ConditionHodgkin Lymphoma, Adult
Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-50
SponsorState Budgetary Healthcare Institution, National Medical Surgical Center N.A. N.I. Pirogov, Ministry of Health of Russia
About this trial
The HL-Russia-1 is a non-randomized, open-label, multicenter, phase III, 3-arm study. The primary objective is to assess efficacy, safety and progression-free survival (PFS) of different approaches (earle favorable, early unfavorable and advanced stages) to first line chemotherapy for classical Hodgkin Lymphoma (HL).
Eligibility criteria
Qualifiers
Histologically confirmed classical HL
Previously untreated disease
Age 18-5 years
Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤2
Disqualifiers
Nodular Lymphocyte Predominant HL
Prior chemotherapy or radiation therapy
Pregnant or lactating females
Cardiac arrhythmia, conduction abnormalities, ischemic cardiopathy, left ventricular hypertrophy or left ventricular ejection fraction (LVEF) ≤50% at echocardiography.
Trial design
Treatments tested in this trial
- Doxorubicin
- Bleomycin
- Vinblastine
- Dacarbazine
- Etoposide
- Doxorubicin
- Cyclophosphamide
- Vincristine
- Dexamethasone
- Dacarbazine
Treatment groups
300 Participants
are divided into 3 treatment groups Source ClinicalTrials.gov