Paganin M, Zecca M, Fabbri G, Polato K, Biondi A, Rizzari C, Locatelli F, Basso G
Laboratorio di Ematologia e Oncologia Pediatrica, Università di Padova, Padova, Italy.
Leukemia. 2008 Dec;22(12):2193-200. doi: 10.1038/leu.2008.227. Epub 2008 Aug 28.
The aim of the study was to analyze the impact of minimal residual disease (MRD) after reinduction therapy on the outcome of children with relapsed 'high-risk' acute lymphoblastic leukemia (ALL). Sixty patients with isolated or combined marrow relapse were studied. All patients belonged to the S3 or S4 groups, as defined by the Berlin-Frankfurt-Münster stratification for relapsed ALL. MRD was studied by real-time quantitative PCR after the first, second and third chemotherapy course (time points 1 (TP1), 2 (TP2) and 3 (TP3), respectively). MRD results, not used for treatment refinement, were categorized as negative (NEG MRD), positive not-quantifiable (POS-NQ MRD) when MRD level was below quantitative range (a level <10(-4)) or positive within quantitative range (POS MRD) when MRD level was >or=10(-4). With a median observation time of 15 months, overall 3-year event-free survival (EFS) was 27%. The 3-year EFS was 73, 45 and 19% for patients with NEG-MRD, POS NQ-MRD and POS-MRD at TP1, respectively (P<0.05). The prognostic predictive value of MRD was statistically confirmed in multivariate analysis. MRD quantitation early and efficiently differentiates patients who benefit from conventional treatment, including allogeneic hematopoietic stem cell transplantation, from those needing innovative, experimental therapies.
本研究旨在分析再诱导治疗后微小残留病(MRD)对复发的“高危”急性淋巴细胞白血病(ALL)患儿预后的影响。对60例孤立性或合并性骨髓复发的患者进行了研究。所有患者均属于复发ALL的柏林-法兰克福-明斯特分层定义的S3或S4组。在第一个、第二个和第三个化疗疗程后(分别为时间点1(TP1)、2(TP2)和3(TP3)),通过实时定量PCR研究MRD。MRD结果未用于治疗调整,当MRD水平低于定量范围(水平<10^(-4))时分类为阴性(NEG MRD),当MRD水平低于定量范围(水平<10^(-4))时分类为阳性不可量化(POS-NQ MRD),当MRD水平≥10^(-4)时分类为定量范围内阳性(POS MRD)。中位观察时间为15个月,总体3年无事件生存率(EFS)为27%。TP1时NEG-MRD、POS NQ-MRD和POS-MRD患者的3年EFS分别为73%、45%和19%(P<0.05)。MRD的预后预测价值在多变量分析中得到统计学证实。MRD定量可早期且有效地将从包括异基因造血干细胞移植在内的传统治疗中获益的患者与需要创新、实验性治疗的患者区分开来。