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Phase II study of R-EPOCH for elderly Burkitt lymphoma and intermediate Burkitt lymphoma /diffuse large B cell lymphoma

Phase II study of R-EPOCH for elderly Burkitt lymphoma and intermediate Burkitt lymphoma /diffuse large B cell lymphoma - EPOCH-BL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007100
Enrollment
40
Registered
2012-01-23
Start date
2012-03-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

elderly Burkitt lymphoma and intermediate Burkitt lymphoma/diffuse large B cell lymphoma

Interventions

6-8 cycles of R-EPOCH are scheduled. The patients achieved CR after 4 cycles recieve total 6cycles, and the patients achieved PR after 4 cycles recieve total 8 cycles.

Sponsors

Clinical Hematology Study Group of National Hospital Organization(CHSG-NHO)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.pathological diagnosis: Burkitt lymphoma or intermediate Burkitt lymphoma/diffuse large B cell lymphoma 2.CD20 antigen positive 3.no prior therapy for lymphoma 4.lymphoma cells less than 5000/mm3 in peripheral blood 5.presence of mesurable lesions 6.age: 65-79 years old 7.PS(ECOG): 0-2 8.adequate organ funcitions 9.informed consented patients

Exclusion criteria

Exclusion criteria: 1.presence of active infeciton 2.presence of central nervous invasion 3.past history of glaucoma. 4.past history of severe drug allergy. 5.HIV Ab positive or HTLV-1 Ab positive. 6.HBsAg positive or HCV Ab positive. 7.severe cardiac disease 8.hepatic cirrhosis 9.uncontrollable diabetis melitus 10.patients with dialysis 11.lung fibrosis or interstitial pneumonitis 12.other active malignancies 13.pregnant or feeding female 14.severe mental disorder 15.judged for inappropriate with other reasons.

Design outcomes

Primary

MeasureTime frame
2 years progression free survival

Secondary

MeasureTime frame
complete remission rate, 2 years over all survival, safety

Countries

Japan

Contacts

Public ContactHirokazu Nagai

National Hospital Organization Nagoya Medical Center Clinical Research Center

nagaih@nnh.hosp.go.jp052-951-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026