Allogeneic Hematopoietic Stem Cell Transplantation
Conditions
Brief summary
Clinical observational studies using epidemiologic theories and methods. Through the collection of various clinically relevant data, specific outcomes are evaluated in hematologic transplant patients, providing high quality real-world data for clinical practice, informing public health decision-making, and reducing the burden of disease
Detailed description
This is a retrospective, prospective, two-way cohort study in which clinical diagnostic and treatment data will be collected on patients enrolled in the study and followed up to characterize the natural course of the patient population as systematically as possible. All treatment decisions and clinical assessments will be made by the treating physician based on conventional treatment criteria and are not required by the study design or protocol. The purpose of this study is to examine the natural course of the disease and current treatments. An in-depth analysis of treatment regimens and treatment duration, as well as the sequence of regimen use, will be conducted to describe treatment modalities and healthcare expenditures for this disease state. No clinical device or laboratory/assessment interventions will be conducted except for disease management requirements based on routine practice requirements or treatment monitoring based on locally approved product characterization requirements. Patients will be required to complete a separate questionnaire containing basic epidemiologic information (demographics, disease history, environmental exposure history). During the duration of this study, some patients may be enrolled in interventional clinical trials. This is allowed and expected to occur in this study. Patients will not be required to withdraw from the cohort study and will continue to be followed up as normal, unless the investigator/patient feels it is more appropriate to withdraw from the study. All requirements of the clinical trial in question are documented according to the trial protocol.
Interventions
None listed
Sponsors
Ruijin Hospital
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
1. At least one visit to a stem cell transplant center beginning January 1, 2021 2. Proposed to undergo or have undergone hematopoietic stem cell transplantation
Exclusion criteria
1. Long-term follow-up information for patients not available for any reason (e.g., unavailable or with serious concomitant disease) according to investigator opinion 2. Due to alcohol and drug addiction thus affecting their ability to follow the requirements of the study 3. Presence of conditions that could jeopardize patient safety or affect their adherence to the protocol, according to the investigator's opinion
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival (OS) | Time Frame: through study completion, an average of 5 year | OS since enrollment |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Complete remission (CR) | Time Frame: through study completion, an average of 5 year | Complete remission (CR) |
| Very Good Partial Relief (VGPR) | Time Frame: through study completion, an average of 5 year | Very Good Partial Relief (VGPR) |
| Partial remission (PR) | Time Frame: through study completion, an average of 5 year | Partial remission (PR) |
| Strictly complete remission (sCR) | Time Frame: through study completion, an average of 5 year | Strictly complete remission (sCR) |
| Disease stabilization (SD) | Time Frame: through study completion, an average of 5 year | Disease stabilization (SD) |
| Progression of Disease (PD) | Time Frame: through study completion, an average of 5 year | Progression of Disease (PD) |
| Minor Relief (MR) | Time Frame: through study completion, an average of 5 year | Minor Relief (MR) |
Countries
China
Contacts
Primary ContactXiaoxia Hu
Backup ContactXiaoxia HU
Outcome results
None listed