Survival outcomes and efficacy of autologous CD19 chimeric antigen receptor-T cell therapy in the patient with diagnosed hematological malignancies: a systematic review and meta-analysis

被引:9
作者
Drokow, Emmanuel Kwateng [1 ,2 ]
Ahmed, Hafiz Abdul Waqas [1 ,2 ]
Amponsem-Boateng, Cecilia [3 ]
Akpabla, Gloria Selorm [4 ]
Song, Juanjuan [1 ,2 ]
Shi, Mingyue [1 ,2 ]
Sun, Kai [1 ,2 ]
机构
[1] Zhengzhou Univ, Dept Hematol, Peoples Hosp, 7 Weiwu Rd, Zhengzhou 450003, Henan, Peoples R China
[2] Henan Prov Peoples Hosp, 7 Weiwu Rd, Zhengzhou 450003, Henan, Peoples R China
[3] Zhengzhou Univ, Coll Publ Hlth, Dept Epidemiol & Biostat, Zhengzhou, Henan, Peoples R China
[4] Tianjin Med Univ, Dept Internal Med, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
autologous; CD19; CAR-T; hematological malignancies; response rate; LYMPHOMA; SAFETY; CYTOTOXICITY; PERSISTENCE; REMISSIONS; TOXICITIES; EXPANSION;
D O I
10.2147/TCRM.S203822
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Purpose: Chimeric Antigen Receptor T(CAR-T) cell therapy is an immunotherapy approach used in treating cancer which has seen rapid development over the decades. It becomes the preferred treatment choice after patients have failed conventional chemotherapy. Methods: We conducted a meta-analysis in 320 patients from 14 studies to estimate the survival outcome, response rate and toxicity of autologous CD19 CAR-T cell therapy and predict other factors associated with a better prognosis. Results: The overall response rate was 71.88% (95% CI: 61.34-80.46%, p<0.01) and CRS toxicity was 60.15% (95% CI: 42.87-75.22%, p<0.01). Patients who received lymphodepletion was associated with a better response rate (77%, 95% CI: 67-83%; p-value = 0.001) in comparison to the other patients who did not (66%, 95% CI: 41-83%). Conclusion: Lymphodepletion regimen may play a crucial role in predicting the prognosis of patients with hematological malignancies. Lymphodepletion patients had better progression-free survival than those who did not.
引用
收藏
页码:637 / 646
页数:10
相关论文
共 30 条
[1]  
[Anonymous], 2014, BLOOD, DOI DOI 10.1182/BLOOD.V124.21.1982.1982
[2]  
[Anonymous], BLOOD
[3]  
[Anonymous], 2015, BLOOD
[4]  
[Anonymous], CLIN IMMUNOLOGY
[5]  
[Anonymous], 2015, BLOOD
[6]   Donor origin CAR T cells: graft versus malignancy effect without GVHD, a systematic review [J].
Anwer, Faiz ;
Shaukat, Al-Aman ;
Zahid, Umar ;
Husnain, Muhammad ;
McBride, Ali ;
Persky, Daniel ;
Lim, Melissa ;
Hasan, Nida ;
Bin Riaz, Irbaz .
IMMUNOTHERAPY, 2017, 9 (02) :123-130
[7]   CD19-Targeted T Cells Rapidly Induce Molecular Remissions in Adults with Chemotherapy-Refractory Acute Lymphoblastic Leukemia [J].
Brentjens, Renier J. ;
Davila, Marco L. ;
Riviere, Isabelle ;
Park, Jae ;
Wang, Xiuyan ;
Cowell, Lindsay G. ;
Bartido, Shirley ;
Stefanski, Jolanta ;
Taylor, Clare ;
Olszewska, Malgorzata ;
Borquez-Ojeda, Oriana ;
Qu, Jinrong ;
Wasielewska, Teresa ;
He, Qing ;
Bernal, Yvette ;
Rijo, Ivelise V. ;
Hedvat, Cyrus ;
Kobos, Rachel ;
Curran, Kevin ;
Steinherz, Peter ;
Jurcic, Joseph ;
Rosenblat, Todd ;
Maslak, Peter ;
Frattini, Mark ;
Sadelain, Michel .
SCIENCE TRANSLATIONAL MEDICINE, 2013, 5 (177)
[8]   IL-7 is superior to IL-2 for ex vivo expansion of tumour-specific CD4+ T cells [J].
Caserta, Stefano ;
Alessi, Patrizia ;
Basso, Veronica ;
Mondino, Anna .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2010, 40 (02) :470-479
[9]   The myth of the second remission of acute leukemia in the adult [J].
Forman, Stephen J. ;
Rowe, Jacob M. .
BLOOD, 2013, 121 (07) :1077-1082
[10]   The inducible caspase-9 suicide gene system as a "safety switch" to limit on-target, off-tumor toxicities of chimeric antigen receptor T cells [J].
Gargett, Tessa ;
Brown, Michael P. .
FRONTIERS IN PHARMACOLOGY, 2014, 5