Clinical Trial: Maintenance Rituximab With mTor Inhibition After High-dose Consolidative Therapy in Lymphoma

Study Status: Recruiting
Recruit Status: Recruiting
Study Type: Interventional

Official Title: A Trial of Maintenance Rituximab With mTor Inhibition After High-dose Consolidative Therapy in CD20+, B-cell Lymphomas, Gray Zone Lymphoma, and Hodgkin's Lymphoma

Brief Summary: This research is being done to determine if combining an investigational drug called Everolimus with Rituximab can reduce the risk of your cancer from returning after high dose chemotherapy.

Detailed Summary:

Everolimus is a pill that interferes with lymphoma cell growth by blocking a cellular pathway important in causing cancer cells to grow, called mTor. Rituximab is an intravenous medication that specifically attacks a protein commonly found on lymphoma cells called CD20.

Rituximab is already widely used to treat multiple forms of lymphoma. Moreover, continuing rituximab after the completion of chemotherapy is already commonly used to help patients stay in remission longer. Everolimus has been shown in many types of relapsed lymphoma to decrease the size of lymph nodes by itself. Everolimus is approved by the Food and Drug Administration (FDA) for the treatment of advanced kidney cancer and subependymal giant cell astocytoma. It is not approved for use in lymphoma. The use of everolimus in this research study is investigational. The word "investigational" means that everolimus is not approved for marketing by the Food and Drug Administration (FDA). The FDA is allowing the use of everolimus in this study.

The combination of everolimus and rituximab for 1 year after high dose therapy is also new. We believe the combination of these medications right after your chemotherapy will be more effective in attacking your remaining cancer before they have time to re-grow.

The usual treatment of lymphoma after high-dose chemotherapy is observation. After your body has fully recovered from the effects of the chemotherapy, you will receive everolimus daily for one year and IV rituximab four times during that year.


Sponsor: Sidney Kimmel Comprehensive Cancer Center

Current Primary Outcome: Number of patients with adverse events when given treatment with maintenance rituximab and prolonged mTOR inhibition with everolimus in CD20+, B cell lymphomas, Gray Zone Lymphoma, and Hodgkin's Lymphoma after high-dose consolidative therapy

• Avoidance of ≥ grade III common toxicities (CTCAE version 4.0)


Original Primary Outcome: Number of patients with adverse events when given treatment with maintenance rituximab and prolonged mTOR inhibition with everolimus in CD20+, B cell lymphomas and Hodgkin's Lymphoma after high-dose consolidative therapy

• Avoidance of ≥ grade III common toxicities (CTCAE version 4.0)


Current Secondary Outcome:

  • 1) Event free survival at three years based on histology [ Time Frame: 3 years ]
    • EFS will be histology grade specific: Mantle cell lymphoma group, low-grade lymphoma group, high-grade lymphoma group
  • 2) Reduction of the frequency of circulating cancer cells due to maintenance rituximab with everolimus treatment
  • 3) Sensitivity, in-vivo, of relapsed disease to mTor kinase inhibition.


Original Secondary Outcome:

  • 1) The secondary endpoint of this study is to evaluate event free survival at three years based on histology [ Time Frame: 3 years ]
    • EFS will be histology grade specific: Mantle cell lymphoma group, low-grade lymphoma group, high-grade lymphoma group
  • 2) To determine whether maintenance rituximab with everolimus treatment reduces the frequency of circulating cancer cells.
  • 3) To determine if relapsed disease is sensitive, in-vivo, to mTor kinase inhibition.


Information By: Sidney Kimmel Comprehensive Cancer Center

Dates:
Date Received: July 27, 2012
Date Started: August 2012
Date Completion: July 2018
Last Updated: May 17, 2016
Last Verified: May 2016