In this first episode, Advances in Non-Hodgkin Lymphoma Care: Navigating New and Emerging Treatments, from the 4-part series Med Table Talk, The Power of the Community: Translating Innovations into Care in NHL and HL, learn from expert faculty about unmet needs for patients with NHL based on an understanding of disease- and patient-related characteristics. Additionally, learn how to best assess eligible patients among new and emerging CAR T-cell and bispecific antibody therapies. Expert faculty will also discuss both the mechanisms of action of CAR T-cell and bispecific antibodies. This episode will conclude with a patient case study, which will consist of a dialogue between faculty.
On May 15, 2024 (after the recording of this activity), the FDA has granted accelerated approval for lisocabtagene maraleucel, a CAR T-cell therapy, for the treatment of adult patients with R/R FL who have received two or more prior lines of systemic therapy.
On May 30, 2024 (after the recording of this activity), the FDA has granted accelerated approval for lisocabtagene maraleucel, a CAR T-cell therapy, for the treatment of adult patients with R/R MCL who have received after at least 2 lines of systemic therapy, including a BTK inhibitor
Speakers
Loretta Nastoupil, MD
Associate Professor
Director of Lymphoma Outcomes Database ad
Section Chief of New Drug Development
Department of Lymphoma – Myeloma, Division of Cancer Medicine
University of Texas MD Anderson Cancer Center
Houston, TX
Loretta J. Nastoupil, MD is an Associate Professor in the Department of Lymphoma/Myeloma at the University of Texas MD Anderson Cancer Center in Houston, TX USA. Dr. Nastoupil received her medical degree from the University of Texas Southwestern Medical School and completed her internal medicine training at Washington University and hematology/medical oncology fellowship at Emory University. She is currently Deputy Chair of the Lymphoma/Myeloma Department and Section Chief of the indolent lymphoma and new drug development teams which are in line with her research interests of designing and conducting prospective trials aimed at exploiting the immune system to eradicate B-cell lymphoma. She has led phase 1, 2, and 3 trials in follicular and diffuse large B-cell lymphoma. She is also interested in real world evidence and has been involved in exploring outcomes among patients treated with standard of care CAR T cell therapy and generating synthetic control arms for single arm phase 2 studies.
Amitkumar Mehta, MD
Director of Lymphoma and CAR T-cell Therapy Program,
University of Alabama at Birmingham
Birmingham, AL
Dr. Mehta is a board-certified hematologist and oncologist with a special interest in Lymphomas. A clinical investigator with a special interest in developing "no chemotherapy" approaches for the treatment of Lymphoma. "No chemotherapy" approaches include immunotherapy, CAR-T therapy, immune-modulating therapy, and targeted therapy. Dr. Mehta is a principal investigator of innovative clinical trials for the treatment of Lymphomas at UAB.
Ann S. LaCasce, MD, MMSc
Institute Physician, Dana-Farber Cancer Institute
Associate Professor of Medicine, Harvard Medical School
Boston, MA
Dr. Ann S. LaCasce earned her medical degree from Tufts University School of Medicine and has a Masters in Medical Science from Harvard/MIT Division of Health Sciences and Technology. She completed training in internal medicine at Brigham and Women's Hospital in Boston, where she later served as a Chief Medical Resident. Since 2003, she has been a member of the Lymphoma Program at Dana-Farber where she performs clinical research. She has a longstanding interest in medical education and is the Program Director of the Dana-Farber/Mass General Brigham Fellowship in hematology/oncology. In addition, she co-directs the Center for Adolescent and young Adult Oncology at Dana-Farber. She is an Associate Professor of Medicine at Harvard Medical School. She is the chair of the Lymphoma Research Foundation Scientific Advisory Board and serves on the ABIM Medical Oncology Board, the National Comprehensive Cancer Network's Lymphoma Guideline Panel, and the Alliance Lymphoma Committee,
Accreditation and Disclosure Information
Target Audience
This educational activity is targeted to hematologic oncology clinicians, nurses, pharmacists, pathologists, and other members of the multi-disciplinary and interprofessional care team who care for individuals with NHL and HL.
Educational Objectives
After completing this CE activity, the participant should be better able to:
- Assess the clinical implications of patient outcomes in the relapsed/refractory setting to support the rationale for new and emerging treatments in NHL.
- Differentiate the mechanisms of action, including therapeutic targets and molecular formats, indications, dosing, and administration requirements of available T-cell mediated treatments in order to tailor personalized treatment strategies.
Agenda
Discuss current unmet needs in NHL patients, across subtypes, and the relevance of new and emerging treatment modalities in NHL
- Understand the clinical implications of these factors on patient prognosis and outcomes, particularly in the relapsed/refractory setting.
