Outcomes with “Off the Shelf” Allogeneic CD19 Chimeric Antigen Receptor T Cell Therapy for Hematological Malignancies: A Systematic Review and Meta-Analysis
Background: Chimeric antigen receptor T cell (CAR-T) therapy is an adoptive T cell immunotherapy that employs the genetically modified T cell to attack the cancer cell. It is widely studied across various hematological and solid organ malignancies. Several autologous CD19 CAR-T cell therapy construc...
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| Veröffentlicht in: | Blood 2021-11, Vol.138 (Supplement 1), p.4831-4831 |
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| creator | Mushtaq, Muhammad Umair Shahzad, Moazzam Hussain, Ali Shah, Amna Y Siddiqui, Raheel S Faisal, Muhammad Salman Anwar, Iqra Chaudhary, Sibgha Gull Mohyuddin, Ghulam Rehman Balusu, Ramesh Tun, Aung M Bansal, Rajat Abdelhakim, Haitham Hoffmann, Marc Singh, Anurag K. Shune, Leyla Abhyankar, Sunil McGuirk, Joseph P. Ahmed, Nausheen |
| description | Background:
Chimeric antigen receptor T cell (CAR-T) therapy is an adoptive T cell immunotherapy that employs the genetically modified T cell to attack the cancer cell. It is widely studied across various hematological and solid organ malignancies. Several autologous CD19 CAR-T cell therapy constructs are now approved for various B cell lymphomas, including aggressive B cell lymphomas, indolent follicular lymphoma and mantle cell lymphoma, and acute lymphoblastic leukemia (ALL). Autologous CD19 CAR-T cell therapy has unprecedented success in relapsed and refractory disease. Long time to manufacture (2-5 weeks) and manufacture failure are challenges associated with risk of interim death and deterioration of CAR-T candidates with rapidly progressive disease. T cell fitness of the autologous product in heavily pretreated patients is also potentially compromised. To overcome these shortcomings, universal “off the shelf” allogeneic CAR-T cell therapy constructs are being developed and studied. Donor sources include healthy donors and cord or induced pluripotent stem cells (iPSCs). These CAR-T constructs have additional gene modifications to mitigate the risk of rejection and graft versus host disease (GVHD). We performed a systematic review and meta-analysis to assess the safety and efficacy of allogeneic CD19 CAR-T cell therapy.
Methods:
Four databases (Web of Science/MEDLINE/PubMed, Embase, and Cochrane Registry of Controlled Trials) were searched for this systematic review and meta-analysis following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines using MeSH terms and keywords for “Receptors, Chimeric antigen” OR “Artificial-T-cell receptor” OR “immunotherapy, adoptive” OR “CD-19”. Our search produced 3506 articles and after removing duplicates, 2243 records were screened. After excluding reviews and irrelevant articles, we included 8 prospective trials of allogeneic CD-19 CAR-T cell therapy enrolling two or more than two patients from Jan 2013 to Nov 2020. We also searched ASH 2020 abstracts to include any additional trials. The methodological quality of the included studies was evaluated using NIH quality assessment tool. Inter-study variance was calculated using the Der Simonian-Laird Estimator. Proportions along with 95% confidence Interval (CI) were extracted to compute pooled analysis using the ‘meta’ package by Schwarzer et al. in the R programming language (version 4.16-2).
