De Paolis Elisa, Perrucci Alessia, Marchetti Claudia, Pietragalla Antonella, Scambia Giovanni, Urbani Andrea, Fagotti Anna, Minucci Angelo
Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Departmental Unit of Molecular and Genomic Diagnostics, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Int J Gynecol Cancer. 2022 Nov 7;32(11):1419-1426. doi: 10.1136/ijgc-2022-003718.
) genetic testing allows patients with high-grade serous ovarian cancer to receive appropriate medical management with molecular target therapy and prevention strategies. Most of the sequencing methods use blood as the primary source of germline DNA. Buccal swab emerged as an alternative collection device due to its convenient and non-invasive characteristics. This study assessed the suitability of buccal swabs as the DNA source in next-generation sequencing-based genotyping.
Matched buccal swabs and blood samples were collected from 51 patients with high-grade serous ovarian cancer, including 29 -mutated patients, from June to December 2021. Buccal swabs were self-collected using COPAN FLOQSwabs hDNA Free. genes were amplified using Devyser's next-generation sequencing kit and sequenced on the Illumina MiSeq platform. We evaluated collection and extraction procedures, amplification and sequencing performances, coverage data, blood/swab variant calling concordance, and interpretation.
Comparable sequencing parameters were observed between the two sample types in term of mean total number of reads passing filter for indexed sample (p>0.05) and sequencing coverage distribution, with a widespread overlap of mean depth of coverage/target region between blood and swab samples. An overall concordance of 100% in both polymorphisms and pathogenic variants calling between the two DNA sources were observed, including the copy number variation prediction.
Data from this study support the use of buccal swabs as an alternative source of DNA for evaluation. The use of this alternative delivery mode of testing may facilitate access to care without compromising patient outcomes.
基因检测可使高级别浆液性卵巢癌患者接受分子靶向治疗和预防策略的适当医疗管理。大多数测序方法以血液作为种系DNA的主要来源。由于其方便且无创的特点,口腔拭子成为一种替代采集工具。本研究评估了口腔拭子作为基于二代测序的基因分型中DNA来源的适用性。
2021年6月至12月,从51例高级别浆液性卵巢癌患者中采集匹配的口腔拭子和血液样本,其中包括29例有突变的患者。口腔拭子使用COPAN FLOQSwabs hDNA Free自行采集。使用Devyser的二代测序试剂盒扩增基因,并在Illumina MiSeq平台上进行测序。我们评估了采集和提取程序、扩增和测序性能、覆盖数据、血液/拭子变异位点检测一致性以及解读情况。
在索引样本通过过滤的平均总读数数量(p>0.05)和测序覆盖分布方面,观察到两种样本类型之间的测序参数具有可比性,血液和拭子样本之间平均覆盖深度/目标区域存在广泛重叠。在两种DNA来源的多态性和致病变异位点检测中,包括拷贝数变异预测,总体一致性均为100%。
本研究数据支持使用口腔拭子作为评估的DNA替代来源。使用这种替代的检测样本递送方式可能有助于患者获得医疗服务,而不会影响患者的治疗结果。