New Horizons in the Treatment of Relapsed and Refractory Myeloma

New Horizons in the Treatment of Relapsed and Refractory Myeloma

On-Demand Webcast
Moderator

Adriana C. Rossi, MD
Weill Cornell Medicine
New York, New York

Faculty

Kenneth C. Anderson, MD
Dana-Farber Cancer Institute
Harvard Medical School
Boston, Massachusetts

Cara A. Rosenbaum, MD
Weill Cornell Medicine
New York, New York

Jesús F. San Miguel, MD
University of Navarra
Pamplona, Spain

Target Audience

Designed for hematologists and hematologic oncologists, medical, radiation, and surgical oncologists, and other healthcare professionals (e.g., physicians, physicians-in-training, oncology nurses, nurse practitioners, pharmacists, physician assistants) who are involved and/or interested in the treatment of patients with hematologic malignancies.

Overview

Multiple myeloma (MM) is an exceedingly challenging condition to treat, for many reasons. There is no cure for MM, and, even if achieved, complete response (CR) will ultimately fail over time. Relapsed/refractory (R/R) MM is treated with combination therapy, and the number of potential combinations can be daunting. Some randomized clinical trials (RCTs) are exploring optimal combination therapies for R/R MM, but, currently, data is sparse. With these challenges in mind, in this on-demand web archive, we focus on proteasome inhibitors (PIs), considered to be a backbone treatment of R/R MM, to better understand within-class differences and opportunities for synergistic combinations with other drugs to overcome these barriers.


Objectives
  1. Identify patient factors that will influence the choice and sequencing of proteasome inhibitor combination medications for optimal individualized treatment of R/R MM
  2. Discuss proteasome inhibitor-based treatment approaches for multidrug-resistant R/R MM based on current data
  3. Evaluate emerging clinical trial data for novel combinations with proteasome inhibitors to overcome resistance in the management of R/R MM

Release Date: October 31, 2018

Expiration Date: October 31, 2019

Hardware/Software Requirements

The evaluation is accessible after the activity via a PC (Windows 7 or newer) or Mac (Mac OS 10.6 or later) computer with current versions of the following browsers: Internet Explorer, Mozilla Firefox, Google Chrome, or Safari. A PDF reader is required for print publications. Please direct technical questions to webmaster@naccme.com.

Support

Supported by educational grants from: Amgen and Takeda Oncology

Accreditation


In support of improving patient care, this activity has been planned and implemented by North American Center for Continuing Medical Education (NACCME) and Imedex. NACCME is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC) to provide continuing education for the healthcare team.

CME

NACCME designates this live activity for a maximum of 1.50 AMA PRA Category 1 Credits™.

Physicians should claim only the credit commensurate with the extent of their participation in the activity.

PHYSICAN ASSISTANTS

NACCME has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with the AAPA CME Criteria. This activity is designated for 1.50 AAPA Category 1 credit(s).

PAs should only claim credit commensurate with the extent of their participation.

CNE

This continuing nursing education activity awards 1.50 contact hours.

Provider approved by the California Board of Registered Nursing, Provider #13255 for 1.50 contact hours.

CPE

This knowledge-based activity (JA0006201-9999-18-218-H01-P) is approved for 1.50 contact hours (0.015 CEUs) of continuing pharmacy education.

This educational activity is a knowledge-based activity.

ACPE Credit Policy

Your official record of ACPE credit will be generated through the CPE Monitor System. The certificate printed from this website after completing the evaluation for this activity is for personal tracking purposes only.

Eligibility for pharmacy credit is contingent upon the successful completion of a post-test and/or evaluation for each activity or session attended. Please note that you must complete the activity evaluation within 60 days of a live activity or within 60 days of beginning the evaluation for an enduring activity. Under ACPE Policy, NACCME will not be able to report your activity completion to CPE Monitor after this 60-day period.

Any participant wanting to file a grievance with respect to any aspect of a continuing pharmacy education activity accredited by NACCME may contact the Senior Manager, Accreditation & Compliance, NACCME, in writing at 104 Windsor Center Drive, East Windsor, NJ 08520. The Senior Manager, Accreditation & Compliance will review the grievance and respond within 30 days of receiving the written statement. If the participant is unsatisfied with the response, an appeal to the Senior Director, Accreditation and Compliance, NACCME, may be made for a second level of review.

Planning Committee

The planning committee comprises Ruben Niesvizky, MD, Adriana C. Rossi, MD, Cara Rosenbaum, MD, Kenneth C. Anderson, MD and Jesus San Miguel, MD; and Chris Bolwell, Monalisa Singh, and Susan Yarbrough, Imedex.

Financial Disclosure and Conflicts of Interest

According to the disclosure policy of NACCME, faculty, editors, managers, and other individuals who are in a position to control content are required to disclose any relevant financial relationships with relevant commercial companies related to this activity. All relevant conflicts of interest that are identified are reviewed for potential conflicts of interest. If a conflict is identified, it is the responsibility of NACCME to initiate a mechanism to resolve the conflict(s). The existence of these interests or relationships is not viewed as implying bias or decreasing the value of the presentation.

All educational materials are reviewed for fair balance, scientific objectivity of studies reported, and levels of evidence.

Kenneth C. Anderson, MD has served as a consultant for Bristol-Myers Squibb, C4 Therapeutics, Celgene, Gilead, Millennium, National Cancer Institute, owns stock in Oncopep and Regenacy, and has received other support from Oncopep and Regenacy.

Cara A. Rosenbaum, MD has recieved research and/or grant support from Takeda Oncology, and has served as a consultant for Celgene Corporation.

Adriana C. Rossi, MD has recieved research and/or grants support from Bristol-Myers Squibb, and has served as a consultant for Amgen, Celgene and Janssen.

Jesús F. San Miguel, MD has served as a consultant for Amgen, Brystol-Myers Squibb, Celgene, Janssen, MSD, Novartis, Takeda, Sanofi and Roche.

Chris Bolwell discloses that he holds shares of stock of GlaxoSmithKline.

Monalisa Singh and Susan Yarbrough disclosed no relevant financial relationships with any commercial interests.

NACCME requires faculty to inform participants whenever off-label/unapproved uses of drugs and/or devices are discussed in their presentations.

Disclosure of off-label/unapproved uses of drugs and/or devices will be provided prior to the symposium.

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Copyright © 2018 by North American Center for Continuing Medical Education, LLC. All rights reserved. No part of this accredited continuing education activity may be reproduced or transmitted in any form or by any means, electronic or mechanical, without first obtaining permission from North American Center for Continuing Medical Education. The opinions expressed in this educational activity are those of the faculty and are not attributable to NACCME. Clinical judgment must guide each professional in weighing the benefits of treatment against the risk of toxicity. Dosages, indications, and methods of use for products referred to in this activity are not necessarily the same as indicated in the package insert for each product, may reflect the clinical experience of the presenters, and may be derived from the professional literature or other clinical sources. Consult complete prescribing information before administering.