Actively Recruiting
Combination of Mitoxantrone Liposome and Etoposide, Dexamethasone, Pegaspargase and Golidocitinib (MEPL-G) in the Treatment of NK/T-cell Lymphoma Associated Hemophagocytic Lymphohistiocytosis (NKTCL-HLH)
Led by Beijing Tongren Hospital · Updated on 2026-04-13
25
Participants Needed
1
Research Sites
130 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Extranodal NK/T-cell lymphoma (NKTCL) is an aggressive EBV-associated lymphoma with poor prognosis, highly prevalent in China. Early-stage NKTCL achieves favorable long-term survival, while advanced disease shows dismal outcomes with no standard therapy. Notably, 10%-20% of patients develop secondary hemophagocytic lymphohistiocytosis (NKTCL-HLH), a life-threatening complication with median survival \<2 months and mortality over 90%. Current treatments fail to simultaneously control lymphoma and hyperinflammation, with poor tolerance and high resistance. The JAK/STAT pathway drives EBV-induced inflammation and tumor progression. Golidocitinib, a selective JAK1 inhibitor, demonstrates potent anti-NKTCL activity and rapid inflammation control. Liposomal mitoxantrone offers targeted efficacy with lower toxicity, while etoposide, methylprednisolone, and pegaspargase provide synergistic anti-tumor and anti-HLH effects. This study proposes the novel MEPL-G regimen (liposomal mitoxantrone, etoposide, methylprednisolone, pegaspargase, golidocitinib) for NKTCL-HLH. By targeting both HLH and NKTCL, this combination aims to achieve rapid disease control, improve tolerance, and prolong survival, addressing the unmet critical clinical need for this high-risk population.
CONDITIONS
Official Title
Combination of Mitoxantrone Liposome and Etoposide, Dexamethasone, Pegaspargase and Golidocitinib (MEPL-G) in the Treatment of NK/T-cell Lymphoma Associated Hemophagocytic Lymphohistiocytosis (NKTCL-HLH)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Histologically confirmed extranodal NK/T-cell lymphoma
- Diagnosis meeting HLH-2004 criteria with at least 5 criteria
- Age 18 years or older, any gender
- Negative HIV antigen or antibody test
- Left ventricular ejection fraction (LVEF) of 50% or higher
- No active visceral bleeding such as gastrointestinal, lung, or brain bleeding
- No uncontrolled infections such as lung or intestinal infections
- Negative hepatitis C antibody or positive antibody with negative hepatitis C RNA
- Negative hepatitis B surface antigen and core antibody; if positive, HBV DNA must be below 1x10^3 copies/mL
- Signed informed consent and ability to follow study procedures
You will not qualify if you...
- New York Heart Association (NYHA) cardiac function class II or higher
- Pregnant or breastfeeding women
- Known allergy to any study drugs
- Other active cancers except non-melanoma skin cancer
- Central nervous system lymphoma involvement
- Severe psychiatric disorders or inability to comply with follow-up
- Severe kidney dysfunction (glomerular filtration rate below 15 mL/min)
- Severe liver cirrhosis (MELD score above 20)
- History of acute or chronic pancreatitis
- Participation in another clinical trial concurrently
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beijing Tongren Hospital, Capital Medical University
Beijing, China, 100730
Actively Recruiting
Research Team
L
Liang Wang, M.D.
CONTACT
J
Jia Cong, M.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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