Lenalidomide Combined With Vorinostat/Gemcitabine/Busulfan/Melphalan With Autologous Stem-Cell Transplantation in Diffuse Large B-Cell Lymphoma of the ABC Subtype

November 26, 2019 updated by: M.D. Anderson Cancer Center
The goal of this clinical research study is to find the highest tolerable dose of lenalidomide that can be given in combination with vorinostat, gemcitabine, busulfan, and melphalan, with a stem cell transplant, and with or without rituximab. Researchers also want to learn about the safety and effectiveness of this combination.

Study Overview

Status

Terminated

Conditions

Intervention / Treatment

Detailed Description

Central Venous Catheter:

Many of the drugs given in this study and the stem cell transplant will be given by vein through a central venous catheter (CVC). A CVC is a sterile flexible tube and needle that will be placed into a large vein while you are under local anesthesia. Blood samples will also be drawn through your CVC. The CVC will remain in your body during treatment. Your doctor will explain this procedure to you in more detail, and you will be required to sign a separate consent form.

Study Groups:

If you are found to be eligible to take part in this study, you will be assigned to a dose level of lenalidomide based on when you join this study. Up to 3 dose levels of lenalidomide will be tested. At least 2 participants will be enrolled at each dose level. The first group of participants will receive the lowest dose level. Each new group will receive a higher dose than the group before it, if no intolerable side effects were seen. This will continue until the highest tolerable dose of lenalidomide is found.

All participants will receive the same dose level of vorinostat, gemcitabine, busulfan, rituximab, and melphalan. However, if the first group of participants have any bad side effects, the dose level of gemcitabine may be lowered for all other groups.

Busulfan Test Dose:

In stem cell transplants, the days before you receive your stem cells are called minus days. The day you receive the stem cells is called Day 0. The days after you receive your stem cells are called plus days.

You will receive a test dose of busulfan by vein over about 60 minutes. This low-level test dose of busulfan is to check how the level of busulfan in your blood levels changes over time. This information will be used to decide the next dose needed to match your body size. You will most likely receive this as an outpatient during the week before you are admitted to the hospital. If it cannot be given as an outpatient, you will be admitted to the hospital on Day -11 (11 days before your stem cells are returned to your body) and the test dose will be given on Day -10.

Blood (about 1 teaspoon each time) will be drawn for pharmacokinetic (PK) testing of busulfan 11 times. PK testing measures the amount of study drug in the body at different time points and will help the study doctor determine what your dose of busulfan should be on study. These blood samples will be drawn at various timepoints before you receive busulfan and over about the next 11 hours. The blood samples will be repeated again on the first day of high-dose busulfan treatment (Day -8). A temporary heparin lock line will be placed in your vein to lower the number of needle sticks needed for these draws. If it is not possible for the PK tests to be performed, you will receive the standard fixed dose of busulfan.

You will also receive palifermin by vein over about 30 seconds each day to help decrease the risk of side effects in the mouth and throat either during the 2 days before you are admitted (inpatient) or during the 3 days before you are admitted (outpatient) You may ask the study staff about the risks of palifermin.

Study Drug Administration (all patients):

Beginning on Day -8, you will swish caphosol and glutamine liquids in your mouth 4 times a day, for about 2 minutes each time. You will swish these liquids every day until you leave the hospital. You will swallow the glutamine. These drugs are used to help decrease the risk of side effects in the mouth and throat.

On Days -9 through Day -2, you will take lenalidomide and vorinostat by mouth, with food.

If you the doctor thinks it is needed, you will receive rituximab by vein over 3-6 hours as part of standard of care, on Day -9.

On Day -8, you will receive gemcitabine by vein over 4½ hours.

On Days -8 through Day -5, you will receive busulfan by vein over 2 hours.

On Day -3, you will receive gemcitabine by vein over 4½ hours and then melphalan by vein over 30 minutes.

On Day -2, you will receive melphalan by vein over 30 minutes.

On Day -1, you will rest (you will not receive chemotherapy).

On Day 0, you will receive your stem cells by vein over about 30-60 minutes.

You will receive 3 more doses of palifermin by vein over 15-30 seconds on Days 0, +1, and +2.

As part of standard care, you will receive G-CSF (filgrastim) as an injection under your skin 1 time each day starting on Day +5 until your blood cell levels return to normal. You may ask the study staff about the risks of filgrastim.

Pregnancy Tests:

If you can become pregnant and have regular menstrual cycles, blood (up to 2 teaspoons) will be drawn for a pregnancy test on the following schedule:

  • Within 10-14 days and within 24 hours before your first dose of lenalidomide, even if you have not had a menstrual period due to treatment or you have only had 1 menstrual period in the past 24 months.
  • One (1) time each week for 4 weeks, then every 4 weeks while taking lenalidomide.
  • Four (4) weeks after you stop taking lenalidomide.

If you have irregular menstrual cycles, you will have pregnancy tests every week for the first 28 days, then every 14 days while you are taking lenalidomide, again when you have been taken off of lenalidomide therapy, and then 14 and 28 days after you have stopped taking lenalidomide.

