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TEST:
Altera

Company:
Natera
Type:
Laboratory Developed Test
Related tests:
Evidence

News

7ms
Analysis of ctDNA assay as a strategy for watchful waiting in locally advanced esophageal cancer. (ASCO 2024)
The clearance of ctDNA favors less clinical disease recurrence in this study. This may indicate that ctDNA clearance confers lower risk of relapase. However, a larger cohort prospective study will be needed to validate the application of ctDNA as an early biomarker.
Circulating tumor DNA • Metastases
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Signatera™ • Altera
over1year
Longitudinal Analysis of Circulating Tumor DNA and Detection of Tumor Genomic Alterations Using Liquid Biopsy in Patients with Locally Advanced Esophagogastric Carcinoma (ASTRO 2023)
Clearance of ctDNA may correlate to a favorable pCR and indicate a lower risk of relapse, guiding the strategy for adjuvant treatment. Personalized, tumor-informed sequence alterations of the 8 patients revealed a high frequency in TP53 alterations, which occurs early during development in esophagogastric cancer. This prospective study seeks to validate the application of ctDNA surveillance and tumor molecular alterations in a larger cohort after 5 years.
Clinical • Tumor mutational burden • Liquid biopsy • Circulating tumor DNA • Metastases • Biopsy
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KRAS (KRAS proto-oncogene GTPase) • TP53 (Tumor protein P53) • PIK3CA (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) • TMB (Tumor Mutational Burden) • CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • MAP2K1 (Mitogen-activated protein kinase kinase 1) • RB1 (RB Transcriptional Corepressor 1) • ARID1A (AT-rich interaction domain 1A) • CCNE1 (Cyclin E1) • PALB2 (Partner and localizer of BRCA2) • RNF43 (Ring Finger Protein 43) • PIK3R1 (Phosphoinositide-3-Kinase Regulatory Subunit 1) • MSH3 (MutS Homolog 3) • MRE11A (MRE11 homolog, double strand break repair nuclease) • CCND3 (Cyclin D3) • MAP3K1 (Mitogen-Activated Protein Kinase Kinase Kinase 1)
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TP53 mutation
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Signatera™ • Altera
2years
Predicting the Risk of Ovarian Cancer Recurrence Using Circulating Tumor DNA to Assess Residual Disease (clinicaltrials.gov)
P=N/A; Not yet recruiting --> Recruiting | Initiation date: Jan 2022 --> Oct 2022 | Trial primary completion date: Dec 2023 --> Dec 2024
Trial primary completion date • Enrollment open • Trial initiation date • Circulating tumor DNA
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MLH1 (MutL homolog 1) • MSH2 (MutS Homolog 2) • MUC16 (Mucin 16, Cell Surface Associated)
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Signatera™ • Altera
over2years
Real World Experience and Feasibility of Tissue Informed CGP and ctDNA Testing in a Cohort of NSCLC Patients (IASLC-WCLC 2022)
Our study shows the feasibility of performing CGP and ctDNA testing using a single source of tissue in patients with NSCLC. CGP allowed for the identification of patients who may derive benefit from targeted therapies and ICIs, while also informing appropriate clinical trials. ctDNA analysis was congruent with clinical findings, and ctDNA dynamics were indicative of response to therapy.
Real-world evidence • Clinical • Tumor mutational burden • Circulating tumor DNA
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TMB (Tumor Mutational Burden) • MSI (Microsatellite instability)
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TMB-H
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Signatera™ • Altera
almost3years
Predicting the Risk of Ovarian Cancer Recurrence Using Circulating Tumor DNA to Assess Residual Disease (clinicaltrials.gov)
P=N/A; N=45; Not yet recruiting; Sponsor:Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
New trial • Circulating tumor DNA
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MLH1 (MutL homolog 1) • MSH2 (MutS Homolog 2) • MUC16 (Mucin 16, Cell Surface Associated)
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Signatera™ • Altera