Clinical trial · Interventional
CEOP/IVE/GDP Compared With CEOP as the First-line Therapy for Newly Diagnosed Adult Patients With PTCL
CEOP/IVE/GDP Compared With CEOP as the First-line Therapy for Newly Diagnosed Adult Patients With Peripheral T-cell Lymphoma (PTCL)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Peripheral T-cell Lymphoma (PTCL) is a heterogenic malignancy with poor outcome. Five-year PFS and OS for these patients received classic CHOP regimen (cyclophosphamide, vincristin, doxorubicin and prednisone) is less than 30%.High dose intensive chemotherapy doesn't demonstrate better response. At present, there is no standardized treatment protocol for this kind of lymphoma. So, clinical trials are encouraged by NCCN for those patients.
Conditions
Conditions (6)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| ALK-negative Anaplastic Large Cell Lymphoma | Anaplastic Large Cell Lymphoma, ALK-Negative | ALIAS | 0.90 |
| Angioimmunoblastic T Cell Lymphoma | Follicular Helper T-Cell Lymphoma, Angioimmunoblastic-Type | ALIAS | 0.90 |
| Enteropathy Associated T Cell Lymphoma | Enteropathy-Associated T-Cell Lymphoma | ONTOLOGY_EXACT | 0.98 |
| Hepatosplenic T-cell Lymphoma | Hepatosplenic T-Cell Lymphoma | ONTOLOGY_EXACT | 0.98 |
| Peripheral T-Cell Lymphoma, Not Otherwise Specified | Peripheral T-Cell Lymphoma, Not Otherwise Specified | ONTOLOGY_EXACT | 0.90 |
| Subcutaneous Panniculitis Like T Cell Lymphoma | Subcutaneous Panniculitis-Like T-Cell Lymphoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CEOP chemotherapy regimen for 6 cycles | Drug | — | UNRESOLVED |
| CEOP/IVE/GDP chemotherapy regimen | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- CEOP/IVE/GDP chemotherapy regimen
- description
- 2 cycles of CEOP(cyclophosphamide,vincristine, epirubucin and prednisone),2 cycles of IVE(ifosfamide, epirubucin, etoposide)and 2 cycles of GDP(gemcitabine, cis-platinum, and dexamethasone)
- interventionNames
- Drug: CEOP/IVE/GDP chemotherapy regimen
- type
- ACTIVE_COMPARATOR
- label
- CEOP chemotherapy regimen for 6 cycles
- description
- 6 cycles of CEOP regimen(cyclophosphamide,vincristin,epirubucin and prednisone)
- interventionNames
- Drug: CEOP chemotherapy regimen for 6 cycles
Primary outcomes (1)
- measure
- Percentage of patients with complete remission (CR)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 16 Years
Show eligibility criteria text
Inclusion Criteria: * Newly diagnosed, histologically confirmed the following pathology subtype according to WHO 2008 classification: peripheral T Cell Lymphoma, not otherwise specified, angioimmunoblastic T cell lymphoma, ALK-negative anaplastic large cell lymphoma, enteropathy associated T cell lymphoma, subcutaneous panniculitis like T cell lymphoma, and hepatosplenic T-cell lymphoma. * ≥ 16 years of age. * Performance status of 2 or less. * Has no history of malignancy. * Has radiologically measurable disease. * Life expectancy ≥6 months. * Voluntarily sign an informed consent. Exclusion Criteria: * Pathology subtype with NK/T cell lymphoma, ALK positive-ALCL. * Primary central nervous system (CNS) lymphoma. * Previous systemic chemotherapy or local therapy. * Has undergone hematopoietic stem-cell transplantation (HSCT). * Has active infectious disease requiring general antibiotics, anti-fungal or anti-virus therapy. * Has uncontrollable cardiocerebrovascular, coagulative, autoimmune, or serious infectious disease. * Echocardiography shows left ventricular ejection fraction (LVEF) ≤ 50%. * Inadequate renal, hepatic or bone marrow function * Active liver or biliary disease. * Has other uncontrollable medical condition that may interfere with their participation in the study. * Woman in pregnancy or lactation. * Patient is known to be positive for Human immunodeficiency virus (HIV) infection.
References
Publications (1)
- DERIVEDCai MC, Cheng S, Wang X, Hu JD, Song YP, Huang YH, Yan ZX, Jiang YJ, Fang XS, Zheng XY, Dong LH, Ji MM, Wang L, Xu PP, Zhao WL. CEOP/IVE/GDP alternating regimen compared with CEOP as the first-line therapy for newly diagnosed patients with peripheral T cell lymphoma: results from a phase 2, multicenter, randomized, controlled clinical trial. Genome Med. 2020 Apr 30;12(1):41. doi: 10.1186/s13073-020-00739-0. PMID 32349779