Length of Study:

As part of standard care, you will remain in the hospital for about 3-4 weeks after the transplant. After you are released from the hospital, you will continue as an outpatient in the Houston area to be monitored for infections and transplant-related complications.

You will be taken off study about 100 days after the transplant. You may be taken off study early if the disease gets worse, if intolerable side effects occur, if you are unable to follow study directions, or if you choose to leave the study early.

If for any reason you want to leave the study early, you must talk to the study doctor. It may be life-threatening to leave the study after you have started to receive the study drugs but before you receive the stem cell transplant because your blood cell counts will be dangerously low.

Follow-Up:

About 100 days after the transplant:

  • You will have a physical exam.
  • Blood (about 4 teaspoons) and urine will be collected for routine tests and to check your kidney and liver function.
  • If the doctor thinks it is needed, you will have computed tomography (CT) and/or positron emission tomography (PET) scans to check the status of the disease.
  • If the doctor thinks it is needed, you may have a bone marrow aspiration and biopsy to check the status of the disease. To collect a bone marrow aspiration/biopsy, an area of the hip is numbed with anesthetic, and a small amount of bone marrow and bone is withdrawn through a large needle.

This is an investigational study. Lenalidomide is FDA approved and commercially available for the treatment of multiple myeloma (MM) and myelodysplastic syndrome (MDS). Rituximab is FDA approved and commercially available for the treatment of non-Hodgkin's lymphoma and certain types of leukemia. Vorinostat is FDA approved and commercially available for the treatment of cutaneous T-cell lymphoma (CTCL). Gemcitabine is FDA approved and commercially available for the treatment of non-small cell lung cancer (NSCLC), breast cancer, pancreatic cancer, and ovarian cancer. Busulfan is FDA approved and commercially available for the treatment of chronic myeloid leukemia (CML). Melphalan is FDA approved and commercially available for the treatment of lymphoma.

The use of these study drugs in combination to treat DLBCL is considered investigational. The study doctor can explain how the study drugs are designed to work.

Up to 30 participants will take part in this study. All will be enrolled at MD Anderson.

Study Type

Interventional

Enrollment (Actual)

8

Phase

  • Phase 2
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Texas
      • Houston, Texas, United States, 77030
        • University of Texas MD Anderson Cancer Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 65 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Age 15-65
  2. Patients with ABC (determined by immunohistochemistry using the Hans algorithmI) DLBCL with primary refractory disease, relapse <12 months after initial therapy, secondary International Prognostic Index (IPI) >1, less than partial response to salvage treatment or exposure to >3 salvage regimens
  3. Adequate renal function, as defined by an estimated serum creatinine clearance >/= 50 ml/min (MDRD method) and/or serum creatinine </= 1.8 mg/dL
  4. Adequate hepatic function (SGOT and/or SGPT </= 3 x ULN; bilirubin and ALP </= 2 x ULN
  5. Adequate pulmonary function with FEV1, FVC and DLCO (corrected for Hgb) >/= 50%
  6. Adequate cardiac function with left ventricular ejection fraction >/= 40%. No uncontrolled arrhythmias or symptomatic cardiac disease
  7. ECOG performance status <2
  8. Negative Beta HCG in woman with child-bearing potential
  9. All study participants must be registered into the mandatory Revlimid REMS program, and be willing and able to comply with the requirements of the REMS program.
  10. Females of reproductive potential must adhere to the scheduled pregnancy testing as required in the Revlimid REMS program.

Exclusion Criteria:

  1. Grade >/= 3 non-hematologic toxicity from previous therapy that has not resolved to </= G1
  2. Prior whole brain irradiation
  3. Active hepatitis B, either active carrier (HBsAg +) or viremic (HBV DNA >/= 10,000 copies/mL, or >/= 2,000 IU/mL)
  4. Evidence of either cirrhosis or stage 3-4 liver fibrosis in patients with chronic hepatitis C or positive hepatitis C serology
  5. Active infection requiring parenteral antibiotics
  6. HIV infection, unless receiving effective antiretroviral therapy with undetectable viral load and normal CD4 counts
  7. Radiation therapy in the month prior to enrollment
  8. History of arterial thromboembolic events in the past 3 months and of venous thromboembolic events in the past month
  9. History of hypersensitivity of lenalidomide or thalidomide

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Lenalidomide + Vorinostat/Gem/Bu/Mel + AutoSCT

Vorinostat and lenalidomide administered orally at the same time within 1 hour before the daily dose of chemotherapy.

Gemcitabine administered as a loading dose of 75 mg/m2 followed by infusion on days -8 and -3.

Busulfan test dose administered as outpatient before admission, or as inpatient on day -10. The "test dose" of 32 mg/m2 based on actual body weight. Doses of days -6 and -5 subsequently adjusted to target an AUC of 4,000 microMol.min-1.

Melphalan administered at 60 mg/m2 on days -3 and -2.

Patients with CD20+ tumors receive rituximab 375 mg/m2 on day -9 in the AM as an inpatient.