- Analyze the distribution of NHL subtypes based on distinct features, such as staging, cytogenic risk factors, and the differentiation between aggressive and indolent lymphomas.
- Reflect upon health disparities that arise across demographics and its implications on access to novel therapies and practical strategies to drive change
Differentiate T-cell mediated treatments, including CART and bispecific antibody therapy
- Describe the therapeutic targets and molecular formats associated with each treatment
- List the indications of these therapies across NHL subtypes to understand their clinical application
- Recognize the unique dosing and administration considerations that are intrinsic to therapy selection
- Incorporate expert guidance in treatment sequencing of bispecific and CAR T
- Case Study: Identify patients that would benefit from CAR-T in the 2L incorporating the latest clinical evidence and NCCN guidelines to ensure timely initiation to appropriate therapy (eg, early relapse and primary refractory disease)
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Physician Continuing Medical Education
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MOC Statement
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Physician Associate
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Nursing Continuing Professional Development
Successful completion of this nursing continuing professional development activity will be awarded 0.25 contact hour and 0.25 contact hour in the area of pharmacology.
ILNA Coding
The program content has been reviewed by the Oncology Nursing Certification Corporation (ONCC) and is acceptable for recertification points in the following ILNA subject areas: 0.25 points: Care Continuum (OCN, CBCN, CPHON, AOCNP); Care of Pediatric Hematology and Oncology Patient (CPHON); Disease Related Biology (CPHON); Foundations of Transplant (BMTCN); Health Maintenance (CPHON) 0.25 points: Oncologic Emergencies (OCN, CPHON, AOCNP); Oncology Nursing Practice (OCN); Pediatric Hematology and Oncology Nursing Practice (CPHON); Professional Practice/Performance (BMTCN, AOCNP); Roles of the APRN (AOCNP); Symptom Management, Palliative Care, Supportive Care (OCN, CPHON, AOCNP); Transplant Process and Infusion (BMTCN); Treatment (OCN, CBCN, AOCNP, CPHON)
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Continuing Pharmacy Education
Medical Learning Institute, Inc. designates this continuing education activity for 0.25 contact hour (.025 CEU) of the Accreditation Council for Pharmacy Education.
Universal Activity Number: JA0007322-0000-24-050-H01-P
Type of Activity: Knowledge
Interprofessional Continuing Education (IPCE) Statement
This activity was planned by and for the healthcare team, and learners will receive 0.25 Interprofessional Continuing Education (IPCE) credit for learning and change.
Support Statement
This activity is supported by an educational grant from Bristol Myers Squibb.
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Faculty Disclosures
Planner/Presenter
Loretta Nastoupil, MD (Chair)
Associate Professor
Director of Lymphoma Outcomes Database ad Section Chief of New Drug Development
Department of Lymphoma – Myeloma, Division of Cancer Medicine
University of Texas MD Anderson Cancer Center
Houston, TX
Loretta Nastoupil, MD, has a financial interest/relationship or affiliation in the form of:
Research Funding: Bristol Myers Squibb, Genentech, Daiichi Sankyo, Genmab, Gilead/Kite, Janssen, Ipsen, Merck, Novartis, Takeda
The following relationships have ended within the last 24 months:
Consultant/Advisor: AstraZeneca, AbbVie, Bristol Myers Squibb
Speakers’ Bureau: Gilead/Kite
Planner/Presenter
Amitkumar Mehta, MD
Director of Lymphoma and CAR T-cell Therapy Program
University of Alabama at Birmingham
Birmingham, AL
Amitkumar Mehta, MD, has a financial interest/relationship or affiliation in the form of:
Consultant/Advisor: Gilead, Seattle Genetics, Incyte, MorphoSys/Incyte, TG Therapeutics, Kyowa Kirin, BeiGene, Roche/Genentech, ADCT
Speakers’ Bureau: Incyte/MorphoSys, BeiGene, Ipsen, Kyowa Kirin
Planner/Presenter
Ann S. LaCasce, MD, MMSc
Institute Physician, Dana-Farber Cancer Institute
Associate Professor of Medicine
Harvard Medical School
Boston, MA
Ann S. LaCasce, MD, MMSc, has a financial interest/relationship or affiliation in the form of:
Consultant/Advisor: Kite Pharma, Seagen
Speakers’ Bureau: Research to Practice
All of the relevant financial relationships of individuals for this activity have been mitigated.
Planning Committee and Content/Peer Reviewers
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Disclosure of Unlabeled Use
This educational activity may contain discussions of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this CE activity do not recommend the use of any agent outside of the labeled indications. The opinions expressed in the CE activity are those of the presenters and do not necessarily represent the views of the planners. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
Disclaimer
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