Catalog Advanced Search

Search by Category
Search by Format
Sort By
Search by Type
Search by Category
Search in Packages
Search by Format
Search by Type
Search by Date Range
Products are filtered by different dates, depending on the combination of live and on-demand components that they contain, and on whether any live components are over or not.
Start
End
Search by Keyword
Sort By
  • Contains 4 Component(s), Includes Credits

    This education session titled 'CD19 Directed Therapy Debate: Blinatumomab vs. CD19 Chimeric Antigen Receptor T-cells (CAR-T) for Acute Lymphoblastic Leukemia (ALL)' is presented by Dr. Anthony J. Perissinotti and Dr. Bernard Lawrence Marini and was originally presented at the 2022 Tandem Meetings Pharmacist Conference.

    Title: CD19 Directed Therapy Debate: Blinatumomab vs. CD19 Chimeric Antigen Receptor T-cells (CAR-T) for Acute Lymphoblastic Leukemia (ALL)

    Speakers: Anthony J. Perissinotti, PharmD, BCOP and Bernard Lawrence Marini, PharmD, BCOP

    This session was originally presented at the 2022 Tandem Meetings Pharmacist Conference.

    Learning Objectives: 

    • Review key background information in the treatment of acute lymphoblastic leukemia (ALL)
    • Appraise the literature surrounding the use of blinatumomab and chimeric antigen receptor T-cell (CAR-T) therapy in the treatment of ALL 
    • Defend the use of either blinatumomab or CAR-T given a patient scenario 
    • Compare and contrast major toxicities of blinatumomab and CAR-T, including financial toxicity

    This session has been accredited for 1 hour of BCOP Credit by HOPA. In order to claim BCOP credit, learners must view the presentation in its entirety and pass the quiz with a minimum score of 80%. You will only have two attempts to pass the quiz.

  • Contains 4 Component(s), Includes Credits

    This education session titled 'Hematopoietic Stem Cell Transplantation for Inherited Bone Marrow Failure Syndromes' is presented by Dr. Binni Kunvarjee and was originally presented at the 2022 Tandem Meetings Pharmacist Conference.

    Title: Hematopoietic Stem Cell Transplantation for Inherited Bone Marrow Failure Syndromes

    Speaker: Binni Kunvarjee, PharmD, BCOP

    This session was originally presented at the 2022 Tandem Meetings Pharmacist Conference.

    Learning Objectives: 

    • Describe the genetic and phenotypic characteristics of various inherited bone marrow failure syndromes (IBMFS) in pediatric patients.
    • Explain the role of hematopoietic stem cell transplantation (HCT) in treatment of the hematologic manifestations of IBMFS.
    • Review available literature on impact of conditioning regimen, graft manipulation, and donor source on outcomes with HCT for IBMFS.
    • Identify the disease-specific pre- and post-transplant considerations in patients receiving HCT for IBMFS.

    This session has been accredited for 1 hour of BCOP Credit by HOPA. In order to claim BCOP credit, learners must view the presentation in its entirety and pass the quiz with a minimum score of 80%. You will only have two attempts to pass the quiz.

  • Contains 3 Component(s)

    This is a recording of the ASTCT Spotlight Session at the 2022 Tandem Meetings of ASTCT and CIBMTR. The workshop comprised short talks by representatives of ASTCT’s six international partner organizations on the subject of access to transplant across the world.

    This workshop comprised short talks by representatives of ASTCT’s six international partner organizations on the subject of access to transplant across the world. Members from APBMT (Asia Pacific Blood and Marrow Transplantation Group); SBTMO (Sociedade Brasileira de Transplante de Medula Óssea); EBMT (European Blood and Marrow Transplantation); ANZTCT (Australia New Zealand Transplantation and Cellular Therapy Group); LABMT (Latin American Blood and Marrow Transplantation Group); and ISTCT (Indian Society for Transplantation and Cellular Therapy) presented on various aspects of access to transplant in their respective regions, such as conflict resolution, workforce development, standardization of processes, and health equity. 

  • Contains 1 Component(s)

    The Pharmacy SIG Online Journal Club session aired on May 11th, 2021 at 3 pm CST.

    The ASTCT Pharmacy SIG May 2022 Journal Club aired on May 11, 2022. This webinar consists of two, 30-minute journal club presentations, which include 20 min for presentation and 10 min for discussion/Q and A.


