and poor response on TP2. Moreover, patients older than 2 years old had a good 5 years OS (84% ± 9% vs. 37% ± 20%, p<0.05) and RFS (84% ± 9% vs. 29% ± 17%, p<0.05). There were no significant differences in the recurrence rate, TRD, 5 years OS and RFS among three groups. For the first group, compared with good response to prednisone, patients with poor response to prednisone had a poor 5 years RFS (41% ± 17% vs. 81% ± 10%, p<0.05). Multivariate Cox regression analysis identified that RFS and OS were influenced by such factors as age, MLL fusion partners, and prednisone response (p<0.05).
Such factors as younger age than 2 years old, MLL/AF4 fusion gene, poor response to prednisone, or no complete remission (CR) on TP3 were poor prognostic parameters in predicting the outcome in childhood ALL with MLL gene rearrangement treated with CCLG-ALL 2008 protocol.
本研究回顾性评估中国儿童白血病协作组-ALL2008(CCLG-ALL2008)方案治疗伴有混合谱系白血病(MLL)基因重排的急性淋巴细胞白血病(ALL)患儿的疗效,以明确其预后因素。
本研究纳入 2008 年 6 月至 2014 年 12 月间 634 例 ALL 患儿。高危组(HR)共 217 例,其中 28 例为 MLL 相关阳性(第 1 组),22 例为 BCR/ABL 阳性(第 2 组),167 例为 MLL 相关或 BCR/ABL 阴性(第 3 组)。根据方案分别在第 8 天(TP1)、第 15 天(TP2)、第 33 天(TP3)和第 12 周(TP4)评估疗效。分析总生存(OS)、无复发生存(RFS)和治疗相关死亡率(TRD)。
第 1 组占所有患者的 4.4%。与第 2 组和第 3 组相比,第 1 组患儿年龄较小(<2 岁)、初诊白细胞≥50×109/L、TP2 时反应不良的比例更高。此外,年龄>2 岁的患儿 5 年 OS(84%±9%比 37%±20%,p<0.05)和 RFS(84%±9%比 29%±17%,p<0.05)较好。三组间复发率、TRD、5 年 OS 和 RFS 差异均无统计学意义。第 1 组中,与泼尼松反应良好的患者相比,反应不良的患者 5 年 RFS 较差(41%±17%比 81%±10%,p<0.05)。多因素 Cox 回归分析显示,年龄、MLL 融合伙伴和泼尼松反应是影响 RFS 和 OS 的因素(p<0.05)。
年龄<2 岁、MLL/AF4 融合基因、泼尼松反应不良或 TP3 时未达完全缓解(CR)等因素是 CCLG-ALL2008 方案治疗伴有 MLL 基因重排的儿童 ALL 预后不良的预测因素。