Meta-Analysis
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©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Stem Cells. Oct 26, 2019; 11(10): 891-903
Published online Oct 26, 2019. doi: 10.4252/wjsc.v11.i10.891
Table 1 Intervention and study population overview
Study Population Intervention Ref. Country Sample size Age (yr) Patient condition Intervention and study groups Application route Type of stem cells Source Origin Dose Chen et al [45 ], 2013 China 60 1-35 CP, GMFCS level 3 to 5 Group 1: SC + rehabilitation Group 2: Rehabilitation only Intrathecal Mesenchymal stem cells in vitro transformed to neural stem cell- like cells Bone marrow Autologous Fixed quantity of 1-2 × 107 cells, twice Huang et al [46 ], 2018 China 56 3-12 CP Group 1: SC + rehabilitation Group 2: Placebo + rehabilitation Intravenous Mesenchymal stem cells Cord blood Allogeneic Fixed quantity of 5 × 107 cells, 4 times Kang et al [47 ], 2015 South Korea 36 0.5-20 CP, GMFCS level 1 to 5 Group 1: SC Group 2: Placebo No rehabilitation Intravenous/intraarterial Mononuclear cells Cord blood Allogeneic1 5.46 × 107 cells/kg, once Liu et al [40 ], 2017 China 105 0.5-12.5 Spastic CP, GMFCS level 2 to 5 Group 1: MNC Group 2: MSC Group 3: rehabilitation Intrathecal Mesenchymal stromal cells and mononuclear cells Bone marrow Autologous 106 cells/kg, 4 times Luan et al [44 ], 2012 China 91 < 0.5-3.5 CP, GMFSC level 1 to 5 Group 1: SC + rehabilitation Group 2: rehabilitation only Intraventricular Neural progenitor cells Aborted healthy fetuses’ forebrains Allogeneic Fixed quantity of 8-10 × 106 cells, once Min et al [39 ], 2013 South Korea 105 0.8-10 CP Group 1: SC+ EPO + rehabilitation Group 2: placebo SC + EPO + rehabilitation Group 3: placebo SC+ placebo + rehabilitation Intravenous Mononuclear cells Cord blood Allogeneic1 ≥ 3 × 107 cells/kg, once Rah et al [42 ], 2017 South Korea 57 2-10 Non-severe CP Group 1: G-CSF at baseline, SC 1 mo later Group 2: G-CSF at baseline, placebo 1 mo later crossover at 7 mo Intravenous Mobilized mononuclear cells Peripheral blood Autologous 5.97 × 108 cells/ kg, once Sun et al [41 ], 2017 USA 63 1-6 CP of any type, GMFCS Level 2 to 4 or 1 with hemiplegia Group 1: SC + rehabilitation Group 2: Placebo + rehabilitation Intravenous Mononuclear cells Cord blood Autologous 2 × 107 cells/kg, once
Table 2 Evaluation of the risk of bias
Ref .Random sequence generation: Selection bias Allocation concealment Blinding of participants and personnel: Performance bias Blinding of outcome assessment: Detection bias Incomplete outcome data: Attrition bias Selective reporting Chen et al [45 ], 2013 High High High Low High High Huang et al [46 ], 2018 Unclear Unclear High Low Low Unclear Kang et al [47 ], 2015 Low Low Low Low Low Unclear Liu et al [40 ], 2017 Low Unclear High Unclear Low Low Luan et al [44 ], 2012 Unclear Unclear High Unclear High Unclear Min et al [39 ], 2013 Low Low Low Low Low Low Rah et al [42 ], 2017 Low Low Low Low High Unclear Sun et al [41 ], 2017 Low Low Low Low Low Unclear
Table 3 Raw motor outcome data
Ref .Follow-up assessments after intervention (mo) Change in GMFM-88/66 after 6 mo ± SD Change in GMFM-88/66 after 12 mo ± SD % improvement compared to baseline after whole observation period Chen et al [45 ], 2013 1, 3, 6 Numbers inaccurately indicated - - Huang et al [46 ], 2018 3, 6, 12, 24 Control: + 2.96 ± 1.66; MSC: + 7.62 ± 2.44 Control: + 4.75 ± 1.45; MSC: + 10.27 ± 2.96 Control: 5.67%; UCB: 14.89% Kang et al [47 ], 2015 1, 3, 6 Control: 3.85 ± 3.75; UCB: 7.08 ± 7.36 Control: 13.1%; UCB: 24.2% Liu et al [40 ], 2017 3,6, 12 Control: + 1.85; BMMNC: + 3.1; BMMSC: + 10.45 Control: + 2.91; BMMNC: + 6.46; BMMSC: + 12.52 Control: 7.84%; BMMSC: 33.76% Luan et al [44 ], 2012 1, 6, 12 Control: not indicated; NPC: + 8.86- - Min et al [39 ], 2013 1, 3, 6 Control: + 7.8 ± 5.1; EPO only: + 9.0 ± 6,3; UCB + EPO: + 9.1 ± 6.7 - No baseline score provided Rah et al [42 ], 2017 12 mo after treatment resp. 6 mo for crossover-group - Transplantation at baseline: + 2.9; Transplantation after 6 mo: + 6.37 No baseline score provided Sun et al [41 ], 2017 12, 24 - Control: + 6.9 ± 5.5; UCB: + 7.5 ± 6.8 (High dose: improvement + 4.3 ± 1.5 greater than expected. Low-dose and placebo: no significant improvement beyond expectation.) Control: 13.3%; UCB: 15.3%
Table 4 Reported serious adverse events
Ref .Serious adverse events in cell recipient group Serious adverse events in control group Allogenic cells Application route Chen et al [45 ], 2013 0/30 0/30 Intrathecal Huang et al [46 ], 2018 0/27 0/27 x Intravenous Kang et al [47 ], 2015 0/18 0/18 x (+ immunosuppressant) Intravenous/intraarterial Liu et al [40 ], 2017 0/68 0/34 Intrathecal Luan et al [44 ], 2012 1/45 0/49 x Intraventricular Min et al [39 ], 2013 3/36 6/70 x (+ immunosuppressant) Intravenous Rah et al [42 ], 2017 0/57 - Intravenous Sun et al [41 ], 2017 0/63 - Intravenous Total 4/344 (1.2%) 6/228 (2.6%)