Non–small-cell lung cancer (NSCLC) is the leading cause of cancer deaths in the United States. Although research on the genetics of lung cancer has led to the development of targeted therapies, many patients with NSCLC lack actionable biomarkers. This program explores options for improving outcomes in NSCLC without an actionable biomarker, including immunotherapy and maintenance therapy, and discusses the identification and optimal management of common side effects of NSCLC therapies.
eNewsletter with interactive benchmarking
After completing this activity, participants should be better able to:
- Discuss current clinical trial data regarding individualization of therapy for patients with non–small-cell lung cancer (NSCLC) based on histology and biomarkers
- Prescribe first-line treatment for patients with NSCLC lacking an activating mutation
- Select maintenance therapy in an evidence-based manner for patients with response or stable disease after upfront therapy
- Prevent and manage adverse events associated with systemic therapy used in the treatment of squamous- and nonsquamous-cell lung cancer
Oncology NPs, PAs, and nurses
There are no prerequisites to participate in this activity.
Continuing Nursing Education Provider Unit, Boston University School of Medicine is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.
This educational activity has been provided by Continuing Nursing Education Provider Unit, Boston University School of Medicine and jointly provided by Practicing Clinicians Exchange.
Contact hours: 1.0, which are eligible for 1.0 pharmacology credits
Course director: J. Mark Sloan, MD, Boston University School of Medicine
CNE course advisor: Jennifer Brock, RN, BSN, OCN, Dana Farber Cancer Institute
This program has been reviewed and is approved for a maximum of 1.00 AAPA Category 1 CME credits by the AAPA Review Panel. Approval is valid for one year from the issue date of July 31, 2017. Participants may submit the post-test at any time during that period.
This program was planned in accordance with AAPA CME Standards for Enduring Material Programs and for Commercial Support of Enduring Material Programs.
This program was cosupported by educational grants from Astellas and Medivation, Inc., a Pfizer Company; Celgene Corporation; Genzyme, a Sanofi Company; Eisai, Inc. and Helsinn; Lilly; Merck & Co., Inc.; Novartis Pharmaceuticals Corporation; Takeda Oncology; and TESARO, Inc.
This activity is supported by an educational grant from Lilly and Novartis Pharmaceuticals Corporation. For further information concerning Lilly grant funding, visit www.lillygrantoffice.com.
The opinions or views expressed in this continuing education activity are those of the faculty and do not necessarily reflect the opinions or recommendations of the American Academy of Physician Assistants, Boston University School of Medicine, Continuing Education Alliance, Practicing Clinicians Exchange, or any educational supporter.
THIS CONTINUING MEDICAL EDUCATION PROGRAM IS INTENDED SOLELY FOR EDUCATIONAL PURPOSES FOR QUALIFIED HEALTH CARE PROFESSIONALS. IN NO EVENT SHALL BOSTON UNIVERSITY BE LIABLE FOR ANY DECISION MADE OR ACTION TAKEN IN RELIANCE ON THE INFORMATION CONTAINED IN THE PROGRAM. IN NO EVENT SHOULD THE INFORMATION CONTAINED IN THE PROGRAM BE USED AS A SUBSTITUTE FOR PROFESSIONAL CARE. NO PHYSICIAN-PATIENT RELATIONSHIP IS BEING ESTABLISHED.
Boston University School of Medicine asks all individuals involved in the development and presentation of Continuing Medical Education (CME) activities to disclose all relevant relationships with commercial interests. This information is disclosed to CME activity participants. Boston University School of Medicine has procedures to resolve any apparent conflicts of interest. In addition, faculty members are asked to disclose when any discussion of unapproved use of pharmaceuticals and devices is being discussed.
This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the US Food and Drug Administration.
Dr Davies: speakers bureau: AstraZeneca, Bristol-Myers Squibb, Genentech, Merck.
Dr Sloan: consultant: Alexion, Incyte, Molecular Templates, Stemline; grant/research support: Gilead.
The Planning Committee for this activity included Jennifer Brock, RN, BSN, OCN, of Dana Farber Cancer Institute; Patti-Ann Collins, DNP, MSN, MBA, RN (Lead Nurse Planner), of Healthcare Advocacy Services; Mark Christiansen, PhD, PA-C, of University of the Pacific; Jason Worcester, MD, Jody Walker, MS, and Julie L. White, MS, of Boston University School of Medicine; and Ruth Cohen, Devera Pine, Warren Beckman, and Margaret Inman of Practicing Clinicians Exchange. None of the aforementioned members of the Planning Committee have any significant relationships to disclose.
Participants wishing to earn CE/CME credit must:
- Read the eNewsletter in its entirety
- Relate the content material to the learning objectives
- Complete the post-test and evaluation form online
Successful completion of the post-test is required to earn CE/CME credit. Successful completion is defined as a cumulative score of at least 70%.
The estimated time to complete this activity is 1.00 hours.
Release date: July 31, 2017
Expiration date: July 30, 2018
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