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Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
Published on: October 19, 2013
Implementation of "clinical sequencing" in cancer genome medicine in Japan
1Division of Genome Biology, National Cancer Center Research Institute, Tokyo, Japan.
Abstract:
In oncology, actionable mutations (alterations) in cancer-associated genes are critical in terms of the selection of therapeutic approaches. Next-generation sequencing of tumor sample DNA (ie, clinical sequencing) can guide clinical management by providing diagnostic or prognostic data, and facilitating the identification of potential treatment regimens, such as molecular-targeted and immune checkpoint blockade therapies. In the USA, a variety of tumor-profiling multiplex gene panels have been developed and implemented for this purpose. In Japan, several academic institutions have now carried out detailed investigations of the feasibility and value of clinical sequencing, and cancer societies have issued consensus clinical practice guidance for next-generation sequencing-based gene panel tests. These efforts will facilitate the implementation of cancer genome medicine in Japan.
Insights
Actionable mutations identified through next-generation sequencing (NGS) guide cancer treatment. Japan is implementing NGS-based gene panel tests and clinical practice guidelines to advance cancer genome medicine.
Area of Science:
- Oncology
- Genomics
- Clinical Diagnostics
Background:
- Actionable mutations in cancer-associated genes are crucial for selecting effective therapeutic strategies.
- Clinical sequencing using next-generation sequencing (NGS) of tumor DNA provides diagnostic and prognostic information.
- NGS facilitates the identification of targeted therapies and immune checkpoint blockade treatments.
Purpose of the Study:
- To assess the implementation and value of clinical sequencing in Japan.
- To align with international standards for molecular-guided cancer therapy.
- To facilitate the adoption of cancer genome medicine in Japan.
Main Methods:
- Review of investigations by Japanese academic institutions on clinical sequencing feasibility.
- Analysis of consensus clinical practice guidance issued by Japanese cancer societies for NGS-based gene panel tests.
- Comparison with established tumor-profiling multiplex gene panel practices in the USA.
Main Results:
- Detailed investigations into the feasibility and value of clinical sequencing have been conducted in Japan.
- Consensus clinical practice guidance for NGS-based gene panel tests has been established by Japanese cancer societies.
- These efforts indicate a strong move towards integrating cancer genome medicine into clinical practice in Japan.
Conclusions:
- Clinical sequencing and NGS-based gene panel tests are becoming integral to oncology in Japan.
- The development of guidelines and feasibility studies supports the advancement of cancer genome medicine.
- These initiatives will enhance personalized therapeutic approaches for cancer patients in Japan.
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