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This study is a prospective single-arm clinical study, focusing on Hemophagocytic lymphohistocytosis,to evaluate the clinical efficacy and safety of zanubrutinib.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| zanubrutinib | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Zanubrutinib | Drug | The dosage of zanubrutinib is 160mg twice a day (80mg twice a day for patients over 75 years old) for 2 months. The remission rate is evaluated after treatment. If it is above PR, continue the dose maintenance treatment. |
| Measure | Description | Time Frame |
|---|---|---|
| evaluation of treatment response | A complete response was defined as normalization of all of the quantifiable symptoms and laboratory markers of HLH, including levels of sCD25, ferritin, and triglyceride; hemoglobin; neutrophil counts; platelet counts; and alanine aminotransferase (ALT). A partial response was defined as at least a 25% improvement in 2 or more quantifiable symptoms and laboratory markers as follows: sCD25 response was>1.5-fold decreased; ferritin and triglyceride decreased at least 25%; for patients with an initial neutrophil count of<0.5 ×109/L, a response was defined as an increase by at least 100% to>0.5×109/L; for patients with a neutrophil count of 0.5 to 2.0× 109/L, an increase by at least 100% to >2.0 × 109/L was considered a response; and for patients with ALT >400 U/L,response was defined as an ALT decrease of at least 50%. | Change from before and 2,4,6 and 8 weeks after initiating therapy |
| Progression Free Survival | from date of inclusion to date of progression, relapse, or death from any cause | 6 months |
| Adverse events | Adverse events including myelosuppression, infection, hemorrhage | 6 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Beijing Friendship Hospital, Capital Medical University | Beijing | China |
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| ID | Term |
|---|---|
| C000629551 | zanubrutinib |
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