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

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-20

Study Completion Date

2027-05-20

Brief Summary

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Adult secondary HLH involves tumors, autoimmune diseases and other causes in addition to infection,Infectious factors, theoretically need different treatment methods for different etiology. But adult HLH itself disease .The situation progresses ferociously, which can cause organ damage and blood coagulation disorder and endanger life quickly, with early mortality (30days).It can be more than 50%. On the other hand, although diagnostic techniques have improved significantly, identifying the cause is still costly Time, such as 1-2 weeks for the pathological diagnosis of lymphoma, leads to more patients losing further treatment due to early death.

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.

Detailed Description

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Conditions

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Hemophagocytic Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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CTX(Cytoxan) group

Group Type EXPERIMENTAL

Cytoxan

Intervention Type DRUG

Cytoxan 40mg/kg iv qd x 2days (day 1 and 2);

Dexamethasone

Intervention Type DRUG

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

Group Type ACTIVE_COMPARATOR

Etoposide

Intervention Type DRUG

etoposide(VP16):150 mg/m2, twice a week, 1-2 weeks; 150mg/m2, once a week for the 3rd to 6th week.

Dexamethasone

Intervention Type DRUG

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)

Intervention Type DRUG

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);

Intervention Type DRUG

Etoposide

etoposide(VP16):150 mg/m2, twice a week, 1-2 weeks; 150mg/m2, once a week for the 3rd to 6th week.

Intervention Type DRUG

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.

Intervention Type DRUG

Cyclosporine (CSA)

Cyclosporine (CSA) 100mg Bid, week 1 to 6 (dosed according to 2004 version).

Intervention Type DRUG

Other Intervention Names

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VP16

Eligibility Criteria

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Inclusion Criteria

1. Age range from 18 to 65 years old (including the critical value), gender is not limited;
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 \&gt; 38.5 ℃, continuous \&gt; 7 d; ② Splenomegaly;

* Hemocytopenia (involving two or three peripheral blood lines) : hemoglobin \&lt; 90 g/L (\&lt; 4 weeks infant, hemoglobin \&lt; 100 g/L), platelet \&lt; 100×109/L, neutrophils \&lt; 1.0×109/L and not caused by reduced hematopoietic function of bone marrow; ④ High triglyceride (TG) sepsis and/or low fibrinogenemia: triglyceride \&gt; 3 mmol/L or 3 standard deviations above the same age, fibrinogen \&lt; 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

1. HLH caused by treatable infectious causes (such as bacteria, fungi, viruses (except Epstein-Barr virus), protozoa, etc.);
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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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shifeng Lou

OTHER

Sponsor Role lead

Responsible Party

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shifeng Lou

Director

Responsibility Role SPONSOR_INVESTIGATOR

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

Site Status RECRUITING

Countries

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China

Central Contacts

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shifeng Lou, master

Role: CONTACT

13508331213

jianchuan Deng, master

Role: CONTACT

15902305571

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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