Haematology, Department of Cellular Biotechnologies and Haematology, "Sapienza" University, Rome, Italy.
GIMEMA Data Centre, GIMEMA Foundation, Rome, Italy.
Br J Haematol. 2018 Jun;181(5):642-652. doi: 10.1111/bjh.15251. Epub 2018 Apr 19.
BCR/ABL1-like acute lymphoblastic leukaemia (ALL) is a subgroup of B-lineage acute lymphoblastic leukaemia that occurs within cases without recurrent molecular rearrangements. Gene expression profiling (GEP) can identify these cases but it is expensive and not widely available. Using GEP, we identified 10 genes specifically overexpressed by BCR/ABL1-like ALL cases and used their expression values - assessed by quantitative real time-polymerase chain reaction (Q-RT-PCR) in 26 BCR/ABL1-like and 26 non-BCR/ABL1-like cases to build a statistical "BCR/ABL1-like predictor", for the identification of BCR/ABL1-like cases. By screening 142 B-lineage ALL patients with the "BCR/ABL1-like predictor", we identified 28/142 BCR/ABL1-like patients (19·7%). Overall, BCR/ABL1-like cases were enriched in JAK/STAT mutations (P < 0·001), IKZF1 deletions (P < 0·001) and rearrangements involving cytokine receptors and tyrosine kinases (P = 0·001), thus corroborating the validity of the prediction. Clinically, the BCR/ABL1-like cases identified by the BCR/ABL1-like predictor achieved a lower rate of complete remission (P = 0·014) and a worse event-free survival (P = 0·0009) compared to non-BCR/ABL1-like ALL. Consistently, primary cells from BCR/ABL1-like cases responded in vitro to ponatinib. We propose a simple tool based on Q-RT-PCR and a statistical model that is capable of easily, quickly and reliably identifying BCR/ABL1-like ALL cases at diagnosis.
BCR/ABL1 样急性淋巴细胞白血病 (ALL) 是一种 B 细胞系急性淋巴细胞白血病亚组,发生于无复发性分子重排的病例中。基因表达谱 (GEP) 可识别这些病例,但费用昂贵且无法广泛应用。我们使用 GEP 鉴定了 10 个在 BCR/ABL1 样 ALL 病例中特异性过表达的基因,并使用定量实时聚合酶链反应 (Q-RT-PCR) 在 26 例 BCR/ABL1 样和 26 例非 BCR/ABL1 样病例中评估其表达值,构建了一个统计“BCR/ABL1 样预测器”,用于识别 BCR/ABL1 样病例。通过对 142 例 B 细胞系 ALL 患者进行“BCR/ABL1 样预测器”筛查,我们鉴定出 28/142 例 BCR/ABL1 样患者 (19.7%)。总体而言,BCR/ABL1 样病例富集 JAK/STAT 突变 (P<0.001)、IKZF1 缺失 (P<0.001) 和涉及细胞因子受体和酪氨酸激酶的重排 (P=0.001),从而证实了预测的有效性。临床上,与非 BCR/ABL1 样 ALL 相比,BCR/ABL1 样预测器鉴定的 BCR/ABL1 样病例的完全缓解率较低 (P=0.014),无事件生存较差 (P=0.0009)。一致地,BCR/ABL1 样病例的原代细胞在体外对 ponatinib 有反应。我们提出了一种基于 Q-RT-PCR 和统计模型的简单工具,能够在诊断时轻松、快速和可靠地识别 BCR/ABL1 样 ALL 病例。