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非小细胞肺癌ROS1融合重排患者酪氨酸激酶抑制剂治疗的检测方法比较及随访研究

Comparison of detection methods and follow-up study on the tyrosine kinase inhibitors therapy in non-small cell lung cancer patients with ROS1 fusion rearrangement.

作者信息

Wu Jieyu, Lin Yunen, He Xinming, Yang Haihong, He Ping, Fu Xinge, Li Guangqiu, Gu Xia

机构信息

Department of Pathology, the First Affiliated Hospital of Guangzhou Medical University, No. 151, Yanjiangxi Road, Guangzhou, 510120, China.

Department of Cardiothoracic Surgery, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

出版信息

BMC Cancer. 2016 Aug 4;16:599. doi: 10.1186/s12885-016-2582-9.

Abstract

BACKGROUND

The screening of ROS proto-oncogene 1, receptor tyrosine kinase(ROS1) fusion rearrangement might be potentially beneficial for an effective therapy against non-small cell lung cancer (NSCLC). However, the three main ROS1 rearrangement detection methods have limitations, and no routine protocol for the detection of ROS1 rearrangement in NSCLC is available. In this study, our aims were to compare immunohistochemistry (IHC), fluorescent in situ hybridization (FISH) and quantitative real-time polymerase chain reaction (qRT-PCR) in their ability to detect ROS1 rearrangement in NSCLC, and discuss the clinical characteristics and histopathology of the patients with ROS1 rearrangement. Moreover, the effects of tyrosine kinase inhibitors (TKIs) therapy on the patients with ROS1 rearrangement and advanced stage disease (III b-IV) were investigated.

METHODS

Patients with a previously diagnosed NSCLC were recruited in this study from November 2013 to October 2015. IHC was performed using the D4D6 monoclonal antibody (mAb) in an automatic IHC instrument, while FISH and qRT-PCR were carried out to confirm the IHC results. FISH and qRT-PCR positive cases underwent direct sequencing. After detection, patients with advanced ROS1 rearranged NSCLC had received TKI therapy.

RESULTS

Two hundred and thirty-eight patients were included in this study. ROS1 rearrangement was detected in 10 patients. The concordant rate of FISH and qRT-PCR results was 100 %, while in the FISH and IHC results high congruence was present when IHC showed a diffusely (≥60 % tumor cells) 2-3+ cytoplasmic reactivity pattern. Patients harboring ROS1 rearrangement were mostly young (8/10), females (7/10) and non-smokers (7/10) with adenocarcinoma (10/10) and acinar pattern. Most of their tumor were in intermediate grade (6/8). Among these 10 patients, three of them in stage IV with ROS1 rearrangement gained benefits from ROS1 TKI therapy.

CONCLUSIONS

IHC, FISH and qRT-PCR can reliably detect ROS1 rearrangement in NSCLC, while IHC can be used as a preliminary screening tool. These results supported the efficacy of ROS1 TKI therapy in treating advanced NSCLC patients with ROS1 rearrangement.

摘要

背景

筛查ROS原癌基因1、受体酪氨酸激酶(ROS1)融合重排可能对非小细胞肺癌(NSCLC)的有效治疗具有潜在益处。然而,三种主要的ROS1重排检测方法都存在局限性,目前尚无检测NSCLC中ROS1重排的常规方案。在本研究中,我们的目的是比较免疫组织化学(IHC)、荧光原位杂交(FISH)和定量实时聚合酶链反应(qRT-PCR)检测NSCLC中ROS1重排的能力,并探讨ROS1重排患者的临床特征和组织病理学。此外,还研究了酪氨酸激酶抑制剂(TKIs)治疗对ROS1重排及晚期疾病(III b-IV期)患者的影响。

方法

2013年11月至2015年10月,本研究招募了先前诊断为NSCLC的患者。使用D4D6单克隆抗体(mAb)在自动免疫组织化学仪器上进行免疫组织化学检测,同时进行荧光原位杂交和定量实时聚合酶链反应以确认免疫组织化学结果。荧光原位杂交和定量实时聚合酶链反应阳性的病例进行直接测序。检测后,晚期ROS1重排的NSCLC患者接受了酪氨酸激酶抑制剂治疗。

结果

本研究共纳入238例患者。10例患者检测到ROS1重排。荧光原位杂交和定量实时聚合酶链反应结果的一致率为100%,而当免疫组织化学显示弥漫性(≥60%肿瘤细胞)2-3+细胞质反应模式时,荧光原位杂交和免疫组织化学结果高度一致。携带ROS1重排的患者大多为年轻人(8/10)、女性(7/10)且不吸烟(7/10),病理类型为腺癌(10/10)且呈腺泡状。他们的大多数肿瘤为中级(6/8)。在这10例患者中,3例IV期ROS1重排患者从ROS1酪氨酸激酶抑制剂治疗中获益。

结论

免疫组织化学、荧光原位杂交和定量实时聚合酶链反应可可靠地检测NSCLC中的ROS1重排,免疫组织化学可作为初步筛查工具。这些结果支持了ROS1酪氨酸激酶抑制剂治疗晚期ROS1重排NSCLC患者的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa5d/4973062/5a38725fd0be/12885_2016_2582_Fig1_HTML.jpg

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