Results:
A total of 68 patients fr |
| doi_str_mv | 10.1182/blood-2021-148999 |
| format | Article |
| fullrecord | <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1182_blood_2021_148999</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006497121067264</els_id><sourcerecordid>S0006497121067264</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1379-2533f66162c54acd53b155be2b2c5c7285666d5839fbc32c0ea3c101e1854fff3</originalsourceid><addsrcrecordid>eNp9kM9u1DAQxq0KJJbCA3CbFwh47DibwCkK0CK1WqldzpHjjBtX3mRlG6q99UFA6rP1SfCynDmN5s_36ZsfY--Qv0esxYfBL8tYCC6wwLJumuaMrVCJuuBc8BdsxTmvirJZ4yv2OsZ7zrGUQq3Y0-ZHMsuOIjy4NMHz46-NtZAmgtuJvH1-_A2t98sdzeQMdJ-xgW5yOwq5a-fk8gJuyNA-LQG20JH3sJ0o6P0BbB5d0k6nJRs4oz1ca-_uZj0bR_EjtHB7iOl4kM1u6KejB9DzCNeUdNHO2h-ii2_YS6t9pLf_6jn7_vXLtrssrjYX37r2qjAo100hlJS2qrASRpXajEoOqNRAYsgDsxa1qqpqVLVs7GCkMJy0NMiRsFaltVaeMzz5mrDEGMj2--B2Ohx65P0Rcf8XcX9E3J8QZ82nk4ZysBw_9DF_NhsaXSCT-nFx_1H_AQgzh1U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Outcomes with “Off the Shelf” Allogeneic CD19 Chimeric Antigen Receptor T Cell Therapy for Hematological Malignancies: A Systematic Review and Meta-Analysis</title><source>Alma/SFX Local Collection</source><source>EZB Electronic Journals Library</source><creator>Mushtaq, Muhammad Umair ; Shahzad, Moazzam ; Hussain, Ali ; Shah, Amna Y ; Siddiqui, Raheel S ; Faisal, Muhammad Salman ; Anwar, Iqra ; Chaudhary, Sibgha Gull ; Mohyuddin, Ghulam Rehman ; Balusu, Ramesh ; Tun, Aung M ; Bansal, Rajat ; Abdelhakim, Haitham ; Hoffmann, Marc ; Singh, Anurag K. ; Shune, Leyla ; Abhyankar, Sunil ; McGuirk, Joseph P. ; Ahmed, Nausheen</creator><creatorcontrib>Mushtaq, Muhammad Umair ; Shahzad, Moazzam ; Hussain, Ali ; Shah, Amna Y ; Siddiqui, Raheel S ; Faisal, Muhammad Salman ; Anwar, Iqra ; Chaudhary, Sibgha Gull ; Mohyuddin, Ghulam Rehman ; Balusu, Ramesh ; Tun, Aung M ; Bansal, Rajat ; Abdelhakim, Haitham ; Hoffmann, Marc ; Singh, Anurag K. ; Shune, Leyla ; Abhyankar, Sunil ; McGuirk, Joseph P. ; Ahmed, Nausheen</creatorcontrib><description>Background:
Chimeric antigen receptor T cell (CAR-T) therapy is an adoptive T cell immunotherapy that employs the genetically modified T cell to attack the cancer cell. It is widely studied across various hematological and solid organ malignancies. Several autologous CD19 CAR-T cell therapy constructs are now approved for various B cell lymphomas, including aggressive B cell lymphomas, indolent follicular lymphoma and mantle cell lymphoma, and acute lymphoblastic leukemia (ALL). Autologous CD19 CAR-T cell therapy has unprecedented success in relapsed and refractory disease. Long time to manufacture (2-5 weeks) and manufacture failure are challenges associated with risk of interim death and deterioration of CAR-T candidates with rapidly progressive disease. T cell fitness of the autologous product in heavily pretreated patients is also potentially compromised. To overcome these shortcomings, universal “off the shelf” allogeneic CAR-T cell therapy constructs are being developed and studied. Donor sources include healthy donors and cord or induced pluripotent stem cells (iPSCs). These CAR-T constructs have additional gene modifications to mitigate the risk of rejection and graft versus host disease (GVHD). We performed a systematic review and meta-analysis to assess the safety and efficacy of allogeneic CD19 CAR-T cell therapy.
Methods:
Four databases (Web of Science/MEDLINE/PubMed, Embase, and Cochrane Registry of Controlled Trials) were searched for this systematic review and meta-analysis following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines using MeSH terms and keywords for “Receptors, Chimeric antigen” OR “Artificial-T-cell receptor” OR “immunotherapy, adoptive” OR “CD-19”. Our search produced 3506 articles and after removing duplicates, 2243 records were screened. After excluding reviews and irrelevant articles, we included 8 prospective trials of allogeneic CD-19 CAR-T cell therapy enrolling two or more than two patients from Jan 2013 to Nov 2020. We also searched ASH 2020 abstracts to include any additional trials. The methodological quality of the included studies was evaluated using NIH quality assessment tool. Inter-study variance was calculated using the Der Simonian-Laird Estimator. Proportions along with 95% confidence Interval (CI) were extracted to compute pooled analysis using the ‘meta’ package by Schwarzer et al. in the R programming language (version 4.16-2).
