Last updated: August 28, 2023
Sponsor: shifeng Lou
Overall Status: Active - Recruiting
Phase
N/A
Condition
Histiocytoma
Treatment
Etoposide
Dexamethasone
Cyclosporine (CSA)
Clinical Study ID
NCT05936086
XYNK 04
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age range from 18 to 65 years old (including the critical value), gender is notlimited;
- According to the diagnostic criteria of HLH-2004, HLH can be diagnosed if any of thefollowing two criteria are met:
- Molecular diagnosis is consistent with HLH: Currently known HLH related pathogenicgenes exist, such as PRF1, UNC13D, STX11, STXBP2, Rab27a, LYST, SH2D1A, BIRC4, ITK,AP3β1, MAGT1, CD27 (cluster of differentiation antigen 27 )and other pathologicalmutations.
- Meet 5 or more of the following 8 indicators:
- Fever: body temperature > 38.5 ℃, continuous > 7 d; ② Splenomegaly;
- Hemocytopenia (involving two or three peripheral blood lines) : hemoglobin < 90 g/L (< 4 weeks infant, hemoglobin < 100 g/L), platelet < 100×109/L, neutrophils < 1.0×109/L and not caused by reducedhematopoietic function of bone marrow; ④ High triglyceride (TG) sepsisand/or low fibrinogenemia: triglyceride > 3 mmol/L or 3 standarddeviations above the same age, fibrinogen < 1.5g /L or less than 3standard deviations for the same age; (5) Hematophagy was found in bonemarrow, spleen, liver or lymph nodes;
- The activity of NK cells is decreased or absent; ⑦ Serum ferritin increase: ferritin ≥500 μg/L; Elevated sCD25 (solubleinterleukin-2 receptor). (3) Those who can understand the researchcontent, agree to comply with the research plan, and voluntarily signthe informed consent.
Exclusion
Exclusion Criteria:
- HLH caused by treatable infectious causes (such as bacteria, fungi, viruses (exceptEpstein-Barr virus), protozoa, etc.);
- Have a history of allergy or contraindications to the drugs involved in the program;
- Organ damage caused by long-term chronic diseases;
- Extreme physical weakness, unstable vital signs and inability to tolerate large dosesof cyclophosphamide;
- Severe and/or uncontrolled co-morbidivities (e.g., uncontrolled diabetes, pulmonaryhypertension, etc.) that the investigator believes may pose an unacceptable safetyrisk or interfere with protocol compliance;
- Mental instability or history of severe mental illness
- Other factors determined by the researcher that subjects are not suitable toparticipate in this study.
Study Design
Total Participants: 160
Treatment Group(s): 4
Primary Treatment: Etoposide
Phase:
Study Start date:
April 20, 2023
Estimated Completion Date:
May 20, 2027
Connect with a study center
The Second affiliated Hosptial of Chongqing medical University
Chongqing,
ChinaActive - Recruiting
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