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Pegaspargase-COEP Chemotherapy Combined With Radiotherapy for Extra-nodal NK/T Cell Lymphoma

Sponsored by Peking University

About this trial

Last updated 5 years ago

Study ID

COEPL for NKTCL

Status

Recruiting

Type

Interventional

Phase

Phase 2

Placebo

No

Accepting

18-75 Years
14 to 80 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Started 14 years ago

What is this trial about?

The optimal first-line treatment for extra-nodal NK/T-cell lymphoma (ENKTL) has not been well-defined. This phase II study aimed to evaluate the efficacy and safety of pegaspargase, cyclophosphamide, vincristine, etoposide and prednisone (COEPL) regimen combined with radiotherapy for patients with newly diagnosed ENKTL.

What are the participation requirements?

Yes

Inclusion Criteria

- patients with confirmed pathological diagnosis of ENKTL as defined by WHO criteria

- age 14-80 years

- no prior chemotherapy or radiotherapy

- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2

- at least one measurable lesion

- adequate bone marrow function (i.e. hemoglobin ≥80 g/l, absolute neutrophil count ≥ 1.0 × 10^9/L, platelets ≥ 100 ×10^9/L), adequate renal function (i.e. serum creatinine ≤177 μmol/L), adequate hepatic function (e.g. total bilirubin ≤ two times the upper limit of normal, and ALT /AST ≤2.5 times the upper limit of normal)

- expected survival of more than three months

No

Exclusion Criteria

- invasion of lymphoma to central nervous system

- pre-existing coagulation disorder

- other concomitant neoplasms

- severe infection

- positive HIV antibody

- HBV DNA titer higher than 10^4 copies /ml in HBsAg-positive patients post antiviral therapy

- pregnant or lactating women

- women of childbearing age unwilling to take contraceptive measures during the study period

Locations

Location

Status

Recruiting