慢性淋巴细胞白血病(CLL)血液和骨髓细胞荧光原位杂交研究标准化

Stephanie A. Smoley , Daniel L. Van Dyke , Neil E. Kay , Nyla A. Heerema , Marie L. Dell’ Aquila , Paola Dal Cin , Prasad Koduru , Ayala Aviram , Laura Rassenti , John C. Byrd , Kanti R. Rai , Jennifer R. Brown , Andrew W. Greaves , Jeanette Eckel-Passow , Donna Neuberg , Thomas J. Kipps , Gordon W. Dewald
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引用次数: 26

摘要

慢性淋巴细胞白血病(CLL)研究联盟(CRC)的五个实验室研究了荧光原位杂交(FISH)结果的标准化和池化作为一个合作研究项目。这项研究使用了固定的骨髓和血细胞,这些细胞可从以前的传统细胞遗传学或FISH研究中获得,在两个试点研究中,为期一天的研讨会和熟练程度测试。多种FISH探针策略用于检测6q-、11q-、+12、13q-、17p-和IGH重排。参与者使用自己的探针研究了10个标本(初步研究1)。在312个FISH解释中,224个(72%)为真阴性,74个(24%)为真阳性,6个(2%)为假阴性,8个(3%)为假阳性。在试点研究中。2、每个参与者使用相同的FISH探针集研究两个标本,以控制探针集和探针策略引起的变化。在80个FISH解释中,没有发现错误的解释。在随后的研讨会上,讨论就评分标准达成了一致。随后的水平测试没有出现假阴性结果,有4%(3/68)的假阳性解释。实验室之间的解释分歧主要是由于正常截止值不足、评分标准不一致以及使用不同的FISH探针策略。使用聚合FISH结果的协作组织可能希望施加更保守的经验正常截止值,或者在正常截止值和异常参考范围之间使用一个模棱两可的范围,以消除假阳性解释。假阴性结果仍然会出现,并且在低百分比阳性病例中是预料之中的;这些结果的临床意义可能不如假阳性结果。个别实验室可以通过严格遵循严格的质量保证指南来提供帮助,以确保在其临床实践和研究中准确和一致的FISH研究。
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Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium

Five laboratories in the Chronic Lymphocytic Leukemia (CLL) Research Consortium (CRC) investigated standardizing and pooling of fluorescence in situ hybridization (FISH) results as a collaborative research project. This investigation used fixed bone marrow and blood cells available from previous conventional cytogenetic or FISH studies in two pilot studies, a one-day workshop, and proficiency test. Multiple FISH probe strategies were used to detect 6q-, 11q-, +12, 13q-, 17p-, and IGH rearrangements. Ten specimens were studied by participants who used their own probes (pilot study 1). Of 312 FISH interpretations, 224 (72%) were true-negative, 74 (24%) true-positive, 6 (2%) false-negative, and 8 (3%) false-positive. In pilot study no. 2, each participant studied two specimens using identical FISH probe sets to control for variation due to probe sets and probe strategies. Of 80 FISH interpretations, no false interpretations were identified. At a subsequent workshop, discussions produced agreement on scoring criteria. The proficiency test that followed produced no false-negative results and 4% (3/68) false-positive interpretations. Interpretation disagreements among laboratories were primarily attributable to inadequate normal cutoffs, inconsistent scoring criteria, and the use of different FISH probe strategies. Collaborative organizations that use pooled FISH results may wish to impose more conservative empiric normal cutoff values or use an equivocal range between the normal cutoff and the abnormal reference range to eliminate false-positive interpretations. False-negative results will still occur, and would be expected in low-percentage positive cases; these would likely have less clinical significance than false positive results. Individual laboratories can help by closely following rigorous quality assurance guidelines to ensure accurate and consistent FISH studies in their clinical practice and research.

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