Difference between revisions of "Lisocabtagene maraleucel (Breyanzi)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
*2/5/2021: Approved for the treatment of adult patients with relapsed or refractory (R/R) large B-cell lymphoma after two or more lines of systemic therapy, including [[Diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL) not otherwise specified]] (including [[Transformed lymphoma|DLBCL arising from indolent lymphoma]]), [[high-grade B-cell lymphoma]], [[Primary mediastinal B-cell lymphoma|primary mediastinal large B-cell lymphoma]], and follicular lymphoma grade 3B. ''(Based on TRANSCEND NHL-001)''
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*2021-02-05: Approved for the treatment of adult patients with relapsed or refractory (R/R) large B-cell lymphoma after two or more lines of systemic therapy, including [[Diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL) not otherwise specified]] (including [[Transformed lymphoma|DLBCL arising from indolent lymphoma]]), [[high-grade B-cell lymphoma]], [[Primary mediastinal B-cell lymphoma|primary mediastinal large B-cell lymphoma]], and follicular lymphoma grade 3B. ''(Based on TRANSCEND NHL-001)''
*6/24/2022: Approved for adult patients with [[Diffuse large B-cell lymphoma|large B-cell lymphoma (LBCL)]] who have refractory disease to first-line chemoimmunotherapy or relapse within 12 months of first-line chemoimmunotherapy. ''(Based on TRANSFORM)''
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*2022-06-24: Approved for adult patients with [[Diffuse large B-cell lymphoma|large B-cell lymphoma (LBCL)]] who have refractory disease to first-line chemoimmunotherapy or relapse within 12 months of first-line chemoimmunotherapy. ''(Based on TRANSFORM)''
*6/24/2022: Approved for adult patients with [[Diffuse large B-cell lymphoma|large B-cell lymphoma (LBCL)]] who have refractory disease to first-line chemoimmunotherapy or relapse after first-line chemoimmunotherapy and are not eligible for hematopoietic stem cell transplantation (HSCT) due to comorbidities or age. ''(Based on TRANSFORM)''
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*2022-06-24: Approved for adult patients with [[Diffuse large B-cell lymphoma|large B-cell lymphoma (LBCL)]] who have refractory disease to first-line chemoimmunotherapy or relapse after first-line chemoimmunotherapy and are not eligible for hematopoietic stem cell transplantation (HSCT) due to comorbidities or age. ''(Based on TRANSFORM)''
 
==History of changes in EMA indication==
 
==History of changes in EMA indication==
*4/4/2022: Breyanzi is indicated for the treatment of adult patients with relapsed or refractory [[Diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL)]], [[Primary mediastinal B-cell lymphoma|primary mediastinal large B-cell lymphoma (PMBCL)]] and follicular lymphoma grade 3B (FL3B), after two or more lines of systemic therapy.
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*2022-04-04: Breyanzi is indicated for the treatment of adult patients with relapsed or refractory [[Diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL)]], [[Primary mediastinal B-cell lymphoma|primary mediastinal large B-cell lymphoma (PMBCL)]] and follicular lymphoma grade 3B (FL3B), after two or more lines of systemic therapy.
 
== Patient Drug Information==
 
== Patient Drug Information==
 
*[https://www.fda.gov/media/145711/download Lisocabtagene maraleucel (Breyanzi) Package Insert]<ref>[https://www.fda.gov/media/145711/download Lisocabtagene maraleucel (Breyanzi) Package Insert]</ref>
 
*[https://www.fda.gov/media/145711/download Lisocabtagene maraleucel (Breyanzi) Package Insert]<ref>[https://www.fda.gov/media/145711/download Lisocabtagene maraleucel (Breyanzi) Package Insert]</ref>

Revision as of 20:54, 5 May 2023

Mechanism of action

From the NCI Drug Dictionary: A preparation of a defined ratio of CD4+ and CD8+ autologous T lymphocytes transduced with a lentiviral vector expressing a chimeric antigen receptor (CAR) containing an anti-CD19 single chain variable fragment (scFv) fused to the signaling domain of 4-1BB (CD137), the zeta chain of the TCR/CD3 complex (CD3-zeta), and a truncated form of the human epidermal growth factor receptor (EGFRt), with potential immunostimulating and antineoplastic activities. Upon intravenous administration, lisocabtagene maraleucel is directed to and induce selective toxicity in CD19-expressing tumor cells.

Toxicity management

Diseases for which it is established (work in progress)

History of changes in FDA indication

History of changes in EMA indication

Patient Drug Information

Also known as

  • Code name: JCAR017
  • Brand names: Breyanzi, Liso-cel

References