November 19th 2024
The FDA has approved FoundationOne Liquid CDx as a companion diagnostic for patients with metastatic non–small cell lung cancer with MET exon 14 skipping alterations eligible for tepotinib.
42nd Annual CFS: Innovative Cancer Therapy for Tomorrow®
November 13-15, 2024
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Community Practice Connections™: 5th Annual Precision Medicine Symposium – An Illustrated Tumor Board
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Annual Hawaii Cancer Conference
January 25-26, 2025
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41st Annual CFS®: Innovative Cancer Therapy for Tomorrow
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Fighting Disparities and Saving Lives: An Exploration of Challenges and Solutions in Cancer Care
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Differentiating Adverse Events for Antibody-Drug Conjugates Across Solid Tumor Management
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Poorer Clinical Outcomes for Certain Patients Shown With ALK-Rearranged NSCLC on Second Line TKIs
February 4th 2022Concomitant mutations, and high PD-L1 expression may be associated with an unfavorable clinical response to second-generation tyrosine kinase inhibitors in patients with ALK-rearrange non–small cell lung cancer.
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Part 2: Rare Mutations and Non-Clinical Barriers for Molecular Testing in NSCLC
December 16th 2021During a live virtual event, Ravi Salgia, MD, PhD, discussed issues with molecular testing and biopsies including delays and affordability, plus identifying and responding to rare mutations detected by molecular testing.
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Repotrectinib Shows Efficacy in Expanded Cohorts of NTRK+ Solid Tumors
December 14th 2021Updated findings from the phase 1/2 TRIDENT-1 trial evaluating repotrectinib showed efficacy in patients with neurotrophic tyrosine receptor kinase fusion-positive advanced solid tumors in expanded cohorts.
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Part 1: Challenges in Performing Biopsies and Molecular Testing in NSCLC
November 12th 2021At a live virtual event, Martin Dietrich, MD, PhD, discusses how to approach biopsies and molecular testing in coordination with pathologists and testing services for patients with non–small cell lung cancer.
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PD-1 Assay to Determine Atezolizumab Eligibility Receives FDA Approval for Use in NSCLC
October 22nd 2021The assay is meant to determine patient eligibility for atezolizumab, which was granted FDA approval in PD-L1-positive lung cancer on October, 15. The assay was used in the IMpower010 study.
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Study Underway to Test ALRN-6924 in p53-Mutated Non–Small Cell Lung Cancer
July 2nd 2021A phase 1b trial is currently recruiting patients with advanced p53-mutated non–small cell lung cancer in order to determine the safety and efficacy of ALRN-6924, and reduce chemotherapy toxicity in this patient population.
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