TY - JOUR
T1 - Severity of Cytokine Release Syndrome Influences Outcome After Axicabtagene Ciloleucel for Large B cell Lymphoma
T2 - Results from the US Lymphoma CAR-T Consortium
AU - Jacobs, Miriam T.
AU - Jain, Michael D.
AU - Gao, Feng
AU - Nastoupil, Loretta J.
AU - Spiegel, Jay Y.
AU - Lin, Yi
AU - Dahiya, Saurabh
AU - Lunning, Matthew
AU - Lekakis, Lazaros
AU - Reagan, Patrick M.
AU - Oluwole, Olalekan O.
AU - McGuirk, Joseph
AU - Deol, Abhinav
AU - Sehgal, Alison
AU - Goy, Andre
AU - Hill, Brian T.
AU - Andreadis, Charalambos
AU - Munoz, Javier
AU - Chavez, Julio C.
AU - Bennani, N. Nora
AU - Rapoport, Aaron P.
AU - Vose, Julie M.
AU - Miklos, David B.
AU - Neelapu, Sattva S.
AU - Ghobadi, Armin
AU - Locke, Frederick L.
N1 - Funding Information:
M.T. Jacobs is partially funded by Conquer Cancer, the ASCO Foundation. M.D. Jain was consulting for Kite Pharma-Gilead, Novartis, BMS and Takeda. L.J. Nastoupil receives research support from Bristol Myers Squib-Celegene, Epizyme, Genentech, Kite Pharma-Gilead, Novartis and TG Therapeutics, Honorarium from Bristol Myers Squib-Celegene, Genentech, Kite Pharma-Gilead, Janssen, Novartis, and TG Therapeutics. Y. Lin receives consulting for Kite Pharma-Gilead, Bristol Myers Squib-Celegene, Bristol Myers Squib –JUNO, BlueBird Bio, Janssen and Legend BioTech, Gamida Cells, Novartis, Iovance, Takeda, Fosun, Kite Pharma-Gilead, receives research support from Kite Pharma-Gilead, Bristol Myers Squib-Celegene, BlueBird Bio, Janssen, Legend Biotech, Merck, Takeda, Boston Scientific, other disclosures DSMB Sorrento. S. Dahiya receives research support from Jazz Pharmaceuticals, Advisory board member for Kite Pharma-Gilead and Atara Biotherapeutics. M. Lunning receives research support from Bristol Myers Squib-Celegene and Curis, consulting for Acrotech, ADC Therapeutics, Astra-Zeneca, BeiGene, Bristol Myers Squib-Celgene-Juno; Diiachi Sankyo, Janssen-Pharmacyclics, Karyopharm, Kite Pharma-Gilead, Legend, Morphosys, Myeloid Therapeutics, Novartis, Spectrum, TG Therapeutics, Verastem. P.M. Reagan receives research support from Seattle Genetics, Genentech, consulting for Kite Pharma-Gilead. O.O. Oluwole receives consulting for Kite Pharma-Gilead, Pfizer, Spectrum, Bayer, Curio science and Legend. J. McGuirk receives research support from AlooVir HCP, Bristol Myers Squib-Juno, Kite Pharma-Gilead, Magenta Therapeutics, consulting for AlooVir HCP, Juno Therapeutics, Kite Pharma-Gilead, Advisory board member for AlooVir HCP, Bristol Myers Squib-Juno Therapeutics, Kite Pharma-Gilead, Magenta Therapeutics, Honorarium from AlooVir HCP, Bristol Myers Squib-Juno, Kite Pharma-Gilead. A. Deol receives consulting for Kite Pharma-Gilead. A. Sehgal receives research funding from Kite Pharma-Gilead and Bristol Myers Squib-Juno Therapeutics. B.T. Hill receives consultancy and research funding from Kite Pharma-Gilead and Novartis. C.Andreadis was Scientific advisor for Kite Pharma-Gilead, Jazz Pharmaceuticals, Astellas, Seattle Genetics, receives research support from Novartis, Amgen, and Merck, spouse employed by Genentech. J. Munoz receives research support from Bayer, Kite Pharma-Gilead, Celgene, Merck, Portola, Incyte, Genentech, Pharmacyclics, Seattle Genetics, Janssen and Millennium, Consulting for Pharmacyclics, Bayer, Kite Pharma-Gilead, Pfizer, Janssen, Bristol Myers Squib-Celegene- Juno- Celgene, Kyowa, Alexion, Beigene, Fosunkite, Innovent, Seattle Genetics and Beigene, Honorarium from Kyowa and Seattle Genetics, Speaker's bureau Kite Pharma-Gilead, Kyowa, Bayer, Pharmacyclics/Janssen, Seattle Genetics, Acrotech/Aurobindo, Beigene, Verastem, AstraZeneca, Bristol Myers Squib-Celegene, Genentech/Roche and Abbvie. J.C. Chavez was consulting for Novartis, Kite Pharma-Gilead, Abbvie, Janssen, Morphosys, Bayer and Karyopharm, receives research support from Merck, Speaker Bureau BeiGene, AstraZeneca, Morphosys and Epyzime. N.N.Bennani receives research funding from Kite Pharma-Gilead and Affimed, Advisory board member for Daiichi Sankyo, Verastem and Purdue Pharma. J.M. Vose receives research support from Acerta/Astra-Zeneca, Bristol Myers Squib-Celegene, Incyte Corp., Kite Pharma-Gilead, Novartis, Seattle Genetics, Inc., LOXO and Epizyme, consulting and honorarium from Abbvie, Epizyme, Vaniam Group, Janssen/Pharmacyclics, Kite Pharma-Gilead, Astra-Zeneca, Verastem, Miltenyi Biotec, Inc, Loxo Oncology, Allogene, Wugene, Bristol Myers Squib-Celegene, Roche, Genentech, Karyopharm, Morphosys/Incyte. D.B.Miklos receives consultancy for Kite Pharma-Gilead, Bristol Myers Squib-Juno-Celgene and Novartis, research funding from Kite Pharma-Gilead. S.S. Neelapu receives research support from Kite Pharma-Gilead, Bristol-Myers Squibb- Celgene, Merck, Poseida, Cellectis, Karus Therapeutics, Unum Therapeutics, Allogene Therapeutics, Precision