A Randomized Controlled Study of High-dose Cyclophosphamide Induction Therapy in Adult Patients With HLH
NCT ID: NCT05936086
Last Updated: 2023-08-30
Study Results
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Basic Information
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RECRUITING
NA
160 participants
INTERVENTIONAL
2023-04-20
2027-05-20
Brief Summary
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The opportunity to heal. Therefore, it is important to explore effective induction therapy for adult HLH. In the majority ,Early (30-day) mortality was as high as 40% after cardiac induction using HLH2004 or CHOP(cyclophosphamide, hydroxydaunomycin, Oncovin, and prednisone) induction. HLH, on the other hand, usually requires prompt treatment before the cause is established. Due to a specific infection HLH can benefit from anti-infective therapy. Therefore, it is necessary to explore more effective induction therapy for adult non-infective HLH.It has very important clinical significance. Adult secondary HLH has the common features of a large number of T cell proliferation and activation and a significant reduction of NK(natural killer) cells, in which the central liNK(natural killer) is a large number of T cells proliferation and secomplete remission etion of cytokines, which can be used as induction therapy.Common target is also the pathological basis for designing unified induction scheme. Cyclophosphamide is a commonly used alkylated chemotherapy drug,It's also an important immunosuppressant. Based on the treatment of regenerative disorders anemia, allogeneic hematopoietic stem cell transplantation prevention.Experience with Plant versus Host disease (GVHD) has shown that the use of cyclophosphamide exceeds a total dose of 25mg/day,Two days can effectively kill CD8(cluster of differentiation 8 )+ or CD4(cluster of differentiation 4
)+T cells, and the maximum tolerated dose of this drug in humans exceeds 50mg/kg/day for two days. Aiming at the central liNK(natural killer) of adult HLH pathogenesis, The investigators designed for the first time to use a large dose of cyclophosphamide (25mg-50mg/kg/day 2days) to inhibit the activation of T cells, inhibit the production of cytokines and block the development mechanism of HLH. This study intends to conduct a randomized controlled study, with HLH2004 scheme as the control, and the observation is large efficacy and safety of dose cyclophosphamide in induction therapy of non-infective adult HLH in order to complete remission eate a new induction Treatment plan.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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CTX(Cytoxan) group
Cytoxan
Cytoxan 40mg/kg iv qd x 2days (day 1 and 2);
Dexamethasone
Dexamethasone: 10 mg/m2/day, week 1 to 2; 5 mg/m2/d for the 3rd to 4th week; 2.5 mg/m2/ day at week 5-6.
Normal treatment group
Etoposide
etoposide(VP16):150 mg/m2, twice a week, 1-2 weeks; 150mg/m2, once a week for the 3rd to 6th week.
Dexamethasone
Dexamethasone: 10 mg/m2/day, week 1 to 2; 5 mg/m2/d for the 3rd to 4th week; 2.5 mg/m2/ day at week 5-6.
Cyclosporine (CSA)
Cyclosporine (CSA) 100mg Bid, week 1 to 6 (dosed according to 2004 version).
Interventions
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Cytoxan
Cytoxan 40mg/kg iv qd x 2days (day 1 and 2);
Etoposide
etoposide(VP16):150 mg/m2, twice a week, 1-2 weeks; 150mg/m2, once a week for the 3rd to 6th week.
Dexamethasone
Dexamethasone: 10 mg/m2/day, week 1 to 2; 5 mg/m2/d for the 3rd to 4th week; 2.5 mg/m2/ day at week 5-6.
Cyclosporine (CSA)
Cyclosporine (CSA) 100mg Bid, week 1 to 6 (dosed according to 2004 version).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. According to the diagnostic criteria of HLH-2004, HLH can be diagnosed if any of the following two criteria are met:
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1. Molecular diagnosis is consistent with HLH: Currently known HLH related pathogenic genes exist, such as PRF1, UNC13D, STX11, STXBP2, Rab27a, LYST, SH2D1A, BIRC4, ITK, AP3β1, MAGT1, CD27 (cluster of differentiation antigen 27 )and other pathological mutations.
2. 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 reduced hematopoietic function of bone marrow; ④ High triglyceride (TG) sepsis and/or low fibrinogenemia: triglyceride \> 3 mmol/L or 3 standard deviations above the same age, fibrinogen \< 1.5g /L or less than 3 standard deviations for the same age; (5) Hematophagy was found in bone marrow, spleen, liver or lymph nodes;
* The activity of NK cells is decreased or absent;
⑦ Serum ferritin increase: ferritin ≥500 μg/L; Elevated sCD25 (soluble interleukin-2 receptor). (3) Those who can understand the research content, agree to comply with the research plan, and voluntarily sign the informed consent.
Exclusion Criteria
2. Have a history of allergy or contraindications to the drugs involved in the program;
3. Organ damage caused by long-term chronic diseases;
4. Extreme physical weakness, unstable vital signs and inability to tolerate large doses of cyclophosphamide;
5. Severe and/or uncontrolled co-morbidivities (e.g., uncontrolled diabetes, pulmonary hypertension, etc.) that the investigator believes may pose an unacceptable safety risk or interfere with protocol compliance;
6. Mental instability or history of severe mental illness
7. Other factors determined by the researcher that subjects are not suitable to participate in this study.
18 Years
65 Years
ALL
Yes
Sponsors
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shifeng Lou
OTHER
Responsible Party
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shifeng Lou
Director
Principal Investigators
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Qing Wen, doctor
Role: STUDY_DIRECTOR
Hematology Medical Center, the Second Affiliated Hospital of PLA Army Medical University
Huaer Shu, bachelor
Role: STUDY_DIRECTOR
Chongqing Kaizhou District People's Hospital
Hongbin Zhang, doctor
Role: STUDY_DIRECTOR
First Affiliated Hospital of Chongqing Medical University
Jinglong Lv, master
Role: STUDY_DIRECTOR
Three Gorges Central Hospital Affiliated to Chongqing University
Zhangqin luo, bachelor
Role: STUDY_DIRECTOR
Yongchuan Hospital affiliated to Chongqing Medical University
Liang Fang, master
Role: STUDY_DIRECTOR
Chongqing Ninth People's Hospital
Yizhi Xu, doctor
Role: STUDY_DIRECTOR
People's Hospital of Chongqing
Zailiang Yang, doctor
Role: STUDY_DIRECTOR
Fuling Hospital affiliated to Chongqing University
Locations
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The Second affiliated Hosptial of Chongqing medical University
Chongqing, , China
Countries
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Central Contacts
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Facility Contacts
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Shifeng Lou, master
Role: primary
Jianchuan Deng
Role: backup
Other Identifiers
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XYNK 04
Identifier Type: -
Identifier Source: org_study_id
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