Oral Lenalidomide and Intravesical BCG for Therapy of Bladder Cancer
Study Details
Study Description
Brief Summary
The purposes of this study are to:
-
find out whether participants' cancer returns or gets worse while they are taking lenalidomide and Bacille Calmette-Guerrin (BCG);
-
evaluate the safety and tolerability of the combination of lenalidomide and BCG;
-
compare the cancer progression of participants taking lenalidomide and BCG versus participants taking only BCG
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Detailed Description
Investigators planned to screen approximately 100 people with bladder cancer who are 18 years of age or older throughout the United States for this study.
This is a multi-center study combining two marketed drugs, one of which has not been used previously in people with transitional cell cancer. Lenalidomide (Revlimid®) is a drug that alters the immune system and it may also interfere with the development of tiny blood vessels that help support tumor growth. Therefore, in theory, it may reduce or prevent the growth of cancer cells. Lenalidomide is approved by the U.S. Food and Drug Administration (FDA) for the treatment of specific types of myelodysplastic syndrome (MDS) and in combination with dexamethasone for patients with multiple myeloma (MM) who have received at least 1 prior therapy. MDS and MM are cancers of the blood. Lenalidomide is currently being tested in a variety of cancer conditions. It is not approved by the FDA for use in people with bladder cancer, so in this case it is considered experimental.
The other drug used in this study is Bacille Calmette-Guerrin (BCG). BCG is approved by the FDA for use in people with bladder cancer.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: A: Combination Arm Bacille Calmette-Guerrin (BCG) and lenalidomide. Participants were assigned to receive BCG or BCG and lenalidomide based on their cancer. This group received BCG + lenalidomide) |
Drug: Bacille Calmette-Guerrin (BCG)
Participants will receive BCG instillations once per week for the first 6 weeks. At 3 months and 6 months, participants will receive BCG instillations once per week for three weeks.
Other Names:
Drug: Lenalidomide
Participants may also receive capsules of lenalidomide 10 mg to swallow once per day for 7 months. The study doctor will tell participants if they will be taking lenalidomide.
Other Names:
|
| Active Comparator: B: Control Arm Bacille Calmette-Guerrin (BCG) only. Participants were assigned to receive BCG or BCG and lenalidomide based on their cancer. This group was not eligible to receive the combination of BCG + lenalidomide. |
Drug: Bacille Calmette-Guerrin (BCG)
Participants will receive BCG instillations once per week for the first 6 weeks. At 3 months and 6 months, participants will receive BCG instillations once per week for three weeks.
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Arm A: Progression Free Survival (PFS) [1 year]
The 1-year progression free/ recurrence free/ bladder-intact survival was tabulated for the experimental arm for a median follow-up period of 369 days. The progression free/ recurrence free/ bladder-intact survival is defined as the time from start of study treatment to first documentation of objective tumor progression, recurrence, bladder resection or irradiation or to death due to any cause, whichever comes first. PFS data was not collected for participants in the Arm B: Control because too few participants were enrolled in Arm B to conduct the planned per Arm comparison
Secondary Outcome Measures
- Treatment Emergent Adverse Events (AEs) or Serious Adverse Events (SAEs) [Duration of study treatment and follow-up - average of 12 months]
Number of participants with treatment emergent AEs or SAEs per category. SAEs will be specifically labeled as such. Participants were assessed at monthly intervals (corresponding to Revlimid™ refill points for adverse events), classified by Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, and these were tabulated.
Other Outcome Measures
- Effect of Addition of Revlimid on Cytokines [Duration of study treatment and follow-up - average of 12 months]
The immunologic impact of the addition of Revlimid™ to BCG for secondary prevention of non-muscle-invasive transitional cell bladder cancer, in terms of a panel of correlative assays. The effect of addition of Revlimid on cytokines associated with generation of immune response and on cytotoxic T lymphocytes and memory phenotype lymphocytes.
- Comparison of the Correlative Assay [1 year post disease response]
For comparing the correlative assay results of ever-relapsers vs non-relapsers, the combined data with the monotherapy and combination therapy groups would be applied. The participants would be categorized based on 1-year relapse.