    Presenters & Articles

    Arthur Nguyen, PharmD 

    PGY2 Oncology Resident, Oregon Health and Science University

    Axicabtagene Ciloleucel as Second-Line Therapy for Large B-Cell Lymphoma

    Elizabeth A. Meszaros, PharmD 

    PGY2 Hematology/Oncology Pharmacy Resident, South Texas Veterans Healthcare System

    Posttransplant Cyclophosphamide for Prevention of Graft-versus-Host Disease: The Prospective Randomized HOVON-96 Trial

     

    Session Learning Objectives:

    Upon completion of the activity, participants should be able to:

    1. Evaluate the safety and efficacy of Axicabtagene Ciloleucel for the treatment of large B-cell lymphomas (LBCL).
    2. Review current standards of care for Graft-versus-Host Disease (GVHD) prevention for Matched Related Donors (MRD) and Matched Unrelated Donor (MUD) peripheral blood allogeneic hematopoietic stem cell transplants (alloHSCT).
    3. Evaluate the utility of post-transplant cyclophosphamide (PTCy) combined with a short course of cyclosporine (CsA) as compared to mycophenolic acid (MPA) with CsA for GVHD prophylaxis in patients receiving MRD and MUD peripheral blood alloHSCT.

    The France Foundation is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education and will award 1.0 CEU to pharmacists who complete the activity, complete the registration and evaluation forms, and successfully pass a posttest (>75%). There is no fee to participate in this activity. This is a knowledge-based educational activity. Your CE credits will be submitted electronically to the CPE Monitor. CE providers must upload participant information within 60 days from the date the participant completed the activity. Please submit all evaluations and credit requests no later than 30 days after you complete this activity to ensure your credit fulfillment, as CE credit cannot be awarded past 60 days from the activity date. 

     

    Full CE information, including presenter disclosures and accreditation information, can be found in the Handouts tab or directly downloaded by clicking here.



  • Contains 4 Component(s)

    This journal club aired live on April 20, 2022, as a part of the expanded ASTCT Journal Club. This webinar consisted of two, 30-minute journal club presentations, which included 20 min for presentation and 10 min for discussion/Q and A.

    ASTCT April Journal Club Session

    This journal club aired live on April 20, 2022, as a part of the expanded ASTCT Journal Club. This webinar consisted of two, 30-minute journal club presentations, which included 20 min for presentation and 10 min for discussion/Q and A.

    Presenters & Articles

    Dr. Patrick Moore, Loyola University Medical Center

    Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell Disease

    Dr. Paramveer Singh, Karmanos Cancer Institute

    Biologic Assignment Trial of Reduced-Intensity Hematopoietic Cell Transplantation Based on Donor Availability in Patients 50-75 Years of Age With Advanced Myelodysplastic Syndrome

  • Contains 4 Component(s), Includes Credits

    This education session titled 'New Drug Updates for Multiple Myeloma' is presented by Dr. Ryan Miller and was originally presented at the 2022 Tandem Meetings Pharmacist Conference.

    Title: New Drug Updates for Multiple Myeloma

    Speaker: Ryan Miller, PharmD, BCOP (Vanderbilt University Medical Center)

    This session was originally presented at the 2022 Tandem Meetings Pharmacist Conference.

    Learning Objectives: 

    • Outline the role of monoclonal antibody based four drug regimens for newly diagnosed multiple myeloma
    • Describe the mechanism of action of newly approved agents for relapsed/refractory multiple myeloma
    • Examine the efficacy and safety data for newly approved anti-BCMA agents for relapsed / refractory multiple myeloma
    • Discuss immunotherapy agents in the pipeline for the treatment of multiple myeloma

    This session has been accredited for 1 hour of BCOP Credit by HOPA. In order to claim BCOP credit, learners must view the presentation in its entirety and pass the quiz with a minimum score of 80%. You will only have two attempts to pass the quiz.

  • Contains 3 Component(s)

    This webinar aired on Wednesday, March 23 at 1 PM CST. This is the second webinar in this series on acute myeloid leukemia (AML) sponsored by Vor Biopharma. This session highlights the current best practices and experimental approaches for treatment of patients who relapse after allo-HSCT.

    On Wednesday, March 23 at 1 PM CST, ASTCT presented the second webinar in its AML webinar series sponsored by Vor Biopharma. 

    Speakers and Moderator:

    Moderator: Antonio Vaz de Macedo, MD; Hospital da Policia Militar

    Presenter: Reshma Ramlal, MD, FACP; University of Kentucky Markey Cancer Center

    Panelists:

    Marcos de Lima, MD; Ohio State University

    Mark Levis, MD, PhD; Johns Hopkins

  • Contains 1 Component(s)

    The 'Recommended Timing for Transplant Consultation' guidelines were updated and published jointly by the National Marrow Donor Program®/Be The Match® (NMDP) and the American Society for Transplantation and Cellular Therapy (ASTCT) in 2022.

