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TEST:
Find It®

Type:
Laboratory Developed Test
Related tests:
Evidence

News

8d
Actionable Mutation Profiling in Solid Tumours in Australia Using Targeted Next-Generation Sequencing Panel (AMP 2024)
We demonstrated the feasibility of obtaining actionable information within a clinically meaningful turnaround time using a robust NGS solution. For samples with sufficient tumour content and DNA for testing (>90% of samples), Find It had an approximately 99% success rate. Actionable information provided by the panel could impact clinical management for 66% of advanced-stage cancer patients.
Next-generation sequencing
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EGFR (Epidermal growth factor receptor) • HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • PIK3CA (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) • NRAS (Neuroblastoma RAS viral oncogene homolog) • RAS (Rat Sarcoma Virus)
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KRAS mutation • EGFR mutation • BRAF mutation • PIK3CA mutation • RAS mutation • EGFR positive
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Find It®
1year
Reference lab experience running FIND IT NGS gene panel for the nation-wide clinical testing of solid tumours in Australia (AMP 2023)
Our targeted NGS panel has proved to be a cost-effective, robust solution, enabling the delivery of actionable information within a clinically meaningful turnaround time. For samples with sufficient neoplastic cell content and DNA quality for testing (>90% of samples), the test success rate with Find It of nearly 99% demonstrates that this targeted panel has met our high standards of molecular testing at Sonic Genetics.
Clinical • Next-generation sequencing
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Find It®
over1year
Harmonized molecular classification; assessment of a single-test ProMisE NGS tool. (PubMed, Gynecol Oncol)
ProMisE NGS is feasible on standard FFPE material, demonstrates high concordance with the original ProMisE classifier and maintains prognostic value in EC. This test has the potential to facilitate implementation of molecular classification of EC at the time of first diagnosis.
Journal • Next-generation sequencing
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TP53 (Tumor protein P53) • MSI (Microsatellite instability) • POLE (DNA Polymerase Epsilon)
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TP53 mutation • POLE mutation
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Find It®
over1year
Development of a one-step molecular classifier for endometrial carcinoma using an amplicon-based gene panel and next generation sequencing technology (AACR 2023)
The one-step NGS molecular classifier demonstrates high concordance with the original ProMisE classifier including between biopsy and hysterectomy samples. This shows that reliable molecular testing could be obtained from time of first diagnosis. Prognostic value of this new one-step classification tool is maintained.
MSi-H Biomarker • Next-generation sequencing
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TP53 (Tumor protein P53) • MSI (Microsatellite instability) • POLE (DNA Polymerase Epsilon)
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TP53 mutation • MSI-H/dMMR • TP53 wild-type • POLE mutation
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Find It®
over1year
Method for identifying microsatellite instability high DNA abnormality samples (AACR 2023)
The MSI detection algorithm can accurately identify samples with MSI-H tumors. When used in a clinical setting, these patients can then be directed to treatments such as immune-checkpoint inhibitors.
Microsatellite instability • MSi-H Biomarker
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MSI (Microsatellite instability)
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MSI-H/dMMR
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Find It®
over2years
PROMISE-2: A ONE STEP DNA-BASED ENDOMETRIAL CANCER MOLECULAR CLASSIFIER (IGCS 2022)
Conclusions We demonstrate high concordance of a one step DNA-based EC molecular classifier when compared to the original ProMisE classifier, importantly maintaining the prognostic value of ProMisE and presenting an option for centers where routine MMR and p53 IHC are not performed. Further validation is needed before implementation into clinical practice.
TP53 (Tumor protein P53) • MSI (Microsatellite instability) • POLE (DNA Polymerase Epsilon)
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TP53 mutation • POLE mutation
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Find It®