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Powering Precision

Learn more about our evolving body of data presented at the 2022 ASCO Congress on June 3- 6, 2022.
Contact us for deeper insight into Signatera's personalized, tumor-informed approach.


Scientific presentations to further validate the utility of Signatera in multiple tumor types

  • Breast Cancer: Serial postoperative ctDNA monitoring of breast cancer recurrence

    Ekaterina Kalashnikova, PhD
    Natera
  • Lung Cancer: Minimal residual disease (MRD) detection by ctDNA in relation to radiographic disease progression in patients with stage I-III non-small cell lung cancer (NSCLC) treated with definitive radiation therapy.

    Emily Lebow, MD
    Memorial Sloan Kettering Cancer Center
  • Sarcoma: Circulating Tumor DNA (ctDNA) detection of Molecular Residual Disease (MRD) as a Potential Biomarker in localized Soft Tissue Sarcoma (STS)

    Abdulazeez Salawu, PhD
    Princess Margaret Cancer Centre and Mount Sinai Hospital
  • Merkel Cell: Circulating tumor DNA to measure Merkel cell carcinoma tumor burden and detect early recurrence

    Richa Rathore, PhD
    Natera
  • Metastatic Renal: Monitoring Efficacy of Neoadjuvant Sunitinib in Metastatic Renal Cell Carcinoma using a Personalized and Tumor Informed ctDNA Assay

    Christine B. Peterson, PhD
    Department of Biostatistics, MD Anderson Cancer Center
  • Colon Cancer: A Single-arm Phase II Study to Evaluate Treatment with Gevokizumab in Patients with Stage II/III Colon Cancer who remain ctDNA+ after Curative Surgery and Adjuvant Chemotherapy

    Thomas George, MD
    Director of the GI Oncology Program, University of Florida
  • Colon Cancer: Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (CIRCULATE-US): NRG-GI008

    N. Arvind Dasari, MD
    Associate Professor Dept of Gastrointestinal Medical Oncology, MD Anderson Cancer Center
  • Immunotherapy: External validation of the VIGex gene-expression signature (GES) as a novel predictive biomarker for immune checkpoint treatment (ICT).

    Alberto Hernando-Calvo
    Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre

Natera led an Industry Expert Theater on June 5

Natera’s Oncology Portfolio

A single tissue source upfront provides a comprehensive genomic profile

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*Reinert T, Henriksen TV, Christensen E, et al. Analysis of Plasma Cell-Free DNA by Ultradeep Sequencing in Patients With Stages I to III Colorectal Cancer. JAMA Oncol. 2019

Learn about Signatera for your clinical trial

Well-designed and successful clinical trials help facilitate earlier “go/no go” decision-making. A trial with Signatera can ultimately enhance the R&D pipeline productivity and impact label expansion of approved oncology drugs to new treatment settings.

Why Partner with us?

  • Experienced team with Global reach: CE Mark, three FDA Breakthrough Device Designations, 8 Non-Significant Risk (NSR) determinations

  • >60 Natera IP assets covering ctDNA MRD and monitoring

  • Clinically validated across multiple solid tumors, Signatera has shown to predict relapse in >98% of patients without further treatment*

Learn More

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Pan Cancer Brochure
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CIRCULATE Japan Sales Aid
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How to Order
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Immunotherapy Brochure
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CRC Brochure
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Patient Brochure
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