This activity is part of PER's Integrated Oncology Learning Series:
A Focus on Thoracic Malignancies
New Developments in Frontline Therapy and Beyond for Metastatic Non–Small-Cell Lung Cancer
Advances in Lung Cancer Vol. 9, No. 1
1 AMA PRA Category 1 Credit(s)™
Release Date: November 24, 2009
Expiration Date: November 24, 2010
Medical writer: Aarati Ranganathan, PhD; Medical writer: Bing-e Xu, PhD; Reviewed by: George Simon, MD, FACP, FCCP; Reviewed by: Giorgio Scagliotti, MD, PhD; Reviewed by: H. Jack West, MD
Most patients with non–small-cell lung cancer (NSCLC) are diagnosed at an advanced stage. Standard frontline treatment of advanced NSCLC includes platinum-based chemotherapy doublets, and to improve the therapeutic ratio of platinum doublets, new cytotoxic agents with similar efficacy but less toxicity compared to old cytotoxic agents have been incorporated into first-line chemotherapy regimens. Targeted agents, such as monoclonal antibodies against vascular endothelial growth factor or epidermal growth factor receptor (EGFR), have improved survival when combined with frontline chemotherapy in eligible patients with advanced NSCLC. Other approaches to improving treatment outcomes of frontline regimens include the administration of maintenance therapy, or early second-line therapy, immediately following first-line treatment in patients with nonprogressive disease. Recent phase III trials have demonstrated a survival benefit with maintenance therapy using either an antifolate or an EGFR tyrosine kinase inhibitor compared to placebo. Personalized therapy based on clinical and/or molecular characteristics of the tumor has also been demonstrated to be feasible. Histological subtypes and biomarkers predictive of efficacy from cytotoxic or targeted agents are now playing important roles in choosing the optimal therapy for individual patients with advanced NSCLC.
The purpose of this activity is to update physicians on frontline regimens, maintenance therapy, and personalized therapy in advanced NSCLC.
This educational activity is intended for medical oncologists involved in the care of patients with NSCLC. No specific skills or knowledge other than a basic training in oncology is required for successful participation in this activity.
Upon completion of this educational activity, you should be able to:
You will be permitted 2 attempts to successfully complete the Posttest.
Complete the test(s) and evaluation by November 24, 2010 to receive your certificate online.
Read all of the conditions in the Activity Terms box below. You must accept the CME Activity Terms in order to continue:
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Aarati Ranganathan, PhD
No relevant relationships to disclose
Bing-e Xu, PhD
No relevant relationships to disclose
Giorgio Scagliotti, MD, PhD
Advisory Board – AstraZeneca, Eli Lilly and Company, Novartis Pharmaceuticals Corporation, Roche Pharmaceuticals, sanofi-aventis U.S.; Speaker’s Bureau – Eli Lilly and Company, GlaxoSmithKline, sanofi-aventis U.S.
H. Jack West, MD
Paid Consultant – Eli Lilly and Company, Bristol-Myers Squibb Company; Speaker’s Bureau – Eli Lilly and Company
George Simon, MD, FACP, FCCP
Paid Consultant – Eli Lilly and Company, Genentech, Inc.; Speaker’s Bureau – Eli Lilly and Company, Genentech, Inc., sanofi-aventis U.S.
Other PER Staff
No relevant relationships to disclose
This CME activity might include discussion of investigational and/or unlabeled uses of drugs. If the activity includes discussion of investigational and/or unlabeled uses of a drug, specific information is located on the title page. Please refer to the full prescribing information for each drug discussed in this activity for FDA-approved dosing, indications, and warnings.
Commercial Support
An educational grant for this activity was provided by Eli Lilly and Company.
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