Advanced Renal Cell Cancer - prIME Oncology
Expert Review
Expert Review

Advanced Renal Cell Cancer

Making Sense of Clinical Trial Results in Clinical Practice

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The information in this activity is intended for healthcare professionals based outside of the United States. This activity may contain information on products outside the approved indications where you practice.

View a comprehensive review and downloadable slides on advanced renal cell cancer (RCC) from leading experts in the field. This activity features a discussion of current standards of care and guidelines, systemic treatment in the real world, and treatment sequencing for patients with RCC.

Interactive Presentation

Interactive Presentation

Downloadable Slides

Downloadable Slides

IME

IME

Release Date

Release Date

Dec 4, 2018

Expiration Date

Dec 4, 2019

Moderator

  • Robert Coleman, MD, FRCP, FRCPEMedical Director, prIME Oncology
    University of Sheffield
    Weston Park Hospital
    Sheffield, United Kingdom

Faculty

  • Bernard Escudier, MDGustave Roussy
    Villejuif, France
  • Elizabeth R. Plimack, MD, MSFox Chase Cancer Center, Temple Health
    Philadelphia, Pennsylvania, United States
  • Manuela Schmidinger, MDMedical University of Vienna
    Vienna, Austria
  • Risk Assessment
  • First-Line Systemic Therapy for Metastatic RCC
  • Second- and Subsequent Lines of Therapy
  • Future Perspectives
  • Munich 2018: Updates on RCC
  • prIME Points™

This educational activity is designed for urologists, medical oncologists, urology and oncology specialist nurses, and other healthcare professionals involved in the management of patients with RCC.

After successful completion of this educational activity, participants should be able to:

  • Describe the clinical relevance of recent findings from clinical trials investigating targeted therapies and immune checkpoint inhibitors either as single agents or in combination for locally advanced and metastatic RCC
  • Identify the subgroups of patients with metastatic RCC best treated in the first-line setting with either tyrosine kinase inhibitors or immunotherapy agents or a combination of the two
  • Define a clinical algorithm to aid the selection and sequencing of available options for the treatment of metastatic RCC

This educational activity is supported by a grant from Pfizer Oncology.

Independent Medical Education (IME)

This IME activity is organized by prIME Oncology. This activity provides content that is evidence-based, balanced, and free of commercial bias, with a primary objective to improve competence and performance of learners in order to improve patient care.

Provider

This activity is provided by prIME Oncology.

Disclosure Information

Disclosure of Relevant Financial Relationships

prIME Oncology assesses relevant financial relationships with its instructors, planners, managers, and other individuals who are in a position to control the content of IME activities. Any potential conflicts of interest that are identified are thoroughly vetted by prIME Oncology for fairness, balance, and scientific objectivity of data, as well as patient care recommendations. prIME Oncology is committed to providing its learners with high-quality IME activities and related materials that promote improvements or quality in healthcare and not a specific proprietary business interest of a commercial entity.

The faculty reported the following financial relationships or relationships to products or devices they or their spouses/life partners have with commercial interest related to the content of this activity:

Dr Escudier has disclosed that he has a board membership with Bristol-Myers Squibb, Ipsen, Pfizer, and Roche. He has received consulting fees from Bristol-Myers Squibb, Ipsen, Novartis, Pfizer, and Roche. He has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in his presentation.

Dr Plimack has disclosed that she has received consulting fees and has a membership on advisory committees or review panels for Bristol-Myers Squibb, Exelixis, Genentech, Incyte, Janssen, Merck, and Pfizer. She has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in her presentation.

Dr Schmidinger has disclosed that she has a board membership with ESMO. She also received consulting fees from Astellas, Bristol-Myers Squibb, Eisai, Eusa, Exelixis, Ipsen, Novartis, Pfizer, and Roche. She has agreed to disclose any unlabeled/unapproved uses of drugs or products referenced in her presentation.

The employees of prIME Oncology have disclosed:

  • Robert Coleman, MD, FRCP, FRCPE (medical director content reviewer/planner) – board membership as chair of Inbiomotion Scientific Advisory Board; consulting fees for advising on clinical trial protocol development from Amgen, Astellas, and Boehringer Ingelheim; intellectual property rights as co-inventor and patent holder of biomarker under development by Inbiomotion; independent medical education lectures at symposia supported by Amgen, Eisai, and Genomic Health; and travel expenses from Amgen for presentation of clinical trial data at ASCO 2018 conference
  • Sanneke Koekkoek, PhD (scientific content reviewer/planner) – no relevant financial relationships
  • Jessica Mastrodomenico, MPH (editorial content reviewer) – no relevant financial relationships

Disclaimer

Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patients’ conditions and possible contraindications or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.

Disclosure Regarding Unlabeled Use

This activity may contain discussion of published and/or investigational uses of agents that are not indicated by the US Food and Drug Administration or European Medicines Agency. Please refer to the official prescribing information for each product discussed for discussions of approved indications, contraindications, and warnings.