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Retrospective and Prospective Longitudinal Observational Study on Invasive Fungal Disease After Allogeneic Hematopoietic Stem Cell Transplantation

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

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
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Since January 1, 2014, patients who underwent allo-HSCT at Peking University People's Hospital and other assistance centers.

Locations
Other Locations
China
Peking University People's Hospital
RECRUITING
Beijing
Contact Information
Primary
Jin Wu, MD
wujin1996@126.com
086-01088326002
Backup
Fanhao Nie
Niefh2003@163.com
086-18887323790
Time Frame
Start Date: 2025-03-15
Estimated Completion Date: 2031-03-14
Participants
Target number of participants: 6000
Treatments
Retrospective cohort
Patients whose first visit to our institution and the termination of follow-up both occurred before the opening of this study will contribute to the retrospective cohort.
Prospective cohort
Patients whose first visit to our institution occur after the opening of this study will contribute to the prospective cohort.
Retrospective/Prospective cohort
Patients whose first visit to our institution occurred before the opening of this study and whose follow-up will terminate after the opening of this study will contribute to the ambispective cohort.
Related Therapeutic Areas
Sponsors
Collaborators: Shanxi Province Cancer Hospital, Zhejiang University, First Affiliated Hospital of Xinjiang Medical University, Jining Medical University, First Affiliated Hospital of Harbin Medical University, The General Hospital of Northern Theater Command, The First Hospital of Jilin University, Qianfoshan Hospital, First Affiliated Hospital of Guangxi Medical University, Shandong Provincial Hospital, Shengjing Hospital
Leads: Peking University People's Hospital

This content was sourced from clinicaltrials.gov