Results:
A total of 68 patients from 8 studies were evaluated. Median age was 22.5 (4.8-64) years. (Table 1) The median follow-up time was 10 (2-18) months with median number of prior therapies of 3.2 (2-11) as reported by 5 studies. Underlying diagnosis was acute lymphocytic lymphoma (n=49, 72%), chronic lymphocytic leukemia (n=6, 9%), and non-Hodgkin lymphoma (n=13, 19%). The pooled overall response rate (ORR) was 77% (95% CI 0.63-0.89, I 2 =22%, n=68) with a complete response (CR) of 75% (95% CI 0.57-0.90, I 2 =48%, n=65). The pooled incidence of cytokine release syndrome grade I/II and grade III/IV was 53% (95% CI 0.16-0.89, I 2 =89%, n=65) and 10% (95% CI 0.01-0.25, I 2 =50%, n=65) respectively. Neurotoxicity grade I/II was 12% (95%CI 0.01-0.30, I 2 =47%, p=0.09, n=47) and GVHD grade I/II was 8% (95%CI 0.01-0.19, I 2 =0%, p=0.57 n=53). None of the clinical trials reported the duration of response.
Conclusion:
“Off the shelf” universal CAR-T therapy is early in development. Our available data suggest that allogeneic CD19 CAR-T constructs offer high ORR and CR rates with acceptable safety profiles. GVHD was mainly low grade (grade I-II). Given these findings, allogeneic CAR-T cell therapy is an attractive option to improve timely access compared to available autologous therapy. Extensive preclinical research to develop novel constructs and several phase I/II clinical trials are ongoing to shape the future of “off the shelf” CAR-T cell therapy.
[Display omitted]
Hoffmann: Pharmcyclics: Consultancy, Honoraria; TG Therapeutics: Consultancy, Honoraria; Novartis: Consultancy, Honoraria; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; celgene: Consultancy, Honoraria. Abhyankar: Incyte/Therakos: Consultancy, Research Funding, Speakers Bureau. McGuirk: Fresenius Biotech: Research Funding; Gamida Cell: Research Funding; Pluristem Therapeutics: Research Funding; EcoR1 Capital: Consultancy; Novartis: Research Funding; Astelllas Pharma: Research Funding; Kite/ Gilead: Consultancy, Honoraria, Other: travel accommodations, expense, Kite a Gilead company, Research Funding, Speakers Bureau; Juno Therapeutics: Consultancy, Honoraria, Research Funding; Magenta Therapeutics: Consultancy, Honoraria, Research Funding; Novartis: Research Funding; Bellicum Pharmaceuticals: Research Funding; Allovir: Consultancy, Honoraria, Research Funding.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2021-148999</identifier><language>eng</language><publisher>Elsevier Inc</publisher><ispartof>Blood, 2021-11, Vol.138 (Supplement 1), p.4831-4831</ispartof><rights>2021 American Society of Hematology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Mushtaq, Muhammad Umair</creatorcontrib><creatorcontrib>Shahzad, Moazzam</creatorcontrib><creatorcontrib>Hussain, Ali</creatorcontrib><creatorcontrib>Shah, Amna Y</creatorcontrib><creatorcontrib>Siddiqui, Raheel S</creatorcontrib><creatorcontrib>Faisal, Muhammad Salman</creatorcontrib><creatorcontrib>Anwar, Iqra</creatorcontrib><creatorcontrib>Chaudhary, Sibgha Gull</creatorcontrib><creatorcontrib>Mohyuddin, Ghulam Rehman</creatorcontrib><creatorcontrib>Balusu, Ramesh</creatorcontrib><creatorcontrib>Tun, Aung M</creatorcontrib><creatorcontrib>Bansal, Rajat</creatorcontrib><creatorcontrib>Abdelhakim, Haitham</creatorcontrib><creatorcontrib>Hoffmann, Marc</creatorcontrib><creatorcontrib>Singh, Anurag K.</creatorcontrib><creatorcontrib>Shune, Leyla</creatorcontrib><creatorcontrib>Abhyankar, Sunil</creatorcontrib><creatorcontrib>McGuirk, Joseph P.</creatorcontrib><creatorcontrib>Ahmed, Nausheen</creatorcontrib><title>Outcomes with “Off the Shelf” Allogeneic CD19 Chimeric Antigen Receptor T Cell Therapy for Hematological Malignancies: A Systematic Review and Meta-Analysis</title><title>Blood</title><description>Background:
