Cutaneous Squamous Cell Carcinoma: Managing Advanced Disease in the Era of Immunotherapy
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Release date: June 30, 2019
Expiration date: June 30, 2020
Most cases of cutaneous squamous cell carcinoma (cSCC), a common cancer, are recognized early and treated successfully with surgery. A small percentage of patients develop advanced or metastatic disease, in which case data to guide treatments are sparse and management depends on a patient’s level of disability and comorbidities. Because patients with de novo or post-surgical advanced or metastatic cSCC are rare, oncologists aren’t always acquainted with pathophysiology, recommendations for diagnostic evaluations, disease staging, management strategies, or agents in clinical trials. Research is contributing to a greater understanding of tumor molecular markers (e.g. overexpression of EGFR) and the role of the programmed death-1 (PD-1) pathway, and has led to the use of targeted agents and the first FDA-approved agent (a PD-1 inhibitor) to treat advanced and metastatic cSCC.
This activity will help clinicians recognize and thoroughly evaluate and stage patients with cSCC who are at high risk of advanced or metastatic disease. Participants should then be able to use this information, in conjunction with expert recommendations and the multidisciplinary team, to develop treatment plans. Up-to-date knowledge of cSCC pathophysiology, including the role of mutations, EGFR overexpression, and the immune system, will give clinicians an understanding of where newly approved and in-development agents fit in treatment strategies.
Welcome and Introductions
Staging of cSCC
Current Understanding of the Pathophysiology of Advanced/Metastatic cSCC
Evolving Paradigm for Managing Advanced/Metastatic cSCC
This activity is intended for oncologists, oncology nurses, pharmacists, and other healthcare professionals involved in the treatment and care of patients with cSCC.
This program is designed to address ACGME and NAM competencies, including delivering patient-centered care and practicing evidence-based medicine.
At the conclusion of this activity, participants should be able to:
- Outline the diagnostic evaluation of patients with cSCC
- Describe commonly used systems for staging cSCC
- Review the current understanding of the pathophysiology of advanced and metastatic cSCC
- Review current recommendations for developing individualized management plans for advanced and metastatic cSCC, including the need for a multidisciplinary team
- Describe the efficacy and safety of immune-targeted agents newly approved for the management of cSCC
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of USF Health and Rockpointe. USF Health is accredited by the ACCME to provide continuing medical education for physicians.
USF Health designates this enduring material for a maximum of 1.0 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity.
For information about accreditation of this activity, please email: email@example.com.
Emily Stamell Ruiz, MD, MPH
Director, Dana‐Farber/Brigham and Women’s High‐Risk Skin Cancer Clinic
Associate Physician, Dana‐Farber/Brigham and Women’s Cancer Center
Instructor in Dermatology, Harvard Medical School
Emily Stamell Ruiz, MD, MPH is Director of the Dana-Farber/Brigham and Women’s High-Risk Skin Cancer Clinic, an Associate Physician at the Mohs and Dermatologic Surgery Center at Dana-Farber/Brigham and Women’s Cancer Center, and an Instructor in Dermatology at Harvard Medical School. Dr. Ruiz received her undergraduate degree from Duke University, her medical degree from New York University School of Medicine, and her Master of Public Health degree from Harvard School of Public Health. She completed an internship in internal medicine at New York University School of Medicine, a dermatology residency at Albert Einstein College of Medicine, and a fellowship in micrographic surgery and dermatologic oncology at Brigham and Women’s Hospital. Dr. Ruiz’s research focuses on the burden of skin cancer through health services research and nonmelanoma skin cancer outcomes studies.
Ann W. Silk, MD, MS
Dana-Farber Cancer Institute
Ann W. Silk, MD, MS is a medical oncologist specializing in the care of patients with advanced skin cancers at Dana‐Farber Cancer Institute, including squamous cell carcinoma, Merkel cell carcinoma, basal cell carcinoma, and melanoma. She conducts clinical trials using immuno‐therapeutics such as immune checkpoint inhibitors, cytokine therapy, and oncolytic viral therapy. Dr. Silk received her medical doctorate and master’s degree in clinical research at the University of Pittsburgh in 2008. She completed a clinical fellowship in hematology and oncology at the University of Michigan in 2014. She joined the faculty at Dana‐Farber Cancer Institute in 2019.
DISCLOSURE/CONFLICT OF INTEREST STATEMENT
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Program Faculty Disclosures
The program faculty reported the following relevant financial relationships that they or their spouse/partner have with commercial interests:
Emily Stamell Ruiz, MD, MPH: Nothing to disclose
Ann W. Silk, MD, MS: Consultant/Independent Contractor: Merck; Grant/Research Support: Bristol-Myers Squibb, Merck
Non-faculty Content Contributors Disclosures
Non-faculty content contributors and/or reviewers reported the following relevant financial relationships that they or their spouse/partner have with commercial interests:
Terry Ann Glauser, MD, MPH; Blair St. Amand; USF Health CPD Staff; Chetasi Talati, MD: Nothing to disclose
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INSTRUCTIONS FOR PARTICIPANTS AND OBTAINING CME CREDIT
There is no fee for this activity. To receive credit, participants must take the pre-test, view this CME activity in its entirety, and then complete the post-test, with a score of 80% or better, and evaluation. The estimated time for completion of this activity is 1 hour. To receive their certificates, participants must demonstrate mastery of the presented material via the post-test. Participant is allowed to take the post-test 2 times.
Jointly provided by USF Health and Rockpointe
This activity is supported by an independent medical education grant from Regeneron Pharmaceuticals, Inc. and Sanofi Genzyme.