Department of Molecular Biotechnologies and Health Sciences - Hematology Division, University of Torino, Torino, Italy.
Department of Computer Sciences, University of Torino, Torino, Italy.
Br J Haematol. 2021 Jul;194(2):378-381. doi: 10.1111/bjh.17519. Epub 2021 May 18.
Minimal residual disease (MRD) determined by classic polymerase chain reaction (PCR) methods is a powerful outcome predictor in mantle cell lymphoma (MCL). Nevertheless, some technical pitfalls can reduce the rate of of molecular markers. Therefore, we applied the EuroClonality-NGS IGH (next-generation sequencing immunoglobulin heavy chain) method (previously published in acute lymphoblastic leukaemia) to 20 MCL patients enrolled in an Italian phase III trial sponsored by Fondazione Italiana Linfomi. Results from this preliminary investigation show that EuroClonality-NGS IGH method is feasible in the MCL context, detecting a molecular IGH target in 19/20 investigated cases, allowing MRD monitoring also in those patients lacking a molecular marker for classical screening approaches.
通过经典聚合酶链反应 (PCR) 方法确定的微小残留病 (MRD) 是套细胞淋巴瘤 (MCL) 的有力预后预测指标。然而,一些技术缺陷会降低分子标志物的检出率。因此,我们将 EuroClonality-NGS IGH(下一代测序免疫球蛋白重链)方法(先前在急性淋巴细胞白血病中发表)应用于 20 名参加意大利三期临床试验的 MCL 患者,该试验由意大利淋巴瘤基金会赞助。这项初步研究的结果表明,EuroClonality-NGS IGH 方法在 MCL 环境中是可行的,在 20 例研究病例中的 19 例中检测到分子 IGH 靶标,允许对那些缺乏经典筛选方法分子标志物的患者进行 MRD 监测。