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Continuing Education Information

Physicians' Education Resource is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

Physicians' Education Resource designates this educational activity for a maximum of 0.5 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

Optimizing Cytotoxic Regimens in Advanced Non–Small-Cell Lung Cancer

Oncology Briefings

Release Date: July 24, 2009
Expiration Date: July 24, 2010

Publication Overview

Authors

Medical writer: Aarati Ranganathan, PhD; Reviewed by: Corey Langer, MD, FACP

Overview and Purpose

Many targeted agents have been developed for the treatment of patients with non–small-cell lung cancer (NSCLC); however, lung cancer is a genetically complex set of diseases, and these agents alone are usually not sufficient to control the disease. Consequently, cytotoxic chemotherapy remains an integral part of the treatment of the majority of patients with advanced NSCLC. Newer chemotherapies are being developed to provide optimum benefit and overcome the disadvantages of existing chemotherapeutic formulations. Strategies include the development of novel formulations of taxanes and the investigation of new microtubule inhibitors, such as epothilones, several of which are being investigated in phase III trials.

The purpose of this activity is to apprise physicians of the mechanisms of delivery and action of and clinical data on novel chemotherapeutic drugs in NSCLC.

Target Audience

This educational activity is intended for medical oncologists involved in the care of patients with lung cancer. No specific skills or knowledge other than a basic training in oncology is required for successful participation in this activity.

Learning Objectives

Upon completion of this educational activity, you should be able to:

  • Assess the efficacy and adverse event profile of albumin-bound paclitaxel formulations in patients with NSCLC
  • Discuss the efficacy and safety of epothilones in patients with previously treated advanced NSCLC
  • Evaluate clinical data on poly-L-glutamic acid–conjugated taxanes in NSCLC

Instructions for Participation

  1. Read the following information before entering the educational activity.
  2. Complete the Pretest.
  3. Study the educational activity.
  4. Complete the Posttest.
  5. Answer the evaluation questions.
  6. After completion of the Pretest and successful completion of the Posttest and evaluation, you will receive your certificate online.

You will be permitted 2 attempts to successfully complete the Posttest.

The tests and evaluation must be completed by July 24, 2010, in order for you to receive your certificate.

CME credit will be granted for only 1 form of participation, either online or via the printed publication.

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Educational Grants

An educational grant for this activity was provided by:


  1. Abraxis BioScience