Chimeric antigen receptor T cell (CAR-T) therapy is an adoptive T cell immunotherapy that employs the genetically modified T cell to attack the cancer cell. It is widely studied across various hematological and solid organ malignancies. Several autologous CD19 CAR-T cell therapy constructs are now approved for various B cell lymphomas, including aggressive B cell lymphomas, indolent follicular lymphoma and mantle cell lymphoma, and acute lymphoblastic leukemia (ALL). Autologous CD19 CAR-T cell therapy has unprecedented success in relapsed and refractory disease. Long time to manufacture (2-5 weeks) and manufacture failure are challenges associated with risk of interim death and deterioration of CAR-T candidates with rapidly progressive disease. T cell fitness of the autologous product in heavily pretreated patients is also potentially compromised. To overcome these shortcomings, universal “off the shelf” allogeneic CAR-T cell therapy constructs are being developed and studied. Donor sources include healthy donors and cord or induced pluripotent stem cells (iPSCs). These CAR-T constructs have additional gene modifications to mitigate the risk of rejection and graft versus host disease (GVHD). We performed a systematic review and meta-analysis to assess the safety and efficacy of allogeneic CD19 CAR-T cell therapy.
Methods:
Four databases (Web of Science/MEDLINE/PubMed, Embase, and Cochrane Registry of Controlled Trials) were searched for this systematic review and meta-analysis following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines using MeSH terms and keywords for “Receptors, Chimeric antigen” OR “Artificial-T-cell receptor” OR “immunotherapy, adoptive” OR “CD-19”. Our search produced 3506 articles and after removing duplicates, 2243 records were screened. After excluding reviews and irrelevant articles, we included 8 prospective trials of allogeneic CD-19 CAR-T cell therapy enrolling two or more than two patients from Jan 2013 to Nov 2020. We also searched ASH 2020 abstracts to include any additional trials. The methodological quality of the included studies was evaluated using NIH quality assessment tool. Inter-study variance was calculated using the Der Simonian-Laird Estimator. Proportions along with 95% confidence Interval (CI) were extracted to compute pooled analysis using the ‘meta’ package by Schwarzer et al. in the R programming language (version 4.16-2).
Results:
A total of 68 patients from 8 studies were evaluated. Median age was 22.5 (4.8-64) years. (Table 1) The median follow-up time was 10 (2-18) months with median number of prior therapies of 3.2 (2-11) as reported by 5 studies. Underlying diagnosis was acute lymphocytic lymphoma (n=49, 72%), chronic lymphocytic leukemia (n=6, 9%), and non-Hodgkin lymphoma (n=13, 19%). The pooled overall response rate (ORR) was 77% (95% CI 0.63-0.89, I 2 =22%, n=68) with a complete response (CR) of 75% (95% CI 0.57-0.90, I 2 =48%, n=65). The pooled incidence of cytokine release syndrome grade I/II and grade III/IV was 53% (95% CI 0.16-0.89, I 2 =89%, n=65) and 10% (95% CI 0.01-0.25, I 2 =50%, n=65) respectively. Neurotoxicity grade I/II was 12% (95%CI 0.01-0.30, I 2 =47%, p=0.09, n=47) and GVHD grade I/II was 8% (95%CI 0.01-0.19, I 2 =0%, p=0.57 n=53). None of the clinical trials reported the duration of response.
Conclusion:
“Off the shelf” universal CAR-T therapy is early in development. Our available data suggest that allogeneic CD19 CAR-T constructs offer high ORR and CR rates with acceptable safety profiles. GVHD was mainly low grade (grade I-II). Given these findings, allogeneic CAR-T cell therapy is an attractive option to improve timely access compared to available autologous therapy. Extensive preclinical research to develop novel constructs and several phase I/II clinical trials are ongoing to shape the future of “off the shelf” CAR-T cell therapy.