Eligibility Criteria
Criteria
Inclusion Criteria - Either control group or combination treatment:
-
Understand and voluntarily sign an informed consent form
-
Able to adhere to the study visit schedule and other protocol requirements
-
Ta high grade, T1 high grade or Tis transitional cell bladder cancer, s/p transurethral resection of bladder tumor (TURBT) with no remaining resectable disease
-
Adequate cardio-pulmonary function (</= Class II ) as defined by New York Heart Association Classification, at the time of screening, and no history of myocardial infarction or heart failure within 6 months of start
-
Laboratory test results within these ranges:
-
Absolute neutrophil count ≥ 1500/mm³
-
Platelet count ≥ 75,000
-
Serum creatinine for which computed creatinine clearance is ≥ 30 ml/min, or directly measured creatinine clearance ≥ 30 ml/min
-
Total bilirubin ≤ 1.5 mg/dL
-
Aspartate transaminase (AST) [serum glutamic oxaloacetic transaminase (SGOT)] and Alanine transaminase (ALT) [serum glutamate pyruvic transaminase (SGPT)] ≤ 2 x upper limit of normal (ULN)
-
Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1 or 2
Inclusion Criteria - Combination treatment:
-
Prior BCG treatment for non-muscle invasive transitional cell carcinoma (TCC) last administered < 2 years for Ta high-grade, T1 high grade, Cis, or combination thereof
-
Must be registered into the mandatory RevAssist® program, and be willing and able to comply with the requirements of RevAssist®
-
Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 50 mIU/mL within 10 - 14 days prior to and again within 24 hours of starting lenalidomide and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable methods of birth control, one highly effective method and one additional effective method AT THE SAME TIME, at least 28 days before she starts taking lenalidomide. FCBP must also agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual contact with a FCBP even if they have had a successful vasectomy.
-
Able to take aspirin (81 or 325 mg) daily as prophylactic anticoagulation (patients intolerant to aspirin may use warfarin or low molecular weight heparin.
Exclusion Criteria:
-
Any serious medical condition, laboratory abnormality, or psychiatric illness that would prevent the participant from providing informed consent
-
Pregnant or breast feeding (lactating females must agree not to breast feed while taking lenalidomide)
-
Any condition, including the presence of laboratory abnormalities, which places the patient at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study
-
Use of any other experimental drug or therapy within 28 days of baseline
-
Known hypersensitivity to thalidomide
-
Known hypersensitivity to BCG or tuberculosis vaccination
-
The development of erythema nodosum if characterized by a desquamating rash while taking thalidomide or similar drugs
-
Any prior use of lenalidomide
-
Concurrent use of other anti-cancer agents or treatments.
-
Known presence of autoimmune disease or immune deficit or chronic disease such as HIV, infectious hepatitis (type B or C), or tuberculosis
-
T2+, or N1+, or M+ disease
-
Ta or T1 low grade disease only
-
Concurrent use of chronic oral steroids, for any indication
-
Recent history of deep venous thrombosis currently receiving anticoagulation therapy, with the clot event being in the last 6 months
-
Diagnosis of any prior malignancies for the last 5 years with exception of definitively treated basal cell, squamous cell carcinoma of the skin, or carcinoma in-situ of the cervix or breast
-
Life expectancy less than 1 year, by treating physician estimate
-
Known exposure to person with active tuberculosis within 48 hours of starting treatment
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | H. Lee Moffitt Cancer Center and Research Institute | Tampa | Florida | United States | 33612 |
Sponsors and Collaborators
