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RANDOMIZED CLINICAL AND BIOLOGICAL STUDY: CHEMOTHERAPY VS CHIMIO-RADIOTERAPIA FOR GASTRIC LYMPHOMA NON-HODGKIN OF HIGH GRADE.

RANDOMIZED CLINICAL AND BIOLOGICAL STUDY: CHEMOTHERAPY VS CHIMIO-RADIOTERAPIA FOR GASTRIC LYMPHOMA NON-HODGKIN OF HIGH GRADE.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REPEC
Registry ID
PER-080-03
Enrollment
Unknown
Registered
2004-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

None listed

Interventions

Cyclophosphamide 750 mg / m2, doxorubicin 50 / m2 mg, vincristine 1.4 mg / m2 and prednisone 100 mg every 21 days are administered. Group name:CHEMOTHERAPY MORE RADIOTERAPY Type of group
Cyclophosphamide 750 mg / m2, doxorubicin 50 / m2 mg, vincristine 1.4 mg / m2 and prednisone 100 mg every 21 days are administered. Radiotherapy includes irradiation of the entire stomach and the primary lymph nodes involved peri gastric, peri hepatic, and / or paraaortic) with high energy photons.

Sponsors

INTERNATIONAL EXTRANODAL LYMPHOMA STUDY GROUP,
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Histological diagnosis of non-Hodgkin lymphoma of high grade primary gastric clinical stage I, ll1, II2, IIE, without indication of emergency surgery. 2 No evidence of other neoplasms. 3 Evidence of measurable or evaluable injuries. 4 No previous treatment. 5 Age 4,000 mm3, neutrophils> 2,000 mm3, platelets> 120,000 min3. 8 Suitable renal and hepatic function 9 Life expectancy of more than three months. 10 Geographic accessibility or treatment. 11 Written consent.

Exclusion criteria

Exclusion criteria: 1 Severe cardiomyopathy. 2 Present or past history of second neoplasia (except carcinoma in-situ of cervix and basal cell carcinoma of skin). 3 Infections or metabolic disorders not controlled. 4 More than one month between the staging and the start of treatment. 5 Previous chemotherapy.

Design outcomes

Primary

MeasureTime frame
Outcome name:- Complete answer - answer parclal - stable inflammation - progression Measure:Evaluation of disease-free survival. Timepoints:one month

Secondary

MeasureTime frame
Outcome name:not contemplated Measure:not contemplated Timepoints:not contemplated

Countries

Peru

Outcome results

None listed

Source: REPEC (via WHO ICTRP)