    The 'Recommended Timing for Transplant Consultation' guidelines were updated and published jointly by the National Marrow Donor Program®/Be The Match® (NMDP) and the American Society for Transplantation and Cellular Therapy (ASTCT) in 2022. 

  • Contains 1 Component(s)

    This article titled 'American Society for Transplantation and Cellular Therapy Guidelines for Fellowship Training in Hematopoietic Cell Transplantation and Immune Effector Cell Therapy' was published in the March 2022 issue of Transplantation and Cellular Therapy Journal.

    This article titled 'American Society for Transplantation and Cellular Therapy Guidelines for Fellowship Training in Hematopoietic Cell Transplantation and Immune Effector Cell Therapy' was published in the March 2022 issue of Transplantation and Cellular Therapy Journal. It is an updated edition of a similar article published back in 2012, but updated to account for best practices. 

  • Contains 1 Component(s)

    Join Dr. Kirk R. Schultz from the University of British Columbia as he discusses new and emerging therapies in cGvHD. In this 20 min. presentation, he focuses on the future directions of treatment for cGvHD, including the idea of synergistic therapy and how biomarkers may be used to personalize therapy.

    Join Dr. Kirk R. Schultz from the University of British Columbia as he discusses new and emerging therapies in cGvHD.  In this 20 min. presentation, he focuses on the future directions of treatment for cGvHD, including the idea of synergistic therapy and how biomarkers may be used to personalize therapy. 

    Activity Title: Emerging Treatments in Chronic GvHD

    Topic: cGVHD

    Accreditation Type: AMA PRA Category 1 Credit(s)™ 

    Release Date: 2/25/2022

    Expiration Date: 2/24/2023

    Estimated Time to Complete Activity: 20 mins

    LEARNING OBJECTIVES
    Upon completion of the activity, participants should be able to:

    • Assess emerging therapies for cGvHD from the standpoint of mechanism of action (MOA), clinical efficacy, and safety

    FACULTY 
    Steven Pavletic, MD, MS
    Head, Graft-Versus-Host Disease and Late Effects Section
    Center for Cancer Research
    National Institute of Health
    Bethesda, MD

    Kirk Schultz, MD
    Investigator, Michael Cuccione Childhood Cancer Research Program
    Director, Michael Cuccione Childhood Cancer Research Program
    British Columbia Children’s Hospital
    Professor, Division of Hematology and Oncology and Department of Pediatrics
    University of British Columbia
    Vancouver, BC

    Kirsten Williams, MD
    Pediatric Hematologist/Oncologist, Aflac Cancer & Blood Disorders Center
    Children’s Healthcare of Atlanta
    Associate Professor of Pediatrics
    Emory University School of Medicine
    Atlanta, GA

    Olaf Penack, MD
    Department of Hematology, Oncology and Tumor Immunology
    Charité-Universitätsmedizin Berlin
    Berlin, Germany 

    METHOD OF PARTICIPATION/HOW TO RECEIVE CREDIT
    Technical Requirements: http://www.francefoundation.co...
    1. There are no fees for participating in and receiving credit for this activity 
    2. Review the activity objectives and CME/CE information
    3. Complete the CME/CE activity 
    4. Complete the online posttest. A score of at least 75% is required to successfully complete this activity. The participant may take the test until successfully passed.
    5. Complete the CME/CE evaluation/attestation form. This form provides each participant with the opportunity to comment on how participating in the activity will affect their professional practice; the quality of the instructional process; the perception of enhanced professional effectiveness; the perception of commercial bias; and his/her views on future educational needs.
    6. Credit documentation/reporting:
    • If you are requesting AMA PRA Category 1 Credits™ or a certificate of participation—your CME/CE certificate will be available for download

    ACCREDITED PROVIDER
    This activity is provided by The France Foundation and produced in collaboration with the American Society for Transplantation and Cellular Therapy (ASTCT).

    TARGET AUDIENCE
    This activity is intended for oncologists, hematologists, physician assistants, nurse practitioners, pharmacists, and other health care professionals involved in treating and managing patients with cGVHD.

    STATEMENT OF NEED
    A significant number of patients—some 30% to 70%—will develop cGVHD after allo-HSCT. It typically manifests during the first year after transplantation, but it can occur several years later. cGVHD is also the leading cause of non-relapse mortality in allo-HSCT patients. The earliest possible diagnosis is critical, as once patients meet diagnostic criteria for GVHD, they may have already developed significant morbidity and possibly even irreversible organ damage. Guidelines and consensus statements from the National Institutes of Health (National Cancer Institute; NIH/NCI), the European Society for Blood and Marrow Transplantation (ESBMT), and the National Comprehensive Cancer Network (NCCN) exist to help diagnose, stage, and manage cGVHD. Unfortunately, uptake and use of guidelines have been inconsistent and variable.