- H. Lee Moffitt Cancer Center and Research Institute
- Celgene Corporation
Investigators
- Principal Investigator: Mayer Fishman, M.D., Ph.D., H. Lee Moffitt Cancer Center and Research Institute
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- MCC-16295
- RV-BLD-PI-0330
Study Results
Participant Flow
| Recruitment Details | Moffitt Cancer Center recruited participants between November 2011 and September 2014. |
|---|---|
| Pre-assignment Detail | Participants were assigned to receive BCG or BCG and lenalidomide based on their cancer. |
| Arm/Group Title | A: Combination Arm | B: Control Arm |
|---|---|---|
| Arm/Group Description | Bacille Calmette-Guerrin (BCG) and lenalidomide. | Bacille Calmette-Guerrin (BCG). |
| Period Title: Overall Study | ||
| STARTED | 15 | 2 |
| COMPLETED | 14 | 2 |
| NOT COMPLETED | 1 | 0 |
Baseline Characteristics
| Arm/Group Title | A: Combination Arm | B: Control Arm | Total |
|---|---|---|---|
| Arm/Group Description | Bacille Calmette-Guerrin (BCG) and lenalidomide. | Bacille Calmette-Guerrin (BCG). | Total of all reporting groups |
| Overall Participants | 15 | 2 | 17 |
| Age (Count of Participants) | |||
| <=18 years |
0
0%
|
0
0%
|
0
0%
|
| Between 18 and 65 years |
3
20%
|
0
0%
|
3
17.6%
|
| >=65 years |
12
80%
|
2
100%
|
14
82.4%
|
| Age (years) [Mean (Full Range) ] | |||
| Mean (Full Range) [years] |
72
|
70
|
71.8
|
| Sex: Female, Male (Count of Participants) | |||
| Female |
1
6.7%
|
0
0%
|
1
5.9%
|
| Male |
14
93.3%
|
2
100%
|
16
94.1%
|
| Region of Enrollment (participants) [Number] | |||
| United States |
15
100%
|
2
100%
|
17
100%
|
Outcome Measures
| Title | Arm A: Progression Free Survival (PFS) |
|---|---|
| Description | The 1-year progression free/ recurrence free/ bladder-intact survival was tabulated for the experimental arm for a median follow-up period of 369 days. The progression free/ recurrence free/ bladder-intact survival is defined as the time from start of study treatment to first documentation of objective tumor progression, recurrence, bladder resection or irradiation or to death due to any cause, whichever comes first. PFS data was not collected for participants in the Arm B: Control because too few participants were enrolled in Arm B to conduct the planned per Arm comparison |
| Time Frame | 1 year |
Outcome Measure Data
| Analysis Population Description |
|---|
| Experimental Arm A Group Only. |
| Arm/Group Title | A: Combination Arm |
|---|---|
| Arm/Group Description | Bacille Calmette-Guerrin (BCG) and lenalidomide. |
| Measure Participants | 15 |
| Number [participants] |
8
53.3%
|
| Title | Treatment Emergent Adverse Events (AEs) or Serious Adverse Events (SAEs) |
|---|---|
| Description | Number of participants with treatment emergent AEs or SAEs per category. SAEs will be specifically labeled as such. Participants were assessed at monthly intervals (corresponding to Revlimid™ refill points for adverse events), classified by Common Terminology Criteria for Adverse Events (CTCAE) version 4.0, and these were tabulated. |
| Time Frame | Duration of study treatment and follow-up - average of 12 months |
Outcome Measure Data
| Analysis Population Description |
|---|
| All participants. |
| Arm/Group Title | A: Combination Arm | B: Control Arm |
|---|---|---|
| Arm/Group Description | Bacille Calmette-Guerrin (BCG) and lenalidomide. | Bacille Calmette-Guerrin (BCG). |
| Measure Participants | 15 | 2 |
| Hematuria |
6
40%
|
1
50%
|
| Urinary frequency |
3
20%
|
0
0%
|
| Urinary urgency |
3
20%
|
1
50%
|
| Urinary tract pain |
2
13.3%
|
0
0%
|
| Bladder spasm |
1
6.7%
|
0
0%
|
| Fatigue |
7
46.7%
|
0
0%
|
| Edema face |
1
6.7%
|
0
0%
|
| Edema limbs |
1
6.7%
|
0
0%
|
| Fever |
1
6.7%
|
0
0%
|
| Pain |
1
6.7%
|
0
0%
|
| Nausea |
2
13.3%
|
0
0%
|
| Erythroderma |
1
6.7%
|
0
0%
|
| Pruritus |
1
6.7%
|
0
0%
|
| Rash acneiform |
1
6.7%
|
0
0%
|
| Rash maculo-papular |
1
6.7%
|
0
0%
|
