April 8th 2025
The FDA is evaluating a new drug application for taletrectinib in patients with ROS1 fusion–positive non–small cell lung cancer.
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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Annual Hawaii Cancer Conference
January 24-25, 2026
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42nd Annual CFS: Chemotherapy Foundation Symposium®: Innovative Cancer Therapy for Tomorrow
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ASCO/CAP Panel Says Evidence Does Not Yet Support ctDNA Testing Outside of Clinical Trials
March 10th 2018After reviewing data from a decade of clinical research, a joint panel from ASCO and the College of American Pathologists concluded that circulating tumor DNA testing should be used only to screen for participation in, or during, a clinical trial.
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Expert Discusses Sequencing With Osimertinib in NSCLC Ahead of FDA's Frontline Decision
March 8th 2018In an interview with<em> Targeted Oncology</em> ahead of the 5th Annual Miami Lung Cancer Conference, Sarah B. Goldberg, MD, discusses the key points of her lecture on testing for and treating resistance to EGFR TKI therapy in NSCLC.
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Growing Role of Immunotherapy as Treatment for Lung Cancer
March 3rd 2018Marina C. Garassino, MD, medical consultant in the Medical Oncology Division, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy, discusses current advancements with immunotherapy as first- and second-line treatments for patients with lung cancer.
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Identifying Patients With Lung Cancer Who Benefit From Immunotherapy
February 24th 2018Hossein Borghaei, DO, MS, chief of the Division of Thoracic Medical Oncology at Fox Chase Cancer Center, discusses biomarkers that may help identify patients with lung cancer who can benefit from immunotherapy agents. Since the introduction of these agents, PD-L1 has been used as a potential biomarker for selecting patients that may benefit from treatment. As PD-L1 is not completely reliable, there is interest in developing additional biomarkers.
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Avelumab Does Not Improve OS Over Docetaxel in NSCLC, Phase III Trial Shows
February 23rd 2018The primary endpoint of improving overall survival was not met in the phase III JAVELIN Lung 200 Trial of avelumab in patients with non–small cell lung cancer, according to Merck KGaA and Pfizer, the co-developers of avelumab.
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Jean-Charles Soria to Receive TAT 2018 Honorary Award for Cancer Drug Development
February 20th 2018Jean-Charles Soria, MD, PhD, will be honored with the Targeted Anticancer Therapies 2018 Honorary Award for cancer drug development. Soria has played a large part in cancer drug development across molecular targeted agents, precision medicine, and immunotherapy for the last 15 years.
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Durvalumab Granted FDA Approval for Locally Advanced NSCLC
February 17th 2018Based on results from the phase III PACIFIC trial, durvalumab has been granted approval by the FDA for the treatment of patients with locally advanced, unresectable stage III non–small cell lung cancer who have not progressed following chemoradiotherapy.
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Promising Activity Seen from ERK1/2 Inhibitor in MAPK/ERK Mutations and BRAF/MEK Resistance
February 17th 2018Ulixertinib, a novel ERK1/2 inhibitor, demonstrated encouraging antitumor activity in patients with solid tumors harboring mutations in the MAPK/ERK pathway, according to the results of a phase I study published in <em>Cancer Discovery</em>.
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What Would CMS Proposed Coverage Decision for Next-Generation Sequencing Mean for Oncologists?
February 16th 2018The day when oncologists can order a Medicare-covered next-generation sequencing diagnostic test may be near at hand, but once this change goes into effect, will oncologists be limited to certain tests, labs, and cancer settings? The answer is unclear.
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Lorlatinib Granted Priority Review by FDA for ALK+ NSCLC
February 13th 2018A new drug application for lorlatinib for use in patients with <em>ALK</em>-positive metastatic non–small cell lung cancer who have progressed on 1 or more ALK tyrosine kinases inhibitors has been granted a priority review by the FDA.
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