Zheng Yu, Sun Yifeng, Kuai Yue, Fu Guoxiang, An Huimin, Chen Jinyun, Chen Jinying, Zhu Jiajun, Wo Yixin, Wu Yiwang, Song Kaibin, Xu Qinghua, Wu Di, Huang Deshuang, Wang Qifeng, Pan Hongming
Department of Medical Oncology, Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, East Qinchun Road 3, Hangzhou, 310016, Zhejiang, China.
Canhelp Genomics Research Center, Xinyan Road 22, Hangzhou, 311100, Zhejiang, China.
Cancer Cell Int. 2021 Jan 12;21(1):47. doi: 10.1186/s12935-021-01748-8.
The incidence of multiple primary malignant tumors (MPMTs) is rising due to the development of screening technologies, significant treatment advances and increased aging of the population. For patients with a prior cancer history, identifying the tumor origin of the second malignant lesion has important prognostic and therapeutic implications and still represents a difficult problem in clinical practice.
In this study, we evaluated the performance of a 90-gene expression assay and explored its potential diagnostic utility for MPMTs across a broad spectrum of tumor types. Thirty-five MPMT patients from Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University and Fudan University Shanghai Cancer Center were enrolled; 73 MPMT specimens met all quality control criteria and were analyzed by the 90-gene expression assay.
For each clinical specimen, the tumor type predicted by the 90-gene expression assay was compared with its pathological diagnosis, with an overall accuracy of 93.2% (68 of 73, 95% confidence interval 0.84-0.97). For histopathological subgroup analysis, the 90-gene expression assay achieved an overall accuracy of 95.0% (38 of 40; 95% CI 0.82-0.99) for well-moderately differentiated tumors and 92.0% (23 of 25; 95% CI 0.82-0.99) for poorly or undifferentiated tumors, with no statistically significant difference (p-value > 0.5). For squamous cell carcinoma specimens, the overall accuracy of gene expression assay also reached 87.5% (7 of 8; 95% CI 0.47-0.99) for identifying the tumor origins.
The 90-gene expression assay provides flexibility and accuracy in identifying the tumor origin of MPMTs. Future incorporation of the 90-gene expression assay in pathological diagnosis will assist oncologists in applying precise treatments, leading to improved care and outcomes for MPMT patients.
由于筛查技术的发展、显著的治疗进展以及人口老龄化加剧,多原发性恶性肿瘤(MPMTs)的发病率正在上升。对于有既往癌症病史的患者,确定第二个恶性病变的肿瘤起源具有重要的预后和治疗意义,并且在临床实践中仍然是一个难题。
在本研究中,我们评估了一种90基因表达检测方法的性能,并探讨了其在广泛肿瘤类型中对MPMTs的潜在诊断效用。招募了来自浙江大学医学院附属邵逸夫医院和复旦大学附属肿瘤医院的35例MPMT患者;73例MPMT标本符合所有质量控制标准,并通过90基因表达检测进行分析。
对于每个临床标本,将90基因表达检测预测的肿瘤类型与其病理诊断进行比较,总体准确率为93.2%(73例中的68例,95%置信区间0.84 - 0.97)。对于组织病理学亚组分析,90基因表达检测对于高-中分化肿瘤的总体准确率为95.0%(40例中的38例;95% CI 0.82 - 0.99),对于低分化或未分化肿瘤的总体准确率为92.0%(25例中的23例;95% CI 0.82 - 0.99),无统计学显著差异(p值>0.5)。对于鳞状细胞癌标本,基因表达检测在识别肿瘤起源方面的总体准确率也达到了87.5%(8例中的7例;95% CI 0.47 - 0.99)。
90基因表达检测在识别MPMTs的肿瘤起源方面提供了灵活性和准确性。未来将90基因表达检测纳入病理诊断将有助于肿瘤学家应用精准治疗,从而改善MPMT患者的护理和预后。