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LVP protocol in combination with radiotherapy for untreated NK/T lymphoma patients

LVP protocol in combination with radiotherapy for untreated NK/T lymphoma patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNC-09000394
Enrollment
Unknown
Registered
2009-05-11
Start date
2009-05-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

NK/T lymphoma (I/II stage)

Interventions

treatment group:LVP(L-asparaginase 6000IU/m2 d1-5+Vincristine 1.4mg/m2 d1,no more than 2mg + prednisoned 45mg d1-5+)repeated every 21 days
radiotherapy

Sponsors

Department of Medical Oncology, Cancer Center, West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
16 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. NK/T lymphoma(Stage I or stage II) proved by pathology and immunohistology; 2. No chemotherapy or radiation was administered since diagnosis; 3. Performance status as ECOG 0-2 and no contraindication to chemotherapy; 4. Expectation of life was over 12 weeks; 5. Voluntary participation and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Patients combined with any unstable systemic diseases; 3. Hypersensitiveness to any kind of trial regime; 4. Any conditions that the investigator regards to be not suitable for current study.

Design outcomes

Primary

MeasureTime frame
Response Rate;Grade 3/4 toxicities;Disease-free survival;

Secondary

MeasureTime frame
Time to progress;overall survival rate;survival rate at year 1 and year 2;

Countries

China

Contacts

Public ContactLiqun Zou
hxlcyxy@163.com+86 028 81812027

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026