Biosciences, and Acerta, served as Advisory Board member or consultant for Kite Pharma-Gilead, Merck, Bristol-Myers Squibb- Celgene, Novartis, Pfizer, Allogene Therapeutics, Cell Medica/Kuur, Incyte, Precision Biosciences, Legend Biotech, Adicet Bio, Calibr, and Unum Therapeutics, received royalties from Takeda Pharmaceuticals and has intellectual property related to cell therapy. A.Ghobadi receives research support from Kite Pharma-Gilead and Amgen, Advisory Board Member/Consultant for Kite Pharma-Gilead, Amgen, Celgene, EUSA, Atara, CRISPR Therapeutics, and Wugen. F.L. Locke was a consultant for Cellular BioMedicine Group Inc., Scientific Advisor/Advisory Board Member for Allogene, Amgen, BlueBird Bio, Iovance, Kite Pharma-Gilead, Novartis, GammaDelta Therapuetics, Calibr, Bristol Myers Squib-Celgene, WuGen; and received research support from Kite Pharma-Gilead, Novartis, CERo Therapuetics, and Bristol-Myers Squibb . All other authors state that they have no conflicts of interest.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/10
Y1 - 2022/10
N2 - Background: The majority of patients with large B-cell lymphoma treated with axicabtagene ciloleucel (axi-cel), an anti-CD19 chimeric antigen receptor (CAR) T-cell therapy, develop cytokine release syndrome (CRS). Whether the lack of development of CRS with axi-cel is associated with inferior lymphoma outcomes is unknown. Additionally, relationship between CRS grade and lymphoma outcome is not well established. Methods: The US Lymphoma CAR T Consortium includes seventeen US academic centers that contribute data independently of manufacturers. We analyzed the modified intent-to-treat population of 275 patients receiving axi-cel in two different ways: 1) Two group analysis comparing no CRS with any grade CRS; 2) Three group analysis comparing grade 0 CRS with grade 1 to 2 CRS, and grade 3-5 CRS. Results: In this large multi-center observational cohort of 275 patients receiving axi-cel, 9% (n = 24) did not develop CRS, 84% (n = 232) developed grade 1-2 CRS, and 7% (n = 19) developed grade 3 to 5 CRS. Patients without CRS, compared with those having any grade CRS, had similar overall response rates (ORR), lower complete response (CR) rates and inferior progression free survival (PFS) with no statistically significant difference in overall survival (OS). Patients experiencing grade 1 to 2 CRS had superior CR rate and PFS, as compared to those without CRS or with grade 3 to 5 CRS. Grade 3 to 5 CRS was associated with a worse OS. Conclusion: Overall, durable responses were seen in patients that did not develop CRS, however grade 1 to 2 CRS was associated with better outcomes while those with grade 3 to 5 experienced the worse outcomes.
AB - Background: The majority of patients with large B-cell lymphoma treated with axicabtagene ciloleucel (axi-cel), an anti-CD19 chimeric antigen receptor (CAR) T-cell therapy, develop cytokine release syndrome (CRS). Whether the lack of development of CRS with axi-cel is associated with inferior lymphoma outcomes is unknown. Additionally, relationship between CRS grade and lymphoma outcome is not well established. Methods: The US Lymphoma CAR T Consortium includes seventeen US academic centers that contribute data independently of manufacturers. We analyzed the modified intent-to-treat population of 275 patients receiving axi-cel in two different ways: 1) Two group analysis comparing no CRS with any grade CRS; 2) Three group analysis comparing grade 0 CRS with grade 1 to 2 CRS, and grade 3-5 CRS. Results: In this large multi-center observational cohort of 275 patients receiving axi-cel, 9% (n = 24) did not develop CRS, 84% (n = 232) developed grade 1-2 CRS, and 7% (n = 19) developed grade 3 to 5 CRS. Patients without CRS, compared with those having any grade CRS, had similar overall response rates (ORR), lower complete response (CR) rates and inferior progression free survival (PFS) with no statistically significant difference in overall survival (OS). Patients experiencing grade 1 to 2 CRS had superior CR rate and PFS, as compared to those without CRS or with grade 3 to 5 CRS. Grade 3 to 5 CRS was associated with a worse OS. Conclusion: Overall, durable responses were seen in patients that did not develop CRS, however grade 1 to 2 CRS was associated with better outcomes while those with grade 3 to 5 experienced the worse outcomes.
KW - Axicabtagene ciloleucel
KW - CRS
KW - Cellular therapy
KW - Lymphoid malignancy
KW - Responses
UR - http://www.scopus.com/inward/record.url?scp=85133386396&partnerID=8YFLogxK
U2 - 10.1016/j.clml.2022.05.004
DO - 10.1016/j.clml.2022.05.004
M3 - Article
C2 - 35780055
AN - SCOPUS:85133386396
SN - 2152-2650
VL - 22
SP - 753
EP - 759
JO - Clinical Lymphoma, Myeloma and Leukemia
JF - Clinical Lymphoma, Myeloma and Leukemia
IS - 10
ER -