[Display omitted]
Hoffmann: Pharmcyclics: Consultancy, Honoraria; TG Therapeutics: Consultancy, Honoraria; Novartis: Consultancy, Honoraria; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; celgene: Consultancy, Honoraria. Abhyankar: Incyte/Therakos: Consultancy, Research Funding, Speakers Bureau. McGuirk: Fresenius Biotech: Research Funding; Gamida Cell: Research Funding; Pluristem Therapeutics: Research Funding; EcoR1 Capital: Consultancy; Novartis: Research Funding; Astelllas Pharma: Research Funding; Kite/ Gilead: Consultancy, Honoraria, Other: travel accommodations, expense, Kite a Gilead company, Research Funding, Speakers Bureau; Juno Therapeutics: Consultancy, Honoraria, Research Funding; Magenta Therapeutics: Consultancy, Honoraria, Research Funding; Novartis: Research Funding; Bellicum Pharmaceuticals: Research Funding; Allovir: Consultancy, Honoraria, Research Funding.</description><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kM9u1DAQxq0KJJbCA3CbFwh47DibwCkK0CK1WqldzpHjjBtX3mRlG6q99UFA6rP1SfCynDmN5s_36ZsfY--Qv0esxYfBL8tYCC6wwLJumuaMrVCJuuBc8BdsxTmvirJZ4yv2OsZ7zrGUQq3Y0-ZHMsuOIjy4NMHz46-NtZAmgtuJvH1-_A2t98sdzeQMdJ-xgW5yOwq5a-fk8gJuyNA-LQG20JH3sJ0o6P0BbB5d0k6nJRs4oz1ca-_uZj0bR_EjtHB7iOl4kM1u6KejB9DzCNeUdNHO2h-ii2_YS6t9pLf_6jn7_vXLtrssrjYX37r2qjAo100hlJS2qrASRpXajEoOqNRAYsgDsxa1qqpqVLVs7GCkMJy0NMiRsFaltVaeMzz5mrDEGMj2--B2Ohx65P0Rcf8XcX9E3J8QZ82nk4ZysBw_9DF_NhsaXSCT-nFx_1H_AQgzh1U</recordid><startdate>20211123</startdate><enddate>20211123</enddate><creator>Mushtaq, Muhammad Umair</creator><creator>Shahzad, Moazzam</creator><creator>Hussain, Ali</creator><creator>Shah, Amna Y</creator><creator>Siddiqui, Raheel S</creator><creator>Faisal, Muhammad Salman</creator><creator>Anwar, Iqra</creator><creator>Chaudhary, Sibgha Gull</creator><creator>Mohyuddin, Ghulam Rehman</creator><creator>Balusu, Ramesh</creator><creator>Tun, Aung M</creator><creator>Bansal, Rajat</creator><creator>Abdelhakim, Haitham</creator><creator>Hoffmann, Marc</creator><creator>Singh, Anurag K.</creator><creator>Shune, Leyla</creator><creator>Abhyankar, Sunil</creator><creator>McGuirk, Joseph P.</creator><creator>Ahmed, Nausheen</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20211123</creationdate><title>Outcomes with “Off the Shelf” Allogeneic CD19 Chimeric Antigen Receptor T Cell Therapy for Hematological Malignancies: A Systematic Review and Meta-Analysis</title><author>Mushtaq, Muhammad Umair ; Shahzad, Moazzam ; Hussain, Ali ; Shah, Amna Y ; Siddiqui, Raheel S ; Faisal, Muhammad Salman ; Anwar, Iqra ; Chaudhary, Sibgha Gull ; Mohyuddin, Ghulam Rehman ; Balusu, Ramesh ; Tun, Aung M ; Bansal, Rajat ; Abdelhakim, Haitham ; Hoffmann, Marc ; Singh, Anurag K. ; Shune, Leyla ; Abhyankar, Sunil ; McGuirk, Joseph P. ; Ahmed, Nausheen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1379-2533f66162c54acd53b155be2b2c5c7285666d5839fbc32c0ea3c101e1854fff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mushtaq, Muhammad Umair</creatorcontrib><creatorcontrib>Shahzad, Moazzam</creatorcontrib><creatorcontrib>Hussain, Ali</creatorcontrib><creatorcontrib>Shah, Amna Y</creatorcontrib><creatorcontrib>Siddiqui, Raheel S</creatorcontrib><creatorcontrib>Faisal, Muhammad Salman</creatorcontrib><creatorcontrib>Anwar, Iqra</creatorcontrib><creatorcontrib>Chaudhary, Sibgha Gull</creatorcontrib><creatorcontrib>Mohyuddin, Ghulam Rehman</creatorcontrib><creatorcontrib>Balusu, Ramesh</creatorcontrib><creatorcontrib>Tun, Aung M</creatorcontrib><creatorcontrib>Bansal, Rajat</creatorcontrib><creatorcontrib>Abdelhakim, Haitham</creatorcontrib><creatorcontrib>Hoffmann, Marc</creatorcontrib><creatorcontrib>Singh, Anurag K.