OPTIMIZATION OF MOLECULAR GENETIC DIAGNOSTICS OF PATIENTS WITH ADVANCED NON-SMALL CELL LUNG CANCER BY INTRODUCING ROS1 TESTING IN THE REPUBLIC OF KAZAKHSTAN

O. Shatkovskaya, D. Kaidarova, M. Orazgaliyeva, E. Satbayeva, S. Ossikbayeva, A. Koishibaeva
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Abstract

Relevance: Currently, molecular diagnosis in NSCLC in Kazakhstan includes detection of EGFR, ALK driver mutations status, and PD-L1-status, but not ROS1, what limits the access of patients with this driver mutation to vital therapy. The study aimed to optimize the methods of molecular genetic diagnosis of patients with NSCLC by introducing ROS1 testing in the Republic of Kazakhstan. Methods: The biopsy and surgical material of non-small cell lung cancer (NSCLC) fixed in 10% buffered formalin was studied. After the initial morphological diagnosis of adenocarcinoma, EGFR, and ALK mutation status determination, EGFR, and ALK-negative tumor assays were sent for further determination of ROS1 mutation status. First, we performed immunohistochemistry (IHC) using the Ventana BenchMark Ultra platform using the ROS1 antibody (SP283) and the OptiView DAB Detection Kit imaging system. After that, samples with positive and doubtful IHC results were sent for RT-PCR (reverse transcriptase polymerase chain reaction) to confirm the ROS1 mutation status. Results: A total of 99 tumor samples from patients with EGFR-negative and ALK-negative lung adenocarcinoma were studied by IHC from January 01 till September 30, 2022. The results of IHC staining were assessed as: 0 (negative) – 59 samples, 1+ (negative) – 25 samples, 2+ (doubtful) – 12 samples, 3+ (positive) – 3 samples. Cases with ≥70% immunostaining were considered positive. Samples with an IHC stain score of 2+ (doubtful), 3+ (positive), and a few samples of 1+ were sent for confirmation by PCR. Overall, 22 samples were tested using RT-PCR, and results were considered as follows:1 (4%) – positive, 13 (59%) – negative, 8 (37%) -– invalid. Conclusion: A large proportion of positive and questionable results were obtained when determining ROS1 mutation status using IHC, and a large proportion of invalid results during subsequent RT-PCR testing. Choosing methods for nationwide ROS1 implementation, one should evaluate the economics of the methods to be implemented and compare them with a standard validated FISH method.
通过在哈萨克斯坦共和国引入ros1检测来优化晚期非小细胞肺癌患者的分子遗传学诊断
相关性:目前,哈萨克斯坦NSCLC的分子诊断包括检测EGFR、ALK驱动突变状态和pd - l1状态,但不包括ROS1,这限制了该驱动突变患者获得重要治疗的机会。本研究旨在通过在哈萨克斯坦共和国引入ROS1检测,优化NSCLC患者的分子遗传学诊断方法。方法:对非小细胞肺癌(NSCLC) 10%缓冲福尔马林固定活检及手术材料进行研究。在腺癌的初步形态学诊断、EGFR和ALK突变状态测定后,进行EGFR和ALK阴性肿瘤检测,进一步测定ROS1突变状态。首先,我们使用Ventana BenchMark Ultra平台使用ROS1抗体(SP283)和OptiView DAB Detection Kit成像系统进行免疫组织化学(IHC)。之后,将IHC结果呈阳性和可疑的样本进行RT-PCR(逆转录酶聚合酶链反应),以确认ROS1突变状态。结果:于2022年1月1日至9月30日对egfr阴性和alk阴性肺腺癌患者共99例肿瘤样本进行免疫组化研究。免疫组化染色结果评估为:0(阴性)- 59例,1+(阴性)- 25例,2+(可疑)- 12例,3+(阳性)- 3例。免疫染色≥70%的病例为阳性。IHC染色评分为2+(可疑)、3+(阳性)和少量1+的样本送PCR确认。总体而言,使用RT-PCR检测了22个样本,结果如下:1个(4%)阳性,13个(59%)阴性,8个(37%)无效。结论:利用免疫组化检测ROS1突变状态时,获得的阳性和可疑结果占很大比例,后续RT-PCR检测中无效结果占很大比例。选择在全国范围内实施ROS1的方法时,应该评估要实施的方法的经济性,并将其与经过标准验证的FISH方法进行比较。
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