Unique ID issued by UMIN | UMIN000045965 |
---|---|
Receipt number | R000052466 |
Scientific Title | Treatment-related mortality with Hematopoietic Stem Cell Transplantation for Progressive Systemic Sclerosis: A Systematic Review and Meta-Analysis |
Date of disclosure of the study information | 2021/11/03 |
Last modified on | 2024/12/16 10:15:57 |
Treatment-related mortality with Hematopoietic Stem Cell Transplantation for Progressive Systemic Sclerosis: A Systematic Review and Meta-Analysis
Systematic review
Treatment-related mortality with Hematopoietic Stem Cell Transplantation for Progressive Systemic Sclerosis: A Systematic Review and Meta-Analysis
Systematic review
Japan |
Systemic sclerosis
Clinical immunology |
Others
NO
Systemic sclerosis (SSc) is an autoimmune disease that causes skin sclerosis as well as damage to the lungs, kidneys, digestive tract, heart, and other organs of the body. Microvascular damage, activation of the immune system, and fibrosis of the skin and organs are the basic pathogenesis of SSc. Severe cases of SSc can be fatal. However, treatment with cyclophosphamide is hampered by its toxicity and restricted possible treatment duration. Hematopoietic stem cell transplantation (HSCT) has been proposed as a therapeutic option for progressive SSc. Therefore, we will conduct systematic review and meta-analysis of treatment-related mortality with HSCT in SSc.
Safety
Overall survival
Treatment related death
Others,meta-analysis etc
18 | years-old | <= |
Not applicable |
Male and Female
(1) The published study including case-control study, cohort study, and randomized clinical trial.
(2) The experimental group of the study was treated by HSCT, with or without control treatment arm.
(3) The patients were clinically diagnosed with SSc.
(5) The study illustrates the safety of HSCT.
(6) Only full-text papers are used to analyze.
(1) Systematic review or meta-analysis articles.
(2) Case reports or case series reporting less than 5 cases.
(3) The republished research literature is excluded unless the research includes new findings related to adverse events listed in inclusion criteria.
(4) Studies with no or insufficient safety results at the time of the literature search.
(5) Studies published in languages other than English.
1st name | Kaoru |
Middle name | |
Last name | Minegishi |
Yokohama City University Graduate School of Medicine
Department of Stem Cell and Immune Regulation
236-0004
3-9, Kanazawa, Fukuura, Yokohama
045-787-2630
kaoru_t@yokohama-cu.ac.jp
1st name | Kaoru |
Middle name | |
Last name | Minegishi |
Yokohama City University Graduate School of Medicine
Department of Stem Cell and Immune Regulation
236-0004
3-9, Kanazawa, Fukuura, Yokohama
045-787-2630
kaoru_t@yokohama-cu.ac.jp
Yokohama City University Graduate School of Medicine, Department of Stem Cell and Immune Regulation
Yokohama City University Graduate School of Medicine, Department of Stem Cell and Immune Regulation
Other
Yokohama City University Graduate School of Medicine
3-9, Kanazawa, Fukuura, Yokohama
045-787-2630
kaoru_t@yokohama-cu.ac.jp
NO
2021 | Year | 11 | Month | 03 | Day |
https://doi.org/10.1093/mr/roac026
Published
https://doi.org/10.1093/mr/roac026
1004
Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.
2024 | Year | 12 | Month | 16 | Day |
2022 | Year | 03 | Month | 12 | Day |
Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.
Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.
Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.
Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.
Completed
2021 | Year | 11 | Month | 03 | Day |
2021 | Year | 11 | Month | 03 | Day |
2021 | Year | 11 | Month | 05 | Day |
2022 | Year | 03 | Month | 31 | Day |
We will search for candidate articles using PubMed, Cochrane, EMBASE, and Web of Science Core Collection in November 2021.
Studies meeting the following criteria will be considered for inclusion:
Participants: The patients were clinically diagnosed with SSc.
Intervention: HSCT.
Comparison: Intravenous cyclophosphamide therapy or no comparison.
Outcome: Treatment-related mortality.
Two investigators independently screened all titles, abstracts, and full texts for eligibility. Final inclusion will be decided after resolving discrepancies between the two investigators.
The risk of bias of each study will be assessed by Cochrane risk of bias (RoB) tool for randomized trials and the Newcastle-Ottawa Scale for cohort studies.
We will conduct subgroup analysis among studies grouped according to the source of information about the cause of death.
2021 | Year | 11 | Month | 03 | Day |
2024 | Year | 12 | Month | 16 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000052466