Clinical Study on the Impact of Covid-19 Vaccine on Allogeneic Hematopoietic Stem Cell Transplantation

Sponsor
The First Affiliated Hospital of Soochow University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05587881
Collaborator
(none)
400
1
22
18.2

Study Details

Study Description

Brief Summary

Aim of this study will evaluate the Impact of Covid-19 vaccine on Safety and Efficacy of Hematological Patients Received Allogeneic Hematopoietic Stem Cell Transplantation.

Condition or Disease Intervention/Treatment Phase
  • Biological: COVID-19 vaccine(donor)
  • Biological: COVID-19 vaccine(patient)

Detailed Description

Since the first detection of a Corona Virus Disease 2019 (COVID-19) infection in late 2019, the syndrome coronavirus-2 (SARS-CoV-2) has spread rapidly across the globe, threatening the health and safety of an increasing number of people. The development of the SARS-CoV-2 vaccine has been shown to be effective in reducing the chance of COVID-19 infection and the severity of the disease. To control the COVID-19 pandemic, an increasing number of studies are calling for people to receive the SARS-CoV-2 vaccine, and the Chinese government is also advocating universal vaccination. However, the investigators have found in our work that as vaccination has become more widespread, clinicians have become somewhat confused about whether they can choose someone who has been vaccinated against SARS-CoV-2 as a donor for a bone marrow transplant, and what is the optimal time for allogeneic hematopoietic stem cell transplantation (allo-HSCT) in vaccined hematological patients. This study will evaluate the impact of Covid-19 vaccine on safety and efficacy of hematological patients received allo-HSCT.

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Clinical Study on the Impact of Covid-19 Vaccine on Safety and Efficacy of Hematological Patients Received Allogeneic Hematopoietic Sem Cell Transplantation
Actual Study Start Date :
Jan 1, 2022
Anticipated Primary Completion Date :
Nov 1, 2023
Anticipated Study Completion Date :
Nov 1, 2023

Arms and Interventions

Arm Intervention/Treatment
donor with vaccine, patient without vaccine

Patients don' t receive COVID-19 vaccine before allo-HSCT but whose donors receive one dose or more doses COVID-19 vaccine(s) before stem cell collection.

Biological: COVID-19 vaccine(donor)
Donor received COVID-19 vaccine before stem cells collection.

donor without vaccine, patient with vaccine

Patients receive one dose or more doses COVID-19 vaccine(s) before allo-HSCT but whose donors don't receive COVID-19 vaccine before stem cell collection.

Biological: COVID-19 vaccine(donor)
Donor received COVID-19 vaccine before stem cells collection.

Biological: COVID-19 vaccine(patient)
Patient received COVID-19 vaccine before allo-HSCT.

donor with vaccine, patient with vaccine

Patients receive one dose or more doses COVID-19 vaccine(s) before allo-HSCT and whose donors also receive one dose or more doses COVID-19 vaccine(s) before stem cell collection.

Biological: COVID-19 vaccine(patient)
Patient received COVID-19 vaccine before allo-HSCT.

donor without vaccine, patient without vaccine

Patients don' t receive COVID-19 vaccine before allo-HSCT and whose donors also don't receive COVID-19 vaccine before stem cell collection.

Outcome Measures

Primary Outcome Measures

  1. Disease-free Survival(PFS) [up to 12 months]

    To measure the duration of response to allo-HSCT over a follow-up period of 12 months.

Secondary Outcome Measures

  1. Overall Survival(OS) [up to 12 months]

    OS will be assessed from the first day of stem cells infused to death or last follow-up.

  2. Adverse events profile [Measured 12 months after stem cells infused]

    Number of participants with adverse events. Frequencies of toxicities based on NCI Common Termeinology Criteria for Adverse Events(CTCAE), version 5.0 will be tabulated.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Allogeneic hematopoietic stem cell transplantation is expected to start in the short term.

  2. Able and willing to provide written informed consent and comply with all requirements for study participation (including all study procedures).

Exclusion Criteria:
  1. Patients or donors with a history of previous infection with SARS-Cov-2.

  2. Patients or donors are currently infected with SARS-Cov-2.

  3. Patients have a history of other malignancies, disease progression, or is currently on systemic therapy.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Soochow University Suzhou Jiangsu China 215000

Sponsors and Collaborators

  • The First Affiliated Hospital of Soochow University

Investigators

  • Study Chair: Depei Wu, M.D, The First Affilated Hospital of Soochow University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The First Affiliated Hospital of Soochow University
ClinicalTrials.gov Identifier:
NCT05587881
Other Study ID Numbers:
  • 2019-nCoVvaccine 01
First Posted:
Oct 20, 2022
Last Update Posted:
Nov 14, 2022
Last Verified:
Jan 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by The First Affiliated Hospital of Soochow University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 14, 2022