Maintenance Rituximab With mTor Inhibition After High-dose Consolidative Therapy in Lymphoma
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
CD20+, B-cell Lymphomas Mantle Cell Lymphoma Non-Mantle Cell Low Grade B Cell Lymphomas (SLL/CLL) Transformed Lymphoma/DLBCL/PMBCL Hodgkin's Disease |
Drug: Everolimus and Rituximab |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Trial of Maintenance Rituximab With mTor Inhibition After High-dose Consolidative Therapy in CD20+, B-cell Lymphomas and Hodgkin's Lymphoma |
- 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 [ Designated as safety issue: Yes ]• Avoidance of ≥ grade III common toxicities (CTCAE version 4.0)
- 1) Event free survival at three years based on histology [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]• 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 [ Designated as safety issue: No ]
- 3) Sensitivity, in-vivo, of relapsed disease to mTor kinase inhibition. [ Designated as safety issue: No ]
| Estimated Enrollment: | 60 |
| Study Start Date: | August 2012 |
| Estimated Primary Completion Date: | July 2017 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Everolimus and Rituximab
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.
|
Drug: Everolimus and Rituximab
Everolimus: 10 mg, orally, every day for one year Rituximab: 375mg/m2 day +1 and then every 90 days for 1 year (a total of 4 infusions)
Other Name: RAD001
|
Detailed Description:
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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age >18 years of age
- ECOG performance status ≤ 2
- INR ≤ 2
- Adequate renal and hepatic function defined as a serum creatinine <2.0mg/dL, total bilirubin <5mg/dL, and AST and ALT ˂ 2.5 ULN.
- Platelet count >75 x 109/L
- Hemoglobin >10mg/dL
- ANC >3.0x109/L
- Fasting serum cholesterol ≤300 mg/dL OR ≤7.75 mmol/L and fasting triglycerides ≤ 2.5 x ULN. NOTE: In case one or both of these thresholds are exceeded, the patient can only be included after initiation of appropriate lipid lowering medication.
- A willingness to use an accepted and effective method of birth control for sexually active women of childbearing potential during the study and for 8 weeks after the end of study drug treatment.
- Ability to sign informed consent
Exclusion Criteria:
- Patient who have previously received an mTor inhibitor
- Patients who are pre-terminal or moribund
- Patients with active bacterial of fungal infections requiring oral or intravenous antimicrobials are not eligible until resolution of the infection
- Female patients who are pregnant or breast feeding, or of reproductive potential who are not using effective birth control methods. Adequate contraception must be used throughout the trial and for 8 weeks after the last dose of study drug.
- Patients with known intolerance to rituximab
- HIV positive, Hepatitis B positive, Hepatitis C positive individuals
Contacts and Locations| Contact: Douglas Gladstone, MD | 410-955-8781 | dgladst1@jhmi.edu |
| United States, Maryland | |
| Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins | Recruiting |
| Baltimore, Maryland, United States, 21231 | |
| Contact: Clinical Trials Office- SKCCC 410-955-8804 jhcccro@jhmi.edu | |
| Principal Investigator: | Douglas Gladstone, MD | Sidney Kimmel Comprehensive Cancer Center |
More Information
No publications provided
| Responsible Party: | Sidney Kimmel Comprehensive Cancer Center |
| ClinicalTrials.gov Identifier: | NCT01665768 History of Changes |
| Other Study ID Numbers: | J1228, NA_00067315 |
| Study First Received: | July 27, 2012 |
| Last Updated: | May 10, 2013 |
| Health Authority: | United States: Institutional Review Board |
Additional relevant MeSH terms:
|
Hodgkin Disease Lymphoma Lymphoma, B-Cell Lymphoma, Mantle-Cell Neoplasms by Histologic Type Neoplasms Lymphoproliferative Disorders Lymphatic Diseases Immunoproliferative Disorders Immune System Diseases Lymphoma, Non-Hodgkin Everolimus Sirolimus |
Rituximab Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Antifungal Agents Anti-Infective Agents Anti-Bacterial Agents Antirheumatic Agents |
ClinicalTrials.gov processed this record on May 16, 2013