Brennan J. Decker, MD, PhD, discusses the role of identifying <em>EGFR</em> mutations in patients with lung cancers. In lung adenocarcinoma, there are many different activating mutations that can lead to the development of cancer, Decker explains.
Brennan J. Decker, MD, PhD, a clinical fellow in the Department of Pathology at Brigham and Women’s Hospital in Boston, Massachusetts, discusses the role of identifyingEGFRmutations in patients with lung cancers. In lung adenocarcinoma, there are many different activating mutations that can lead to the development of cancer, Decker explains.
Molecular mutations, such as theEGFRmutation, can be thought of like flipping a switch that activates cancer in some way. The major breakthrough in the treatment of patients with EGFR-positive lung cancer has been the development of osimertinib (Tagrisso) and otherEGFR-targeted therapies, according to Decker.
The EGFR gene is a signaling molecule, and when this “switch” is turned on in patients with lung cancer, it can cause uncontrollable cancer growth, Decker says. TheseEGFR-directed therapies help in slowing down the signaling and has been beneficial in terms of overall prognosis in patients. However, Decker notes that these treatments only benefit patients with theEGFR
Acalabrutinib/Obinutuzumab Shows Improved PFS in Treatment-Naive CLL
April 10th 2024In an interview with Targeted Oncology, Jeff Sharman, MD, discussed the results of the ELEVATE-TN trial of acalabrutinib with or without obinutuzumab at 74.5 months of follow-up among patients with chronic lymphocytic leukemia.
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