Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis
Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had...
Ausführliche Beschreibung
Autor*in: |
Abbasi, Ahmed [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2020 |
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Anmerkung: |
© The Author(s). 2020 |
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Übergeordnetes Werk: |
Enthalten in: Journal of hematology & oncology - London : Biomed Central, 2008, 13(2020), 1 vom: 03. Jan. |
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Übergeordnetes Werk: |
volume:13 ; year:2020 ; number:1 ; day:03 ; month:01 |
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DOI / URN: |
10.1186/s13045-019-0838-y |
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Katalog-ID: |
SPR029625378 |
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520 | |a Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. | ||
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10.1186/s13045-019-0838-y doi (DE-627)SPR029625378 (SPR)s13045-019-0838-y-e DE-627 ger DE-627 rakwb eng Abbasi, Ahmed verfasserin aut Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2020 Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. CD19 CAR-T (dpeaa)DE-He213 HIV and CD-19 CAR-T (dpeaa)DE-He213 CNS and CD-19 CAR-T (dpeaa)DE-He213 Axi-cel (dpeaa)DE-He213 Hepatitis B and CD-19 CAR-T (dpeaa)DE-He213 Peeke, Stephen aut Shah, Nishi aut Mustafa, Jennat aut Khatun, Fariha aut Lombardo, Amanda aut Abreu, Michelly aut Elkind, Richard aut Fehn, Karen aut de Castro, Alyssa aut Wang, Yanhua aut Derman, Olga aut Nelson, Randin aut Uehlinger, Joan aut Gritsman, Kira aut Sica, R. Alejandro aut Kornblum, Noah aut Mantzaris, Ioannis aut Shastri, Aditi aut Janakiram, Murali aut Goldfinger, Mendel aut Verma, Amit aut Braunschweig, Ira aut Bachier-Rodriguez, Lizamarie aut Enthalten in Journal of hematology & oncology London : Biomed Central, 2008 13(2020), 1 vom: 03. Jan. (DE-627)568914813 (DE-600)2429631-4 1756-8722 nnns volume:13 year:2020 number:1 day:03 month:01 https://dx.doi.org/10.1186/s13045-019-0838-y kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2020 1 03 01 |
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10.1186/s13045-019-0838-y doi (DE-627)SPR029625378 (SPR)s13045-019-0838-y-e DE-627 ger DE-627 rakwb eng Abbasi, Ahmed verfasserin aut Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2020 Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. CD19 CAR-T (dpeaa)DE-He213 HIV and CD-19 CAR-T (dpeaa)DE-He213 CNS and CD-19 CAR-T (dpeaa)DE-He213 Axi-cel (dpeaa)DE-He213 Hepatitis B and CD-19 CAR-T (dpeaa)DE-He213 Peeke, Stephen aut Shah, Nishi aut Mustafa, Jennat aut Khatun, Fariha aut Lombardo, Amanda aut Abreu, Michelly aut Elkind, Richard aut Fehn, Karen aut de Castro, Alyssa aut Wang, Yanhua aut Derman, Olga aut Nelson, Randin aut Uehlinger, Joan aut Gritsman, Kira aut Sica, R. Alejandro aut Kornblum, Noah aut Mantzaris, Ioannis aut Shastri, Aditi aut Janakiram, Murali aut Goldfinger, Mendel aut Verma, Amit aut Braunschweig, Ira aut Bachier-Rodriguez, Lizamarie aut Enthalten in Journal of hematology & oncology London : Biomed Central, 2008 13(2020), 1 vom: 03. Jan. (DE-627)568914813 (DE-600)2429631-4 1756-8722 nnns volume:13 year:2020 number:1 day:03 month:01 https://dx.doi.org/10.1186/s13045-019-0838-y kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2020 1 03 01 |
