Normanno Nicola, Pinto Carmine, Castiglione Francesca, Fenizia Francesca, Barberis Massimo, Marchetti Antonio, Fontanini Gabriella, De Rosa Gaetano, Taddei Gian Luigi
Cell Biology and Biotherapy Unit, Istituto Nazionale per lo Studio e la Cura dei Tumori "Fondazione Giovanni Pascale"-IRCCS, Via M. Semmola, 80131, Naples, Italy.
Laboratory of Pharmacogenomics, Centro di Ricerche Oncologiche di Mercogliano (CROM), Istituto Nazionale Tumori "Fondazione Giovanni Pascale" IRCCS, Naples, Italy.
J Transl Med. 2015 Sep 3;13:287. doi: 10.1186/s12967-015-0655-1.
In 2014 the European Medicines Agency included exon 2, 3 and 4 KRAS and NRAS testing for the selection of metastatic colorectal cancer (mCRC) patients eligible for the therapy with anti-EGFR monoclonal antibodies. The Italian Association of Medical Oncology (AIOM) and the Italian Society of Pathology and Cytology (SIAPEC) organized an external quality assessment (EQA) scheme for CRC to evaluate inter-laboratory consistency and to ensure standardization of the results in the transition from KRAS to all-RAS testing.
Ten formalin fixed paraffin embedded specimens including KRAS/NRAS (exons 2, 3, 4) and BRAF (codon 600) mutations were validated by three referral laboratories and sent to 88 participant centers. Molecular pathology sample reports were also requested to each laboratory. A board of assessors from AIOM and SIAPEC evaluated the results according to a predefined scoring system. The scheme was composed of two rounds.
In the first round 36% of the 88 participants failed, with 23 centers having at least one false positive or false negative while 9 centers did not meet the deadline. The genotyping error rate was higher when Sanger sequencing was employed for testing as compared with pyrosequencing (3 vs 1.3%; p = 0.01; Pearson Chi Square test). In the second round, the laboratories improved their performance, with 23/32 laboratories passing the round. Overall, 79/88 participants passed the RAS EQA scheme. Standardized Human Genome Variation Society nomenclature was incorrectly used to describe the mutations identified and relevant variations were noticed in the genotype specification.
The results of the Italian RAS EQA scheme indicate that the mutational analyses are performed with good quality in many Italian centers, although significant differences in the methods used were highlighted. The relatively high number of centers failing the first round underlines the fundamental role in continued education covered by EQA schemes.
2014年,欧洲药品管理局将KRAS和NRAS基因外显子2、3和4检测纳入其中,用于筛选适合接受抗表皮生长因子受体(EGFR)单克隆抗体治疗的转移性结直肠癌(mCRC)患者。意大利医学肿瘤学会(AIOM)和意大利病理与细胞学会(SIAPEC)组织了一项针对结直肠癌的外部质量评估(EQA)计划,以评估实验室间的一致性,并确保在从KRAS检测过渡到全RAS检测过程中结果的标准化。
十个经福尔马林固定石蜡包埋的标本,包括KRAS/NRAS(外显子2、3、4)和BRAF(密码子600)突变,经三个参比实验室验证后,发送至88个参与中心。同时要求每个实验室提交分子病理学样本报告。由AIOM和SIAPEC的评估委员会根据预定义的评分系统对结果进行评估。该计划由两轮组成。
在第一轮中,88名参与者中有36%未通过,23个中心至少有一个假阳性或假阴性结果,9个中心未在截止日期前完成。与焦磷酸测序相比,采用桑格测序法进行检测时基因分型错误率更高(3%对1.3%;p = 0.01;Pearson卡方检验)。在第二轮中,各实验室改进了表现,32个实验室中有23个通过了本轮。总体而言,88名参与者中有79名通过了RAS EQA计划。在描述所识别的突变时,错误地使用了标准化的人类基因组变异协会命名法,并且在基因型规范中发现了相关差异。
意大利RAS EQA计划的结果表明,许多意大利中心的突变分析质量良好,尽管所使用的方法存在显著差异。第一轮中未通过的中心数量相对较多,凸显了EQA计划在继续教育中所起的重要作用。