Longitudinal Cohort Study on Invasive Fungal Disease After Allogeneic Hematopoietic Stem Cell Transplantation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorPeking University People's Hospital

About this trial

Invasive fungal disease (IFD) is one of the serious complications after hematopoietic stem cell transplantation (HSCT), characterized by high incidence and high mortality. According to the data from a multi-center study in China (CAESAR 2.0), even with the extensive use of antifungal active drugs for prevention, the cumulative incidence of IFD one year after HSCT still reached 6.3%, and the IFD-related mortality rate was 48.28%. In recent years, with the improvement of transplantation techniques, the application of new antifungal drugs and the optimization of diagnostic methods, the pathogen spectrum and clinical characteristics of IFD have undergone significant changes. Compared with ten years ago, the proportion of non-Aspergillus pathogens (such as Candida and Mucophora) has significantly increased, while the proportion of Aspergillus has relatively decreased. In addition, different types of invasive mycosis (such as invasive aspergillosis and invasive fusarium) show significant differences in clinical manifestations, onset time and prognosis. However, at present, large-scale prospective cohort studies on IFD after HSCT in China are still relatively scarce, and the diagnosis and treatment norms and prevention strategies in clinical practice still need to be further optimized. This study intends to conduct a multi-center retrospective and prospective combined longitudinal cohort study to comprehensively register the basic information, diagnosis, treatment and prognosis of IFD patients after HSCT, providing evidence-based medical basis for establishing new clinical diagnosis and treatment technologies and improving the long-term survival rate of patients.

Eligibility criteria

Qualifiers

None

Disqualifiers

For any reason, such as the occurrence of severe mental disorders, the follow-up information may be unavailable;

Patients deemed unsuitable for the study by the researchers.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

6,000 Participants
are grouped into 3 trial groups

Sponsors and collaborators

Peking University People's Hospital

Lead sponsor

First Affiliated Hospital of Guangxi Medical University

Collaborator

First Affiliated Hospital of Harbin Medical University

Collaborator

The First Hospital of Jilin University

Collaborator

Jining Medical University

Collaborator

Qianfoshan Hospital

Collaborator

Shandong Provincial Hospital

Collaborator

Shanxi Province Cancer Hospital

Collaborator

Shengjing Hospital

Collaborator

First Affiliated Hospital of Xinjiang Medical University

Collaborator

Zhejiang University

Collaborator

The General Hospital of Northern Theater Command

Collaborator