</creatorcontrib><creatorcontrib>Shune, Leyla</creatorcontrib><creatorcontrib>Abhyankar, Sunil</creatorcontrib><creatorcontrib>McGuirk, Joseph P.</creatorcontrib><creatorcontrib>Ahmed, Nausheen</creatorcontrib><collection>CrossRef</collection><jtitle>Blood</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mushtaq, Muhammad Umair</au><au>Shahzad, Moazzam</au><au>Hussain, Ali</au><au>Shah, Amna Y</au><au>Siddiqui, Raheel S</au><au>Faisal, Muhammad Salman</au><au>Anwar, Iqra</au><au>Chaudhary, Sibgha Gull</au><au>Mohyuddin, Ghulam Rehman</au><au>Balusu, Ramesh</au><au>Tun, Aung M</au><au>Bansal, Rajat</au><au>Abdelhakim, Haitham</au><au>Hoffmann, Marc</au><au>Singh, Anurag K.</au><au>Shune, Leyla</au><au>Abhyankar, Sunil</au><au>McGuirk, Joseph P.</au><au>Ahmed, Nausheen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcomes with “Off the Shelf” Allogeneic CD19 Chimeric Antigen Receptor T Cell Therapy for Hematological Malignancies: A Systematic Review and Meta-Analysis</atitle><jtitle>Blood</jtitle><date>2021-11-23</date><risdate>2021</risdate><volume>138</volume><issue>Supplement 1</issue><spage>4831</spage><epage>4831</epage><pages>4831-4831</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Background:
Chimeric antigen receptor T cell (CAR-T) therapy is an adoptive T cell immunotherapy that employs the genetically modified T cell to attack the cancer cell. It is widely studied across various hematological and solid organ malignancies. Several autologous CD19 CAR-T cell therapy constructs are now approved for various B cell lymphomas, including aggressive B cell lymphomas, indolent follicular lymphoma and mantle cell lymphoma, and acute lymphoblastic leukemia (ALL). Autologous CD19 CAR-T cell therapy has unprecedented success in relapsed and refractory disease. Long time to manufacture (2-5 weeks) and manufacture failure are challenges associated with risk of interim death and deterioration of CAR-T candidates with rapidly progressive disease. T cell fitness of the autologous product in heavily pretreated patients is also potentially compromised. To overcome these shortcomings, universal “off the shelf” allogeneic CAR-T cell therapy constructs are being developed and studied. Donor sources include healthy donors and cord or induced pluripotent stem cells (iPSCs). These CAR-T constructs have additional gene modifications to mitigate the risk of rejection and graft versus host disease (GVHD). We performed a systematic review and meta-analysis to assess the safety and efficacy of allogeneic CD19 CAR-T cell therapy.
Methods:
Four databases (Web of Science/MEDLINE/PubMed, Embase, and Cochrane Registry of Controlled Trials) were searched for this systematic review and meta-analysis following the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines using MeSH terms and keywords for “Receptors, Chimeric antigen” OR “Artificial-T-cell receptor” OR “immunotherapy, adoptive” OR “CD-19”. Our search produced 3506 articles and after removing duplicates, 2243 records were screened. After excluding reviews and irrelevant articles, we included 8 prospective trials of allogeneic CD-19 CAR-T cell therapy enrolling two or more than two patients from Jan 2013 to Nov 2020. We also searched ASH 2020 abstracts to include any additional trials. The methodological quality of the included studies was evaluated using NIH quality assessment tool. Inter-study variance was calculated using the Der Simonian-Laird Estimator. Proportions along with 95% confidence Interval (CI) were extracted to compute pooled analysis using the ‘meta’ package by Schwarzer et al. in the R programming language (version 4.16-2).
