Phase 2
N=58
Combination Chemotherapy With or Without Rituximab in Treating Participants With Stage III-IV Classic Hodgkin Lymphoma
Classic Hodgkin Lymphoma · Lugano Classification Stage III Hodgkin Lymphoma AJCC v8 · Lugano Classification Stage IV Hodgkin Lymphoma AJCC v8
Bottom Line
View on ClinicalTrials.gov: NCT00654732 ↗Enrolled (actual)
58
Serious AEs
44.8%
Results posted
Feb 2020
Primary outcome: Primary: Event-free Survival (EFS) Rate — 17; 20 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Bleomycin (Drug); Dacarbazine (Drug); Doxorubicin Hydrochloride (Drug); Rituximab (Biological); Vinblastine (Drug)
- Age
- Pediatric, Adult, Older Adult · 17+ yrs
- Sex
- All
- Sponsor
- M.D. Anderson Cancer Center
- Primary completion
- Sep 2018
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Event-free Survival (EFS) Rate |
17; 20 | — |
Summary
This phase II trial studies how well combination chemotherapy with or without rituximab works in treating participants with stage III-IV classic Hodgkin lymphoma. Monoclonal antibodies, such as rituximab, may interfere with the ability of tumor cells to grow and spread. Drugs used in chemotherapy, such as doxorubicin hydrochloride, bleomycin, vinblastine, and dacarbazine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving rituximab with combination chemotherapy may work better in treating participants with classic Hodgkin lymphoma.
Eligibility Criteria
Inclusion Criteria
- Previously untreated patient with classical Hodgkin's lymphoma patients with stage III and IV
- International Prognostic Score of > 2 (patient must have > 2 of the following risk features: Male, >= 45 years of age, stage IV, albumin = 15, lymphocytes = 1,500/microL
- Platelet > 100,000/microL
- Left ventricular ejection fraction (LVEF) >= 50% by multigated acquisition (MUGA) scan or echocardiogram
- Serum creatinine < 2 mg/dl
- Serum bilirubin < 2 mg/dl
- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) < 2 x upper limit of normal (ULN)
- Bi-dimensionally measurable disease
Exclusion Criteria
- Lymphocyte predominant Hodgkin's lymphoma
- Known human immunodeficiency virus (HIV) infection
- Pregnant women and women of child bearing age who are not practicing adequate contraception
- Prior chemotherapy or radiation therapy
- Severe pulmonary disease as judged by the principal investigator (PI) including chronic obstructive pulmonary disease (COPD) and asthma
- Active infection requiring treatment with intravenous therapy
- Presence of central nervous system (CNS) lymphoma
- Concomitant malignancies or previous malignancies within the last 5 years (exception made for adequately treated basal or squamous cell carcinoma of the skin or carcinoma in situ of cervix)
- Active hepatitis B or C infection
Data sourced from ClinicalTrials.gov (NCT00654732). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.