Kabatas S, Civelek E, Savrunlu EC, Kaplan N, Boyalı O, Diren F, Can H, Genç A, Akkoç T, Karaöz E. Feasibility of allogeneic mesenchymal stem cells in pediatric hypoxic-ischemic encephalopathy: Phase I study. World J Stem Cells 2021; 13(5): 470-484 [PMID: 34136076 DOI: 10.4252/wjsc.v13.i5.470]
Corresponding Author of This Article
Serdar Kabatas, MD, Full Professor, Department of Neurosurgery, University of Health Sciences, Gaziosmanpaşa Training and Research Hospital, Karayolları Mahallesi, Osmanbey Caddesi 616. Sokak No. 10, Gaziosmanpaşa, Istanbul 34255, Turkey. kabatasserdar@hotmail.com
Research Domain of This Article
Neurosciences
Article-Type of This Article
Retrospective Study
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Stem Cells. May 26, 2021; 13(5): 470-484 Published online May 26, 2021. doi: 10.4252/wjsc.v13.i5.470
Table 1 Enrollment criteria
No.
Inclusion criteria
1
Age < 18
2
HIE radiologically confirmed at initial diagnosis and at study enrollment
3
The patients who does not have any chronic illness (cancer, kidney, heart/hepatic failure etc.) other than HIE. Adequate systemic organ function confirmed by normal ranged laboratory values
4
Life expectancy > 12 mo
5
No substiantial improvement despite of a treatment in neurological/functional status for the 3 mo before study enrollment
6
Severe disability defined as subject confined to a wheelchair/required to have home nursing care/needing assistance with activities of daily living
7
Expectation that the patient will receive standard post-treatment care and attend all visits
8
Signing in the written informed consent form for confirming to that know the treatment to be applied and to be willing by their parents/a surrogate
Exclusion criteria
1
Presence of any other clinically significant medical/psychiatric condition, or laboratory abnormality, for which study participation would pose a safety risk in the judgment of the investigator/sponsor or history within the past year of drug/alcohol abuse
2
Recently diagnosed severe infection (meningitis, etc.)/development of liver, kidney/heart failure/sepsis or skin infection at the i.v. infusion site or positive for hepatitis B, C/HIV
3
History of uncontrolled seizure disorder
4
History of cerebral neoplasm, or cancer within the past 5 yr, with the exception of localized basal or squamous cell carcinoma
5
Having clinic symptoms that formation of white sphere number ≥ 15000/μL or platelet count ≤ 100.000/μL
6
Serum aspartate aminotransferase and serum alanine aminotransferase > 3× upper limit of normal/creatinine > 1.5× upper limit of normal
7
Participation in an another investigational stem cell study before treatment
8
The patient/parents decides to abandon the treatment or the patient death
Table 2 Study population
Frequency
Percent
Age
1.00
1
16.7
6.00
2
33.3
7.00
1
16.7
9.00
1
16.7
12.00
1
16.7
Sex
F
4
66.7
M
2
33.3
Cause of hypoxia
Acute meningitis
1
16.7
Cardiac arrest after an orthopedic surgery
1
16.7
Cardiac arrest due to long QT syndrome
1
16.7
Cardiac arrest, unknown etiology
1
16.7
Drowning in water
1
16.7
Foreign body aspiration
1
16.7
Duration of Hypoxia
25.00
1
16.7
30.00
3
50.0
45.00
1
16.7
75.00
1
16.7
Comorbidity
Long QT syndrome
1
16.7
no
4
66.7
Osteogenesis imperfecta
1
16.7
Duration Between Hypoxia & First SCT
6.00
3
50.0
9.00
1
16.7
32.00
1
16.7
72.00
1
16.7
Table 3 Administration schedule
Rounds
Route
WJ-MSC
Round 1
IT
1 × 106/kg in 3 mL
IV
1 × 106/kg in 30 mL
IM
1 × 106/kg in 20 mL
Round 2 (2nd week)
IT
1 × 106/kg in 3 mL
IV
1 × 106/kg in 30 mL
IM
1 × 106/kg in 20 mL
Round 3 (4th week)
IT
1 × 106/kg in 3 mL
IV
1 × 106/kg in 30 mL
IM
1 × 106/kg in 20 mL
Round 4 (6th week)
IT
1 × 106/kg in 3 mL
IV
1 × 106/kg in 30 mL
IM
1 × 106/kg in 20 mL
Table 4 Early and late complications of the procedures
Complications
Patient No. 1
Patient No. 2
Patient No. 3
Patient No. 4
Patient No. 5
Patient No. 6
Administration
Administration
Administration
Administration
Administration
Administration
1st
2nd
3rd
4th
1st
2nd
3rd
4th
1st
2nd
3rd
4th
1st
2nd
3rd
4th
1st
2nd
3rd
4th
1st
2nd
3rd
4th
Early
Infection
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Fever
-
-
-
-
-
-
-
-
-
+
-
-
-
+
-
-
+
+
-
-
-
-
-
-
Pain
-
-
-
-
-
-
-
-
+
-
+
-
+
+
-
-
+
-
-
-
-
-
-
-
Headache
-
-
-
-
-
-
-
-
-
-
+
-
+
-
-
-
-
-
-
-
-
-
-
-
Increased level of C-reactive protein
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Leukocytosis
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Allergic reaction or shock
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Perioperative complications
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Late
Secondary infections
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Urinary tract infections
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Deterioration of neurological status
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Neuropathic pain
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Carcinogenesis
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
Table 5 Friedman test results regarding the change in the Wee Functional Independence Measure Motor scores of the patients before and after the operation
n
Mean
SD
Mean rank
χ2
df
P value
Pre-test
6
8.00
0.00
2.50
23.444
5
0.000
Post-test 1 wk
6
8.00
0.00
2.50
Post-test 1 mo
6
8.00
0.00
2.50
Post-test 2 mo
6
8.33
0.52
3.17
Post-test 4 mo
6
9.67
0.82
4.92
Post-test 12 mo
6
10.50
1.52
5.42
Table 6 Friedman test results regarding the change in the Wee Functional Independence Measure cognitive scores of the patients before and after the operation
n
Mean
SD
Mean rank
χ2
df
P value
Pre-test
6
5.50
0.55
1.67
28.255
5
0.000
Post-test 1 wk
6
5.67
0.82
1.83
Post-test 1 mo
6
7.17
1.60
2.75
Post-test 2 mo
6
8.33
2.25
3.83
Post-test 4 mo
6
10.17
3.06
4.92
Post-test 12 mo
6
13.00
2.83
6.00
Table 7 Friedman test results regarding the change in the macrophage activation syndrome right scores of the patients before and after the operation
n
Mean
SD
Mean rank
χ2
df
P value
Pre-test
6
18.67
4.72
5.83
29.439
5
0.000
Post-test 1 wk
6
16.83
6.15
5.17
Post-test 1 mo
6
14.00
7.62
3.92
Post-test 2 mo
6
12.17
6.94
2.92
Post-test 4 mo
6
10.17
6.65
2.17
Post-test 12 mo
6
7.67
6.12
1.00
Table 8 Friedman test results regarding the change in the macrophage activation syndrome left scores of the patients before and after the operation
n
Mean
SD
Mean rank
χ2
df
P value
Pre-test
6
16.33
5.13
5.58
29.000
5
0.000
Post-test 1 wk
6
15.67
5.89
5.25
Post-test 1 mo
6
13.17
7.33
4.08
Post-test 2 mo
6
11.33
6.31
2.92
Post-test 4 mo
6
9.17
5.74
2.17
Post-test 12 mo
6
7.00
5.33
1.00
Citation: Kabatas S, Civelek E, Savrunlu EC, Kaplan N, Boyalı O, Diren F, Can H, Genç A, Akkoç T, Karaöz E. Feasibility of allogeneic mesenchymal stem cells in pediatric hypoxic-ischemic encephalopathy: Phase I study. World J Stem Cells 2021; 13(5): 470-484