Breyanzi (lisocabtagene maraleucel) / BMS 
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 5 Diseases   11 Trials   11 Trials   982 News 


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  • ||||||||||  Uncovering Prescription Drug Pricing: Insights from Payer Price Transparency Regulations () -  Mar 9, 2023 - Abstract #ISPOR2023ISPOR_773;    
    Prescription drug prices negotiated between payers and manufacturers are not yet required for release under the Transparency in Coverage regulations, but are nonetheless beginning to appear in publicly released data. Increased reporting efforts have the potential to inform the industry regarding historically concealed negotiated rates for prescription drugs.
  • ||||||||||  Journal:  CD19 CAR antigen engagement mechanisms and affinity tuning. (Pubmed Central) -  Mar 7, 2023   
    The CAR T cells exhibited different antigen density requirements to trigger cytolysis and differed in their propensity to prompt trogocytosis upon contacting tumor cells. Our work shows how structural information can be applied to tune CAR T cell performance to specific target antigen densities.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS
    Journal:  Lisocabtagene maraleucel for relapsed or refractory large B-cell non-Hodgkin lymphoma. (Pubmed Central) -  Mar 4, 2023   
    When evaluated in the second line setting in LBCL, liso-cel demonstrated superior event-free survival (EFS) versus standard of care. While acknowledging that choice of a particular CAR T-cell is based chiefly on familiarity of the treating physician with a specific product, liso-cel definitely represents an important addition to the treatment armamentarium of R/R LBCL whether in the second-line setting or beyond.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS
    Changing Lanes: CAR T-cell therapy Turns to the Ambulatory Care Setting (ePoster Station #4) -  Feb 28, 2023 - Abstract #ONS2023ONS_289;    
    Interventions We selected the CAR T-cell product Lisocabtagene Maraleucel, for use after two lines of therapy, as the first product to administer in the ambulatory setting based on its safety profile...Outpatient education and administration of this therapy shows promising outcomes for decreasing hospitalization and increasing patient satisfaction without compromising safety. Additional considerations are to discuss the increased burden on caregivers.
  • ||||||||||  Yescarta (axicabtagene ciloleucel) / Gilead
    Journal:  Safety evaluation of axicabtagene ciloleucel for relapsed or refractory large B-cell lymphoma. (Pubmed Central) -  Feb 27, 2023   
    A thorough understanding of the toxicities associated with CD19-directed CAR T-cell therapy will facilitate the optimal selection of patients for this therapy. Furthermore, knowledge of preventative measures of CAR T-cell related complications, and early recognition and appropriate intervention will lead to the safe administration of these therapies, and ultimately improved outcomes for our patients.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS
    LISOCABTAGENE MARALEUCEL FOR RELAPSED OR REFRACTORY LARGE B-CELL LYMPHOMA: FEASIBILITY, SAFETY AND EFFICACY IN A REAL-WORLD SETTING (ePoster Area) -  Feb 11, 2023 - Abstract #EBMT2023EBMT_1225;    
    P1
    Tocilizumab and steroids were administered to 5 (21.7%) and 7 (30.4%), respectively.Among infused patients (n=23), the best overall response (ORR) and complete response rates were 78.3% (ITT, 69.2%) and 56.5% (ITT, 50.0%), respectively. Our ITT analysis in an older patient population referred to our center for CD19 CAR-T therapy for R/R LBCL in the non-trial setting showed high rates of durable response after liso-cel with an acceptable safety profile.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS, Tecartus (brexucabtagene autoleucel) / Gilead, Yescarta (axicabtagene ciloleucel) / Gilead
    A REPRODUCIBLE INFLAMMATORY BIOMARKER SIGNATURE IDENTIFIES NON-HODGKIN LYMPHOMA PATIENTS AT HIGH RISK OF CAR-T TREATMENT FAILURE ACROSS DIFFERENT COHORTS (Room 251) -  Feb 11, 2023 - Abstract #EBMT2023EBMT_992;    
