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|a Axicabtagene ciloleucel for large B-cell lymphoma: Health technology assessment introduction and clinical review protocol
|h Elektronische Ressource
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|a Health technology assessment introduction and clinical review protocol
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|a Ottawa (ON)
|b Canadian Agency for Drugs and Technologies in Health
|c May 2019, 2019
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|a 1 PDF file (29 pages)
|b illustrations
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|a Includes bibliographical references
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|a Immunotherapy, Adoptive
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|a Lymphoma, Large B-Cell, Diffuse / drug therapy
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|a Canada
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|a Technology Assessment, Biomedical
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|a Treatment Outcome
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|a Antineoplastic Protocols
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|a Antigens, CD19 / therapeutic use
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|a Canadian Agency for Drugs and Technologies in Health
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a CADTH optimal use report
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|a "PROSPERO registration number: CRD42019119293."
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|u http://www.ncbi.nlm.nih.gov/books/NBK550126
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 600
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|a Lymphomas are blood cancers that develop in the lymphatic system and are divided into Hodgkin lymphoma and non-Hodgkin lymphomas (NHL). NHLs are categorized as B-cell, Tcell, or natural killer/T-cell lymphoma, depending on the cell implicated in the disease. While B-cell NHLs display a wide range of clinical behaviours, there are several subtypes that have a roughly similar clinical course and are treated in a similar manner. These subtypes include diffuse large B-cell lymphoma (DLBCL), primary mediastinal B-cell lymphoma, high-grade B-cell lymphoma, and DLBCL arising from follicular lymphoma. In Canada, NHL accounts for 83% of all cases of lymphomas. In this context, axicabtagene ciloleucel is a chimeric antigen receptor (CAR) T-cell therapy that has been approved by the FDA for use in "adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including DLBCL not otherwise specified, primary mediastinal large B-cell lymphoma, high-grade B-cell lymphoma, and DLBCL arising from follicular lymphoma." As Health Canada approval for axicabtagene ciloleucel is pending, the final indication remains to be confirmed; however, based on the available evidence and existing approvals for this therapy (i.e., by the FDA and the European Union), potentially eligible indications are these types of relapsed or refractory large B-cell lymphomas: DLBCL, primary mediastinal B-cell lymphoma, high-grade B-cell lymphoma, and DLBCL arising from follicular lymphoma
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