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10.1186/s13045-019-0838-y doi (DE-627)SPR029625378 (SPR)s13045-019-0838-y-e DE-627 ger DE-627 rakwb eng Abbasi, Ahmed verfasserin aut Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2020 Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. CD19 CAR-T (dpeaa)DE-He213 HIV and CD-19 CAR-T (dpeaa)DE-He213 CNS and CD-19 CAR-T (dpeaa)DE-He213 Axi-cel (dpeaa)DE-He213 Hepatitis B and CD-19 CAR-T (dpeaa)DE-He213 Peeke, Stephen aut Shah, Nishi aut Mustafa, Jennat aut Khatun, Fariha aut Lombardo, Amanda aut Abreu, Michelly aut Elkind, Richard aut Fehn, Karen aut de Castro, Alyssa aut Wang, Yanhua aut Derman, Olga aut Nelson, Randin aut Uehlinger, Joan aut Gritsman, Kira aut Sica, R. Alejandro aut Kornblum, Noah aut Mantzaris, Ioannis aut Shastri, Aditi aut Janakiram, Murali aut Goldfinger, Mendel aut Verma, Amit aut Braunschweig, Ira aut Bachier-Rodriguez, Lizamarie aut Enthalten in Journal of hematology & oncology London : Biomed Central, 2008 13(2020), 1 vom: 03. Jan. (DE-627)568914813 (DE-600)2429631-4 1756-8722 nnns volume:13 year:2020 number:1 day:03 month:01 https://dx.doi.org/10.1186/s13045-019-0838-y kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2020 1 03 01 |
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10.1186/s13045-019-0838-y doi (DE-627)SPR029625378 (SPR)s13045-019-0838-y-e DE-627 ger DE-627 rakwb eng Abbasi, Ahmed verfasserin aut Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2020 Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. CD19 CAR-T (dpeaa)DE-He213 HIV and CD-19 CAR-T (dpeaa)DE-He213 CNS and CD-19 CAR-T (dpeaa)DE-He213 Axi-cel (dpeaa)DE-He213 Hepatitis B and CD-19 CAR-T (dpeaa)DE-He213 Peeke, Stephen aut Shah, Nishi aut Mustafa, Jennat aut Khatun, Fariha aut Lombardo, Amanda aut Abreu, Michelly aut Elkind, Richard aut Fehn, Karen aut de Castro, Alyssa aut Wang, Yanhua aut Derman, Olga aut Nelson, Randin aut Uehlinger, Joan aut Gritsman, Kira aut Sica, R. Alejandro aut Kornblum, Noah aut Mantzaris, Ioannis aut Shastri, Aditi aut Janakiram, Murali aut Goldfinger, Mendel aut Verma, Amit aut Braunschweig, Ira aut Bachier-Rodriguez, Lizamarie aut Enthalten in Journal of hematology & oncology London : Biomed Central, 2008 13(2020), 1 vom: 03. Jan. (DE-627)568914813 (DE-600)2429631-4 1756-8722 nnns volume:13 year:2020 number:1 day:03 month:01 https://dx.doi.org/10.1186/s13045-019-0838-y kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2020 1 03 01 |
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10.1186/s13045-019-0838-y doi (DE-627)SPR029625378 (SPR)s13045-019-0838-y-e DE-627 ger DE-627 rakwb eng Abbasi, Ahmed verfasserin aut Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s). 2020 Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. CD19 CAR-T (dpeaa)DE-He213 HIV and CD-19 CAR-T (dpeaa)DE-He213 CNS and CD-19 CAR-T (dpeaa)DE-He213 Axi-cel (dpeaa)DE-He213 Hepatitis B and CD-19 CAR-T (dpeaa)DE-He213 Peeke, Stephen aut Shah, Nishi aut Mustafa, Jennat aut Khatun, Fariha aut Lombardo, Amanda aut Abreu, Michelly aut Elkind, Richard aut Fehn, Karen aut de Castro, Alyssa aut Wang, Yanhua aut Derman, Olga aut Nelson, Randin aut Uehlinger, Joan aut Gritsman, Kira aut Sica, R. Alejandro aut Kornblum, Noah aut Mantzaris, Ioannis aut Shastri, Aditi aut Janakiram, Murali aut Goldfinger, Mendel aut Verma, Amit aut Braunschweig, Ira aut Bachier-Rodriguez, Lizamarie aut Enthalten in Journal of hematology & oncology London : Biomed Central, 2008 13(2020), 1 vom: 03. Jan. (DE-627)568914813 (DE-600)2429631-4 1756-8722 nnns volume:13 year:2020 number:1 day:03 month:01 https://dx.doi.org/10.1186/s13045-019-0838-y kostenfrei Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2020 1 03 01 |
