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LIVE WEBINAR SERIES

Are you getting the full picture?
The power of comprehensive intelligent diagnostics

Webinar #1: Friday, April 11
9:00 AM PT / 11:00 AM CT / 12:00 PM ET
Webinar #2: Tuesday, April 22
9:00 AM PT / 11:00 AM CT / 12:00 PM ET

REGISTER NOW

All registrants will be sent the webinar recording shortly following the completion of the session.

what you’ll learn

Join us for an engaging two-part webinar series exploring the power of comprehensive testing, spanning the cancer continuum. When you sign up for Part 1, you’ll be automatically registered for Part 2.

  • One Blood Sample, Many Options: The Benefits of Tumor + Normal Match

    April 11
    9:00 AM PT / 11:00 AM CT / 12:00 PM ET

    In Part 1, we’ll explore the benefits of a tumor + normal matched sequencing approach. Learn how a single blood sample can generate insights that may guide more personalized treatment plans while offering flexible ordering options like automatic conversion and concurrent solid tumor and liquid biopsy testing. Our expert speakers, Dr. Ezra Cohen and Dr. Rena Callahan, will highlight clinical decision making with a tumor + normal matched approach, showcasing its real-world impact through a live case review.
  • Alterations Drive Decisions: Advancing personalized care with comprehensive genomic profiling

    April 22
    9:00 AM PT / 11:00 AM CT / 12:00 PM ET

    In Part 2, we’ll explore how understanding genomic alterations can drive clinical decisions. We'll discuss the importance of a comprehensive testing approach, with a deep dive into xT CDx and its role within our broader portfolio—including MRD, solid tumor, liquid biopsy, RNA, and tailored testing options such as IHCs and algorithmic tests. Dr. Ezra Cohen and Dr. Frank Weinberg will explore this topic in detail and lead a live case review to demonstrate its real-world clinical impact.
    xT CDx is a qualitative Next Generation Sequencing (NGS)-based in vitro diagnostic device intended for use in the detection of substitutions (single nucleotide variants (SNVs) and multi-nucleotide variants (MNVs)) and insertion and deletion alterations (INDELs) in 648 genes, as well as microsatellite instability (MSI) status, using DNA isolated from Formalin-Fixed Paraffin Embedded (FFPE) tumor tissue specimens, and DNA isolated from matched normal blood or saliva specimens, from previously diagnosed cancer patients with solid malignant neoplasms. The test is intended as a companion diagnostic (CDx) to identify patients who may benefit from treatment with the targeted therapies listed in the Companion Diagnostic Indications table in accordance with the approved therapeutic product labeling. Additionally, xT CDx is intended to provide tumor mutation profiling to be used by qualified health care professionals in accordance with professional guidelines in oncology for patients with previously diagnosed solid malignant neoplasms. Genomic findings other than those listed in the Companion Diagnostic Indications table are not prescriptive or conclusive for labeled use of any specific therapeutic product. xT CDx is a single-site assay performed at Tempus Labs, Inc., Chicago, IL. For the complete xT CDx label, including companion diagnostic indications and important risk information, please visit tempus.com/xt-cdx-label/.

SPEAKERS

Rena D. Callahan, MD Associate Clinical Professor of Medicine, University of California, Los Angeles, Jonsson Comprehensive Cancer Center
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Frank Weinberg, MD Assistant Professor, University of Illinois College of Medicine
Lead, Thoracic Oncology Program UI Health

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MODERATOR
Ezra Cohen, MD Chief Medical Officer of Oncology, Tempus

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