    ACCREDITATION STATEMENT  
    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 The France Foundation and American Society for Transplantation and Cellular Therapy. The France Foundation is accredited by the ACCME to provide continuing medical education for physicians.

    CREDIT DESIGNATION
    Physicians
    The France Foundation designates this enduring activity for a maximum of 0.25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

    DISCLOSURE POLICY
    In accordance with the ACCME Standards for Commercial Support, The France Foundation (TFF) and American Society for Transplantation and Cellular Therapy (ASTCT) require that individuals in a position to control the content of an educational activity disclose all relevant financial relationships with any commercial interest. TFF and ASTCT resolve all conflicts of interest to ensure independence, objectivity, balance, and scientific rigor in all their educational programs. Furthermore, TFF and ASTCT seek to verify that all scientific research referred to, reported, or used in a CME/CE activity conforms to the generally accepted standards of experimental design, data collection, and analysis. TFF and ASTCT are committed to providing learners with high-quality CME/CE activities that promote improvements in health care and not those of a commercial interest.

    Activity Staff Disclosures 
    The planners, reviewers, editors, staff, CME committee, or other members at The France Foundation who control content have no relevant financial relationships to disclose.

    The planners, reviewers, staff, or other members at American Society for Transplantation and Cellular Therapy who control content have no relevant financial relationships to disclose.

    Faculty Disclosures - Content Creators 
    The faculty listed below report that they have no relevant financial relationships to disclose:
    • Kirsten Williams, MD
    • Kirk Schultz, MD

    The following faculty report that they have relevant financial relationships to disclose: 
    • Olaf Penack, MD, has done non-CE consulting for Jazz, Gilead, MSD, Omeros, Priothera, Shionogi, and SOBI. He has served on the speaker’s bureau for Astellas, Gilead, Jazz, MSD, Neovii Biotech, Novartis, Pfizer, and Therakos. He has also done contract research for Gilead, Incyte, Jazz, Neovii Biotech, and Takeda.
    • Steven Pavletic, MD, MS has done contract research for Kadmon, Eli Lilly, and Pharmacyclins.

    DISCLOSURE OF UNLABELED USE
    TFF and ASTCT require CME faculty (speakers) to disclose when products or procedures being discussed are off label, unlabeled, experimental and/or investigational, and any limitations on the information that is presented, such as data that are preliminary, or that represent ongoing research, interim analyses, and/or unsupported opinion. Faculty in this activity may discuss information about pharmaceutical agents that is outside of US Food and Drug Administration approved labeling. This information is intended solely for continuing medical education and is not intended to promote off-label use of these medications. TFF and ASTCT do not recommend the use of any agent outside of the labeled indications. If you have questions, contact the Medical Affairs Department of the manufacturer for the most recent prescribing information. 

    COMMERCIAL SUPPORT ACKNOWLEDGMENT
    This activity is supported by an educational grant from Incyte.

    DISCLAIMER 
    The France Foundation and American Society for Transplantation and Cellular Therapy present this information for educational purposes only. The content is provided solely by faculty who have been selected because of recognized expertise in their field. Participants have the professional responsibility to ensure that products are prescribed and used appropriately on the basis of their own clinical judgment and accepted standards of care. The France Foundation, American Society for Transplantation and Cellular Therapy, and the commercial supporter(s) assume no liability for the information herein.

    COPYRIGHT INFORMATION
    Copyright © 2021 The France Foundation. Any unauthorized use of any materials on the site may violate copyright, trademark, and other laws. You may view, copy, and download information or software ("Materials") found on the Site subject to the following terms, conditions, and exceptions: 
    • The materials are to be used solely for personal, noncommercial, informational, and educational purposes. The materials are not to be modified. They are to be distributed in the format provided with the source clearly identified. The copyright information or other proprietary notices may not be removed, changed, or altered. 
    • Materials may not be published, uploaded, posted, or transmitted (other than as set forth herein), without The France Foundation's prior written permission 

    PRIVACY POLICY
    The France Foundation protects the privacy of personal and other information regarding participants and educational collaborators. The France Foundation will not release personally identifiable information to a third party without the individual's consent, except when such information is required for reporting purposes to the ACCME.

    The France Foundation maintains physical, electronic, and procedural safeguards that comply with federal regulations to protect against the loss, misuse, or alteration of information that we have collected from you.

    Additional information regarding The France Foundation’s Privacy Policy can be viewed at http://www.francefoundation.com/privacy. 

    CONTACT INFORMATION
    If you have questions about this CME activity, please contact The France Foundation at 860-434-1650 or info@francefoundation.com.