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Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis CD19 CAR-T (dpeaa)DE-He213 HIV and CD-19 CAR-T (dpeaa)DE-He213 CNS and CD-19 CAR-T (dpeaa)DE-He213 Axi-cel (dpeaa)DE-He213 Hepatitis B and CD-19 CAR-T (dpeaa)DE-He213 |
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Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis |
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Abbasi, Ahmed |
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Abbasi, Ahmed Peeke, Stephen Shah, Nishi Mustafa, Jennat Khatun, Fariha Lombardo, Amanda Abreu, Michelly Elkind, Richard Fehn, Karen de Castro, Alyssa Wang, Yanhua Derman, Olga Nelson, Randin Uehlinger, Joan Gritsman, Kira Sica, R. Alejandro Kornblum, Noah Mantzaris, Ioannis Shastri, Aditi Janakiram, Murali Goldfinger, Mendel Verma, Amit Braunschweig, Ira Bachier-Rodriguez, Lizamarie |
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10.1186/s13045-019-0838-y |
title_sort |
axicabtagene ciloleucel cd19 car-t cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large b cell lymphoma including two with hiv and viral hepatitis |
title_auth |
Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis |
abstract |
Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. © The Author(s). 2020 |
abstractGer |
Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. © The Author(s). 2020 |
abstract_unstemmed |
Abstract Axicabtagene ciloleucel (Axi-cel) is a CD-19 Chimeric Antigen Receptor T cell therapy approved for the treatment of relapsed/refractory diffuse large B cell lymphoma. We treated ten patients with DLBCL post-FDA approval in an inner-city tertiary center in the Bronx. Eight patients (80%) had received ≥ 3 lines of therapy, six patients had received prior radiation, and seven had recurrent disease after prior autologous hematopoietic stem cell transplant (AHCT). Our cohort included one patient with HIV, two patients with hepatitis B, and two patients with CNS involvement of lymphoma. Axi-cel treatment led to significant responses with 8/10 patients achieving a complete remission at 3 months, including both patients with prior CNS involvement. The treatment was generally well tolerated with 20% of patients experiencing grade ≥ 2 CRS. One patient each with HIV and hepatitis B responded without significant toxicities. In conclusion, Axi-cel led to significant efficacy with manageable toxicity in DLBCL in a real-world setting. © The Author(s). 2020 |
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title_short |
Axicabtagene ciloleucel CD19 CAR-T cell therapy results in high rates of systemic and neurologic remissions in ten patients with refractory large B cell lymphoma including two with HIV and viral hepatitis |
url |
https://dx.doi.org/10.1186/s13045-019-0838-y |
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Peeke, Stephen Shah, Nishi Mustafa, Jennat Khatun, Fariha Lombardo, Amanda Abreu, Michelly Elkind, Richard Fehn, Karen de Castro, Alyssa Wang, Yanhua Derman, Olga Nelson, Randin Uehlinger, Joan Gritsman, Kira Sica, R. Alejandro Kornblum, Noah Mantzaris, Ioannis Shastri, Aditi Janakiram, Murali Goldfinger, Mendel Verma, Amit Braunschweig, Ira Bachier-Rodriguez, Lizamarie |
author2Str |
Peeke, Stephen Shah, Nishi Mustafa, Jennat Khatun, Fariha Lombardo, Amanda Abreu, Michelly Elkind, Richard Fehn, Karen de Castro, Alyssa Wang, Yanhua Derman, Olga Nelson, Randin Uehlinger, Joan Gritsman, Kira Sica, R. Alejandro Kornblum, Noah Mantzaris, Ioannis Shastri, Aditi Janakiram, Murali Goldfinger, Mendel Verma, Amit Braunschweig, Ira Bachier-Rodriguez, Lizamarie |
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up_date |
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