The initial assessment of expert panel performance in core hospitals for cancer genomic medicine in Japan
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Updated: Nov 23, 2025

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
Published on: October 11, 2018
Kuniko Sunami1, Yoichi Naito2, Eriko Aimono3
1Department of Laboratory Medicine, National Cancer Center Hospital, Tokyo, Japan.
Insights
Cancer genomic profiling (CGP) in Japan shows low treatment matching rates but highlights the need for standardized expert panels (EPs) to improve precision oncology implementation and genetic counseling referrals.
Area of Science:
- Oncology
- Genomics
- Healthcare Policy
Background:
- Japan's National Health Insurance covers cancer genomic profiling (CGP) since June 2019.
- Implementation is restricted to designated hospitals with molecular tumor boards (expert panels, EPs).
- Standardizing EPs is crucial for advancing precision oncology.
Purpose of the Study:
- To evaluate the real-world application of CGP in Japan.
- To assess treatment matching and genetic counseling referrals post-CGP.
- To analyze the efficiency and standardization of expert panels.
Main Methods:
- Collected data from 747 consecutive CGP cases across 11 hospitals (June 2019-Jan 2020).
- Assessed genomically matched treatments, including investigational new drugs (INDs), and genetic counseling recommendations.
- Evaluated simulated cases annotated by multiple EPs.
Main Results:
- 3.7% of cases received genomically matched treatment; 2.3% were referred for genetic counseling.
- EP discussions focused on treatment applicability and genetic counseling needs.
- EP annotation variability, especially for IND trials, was observed, potentially impacting trial enrollment.
Conclusions:
- CGP application in Japan provides valuable reference data for precision oncology.
- Further research is needed to standardize clinical annotations by EPs.
- Optimizing EP function is key to maximizing the benefits of CGP.
Background:
Since June 2019, cancer genomic profiling (CGP) tests have been reimbursed by the National Health Insurance system in Japan, with restrictions for government-designated hospitals with a molecular tumor board composed of multidisciplinary specialists, known as an expert panel (EP). The standardization of EPs is a critical challenge for implementing precision oncology in the clinical setting.
Methods:
Data on consecutive cases who underwent the CGP tests at 11 core hospitals between June 2019 and January 2020 were collected. We evaluated the proportions of cases that received genomically matched treatments, including investigational new drugs (INDs) based on CGP results, and/or for which genetic counseling was recommended. Two simulated cases were annotated by each EP. The annotated reports were then centrally assessed.
Results:
Each EP mainly discussed the applicability to genomically matched treatments and the necessity of performing genetic counseling. A pre-review of the report by key members in each EP reportedly made the EP conference more interactive and efficient, and thereby saved time. A total of 747 cases underwent CGP tests, 28 cases (3.7%) received genomically matched treatment, and 17 cases (2.3%) were referred for genetic counseling. Annotated reports for the simulated cases varied across the EPs, particularly the number of recommended IND trials, which seemed to be associated with the actual number of participants in IND trials.
Conclusions:
This investigation provides reference data for the application of precision oncology in a clinical setting. Further investigations on the standardization of clinical annotations are warranted.
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