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NARecruitingPriority 4 · Lower priorityNCT06069830

PET and EBV DNA-directed Therapy for Localized Nasal Extranodal NK/T Cell Lymphoma

ClinicalTrials.gov

Plain-language summary

This NA trial is evaluating 4 cycles of ESA regimen with sandwiched radiotherapy, 2 cycles of ESA regimen sequential radiotherapy and 2 cycles of PD-1 monoclonal antibody combined with pegaspargase, and other medications as a treatment for people newly diagnosed with NK/T-cell lymphoma. The study measures how well this treatment works and monitors for side effects. This trial does not currently list US sites.

Who can join (key eligibility)

  • Age 18 Years or older
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

Final eligibility is determined by the trial team. This list is a starting point only.

What's being tested

4 cycles of ESA regimen with sandwiched radiotherapy (DRUG): Pegaspargase, 2500U/m2, i.m. d1; etoposide, 200mg, p.o., d2-d4; Dexamethasone, 40mg, p.o. d2-d4; | 2 cycles of ESA regimen sequential radiotherapy and 2 cycles of PD-1 monoclonal antibody combined with pegaspargase (DRUG): Pegaspargase, 2500U/m2, IM, d1; PD-1 monoclonal antibody, 200mg, i.v. d2; | 2 cycles of ESA regimen, 2 cycles of PD-1 monoclonal antibody and concurrent radiotherapy, 2 cycles of PD-1 monoclonal antibody combined with pegaspargase (DRUG): PD-1 monoclonal antibody, 200mg, i.v. d1

Drugs / treatments
4 cycles of ESA regimen with sandwiched radiotherapy, 2 cycles of ESA regimen sequential radiotherapy and 2 cycles of PD-1 monoclonal antibody combined with pegaspargase, 2 cycles of ESA regimen, 2 cycles of PD-1 monoclonal antibody and concurrent radiotherapy, 2 cycles of PD-1 monoclonal antibody combined with pegaspargase
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
NA
Status
Recruiting
Design
Non-randomized, open-label
Enrollment target
89 patients
Primary endpoint
2-year progression-free survival rate
Ages
18 Years to —
Start date
2023-12-06
Est. completion
2026-10

Locations

0 US sites · 1 total

No US sites currently listed.

Contact

Sponsor
Ruijin Hospital (OTHER)
Contact
Weili Zhao | zwl_trial@163.com | +862164370045

Tags

ENKTLNewly diagnosed
TrialCompass — Clinical Trial Summary

PET and EBV DNA-directed Therapy for Localized Nasal Extranodal NK/T Cell Lymphoma

NCT06069830

Phase: NA | Status: Recruiting | Priority: Lower

Plain-language summary

This NA trial is evaluating 4 cycles of ESA regimen with sandwiched radiotherapy, 2 cycles of ESA regimen sequential radiotherapy and 2 cycles of PD-1 monoclonal antibody combined with pegaspargase, and other medications as a treatment for people newly diagnosed with NK/T-cell lymphoma. The study measures how well this treatment works and monitors for side effects. This trial does not currently list US sites.

Who can join

  • Age 18 Years or older
  • Newly diagnosed, not yet treated
  • Must be well enough for treatment (adequate performance status)

What's being tested

4 cycles of ESA regimen with sandwiched radiotherapy (DRUG): Pegaspargase, 2500U/m2, i.m. d1; etoposide, 200mg, p.o., d2-d4; Dexamethasone, 40mg, p.o. d2-d4; | 2 cycles of ESA regimen sequential radiotherapy and 2 cycles of PD-1 monoclonal antibody combined with pegaspargase (DRUG): Pegaspargase, 2500U/m2, IM, d1; PD-1 monoclonal antibody, 200mg, i.v. d2; | 2 cycles of ESA regimen, 2 cycles of PD-1 monoclonal antibody and concurrent radiotherapy, 2 cycles of PD-1 monoclonal antibody combined with pegaspargase (DRUG): PD-1 monoclonal antibody, 200mg, i.v. d1

Drugs / treatments: 4 cycles of ESA regimen with sandwiched radiotherapy, 2 cycles of ESA regimen sequential radiotherapy and 2 cycles of PD-1 monoclonal antibody combined with pegaspargase, 2 cycles of ESA regimen, 2 cycles of PD-1 monoclonal antibody and concurrent radiotherapy, 2 cycles of PD-1 monoclonal antibody combined with pegaspargase

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Non-randomized, open-label

Enrollment target: 89 patients

Primary endpoint: 2-year progression-free survival rate

Ages: 18 Years to —

Start date: 2023-12-06 | Est. completion: 2026-10

Locations

0 US sites · 1 total

Contact

Weili Zhao | zwl_trial@163.com | +862164370045

Sponsor: Ruijin Hospital (OTHER)

Tags

ENKTL · Newly diagnosed

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT06069830

Prepared using TrialCompass (trialcompass.com) on June 19, 2026. For informational purposes only. Always discuss with your healthcare team.
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Data sourced from ClinicalTrials.gov.

For informational purposes only. Not medical advice — always consult your healthcare team.

Built with care for the rare cancer community.

Data last updated: June 2026

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