UMIN-CTR Clinical Trial

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

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Treatment-related mortality with Hematopoietic Stem Cell Transplantation for Progressive Systemic Sclerosis: A Systematic Review and Meta-Analysis

Acronym

Systematic review

Scientific Title

Treatment-related mortality with Hematopoietic Stem Cell Transplantation for Progressive Systemic Sclerosis: A Systematic Review and Meta-Analysis

Scientific Title:Acronym

Systematic review

Region

Japan


Condition

Condition

Systemic sclerosis

Classification by specialty

Clinical immunology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

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.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Overall survival

Key secondary outcomes

Treatment related death


Base

Study type

Others,meta-analysis etc


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

(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.

Key exclusion criteria

(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.

Target sample size



Research contact person

Name of lead principal investigator

1st name Kaoru
Middle name
Last name Minegishi

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Stem Cell and Immune Regulation

Zip code

236-0004

Address

3-9, Kanazawa, Fukuura, Yokohama

TEL

045-787-2630

Email

kaoru_t@yokohama-cu.ac.jp


Public contact

Name of contact person

1st name Kaoru
Middle name
Last name Minegishi

Organization

Yokohama City University Graduate School of Medicine

Division name

Department of Stem Cell and Immune Regulation

Zip code

236-0004

Address

3-9, Kanazawa, Fukuura, Yokohama

TEL

045-787-2630

Homepage URL


Email

kaoru_t@yokohama-cu.ac.jp


Sponsor or person

Institute

Yokohama City University Graduate School of Medicine, Department of Stem Cell and Immune Regulation

Institute

Department

Personal name



Funding Source

Organization

Yokohama City University Graduate School of Medicine, Department of Stem Cell and Immune Regulation

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Yokohama City University Graduate School of Medicine

Address

3-9, Kanazawa, Fukuura, Yokohama

Tel

045-787-2630

Email

kaoru_t@yokohama-cu.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2021 Year 11 Month 03 Day


Related information

URL releasing protocol

https://doi.org/10.1093/mr/roac026

Publication of results

Published


Result

URL related to results and publications

https://doi.org/10.1093/mr/roac026

Number of participants that the trial has enrolled

1004

Results

Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.

Results date posted

2024 Year 12 Month 16 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results

2022 Year 03 Month 12 Day

Baseline Characteristics

Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.

Participant flow

Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.

Adverse events

Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.

Outcome measures

Please refer to the following:
Mod Rheumatol. 2023 Mar 2;33(2):330-337. doi: 10.1093/mr/roac026.

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2021 Year 11 Month 03 Day

Date of IRB

2021 Year 11 Month 03 Day

Anticipated trial start date

2021 Year 11 Month 05 Day

Last follow-up date

2022 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

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.


Management information

Registered date

2021 Year 11 Month 03 Day

Last modified on

2024 Year 12 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000052466