    Our ITT analysis in an older patient population referred to our center for CD19 CAR-T therapy for R/R LBCL in the non-trial setting showed high rates of durable response after liso-cel with an acceptable safety profile. Population CharacteristicsCenter 1 DevelopmentCenter 1 ValidationCenter 2 ValidationSample size, n17154141Disease, n (%)Large B-Cell Lymphoma171 (100)26 (48)141 (100)Mantle Cell Lymphoma0 (0)28 (52)0 (0)Age, median (IQR)66 (56
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS, Kymriah (tisagenlecleucel-T) / Novartis, Yescarta (axicabtagene ciloleucel) / Gilead
    ASCT before Lymphocyte-apheresis Results in a More "Exhausted" T-cells Repertoire (Poster Area) -  Jan 24, 2023 - Abstract #EHAEBMTCART2023EHA_EBMT_CART_109;    
    P
    The use of CAR-T in second line in refractory or early relapse DLBCL patients, recently approved by FDA (Axi-cel and Liso-cel) and EMA (Axi-cel), would help to collect more "fit" Ly. Likewise, in high-risk DLBCL patients, timely pre-ASCT Ly-apheresis would be considered (Tisa-cel allow cryopreservation of Ly) in order to improve the quality of collected Lymphocyte for CAR-T manufacturing.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS, Kymriah (tisagenlecleucel-T) / Novartis, Yescarta (axicabtagene ciloleucel) / Gilead
    Cytotoxicity of CAR-T-cells from DLBCL Patients in High Resolution Microscopy (Poster Area) -  Jan 24, 2023 - Abstract #EHAEBMTCART2023EHA_EBMT_CART_71;    
    Up to date, three different CD19 CAR (chimeric antigen receptor)-T-cell products, Axi-cel, Tisa-cel and Liso-cel have been tested in these patients as second- or third-line therapies and have shown promising outcome. Our analysis provides insights into the killing mechanism and the cytotoxic efficiency of CD19 CAR-T-cells isolated from DLBCL patients.
  • ||||||||||  Kymriah (tisagenlecleucel-T) / Novartis, Yescarta (axicabtagene ciloleucel) / Gilead
    Systematic Literature Review of Real-world Evidence on Axicabtagene-ciloleucel and Tisagenlecleucel (Poster Area) -  Jan 24, 2023 - Abstract #EHAEBMTCART2023EHA_EBMT_CART_65;    
    Patients receiving CAR-T cell therapy in real-world settings had similar outcomes as patients who received CAR-T cell therapy in the pivotal clinical trials. Axi-cel led to improved OS and other effectiveness outcomes compared with tisa-cel in the real-world setting, although axi-cel was also associated with higher risks of CRS and ICANS.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS
    Trial completion:  Lisocabtagene Maraleucel (JCAR017) as Second-Line Therapy (TRANSCEND-PILOT-017006) (clinicaltrials.gov) -  Jan 13, 2023   
    P2,  N=74, Completed, 
    Trial completion date: Jul 2025 --> Jan 2023 | Trial primary completion date: Jul 2025 --> Jan 2023 Active, not recruiting --> Completed
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS
    Review, Journal:  CD19 CAR-T therapy in solid organ transplant recipients: case report and systematic review. (Pubmed Central) -  Dec 28, 2022   
    We report the first case of diffuse large B-cell lymphoma (DLBCL) PTLD treated with lisocabtagene maraleucel and present a systematic literature review of SOTRs with PTLD treated with CD19 CAR-T therapy...Our analysis suggests that CD19 CAR-T therapy offers short-term effectiveness and manageable toxicity in SOTRs with R/R PTLD. Further investigation through larger datasets and prospective study is needed.
  • ||||||||||  Journal, CAR T-Cell Therapy:  Next-Generation Chimeric Antigen Receptor T-cells. (Pubmed Central) -  Dec 21, 2022   
    Furthermore, CAR T-cell therapy is not broadly utilized in solid tumors due to various barriers. This review discusses the evolution of CAR T-cell therapies and how the "younger-generation" CAR T cells counteract these challenges to potentially broaden their applications in the future.
  • ||||||||||  Breyanzi (lisocabtagene maraleucel) / BMS, Kymriah (tisagenlecleucel-T) / Novartis, Yescarta (axicabtagene ciloleucel) / Gilead
    Severe Persistent Cytopenias Following CAR T-Cell Therapy in Patients with Large B-Cell Lymphoma () -  Dec 16, 2022 - Abstract #TCTASTCTCIBMTR2023TCT_ASTCT_CIBMTR_898;    
    CONCLUSION Severe cytopenias following CD19-CAR-T are common, with an estimated incidence of 25% and 80% incidence of profound thrombocytopenia and neutropenia, respectively. Our data suggest that clinical features, baseline counts, and the inflammatory profile before infusion are important determinants of cytopenia risk in CAR-T recipients.