an overview of chimeric antigen receptor t-cells · an overview of chimeric antigen receptor...
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An Overview of Chimeric Antigen Receptor T-cells:
Maxwell Brown, PharmD
Clinical Pharmacy Manager, Hematopoietic Stem Cell Transplantation
NewYork-Presbyterian/Weill Cornell Medical Center
“CAR-T-ing Away Cancer”
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Conflict of Interest Disclosure
I have no actual or potential conflicts of interest to disclose regarding this presentation.
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Objectives
1. Discuss the structure and mechanism of action of chimeric antigen receptor (CAR) T-cells.
2. Describe the pathophysiology and management of cytokine release syndrome (CRS) and CAR-T related encephalopathy syndrome (CRES)
3. Summarize key clinical trials assessing the use of CAR-T cell therapy in acute lymphoblastic leukemia (ALL) and B-cell lymphomas
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Audience Response Question #1
What does CAR-T cell stand for?
1. Carrier T cell
2. Chemotherapy/antibody receptor T cell
3. Chimeric antigen receptor T cell
4. Chimeric antibody receptor T cell
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Audience Response Question #1
What does CAR-T cell stand for?
1. Carrier T cell
2. Chemotherapy/antibody receptor T cell
3. Chimeric antigen receptor T cell
4. Chimeric antibody receptor T cell
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Chimeric: combination of different genes
Antigen: substance which initiates an immune response
Receptor: molecule which binds a particular substance resulting in a specific effect
T cell: type of white blood cell or lymphocyte; component of the adaptive immune system
C
A
R
T
CAR-T cells
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What is a CAR-T cell?
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Hematopoiesis
https://en.wikipedia.org/wiki/Haematopoiesis#/media/File:Hematopoiesis_simple.svg
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Antigen Recognition and Processing
Bacteria Viruses
APC
Phagocytosis of bacterial cells by antigen presenting cells (APC).
Antigen processing into peptide fragments for presentation via the major histocompatibility complex (MHC).
Healthy Cell
Virus invades healthy cell and begins replicating.
Degradation of viral proteins by the proteasome for presentation via the MHC.
Curr Res Transl Med. 2017;65(3):93-102.
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Endogenous T-cell Activation
T-cellα β
Variable Region
Constant Region
APC
Co-Receptor(e.g. CD4, CD8)
MHC- Class I: cytotoxic T-cell- Class II: helper T-cell
T-cell Receptor
Curr Res Transl Med. 2017;65(3):93-102.
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CAR-T cell Activation
CAR-T cellα β
Variable Region
Constant Region
APC
Co-Receptor(e.g. CD4, CD8)
MHC- Class I: cytotoxic T-cell- Class II: helper T-cell
Tumor Cell
Tumor Cell Antigen(e.g. CD19)
scFv = single chain fragment variable
scFv
Linker
Hinge
Transmembrane Domain
Signaling Domain
CAR-T cell Receptor
Curr Res Transl Med. 2017;65(3):93-102.
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Engineering of CAR-T cells
- Cytotoxicity- Proliferation & Persistence- Cytokine Production
TRUCK =T cell redirected for universal cytokine-mediated killing Curr Res Transl Med. 2017;65(3):93-102.
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CAR-T cell Manufacturing and Administration
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T-cell Collection CAR
TransductionCAR-T
Expansion CAR-T Infusion
Apheresis
T-cell selection
Autologous versus
Allogeneic?
Lentiviral/retroviral DNA vectors
Gene transfer
CAR expression
APCs, activation reagents, antibody-coated microbeads
Cryopreservation
Administration of lymphodepleting chemotherapy
Infusion of CAR-T product
CAR-T cell Manufacturing Process
Mol Ther Oncolytics. 2016;3:16015.
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Autologous versus Allogeneic CAR-T cells
Autologous Allogeneic
Ability to collect Persistence of CAR-T cells
Quality & functionality Risk of graft-versus-host disease
Production time
Delays in treatment
Curr Opin Hematol. 2015;22(6):509-15.
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Lymphodepleting Chemotherapy
Cyclophosphamide 500 mg/m2 IV once daily Rest
Fludarabine 30 mg/m2 IV once daily CAR-T cell Infusion
Day -5 Day -4 Day -3 Day -2 Day -1
Day -5 Day -4 Day -3 Day 0
YESCARTA (axicabtagene ciloleucel suspension) [package insert].
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Commercially Available CAR-T Products
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Audience Response Question #2
For which disease states are CAR-T cells currently FDA approved?
1. Acute lymphoblastic leukemia (relapsed or refractory)
2. Large B-cell lymphoma (relapsed or refractory)
3. Acute myeloid leukemia (relapsed or refractory)
4. Both A and B
5. All of the above
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Audience Response Question #2
For which disease states are CAR-T cells currently FDA approved?
1. Acute lymphoblastic leukemia (relapsed or refractory)
2. Large B-cell lymphoma (relapsed or refractory)
3. Acute myeloid leukemia (relapsed or refractory)
4. Both A and B
5. All of the above
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Currently Available CAR-T cell Products
YESCARTA (axicabtagene ciloleucel)
• FDA Approval: treatment of adults with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy
• Autologous CAR-T cell product targeting CD19
KYMRIAH (tisagenlecleucel)
• FDA Approval: treatment of patients up to 25 years of age with relapsed or refractory B-cell precursor acute lymphoblastic leukemia
• Autologous CAR-T cell product targeting CD19YESCARTA (axicabtagene ciloleucel suspension) [package insert].
KYMRIAH (tisagenlecleucel) [package insert].
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What’s in a name?
axicabtagene ciloleucel
• First Word: corresponds to gene component
• Second Word: corresponds to vector and cell component
World Health Organization 2017.
