High clinical actionability of a pan-cancer tissue-based combined DNA and RNA next generation sequencing assay in a diverse Asian population

Advancements in next-generation sequencing have facilitated tumour-agnostic approaches for cancer therapy. Here, we demonstrate the clinical utility of molecularly guided tumour-agnostic precision medicine in an Asian cohort, leveraging an Asian-centric DNA/RNA comprehensive genomic profiling (CGP) panel. A total of 1166 tissue samples encompassing 29 cancer types underwent real-world CGP testing. Actionable biomarkers were identified in 62.3% of samples, including 1291 (4.7%) somatic variants potentially targetable by regulatory-approved therapies. At least one tumour-agnostic biomarker, including high tumour mutation burden (TMB-high), microsatellite instability (MSI-high), NTRK/RET fusions, and BRAF V600E was identified in 98 samples across 26 cancer types (8.4%). ERBB2 amplification was identified in 42 samples (3.6%) and was most frequently detected in breast (15.0%), followed by endometrial (11.8%) and ovarian tumours (8.9%). Homologous recombination deficiency (HRD) was observed in 407 samples (34.9%). The high prevalence of actionable biomarkers underscores the significance of CGP in facilitating precision medicine in an Asian setting.

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Publication Details

Journal
npj Precision Oncology
Published
2025-11-13
DOI
https://doi.org/10.1038/s41698-025-01126-x
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

High clinical actionability of a pan-cancer tissue-based combined DNA and RNA next generation sequencing assay in a diverse Asian population

Zi Yi Wan, Su Pin Choo, Ross Andrew Soo, Joseph S. K. Au et al.
npj Precision Oncology
Cancer Genomics and Diagnostics
article

High clinical actionability of a pan-cancer tissue-based combined DNA and RNA next generation sequencing assay in a diverse Asian population

Zi Yi Wan, Su Pin Choo, Ross Andrew Soo, Joseph S. K. Au, Ravindran Kanesvaran, Bin Tean Teh, Jens Samol, Ruifen Weng, Aya El Helali, Daniel S.W. Tan, Jonathan Poh, Cheng-Vai Hui, Jing Yi Lee, Jason Yongsheng Chan, Timothy T. C. Yip, Min-Han Tan, Michelle Pek, Donald Poon, Tsz Him So
article en

Abstract

Advancements in next-generation sequencing have facilitated tumour-agnostic approaches for cancer therapy. Here, we demonstrate the clinical utility of molecularly guided tumour-agnostic precision medicine in an Asian cohort, leveraging an Asian-centric DNA/RNA comprehensive genomic profiling (CGP) panel. A total of 1166 tissue samples encompassing 29 cancer types underwent real-world CGP testing. Actionable biomarkers were identified in 62.3% of samples, including 1291 (4.7%) somatic variants potentially targetable by regulatory-approved therapies. At least one tumour-agnostic biomarker, including high tumour mutation burden (TMB-high), microsatellite instability (MSI-high), NTRK/RET fusions, and BRAF V600E was identified in 98 samples across 26 cancer types (8.4%). ERBB2 amplification was identified in 42 samples (3.6%) and was most frequently detected in breast (15.0%), followed by endometrial (11.8%) and ovarian tumours (8.9%). Homologous recombination deficiency (HRD) was observed in 407 samples (34.9%). The high prevalence of actionable biomarkers underscores the significance of CGP in facilitating precision medicine in an Asian setting.

npj Precision OncologyVol. 9(1)
Agency for Science, Technology and Research (SG), Johns Hopkins University (US), Tan Tock Seng Hospital (SG), Mount Elizabeth Novena Hospital (SG), National University Cancer Institute, Singapore (SG), Hong Kong Design Centre (CN), Experimental Drug Development Centre (SG), Society of Hong Kong Scholars (CN), National Cancer Centre Singapore (SG), Hospital Conde S. Januário (CN), University of Hong Kong (HK)
Duke-NUS Medical School, Medical Research Council, National Medical Research Council
Openalex Percentile: Top 58%
Cancer Genomics and Diagnostics
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