Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT07525466

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Beijing Tongren Hospital, Capital Medical University

Beijing, China, 100730

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here