วางแผนการรักษาอย่างชาญฉลาดด้วยจีโนมิกส์

การรักษา

ACTOnco®+ analyzes >400 genes and 13 fusion genes to assist physicians identify the most suitable therapies. Treatment evaluations include targeted therapy, immunotherapy, hormone therapy, and chemotherapy.

การรักษา

ACT Nonet™ is an RT-PCR customizable tissue panel. It covers 167 variants of 11 genes with U.S. FDA-approved targeted treatments. Including all NCCN guideline-recommended genes and high sensitivity (1~5% of DNA, 125 copies/reaction for RNA).

การรักษา

ACTLiquid™ Pro is a comprehensive NGS-based liquid biopsy assay for pan-solid tumors covering 523 genes and 23 fusion gene variants in circulating tumor DNA. Treatment evaluations include targeted therapy, immunotherapy, and hormone therapy.

การคาดการณ์

ACTRisk™ hereditary gene testing decodes 67 cancer genes associated with 9 common hereditary cancers and 11 cancer syndromes, which provides additional information to a health management strategy.

การรักษา

ACT EGFR™ analyze EGFR gene mutations in cell-free DNA or FFPE DNA for non-small cell lung patients.

การตรวจสอบ

ACTMonitor® Colon analyzes 13 forms of circulating tumor DNA in the bloodstream to provide real-time monitoring of drug resistance, early detection of cancer recurrence, and evaluation of treatment response.

การตรวจสอบ

ACTMonitor® Breast analyzes 8 forms of circulating tumor DNA in the bloodstream to provide real-time monitoring of drug resistance, early detection of cancer recurrence, and evaluation of treatment response.

การตรวจสอบ

ACTMonitor® Lung analyzes 11 forms of circulating tumor DNA in the bloodstream to provide real-time monitoring of drug resistance, early detection of cancer recurrence, and evaluation of treatment response.

การตรวจสอบ

ACTMonitor®+ analyzes 50 forms of circulating tumor DNA in the bloodstream to provide real-time monitoring of drug resistance, early detection of cancer recurrence, and evaluation of treatment response.

การรักษา

ACTCerebra™ sequences 40 druggable genes from Cerebrospinal Fluid (CSF) to identify the most effective targeted therapies based on medical history.

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ACTHRD™ detects HRD status by LOH score and 24 HRR-related genes to evaluate whether a tumor is suitable for PARP inhibitors.

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ACTBRCA® genetic tests detect mutations in BRCA1/2 genes, which can provide genetic information to evaluate whether a tumor is suitable for PARP inhibitors.

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ACTFusion™ is a targeted, multi-biomarker assay that examines 13 druggable fusion genes, and more than 350 known and novel transcripts.

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ACTLung™ targets 13 common driver genes and assists newly diagnosed lung cancer patients to rapidly determine a first-line targeted therapy opportunity.

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ACTDrug®+ is an NGS-based test, which sequences 40 druggable genes, 13 fusion genes, and more than 350 fusion transcripts simultaneously from cancer specimens.