Rituximab and ABVD for Hodgkin's Patients

This study has been completed.
Sponsor:
Collaborator:
Genentech
Information provided by (Responsible Party):
M.D. Anderson Cancer Center
ClinicalTrials.gov Identifier:
NCT00504504
First received: July 19, 2007
Last updated: March 6, 2013
Last verified: March 2013

July 19, 2007
March 6, 2013
March 2001
March 2012   (final data collection date for primary outcome measure)
5-year failure-free survival rate for patients with Hodgkin's disease given Rituximab with ABVD [ Time Frame: Baseline to 5 Years or until disease progression ] [ Designated as safety issue: No ]
Event free survival (EFS) using Rituximab+ABVD (RABVD) in newly diagnosed patients with advanced stage classical Hodgkin lymphoma (HL). Event-free Survival (EFS) analyzed every 6 months.
Not Provided
Complete list of historical versions of study NCT00504504 on ClinicalTrials.gov Archive Site
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Rituximab and ABVD for Hodgkin's Patients
A Phase II Study of Rituximab + ABVD for Patients With Hodgkin's Disease

Primary Objective:

- To determine the feasibility, toxicity, and efficacy of Rituximab with standard dose ABVD combination chemotherapy.

ABVD combination chemotherapy consists of Adriamycin, Bleomycin, Vinblastine and DTIC.

Before treatment starts, patients will have a physical exam. Bone marrow samples will be taken. Blood samples (4 to 8 tablespoons) will be taken before and during the study. A chest x-ray, CT scans of the abdomen and pelvis, and a gallium scan will be done if necessary.

Patients in this study will receive rituximab by vein over 3 to 8 hours weekly for 6 weeks in a row. ABVD will be injected over 3 hours every other week for a total of 12 treatments. On the cycles where both rituximab and ABVD are given, rituximab will be given on day 1, and ABVD will be given on day 2. Response to therapy will be determined after 3 months and at the end of therapy (6 months). At the end, patients may receive radiation therapy to areas of large masses. All treatments can be given in an outpatient setting.

Scans and x-rays will be repeated if needed after completion of therapy and every 3 months from then on. If tumors do not shrink after 3 months of therapy, patients will be offered a different treatment.

This is an investigational study. Although ABVD is considered the standard treatment for patients with Hodgkin's disease, the combination of ABVD with rituximab is considered investigational. All drugs involved in this study are commercially available and are approved by the FDA. Up to 85 patients will take part in this study. All will be enrolled at M. D. Anderson. This protocol is partially funded by a research grant from Genentech.

Interventional
Phase 2
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Lymphoma
  • Drug: Rituximab
    375 mg/m^2 by vein over 3 to 8 hours weekly for 6 weeks in a row.
    Other Name: Rituxan
  • Drug: Adriamycin
    25 mg/m^2 injected by vein over 3 hours every other week for a total of 12 treatments.
    Other Names:
    • Doxorubicin
    • Rubex
  • Drug: Bleomycin
    10 U/m^2 injected by vein over 3 hours every other week for a total of 12 treatments.
    Other Names:
    • Bleomycin sulfate
    • Blenoxane
    • BLM
  • Drug: Vinblastine
    6 mg/m^2 injected by vein over 3 hours every other week for a total of 12 treatments.
    Other Names:
    • Vinblastine Sulfate
    • Velban
  • Drug: Dacarbazine (DTIC)
    375 mg/m^2 injected by vein over 3 hours every other week for a total of 12 treatments.
    Other Name: DTIC-Dome
Experimental: Rituximab + ABVD Chemotherapy
Rituximab 375 mg/m^2 by vein (IV) over 3 to 8 hours weekly for 6 weeks in a row. ABVD Chemo: Adriamycin 25 mg/m^2 IV, Bleomycin 10 U/m^2 IV, Vinblastine 6 mg/m^2 IV, DTIC 375 mg/m^2 IV. Each but Rituximab over 3 hours every other week for a total of 12 treatments.
Interventions:
  • Drug: Rituximab
  • Drug: Adriamycin
  • Drug: Bleomycin
  • Drug: Vinblastine
  • Drug: Dacarbazine (DTIC)
Younes A, Oki Y, McLaughlin P, Copeland AR, Goy A, Pro B, Feng L, Yuan Y, Chuang HH, Macapinlac HA, Hagemeister F, Romaguera J, Samaniego F, Fanale MA, Dabaja BS, Rodriguez MA, Dang N, Kwak LW, Neelapu SS, Fayad LE. Phase 2 study of rituximab plus ABVD in patients with newly diagnosed classical Hodgkin lymphoma. Blood. 2012 May 3;119(18):4123-8. Epub 2012 Feb 27.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
85
March 2012
March 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Hodgkin's disease patients who relapse after radiation therapy alone and previously untreated patients with stage II bulky, III and IV who are eligible for ABVD.
  2. Must have histologically proven diagnosis of Hodgkin's disease (Nodular sclerosis or mixed cellularity).
  3. Must have bidimensionally measurable disease.
  4. Must sign a consent form.
  5. Must be older than 16 years of age.
  6. Must have adequate bone marrow reserve (ANC > 1,000/microL, Platelet > 100,000/microL
  7. Left Ventricular Ejection Fraction (LVEF) >/= 50% by multigated acquisition (MUGA) scan or echocardiogram.
  8. Serum creatinine < 2 mg/dl, serum bilirubin < 2 mg/dl

Exclusion Criteria:

  1. HIV positive.
  2. Pregnant women and women of child bearing age who are not practicing adequate contraception.
  3. Prior chemotherapy.
  4. Severe pulmonary disease including Chronic obstructive pulmonary disease (COPD) and asthma.
Both
16 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00504504
ID00-218
No
M.D. Anderson Cancer Center
M.D. Anderson Cancer Center
Genentech
Principal Investigator: Anas Younes, MD M.D. Anderson Cancer Center
M.D. Anderson Cancer Center
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP