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Assessment of IgH PCR strategies in multiple myeloma.

机译:多发性骨髓瘤中IgH PCR策略的评估。

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AIMS: To compare the ability of four commonly used PCR techniques to demonstrate clonal IgH rearrangements in multiple myeloma. METHODS: Bone marrow samples (containing a minimum of 10% plasma cells) were obtained from 127 patients with confirmed multiple myeloma. Framework 3 (Fr3) PCR was performed in all cases and the Framework 1 (Fr1f) PCR, which utilises six VH family specific primers, in 98 cases. In addition, 44 cases were assessed by Fr3, Fr1f, Framework 2 (Fr2) and Framework 1 consensus (Fr1 con) PCR techniques. JH primer selection was also assessed such that each PCR strategy was performed twice in each of the 44 cases, using the JH consensus primer (JH con) alone and then repeated with an equimolar mixture of JH con, JH3 and JH6 (JH mix). RESULTS: Clonal rearrangements were demonstrated in 71 (56%) of 127 cases with the Fr3 PCR and in 52 (53%) of 98 with the Fr1f PCR. However, by using both techniques it was possible to demonstrate clonal IgH rearrangements in 92 (75%) of 122 cases. Forty four cases were assessed by all four PCR techniques; in these cases the Fr3 and Fr1f PCRs demonstrated clonal rearrangements in 26 (59%) cases with a combined yield of 34 (77%). The Fr2 and Fr1 con PCR techniques had inferior pick up rates, demonstrating clonal rearrangements in 21 (48%) of 44 cases and a combined yield of 28 (63%). The Fr2 PCR did, however, demonstrate a clonal rearrangement in one case negative by both Fr3 and Fr1f. Two additional rearrangements were demonstrated by using JH mix; one became positive by Fr3, Fr1f and Fr2 and the other positive by Fr1f, Fr1 con and Fr2. CONCLUSIONS: By utilising both the Fr3 and Fr1f PCR techniques it is possible to demonstrate definitive clonal rearrangements in the majority of patients with multiple myeloma. The Fr1 con and Fr2 PCR techniques have inferior pick up rates but may detect some additional rearrangements.
机译:目的:比较四种常用PCR技术证明多发性骨髓瘤中克隆IgH重排的能力。方法:从127例确诊的多发性骨髓瘤患者中获取骨髓样本(至少含有10%的浆细胞)。在所有情况下均进行框架3(Fr3)PCR,在98例中使用6个VH家族特异性引物的框架1(Fr1f)PCR。此外,通过Fr3,Fr1f,框架2(Fr2)和框架1共有(Fr1 con)PCR技术评估了44例病例。还评估了JH引物的选择,以使得在44例中的每种情况下,均单独使用JH共有引物(JH con)对每种PCR策略进行两次,然后用JH con,JH3和JH6等摩尔混合物(JH mix)重复进行。结果:127例Fr3 PCR证实了克隆重排(56%),98例Fr1f PCR证实了52(53%)克隆重排。但是,通过使用这两种技术,有可能在122例病例中的92例(75%)中证实克隆IgH重排。通过全部四种PCR技术评估了44例病例。在这些情况下,Fr3和Fr1f PCR在26(59%)个病例中显示出克隆重排,总产量为34(77%)。 Fr2和Fr1 con PCR技术的回收率较差,在44例病例中有21例(48%)发生了克隆重排,而联合收率为28例(63%)。但是,Fr2 PCR确实显示了在Fr3和Fr1f均为阴性的情况下克隆重排。使用JH mix演示了另外两个重排;一个由Fr3,Fr1f和Fr2变为正,另一个由Fr1f,Fr1 con和Fr2变为正。结论:通过同时使用Fr3和Fr1f PCR技术,可以在大多数多发性骨髓瘤患者中证明确切的克隆重排。 Fr1 con和Fr2 PCR技术的提取率较低,但可能检测到一些其他的重排。

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