Efficacy and safety of chimeric antigen receptor T-cell (CAR-T) therapy in patients with haematological and solid malignancies: protocol for a systematic review and meta-analysis

Introduction Patients with relapsed or refractory malignancies have a poor prognosis. Immunotherapy with chimeric antigen receptor T (CAR-T) cells redirects a patient’s immune cells against the tumour antigen. CAR-T cell therapy has demonstrated promise in treating patients with several haematological malignancies, including acute B-cell lymphoblastic leukaemia and B-cell lymphomas. CAR-T cell therapy for patients with other solid tumours is also being tested. Safety is an important consideration in CAR-T cell therapy given the potential for serious adverse events, including death. Previous reviews on CAR-T cell therapy have been limited in scope and methodology. Herein, we present a protocol for a systematic review to identify CAR-T cell interventional studies and examine the safety and efficacy of this therapy in patients with haematology malignancies and solid tumours. Methods and analysis We will search MEDLINE, including In-Process and Epub Ahead of Print, EMBASE and the Cochrane Central Register of Controlled Trials from 1946 to 22 February 2017. Studies will be screened by title, abstract and full text independently and in duplicate. Studies that report administering CAR-T cells of any chimeric antigen receptor construct targeting antigens in patients with haematological malignancies and solid tumours will be eligible for inclusion. Outcomes to be extracted will include complete response rate (primary outcome), overall response rate, overall survival, relapse and adverse events. A meta-analysis will be performed to synthesise the prevalence of outcomes reported as proportions with 95% CIs. The potential for bias within included studies will be assessed using a modified Institute of Health Economics tool. Heterogeneity of effect sizes will be determined using the Cochrane I 2 statistic. Ethics and dissemination The review findings will be submitted for peer-reviewed journal publication and presented at relevant conferences and scientific meetings to promote knowledge transfer. PROSPERO registration number CRD42017075331.

[1]  A. Esmaeilzadeh,et al.  Immune Cell Hacking: Challenges and Clinical Approaches to Create Smarter Generations of Chimeric Antigen Receptor T Cells , 2018, Front. Immunol..

[2]  J. Peters,et al.  Molecular Regulation of Carcinogenesis: Friend and Foe. , 2018, Toxicological sciences : an official journal of the Society of Toxicology.

[3]  B. Bonavida Linking Autophagy and the Dysregulated NFκB/ SNAIL/YY1/RKIP/PTEN Loop in Cancer: Therapeutic Implications. , 2018, Critical reviews in oncogenesis.

[4]  Anping Li,et al.  Chimeric antigen receptor T cells: a novel therapy for solid tumors , 2017, Journal of Hematology & Oncology.

[5]  I. Riaz,et al.  Donor origin CAR T cells: graft versus malignancy effect without GVHD, a systematic review. , 2017, Immunotherapy.

[6]  Hanmei Xu,et al.  A new insight in chimeric antigen receptor-engineered T cells for cancer immunotherapy , 2017, Journal of Hematology & Oncology.

[7]  H. Abken,et al.  The growing world of CAR T cell trials: a systematic review , 2016, Cancer Immunology, Immunotherapy.

[8]  J. McGowan,et al.  PRESS Peer Review of Electronic Search Strategies: 2015 Guideline Statement. , 2016, Journal of clinical epidemiology.

[9]  Renier J. Brentjens,et al.  Driving CAR T-cells forward , 2016, Nature Reviews Clinical Oncology.

[10]  Qing Zhang,et al.  Anti‐CD19 chimeric antigen receptor‐modified T cells for B‐cell malignancies: a systematic review of efficacy and safety in clinical trials , 2016, European journal of haematology.

[11]  S. Maude,et al.  Current status of chimeric antigen receptor therapy for haematological malignancies , 2016, British journal of haematology.

[12]  C. Moga,et al.  A principal component analysis is conducted for a case series quality appraisal checklist. , 2016, Journal of clinical epidemiology.

[13]  W. Han,et al.  Efficiency of CD19 chimeric antigen receptor-modified T cells for treatment of B cell malignancies in phase I clinical trials: a meta-analysis , 2015, Oncotarget.

[14]  Seth M Steinberg,et al.  T cells expressing CD19 chimeric antigen receptors for acute lymphoblastic leukaemia in children and young adults: a phase 1 dose-escalation trial , 2015, The Lancet.

[15]  P. Shekelle,et al.  Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement , 2015, Systematic Reviews.

[16]  A. Sutton,et al.  In meta-analyses of proportion studies, funnel plots were found to be an inaccurate method of assessing publication bias. , 2014, Journal of clinical epidemiology.

[17]  Qing He,et al.  Efficacy and Toxicity Management of 19-28z CAR T Cell Therapy in B Cell Acute Lymphoblastic Leukemia , 2014, Science Translational Medicine.

[18]  B. Levine,et al.  T Cells Expressing Chimeric Antigen Receptors Can Cause Anaphylaxis in Humans , 2013, Cancer Immunology Research.

[19]  J. Higgins,et al.  Cochrane Handbook for Systematic Reviews of Interventions, Version 5.1.0. The Cochrane Collaboration , 2013 .

[20]  A. Bagg,et al.  Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia. , 2011, The New England journal of medicine.

[21]  R. Gambari,et al.  Induction by TNF-α of IL-6 and IL-8 in Cystic Fibrosis Bronchial IB3-1 Epithelial Cells Encapsulated in Alginate Microbeads , 2010, Journal of biomedicine & biotechnology.

[22]  A. D. Van den Abbeele,et al.  Revised RECIST guideline version 1.1: What oncologists want to know and what radiologists need to know. , 2010, AJR. American journal of roentgenology.

[23]  T. Asai,et al.  Role of Antimicrobial Selective Pressure and Secondary Factors on Antimicrobial Resistance Prevalence in Escherichia coli from Food-Producing Animals in Japan , 2010, Journal of Biomedicine and Biotechnology.

[24]  A. Temme,et al.  Chimeric Antigen Receptor-Engineered T Cells for Immunotherapy of Cancer , 2010, Journal of biomedicine & biotechnology.

[25]  D. Moher,et al.  Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. , 2010, International journal of surgery.

[26]  A. Quittner,et al.  Lung transplantation for cystic fibrosis , 2006, Current opinion in pulmonary medicine.

[27]  Michael Hallek,et al.  Guidelines for the diagnosis and treatment of chronic lymphocytic leukemia: a report from the International Workshop on Chronic Lymphocytic Leukemia updating the National Cancer Institute-Working Group 1996 guidelines. , 2008, Blood.

[28]  G. Guyatt,et al.  GRADE: an emerging consensus on rating quality of evidence and strength of recommendations , 2008, BMJ : British Medical Journal.

[29]  Angela Coulter,et al.  The Picker Patient Experience Questionnaire: development and validation using data from in-patient surveys in five countries. , 2002, International journal for quality in health care : journal of the International Society for Quality in Health Care.

[30]  A. Laupacis,et al.  WHAT SHOULD BE INCLUDED IN META-ANALYSES? , 2000, International Journal of Technology Assessment in Health Care.