Results:
A total of 68 patients from 8 studies were evaluated. Median age was 22.5 (4.8-64) years. (Table 1) The median follow-up time was 10 (2-18) months with median number of prior therapies of 3.2 (2-11) as reported by 5 studies. Underlying diagnosis was acute lymphocytic lymphoma (n=49, 72%), chronic lymphocytic leukemia (n=6, 9%), and non-Hodgkin lymphoma (n=13, 19%). The pooled overall response rate (ORR) was 77% (95% CI 0.63-0.89, I 2 =22%, n=68) with a complete response (CR) of 75% (95% CI 0.57-0.90, I 2 =48%, n=65). The pooled incidence of cytokine release syndrome grade I/II and grade III/IV was 53% (95% CI 0.16-0.89, I 2 =89%, n=65) and 10% (95% CI 0.01-0.25, I 2 =50%, n=65) respectively. Neurotoxicity grade I/II was 12% (95%CI 0.01-0.30, I 2 =47%, p=0.09, n=47) and GVHD grade I/II was 8% (95%CI 0.01-0.19, I 2 =0%, p=0.57 n=53). None of the clinical trials reported the duration of response.
Conclusion:
“Off the shelf” universal CAR-T therapy is early in development. Our available data suggest that allogeneic CD19 CAR-T constructs offer high ORR and CR rates with acceptable safety profiles. GVHD was mainly low grade (grade I-II). Given these findings, allogeneic CAR-T cell therapy is an attractive option to improve timely access compared to available autologous therapy. Extensive preclinical research to develop novel constructs and several phase I/II clinical trials are ongoing to shape the future of “off the shelf” CAR-T cell therapy.
[Display omitted]
Hoffmann: Pharmcyclics: Consultancy, Honoraria; TG Therapeutics: Consultancy, Honoraria; Novartis: Consultancy, Honoraria; Janssen: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; celgene: Consultancy, Honoraria. Abhyankar: Incyte/Therakos: Consultancy, Research Funding, Speakers Bureau. McGuirk: Fresenius Biotech: Research Funding; Gamida Cell: Research Funding; Pluristem Therapeutics: Research Funding; EcoR1 Capital: Consultancy; Novartis: Research Funding; Astelllas Pharma: Research Funding; Kite/ Gilead: Consultancy, Honoraria, Other: travel accommodations, expense, Kite a Gilead company, Research Funding, Speakers Bureau; Juno Therapeutics: Consultancy, Honoraria, Research Funding; Magenta Therapeutics: Consultancy, Honoraria, Research Funding; Novartis: Research Funding; Bellicum Pharmaceuticals: Research Funding; Allovir: Consultancy, Honoraria, Research Funding.</abstract><pub>Elsevier Inc</pub><doi>10.1182/blood-2021-148999</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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| identifier | ISSN: 0006-4971 |
| ispartof | Blood, 2021-11, Vol.138 (Supplement 1), p.4831-4831 |
| issn | 0006-4971 1528-0020 |
| language | eng |
| recordid | cdi_crossref_primary_10_1182_blood_2021_148999 |
| source | Alma/SFX Local Collection; EZB Electronic Journals Library |
| title | Outcomes with “Off the Shelf” Allogeneic CD19 Chimeric Antigen Receptor T Cell Therapy for Hematological Malignancies: A Systematic Review and Meta-Analysis |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-20T23%3A33%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Outcomes%20with%20%E2%80%9COff%20the%20Shelf%E2%80%9D%20Allogeneic%20CD19%20Chimeric%20Antigen%20Receptor%20T%20Cell%20Therapy%20for%20Hematological%20Malignancies:%20A%20Systematic%20Review%20and%20Meta-Analysis&rft.jtitle=Blood&rft.au=Mushtaq,%20Muhammad%20Umair&rft.date=2021-11-23&rft.volume=138&rft.issue=Supplement%201&rft.spage=4831&rft.epage=4831&rft.pages=4831-4831&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood-2021-148999&rft_dat=%3Celsevier_cross%3ES0006497121067264%3C/elsevier_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_els_id=S0006497121067264&rfr_iscdi=true |