BCMA CAR-T cells in multiple myeloma-ready for take-off? (Record no. 27976)

MARC details
000 -LEADER
fixed length control field 02159nam a22003497a 4500
001 - CONTROL NUMBER
control field 20240607164401.0
003 - CONTROL NUMBER IDENTIFIER
control field 20240607164401.0
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240607165345.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
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040 ## - CATALOGING SOURCE
Transcribing agency ddc
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title English
100 ## - MAIN ENTRY--PERSONAL NAME
Fuller form of name Lukas Scheller
245 ## - TITLE STATEMENT
Title BCMA CAR-T cells in multiple myeloma-ready for take-off?
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mwanza, Tanzania :
Name of publisher, distributor, etc. Catholic University of Health and Allied Sciences [CUHAS-Bugando] :
Date of publication, distribution, etc. 2023
300 ## - PHYSICAL DESCRIPTION
Extent Pages 143-157
Extent Includes References
490 ## - SERIES STATEMENT
Volume/sequential designation Leukemia & Lymphoma Volume 65, 2024 - Issue 2
520 ## - SUMMARY, ETC.
Summary, etc. Abstract :<br/><br/>Although the approval of new drugs has improved the clinical outcome of multiple myeloma (MM), it was widely regarded as incurable over the past decades. However, recent advancements in groundbreaking immunotherapies, such as chimeric antigen receptor T cells (CAR-T), have yielded remarkable results in heavily pretreated relapse/refractory patients, instilling hope for a potential cure. CAR-T are genetically modified cells armed with a novel receptor to specifically recognize and kill tumor cells. Among the potential targets for MM, the B-cell maturation antigen (BCMA) stands out since it is highly and almost exclusively expressed on plasma cells. Here, we review the currently approved BCMA-directed CAR-T products and ongoing clinical trials in MM. Furthermore, we explore innovative approaches to enhance BCMA-directed CAR-T and overcome potential reasons for treatment failure. Additionally, we explore the side effects associated with these novel therapies and shed light on accessibility of CAR-T therapy around the world.
600 ## - SUBJECT ADDED ENTRY--PERSONAL NAME
General subdivision BCMA
General subdivision multiple myeloma
General subdivision clinical trials
General subdivision CAR-T
General subdivision chimeric antigen receptor T cell
700 ## - ADDED ENTRY--PERSONAL NAME
Fuller form of name Erius Tebuka
Fuller form of name Peter Fabian Rambau
Fuller form of name Hermann Einsele
Fuller form of name Michael Hudecek
Fuller form of name Sabrina Rebecca Prommersberger
Fuller form of name Sophia Danhof
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1080/10428194.2023.2276676 ">https://doi.org/10.1080/10428194.2023.2276676 </a>
Link text https://doi.org/10.1080/10428194.2023.2276676
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme ddc
Koha item type RESEARCH ARTICLES
Suppress in OPAC
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Date acquired Total checkouts Barcode Date last seen Price effective from Koha item type
          MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO MWALIMU NYERERE LEARNING RESOURCES CENTRE-CUHAS BUGANDO 06/07/2024   20240607164401.0 06/07/2024 06/07/2024 RESEARCH ARTICLES
Catholic University of  Health and Allied Sciences - CUHAS
Directorate of ICT @ 2024