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日本肺癌驱动基因突变化诊断检测的真实世界证据

Real-World Evidence of Diagnostic Testing for Driver Oncogene Mutations in Lung Cancer in Japan.

作者信息

Yatabe Yasushi, Yoshiki Yasumasa, Matsumura Koichi, Togo Kanae, Kikkawa Hironori, Iadeluca Laura, Li Benjamin, Nishio Kazuto

机构信息

Department of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.

Pfizer Japan, Inc., Tokyo, Japan.

出版信息

JTO Clin Res Rep. 2020 Dec 29;2(3):100136. doi: 10.1016/j.jtocrr.2020.100136. eCollection 2021 Mar.

Abstract

INTRODUCTION

Diagnostic testing is important in determining appropriate treatment for individuals with lung cancer. In 2018, testing of five biomarkers (, , , , programmed cell death-ligand 1 [PD-L1]) was approved in Japan. Information is lacking regarding real-world testing patterns.

METHODS

This descriptive, retrospective observational study used the Japan Medical Data Vision Co., Ltd. (MDV), database (June 2017-November 2018) and covered data for , , , and PD-L1; records on testing were not yet available. Adults diagnosed with having lung cancer (International Classification of Diseases-10 C34) with record of any biomarker test ordered were included.

RESULTS

Of 8323 patients with any biomarker test, 83.2% were tested for , 55.3% for , 32.2% , and 77.2% PD-L1. Combinations of with other biomarkers accounted for approximately 80% of the testing patterns; 1427 patients (17.1%) had combination testing ordered for ///PD-L1, but some biomarker combinations were tested in less than 1% of the cases. Median time from first testing order to treatment order was 22 (range: 2-525) days overall and increased with number of testing instances: 21 (2-509) days for patients with one, 28 (3-525) days for patients with two, and 30 (9-502) days for patients with three. A 7-day pattern of peaks was observed in the test order date and time to treatment.

CONCLUSIONS

This real-world evidence revealed variations in diagnostic testing patterns, which could affect time to treatment in Japan. Variations are likely influenced by individual biomarker prioritization considering limited tissue samples in clinical practice.

摘要

引言

诊断检测对于确定肺癌患者的合适治疗方法至关重要。2018年,五种生物标志物(、、、、程序性细胞死亡配体1[PD-L1])的检测在日本获得批准。目前缺乏关于实际检测模式的信息。

方法

这项描述性、回顾性观察性研究使用了日本医疗数据视觉有限公司(MDV)的数据库(2017年6月至2018年11月),涵盖了、、和PD-L1的数据;关于检测的记录尚不可用。纳入了被诊断患有肺癌(国际疾病分类-10 C34)且有任何生物标志物检测记录的成年人。

结果

在8323例进行了任何生物标志物检测的患者中,83.2%进行了检测,55.3%进行了检测,32.2%进行了检测,77.2%进行了PD-L1检测。与其他生物标志物的组合占检测模式的约80%;1427例患者(17.1%)进行了///PD-L1的联合检测,但某些生物标志物组合的检测病例不到1%。从首次检测医嘱到治疗医嘱的中位时间总体为22天(范围:2-525天),并随着检测次数的增加而增加:进行一次检测的患者为21天(2-509天),进行两次检测的患者为28天(3-525天),进行三次检测的患者为30天(9-502天)。在检测医嘱日期和治疗时间中观察到了7天的峰值模式。

结论

这一实际证据揭示了诊断检测模式的差异,这可能会影响日本的治疗时间。考虑到临床实践中组织样本有限,这些差异可能受到个体生物标志物优先级的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5dc/8474388/20436023ef9c/gr1.jpg

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