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What’s in a name?
axicabtagene ciloleucel
Prefix is random
World Health Organization 2017.
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First Word Infix identifies the gene component
‘cabta’ = cell expressed antibody and T cell activation
Second Word Infix identifies the cell type
‘leu’ = lymphocytes/monocytes/APC (white cells)
What’s in a name?
axicabtagene ciloleucel
World Health Organization 2017.
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First Word Suffix Second Word Suffix
Designate the product as a genetically modified cell-based therapy
What’s in a name?
axicabtagene ciloleucel
World Health Organization 2017.
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ZUMA-1 Trial
N Engl J Med 2017; 377:2531-44.
Design ▪ Multicenter, phase II clinical trial
Population▪ n = 111▪ Adult patients with relapsed or refractory B cell lymphomas*
Intervention ▪ Axicabtagene ciloleucel
Efficacy
▪ ORR = 82%; CR = 52%; median duration of response = 8.1 months▪ At 15 months:
o Median PFS = 44%o Median OS = 52%
Safety▪ CRS occurred in 93% of patients, 13% of grade 3 or higher
▪ Neurotoxicity occurred in 64% of patients, 28% of grade 3 or higher
ORR = overall response rate; PFS = progression-free survival; OS = overall survival; CRS = cytokine release syndrome
*diffuse large B-cell lymphoma, primary mediastinal B-cell lymphoma, or transformed follicular lymphoma
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N Engl J Med 2018; 378:439-48.
Design ▪ Multicenter, phase II clinical trial
Population▪ n = 92▪ Pediatric and young adults (≤25 years) with CD19+ relapsed or refractory B-cell ALL
Intervention ▪ Tisagenlecleucel
Efficacy
▪ ORR = 81%; CR = 45%; CRi = 21%; Median duration of response not reached ▪ At 12 months:
o Median EFS = 50%o Median OS = 76%
Safety▪ CRS occurred in 77% of patients, 46% of grade 3 or higher
▪ Neurotoxicity occurred in 40% of patients, 10% of grade 3
ELIANA Trial
CRi = complete response with incomplete hematologic recovery; EFS = event free survival
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Black Box Warnings
• Fever, hypoxia, hypotension, coagulopathy, acute kidney injury, transaminitis, hyperbilirubinemia
Cytokine Release Syndrome
• Headache, encephalopathy, delirium, anxiety, tremor
Neurologic Toxicities
• Patient wallet card
• Minimum of two doses of tocilizumab available for each patient
REMS Program
YESCARTA (axicabtagene ciloleucel suspension) [package insert].KYMRIAH (tisagenlecleucel) [package insert].
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Cytokine Release Syndrome (CRS)
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Pathophysiology of CRS
APC
T-cell
T
T
T
TT
T
Tumor Cell
Blood. 2014;124(2):188-95.
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Tocilizumab
Blood. 2014;124(2):188-95.
IL-6R
IL-6
IL-6R = interleukin-6 receptor; IL-6 = interleukin-6
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Tocilizumab
Blood. 2014;124(2):188-95.
IL-6R
IL-6
IL-6R = interleukin-6 receptor; IL-6 = interleukin-6
Tocilizumab
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Siltuximab
Blood. 2014;124(2):188-95.
IL-6R
IL-6
IL-6R = interleukin-6 receptor; IL-6 = interleukin-6
Siltuximab
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Conclusion
▪CAR-T cells are a novel therapeutic approach to cancer therapy
▪Over 200 clinical trials actively recruiting participants
▪Proper management of CAR-T cell toxicities is critical▪ CRS / Neurotoxicity
▪ “On-target, off-tumor” toxicities
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An Overview of Chimeric Antigen Receptor T-cells:
Maxwell Brown, PharmD
Clinical Pharmacy Manager, Hematopoietic Stem Cell Transplantation
NewYork-Presbyterian/Weill Cornell Medical Center
“CAR-T-ing Away Cancer”
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References1. Wikipedia: The Free Encyclopedia [Internet]. Wikimedia Foundation Inc. Updated 4 January 2017. Encyclopedia
on-line. Available from https://en.wikipedia.org/wiki/Haematopoiesis#/media/File: Hematopoiesis_simple.svg. Retrieved 7 January 2017.
2. Gauthier J, Yakoub-Agha I. Chimeric antigen-receptor T-cell therapy for hematological malignancies and solid tumors: Clinical data to date, current limitations and perspectives.Curr Res Transl Med. 2017;65(3):93-102.
3. Wang X and Rivière I. Clinical manufacturing of CAR T cells: foundation of a promising therapy. Mol TherOncolytics. 2016;3:16015.
4. Yang Y, Jacoby E, and Fry TJ. Challenges and opportunities of allogeneic donor-derived CAR T cells. Curr Opin Hematol. 2015;22(6):509-15.
5. YESCARTA (axicabtagene ciloleucel suspension) [package insert]. El Segundo, CA: Kite Pharma, Inc.; 2017.6. KYMRIAH (tisagenlecleucel) [package insert]. Morris Plans, NJ: Novartis Pharmaceuticals Corporation; 2017.7. Guidance on the use of international nonproprietary names (INNs) for pharmaceutical substances. Geneva:
World Health Organization; 2017. 8. Neelapu SS, Locke FL, Bartlett NL et al. Axicabtagene ciloleucel CAR T-cell therapy in refractory large B-cell
lymphoma. N Engl J Med 2017; 377:2531-44.9. Maude SL, Laetsch TW, Buechner J et al. Tisagenlecleucel in children and young adults with B-cell lymphoblastic
leukemia. N Engl J Med 2018; 378:439-48.10. Lee DW, Gardner R, Porter DL et al. Current concepts in the diagnosis and management of cytokine release
syndrome. Blood. 2014;124(2):188-95.