Pennell Nancy, Woods Anthony, Reis Marciano, Buckstein Rena, Spaner David, Imrie Kevin, Hewitt Karen, Boudreau Angela, Seth Arun, Berinstein Neil L
Advanced Therapeutics Program, Toronto-Sunnybrook Regional Cancer Centre, Sunnybrook and Women's College Health Sciences Centre, 2075 Bayview Ave., Toronto, ON Canada M4N 3M5.
J Mol Diagn. 2006 Feb;8(1):40-50. doi: 10.2353/jmoldx.2006.050050.
Molecular remission in the autograft and bone marrow after transplant are predictive of durable clinical remission in relapsed follicular lymphoma. Thus, a simple reliable method to quantify minimal residual disease (MRD) would improve prognostication in these patients. Fluorescent hybridization probes have been used in real-time quantitative polymerase chain reaction (RQ-PCR) to monitor MRD with a reproducible sensitivity of 0.01%; however, these techniques are expensive and require additional experiments to examine clonality. We describe a SYBR Green I detection method that is more universal, checks clonal identity, yields the same sensitivity for monitoring MRD, and is more economically attractive. Using this method to follow 14 follicular lymphoma patients treated with autologous stem cell transplantation, molecular markers were successfully defined for 12 patients. Median contamination of stem-cell grafts was 0.1% (range, 0 to 13%). Six patients with measurable graft contamination became PCR-negative in blood and bone marrow within 12 months after autologous stem cell transplantation. Three patients free of disease progression (median follow-up of 75 months) are in molecular remission. Increasing fractions of RQ-PCR-positive blood and bone marrow cells reliably predicted morphological and clinical relapse. In one case, both clinical relapse and spontaneous regression were reflected by changes in MRD levels. Thus, our RQ-PCR method reproducibly distinguishes different levels of MRD.
自体移植及移植后骨髓中的分子缓解可预测复发性滤泡性淋巴瘤的持久临床缓解。因此,一种简单可靠的微小残留病(MRD)定量方法将改善这些患者的预后。荧光杂交探针已用于实时定量聚合酶链反应(RQ-PCR)来监测MRD,其可重复性灵敏度为0.01%;然而,这些技术昂贵且需要额外实验来检测克隆性。我们描述了一种SYBR Green I检测方法,该方法更通用,可检查克隆身份,监测MRD时灵敏度相同,且在经济上更具吸引力。使用该方法对14例接受自体干细胞移植治疗的滤泡性淋巴瘤患者进行随访,成功为12例患者确定了分子标志物。干细胞移植物的中位污染率为0.1%(范围为0至13%)。6例有可测量移植物污染的患者在自体干细胞移植后12个月内血液和骨髓中的PCR检测转为阴性。3例无疾病进展(中位随访75个月)的患者处于分子缓解状态。RQ-PCR阳性的血液和骨髓细胞比例增加可可靠地预测形态学和临床复发。在1例患者中,临床复发和自发缓解均由MRD水平的变化反映。因此,我们的RQ-PCR方法可重复性地区分不同水平的MRD。