Biomarker testing for personalized, first-line therapy in advanced nonsquamous non-small cell lung cancer patients in the real world setting in Japan: a retrospective, multicenter, observational study (the BRAVE study)

Author:

Shimizu Junichi1,Masago Katsuhiro2ORCID,Saito Haruhiro3,Nishino Kazumi4,Kurata Takayasu5,Itoh Yohji6,Yoshimura Yoko7,Yabuki Yutaka7,Dosaka-Akita Hirotoshi8

Affiliation:

1. Department of Thoracic Oncology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya, Aichi 464-8681, Japan

2. Department of Pathology and Molecular Diagnosis, Aichi Cancer Center Hospital, Nagoya, Aichi, Japan

3. Department of Thoracic Oncology, Kanagawa Cancer Center, Asahi-ku, Yokohama, Japan

4. Department of Thoracic Oncology, Osaka International Cancer Institute, Chuo-ku, Osaka, Japan

5. Department of Thoracic Oncology, Kansai Medical University Hospital, Hirakata, Osaka, Japan

6. Statistics Group, AstraZeneca, Kita-ku, Osaka, Japan

7. Medical Department, AstraZeneca, Kita-ku, Osaka, Japan

8. Department of Medical Oncology, Faculty of Medicine & Graduate School of Medicine, Hokkaido University, Sapporo, Japan

Abstract

Background: Molecular diagnostic testing is necessary to guide optimal first-line treatment. The number of patients who receive first-line treatment based on biomarker analysis in Japan is unknown. We aimed to determine the proportion of nonsquamous non-small cell lung cancer (NSCLC) patients for whom first-line treatment was selected based on biomarker testing. Methods: This retrospective, multicenter, observational study registered patients aged ⩾20 years with locally advanced or metastatic nonsquamous NSCLC who started first-line treatment between August and December 2017 in Japan. Data were collected from medical records between January and May 2018. The primary endpoint was the proportion of patients with confirmed biomarker status for first-line treatment decision. Results: Among 202 patients enrolled from 11 centers, 161 (79.7%; 95% confidence interval, 74.2–85.2%) had confirmed biomarker status. The testing rate was highest for epidermal growth factor receptor ( EGFR; 97.5%), followed by anaplastic lymphoma kinase ( ALK; 88.1%), programmed death ligand-1 (PD-L1; 87.1%), and ROS1 (67.3%). For first-line treatment, 70/75 patients with EGFR-positive tumors were administered an EGFR-TKI; 14/15 patients with ALK-positive tumors received an ALK inhibitor; 2/2 patients with ROS1-positive tumors received a ROS1 inhibitor; and 29/36 driver mutation-negative patients with a PD-L1 tumor proportion score ⩾50% were administered an anti-PD-1 monoclonal antibody. Median times from confirmed diagnosis date to first-line treatment initiation, and from first biomarker test order to last biomarker test result were 19 and 11 days, respectively. Conclusions: The proportion of nonsquamous NSCLC patients with confirmed biomarker status for first-line treatment was considered insufficient and in need of improvement.

Funder

AstraZeneca

Publisher

SAGE Publications

Subject

Oncology

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