Dexamethasone 8 mg by vein twice a day from day -8 to day -2. Caphosol oral rinses 30 mL four times a day used from day -8. Oral glutamine, 15 g four times a day, swished, gargled and swallowed started on day -8.

Pyridoxine 100 mg by vein or mouth three times a day from day -1. Enoxaparin 40 mg subcutaneously daily from admission until platelet count drops below 50,000/mm3.
Drug: Dexamethasone
8 mg by vein twice a day from Day -8 AM to Day -2 PM.
Other Names:
  • Decadron
Drug: Caphosol
Caphosol oral rinses 30 mL four times a day used from Day -8.
Drug: Lenalidomide

Dose Escalation Phase Starting dose of Lenalidomide: 50 mg by mouth on Days -9 to -2.

Dose Expansion Phase Starting Dose: Maximum tolerated dose from Phase I.

Other Names:
  • CC-5013
  • Revlimid
Drug: Vorinostat
1000 mg by mouth on Days -9 to -2.
Other Names:
  • SAHA
  • Suberoylanilide Hydroxamic Acid
  • MSK-390
  • Zolinza
Drug: Gemcitabine
Gemcitabine administered as a loading dose of 75 mg/m2 by vein on Day -8 and 2775 mg by vein on Day -3.
Other Names:
  • Gemzar
  • Gemcitabine Hydrochloride
Drug: Busulfan
Busulfan test dose administered by vein either as outpatient before admission, or as inpatient on day -10. The "test dose" of 32 mg/m2 based on actual body weight. Doses of days -6 and -5 subsequently adjusted to target an AUC of 4,000 microMol.min-1.
Other Names:
  • Busulfex
  • Myleran
Drug: Melphalan
60 mg/m2 by vein on days -3 and -2.
Other Names:
  • Alkeran
Drug: Rituximab
Patients with CD20+ tumors receive Rituximab 375 mg/m2 by vein on day -9 in the AM as an inpatient.
Other Names:
  • Rituxan
Drug: Glutamine
Oral glutamine, 15 g four times a day, swished, gargled and swallowed started on Day -8.
Other Names:
  • Enterex
  • Glutapak-10
  • NutreStore
  • Resource
  • GlutaSolve
  • Sympt-X G.I.
  • Symptx-X
Drug: Pyridoxine
100 mg by vein or mouth three times a day from Day -1
Drug: Enoxaparin
40 mg subcutaneously daily from admission until platelet count drops below 50,000/mm3.
Other Names:
  • Lovenox Injection
Procedure: Stem Cell Transplant
Stem cell transplant performed on Day 0.
Other Names:
  • SCT
Drug: Palifermin
Palifermin per departmental standard of care with 3 doses to be administered prior to starting chemotherapy and 3 doses starting on day 0.
Other Names:
  • Kepivance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maximum Tolerated Dose (MTD)
Time Frame: Enrollment up to day 30 post transplant for each dosing cohort
Established the maximum tolerated dose (MTD) of lenalidomide combined with vorinostat/gemcitabine/busulfan/melphalan with autologous stem-cell transplant ASCT). Maximum tolerated dose (MTD) of lenalidomide based on DLT was defined as any Grade 4 or 5 nonhematologic, noninfectious toxicity or any grade 3 mucositis or skin toxicity lasting > 5 days at their peak severity. Lenalidomide doses were chosen adaptively for successive cohorts with a minimum size of 2 patients. Toxicity scoring followed the National Cancer Institute Common Toxicity Criteria, version 4.
Enrollment up to day 30 post transplant for each dosing cohort
Event-free Survival (EFS)
Time Frame: Up to 2 years post transplant
Determined the 2-year event-free survival (EFS)
Up to 2 years post transplant

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall Survival (OS)
Time Frame: Up to 2 years post transplant
Assessed the 2-year overall survival (OS)
Up to 2 years post transplant
Complete Remission (CR) Rate
Time Frame: Up to 2 years post transplant
Determined complete remission (CR) rate
Up to 2 years post transplant
Overall Remission Rate (ORR)
Time Frame: Up to 2 years post transplant
Determined overall remission rate (ORR) rate
Up to 2 years post transplant
Toxicity Profile
Time Frame: Up to 2 years post transplant
Determined the toxicity profile
Up to 2 years post transplant
Pharmacodynamic Studies
Time Frame: Up to 2 years post transplant
Evaluated IRF4, SPIB, STAT1, p-STAT1, CARD11, I-kappa-Kinase-beta and p-I-kappa-Kinase-beta in PBMNC pre- and post-treatment (at baseline and on day -1).
Up to 2 years post transplant

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

M.D. Anderson Cancer Center

Collaborators

Celgene Corporation

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 22, 2016

Primary Completion (Actual)

April 8, 2019

Study Completion (Actual)

April 8, 2019

Study Registration Dates

First Submitted

October 26, 2015

First Submitted That Met QC Criteria

October 26, 2015

First Posted (Estimate)

October 28, 2015

Study Record Updates

Last Update Posted (Actual)

December 13, 2019

Last Update Submitted That Met QC Criteria

November 26, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2015-0558
  • NCI-2015-01938 (Registry Identifier: NCI CTRP)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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