| Urinary tract infection |
2
13.3%
|
0
0%
|
| Pharyngitis |
1
6.7%
|
0
0%
|
| Platelet count decreased |
1
6.7%
|
0
0%
|
| SAE: Grade 3 Myocardial infarction |
1
6.7%
|
0
0%
|
| Headache |
1
6.7%
|
0
0%
|
| Peripheral sensory neuropathy |
1
6.7%
|
0
0%
|
| Title | Effect of Addition of Revlimid on Cytokines |
|---|---|
| Description | The immunologic impact of the addition of Revlimid™ to BCG for secondary prevention of non-muscle-invasive transitional cell bladder cancer, in terms of a panel of correlative assays. The effect of addition of Revlimid on cytokines associated with generation of immune response and on cytotoxic T lymphocytes and memory phenotype lymphocytes. |
| Time Frame | Duration of study treatment and follow-up - average of 12 months |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
| Title | Comparison of the Correlative Assay |
|---|---|
| Description | For comparing the correlative assay results of ever-relapsers vs non-relapsers, the combined data with the monotherapy and combination therapy groups would be applied. The participants would be categorized based on 1-year relapse. |
| Time Frame | 1 year post disease response |
Outcome Measure Data
| Analysis Population Description |
|---|
| [Not Specified] |
| Arm/Group Title |
|---|
| Arm/Group Description |
Adverse Events
| Time Frame | 36 months | |||
|---|---|---|---|---|
| Adverse Event Reporting Description | ||||
| Arm/Group Title | A: Combination Arm | B: Control Arm | ||
| Arm/Group Description | Bacille Calmette-Guerrin (BCG) and lenalidomide. | Bacille Calmette-Guerrin (BCG). | ||
All Cause Mortality |
||||
| A: Combination Arm | B: Control Arm | |||
| Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
| Total | / (NaN) | / (NaN) | ||
Serious Adverse Events |
||||
| A: Combination Arm | B: Control Arm | |||
| Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
| Total | 2/15 (13.3%) | 0/2 (0%) | ||
| Cardiac disorders | ||||
| Myocardial infarction | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Nervous system disorders | ||||
| Dizziness | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Vascular disorders | ||||
| Hypertension | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
Other (Not Including Serious) Adverse Events |
||||
| A: Combination Arm | B: Control Arm | |||
| Affected / at Risk (%) | # Events | Affected / at Risk (%) | # Events | |
| Total | 15/15 (100%) | 1/2 (50%) | ||
| Blood and lymphatic system disorders | ||||
| Blood and lymphatic system disorders - Other, blood clots in urine | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Cardiac disorders | ||||
| Atrial flutter | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Gastrointestinal disorders | ||||
| Constipation | 3/15 (20%) | 5 | 0/2 (0%) | 0 |
| Diarrhea | 3/15 (20%) | 3 | 0/2 (0%) | 0 |
| Nausea | 2/15 (13.3%) | 2 | 0/2 (0%) | 0 |
| Gastrointestinal disorders - Other, soreness over suprapubic area | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| General disorders | ||||
| Fatigue | 7/15 (46.7%) | 9 | 0/2 (0%) | 0 |
| Edema face | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Edema limbs | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Fever | 1/15 (6.7%) | 2 | 0/2 (0%) | 0 |
| Pain | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Infections and infestations | ||||
| Urinary tract infection | 3/15 (20%) | 4 | 0/2 (0%) | 0 |
| Pharyngitis | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Investigations | ||||
| Weight loss | 2/15 (13.3%) | 2 | 0/2 (0%) | 0 |
| Platelet count decreased | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Musculoskeletal and connective tissue disorders | ||||
| Generalized muscle weakness | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Nervous system disorders | ||||
| Headache | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Peripheral sensory neuropathy | 1/15 (6.7%) | 2 | 0/2 (0%) | 0 |
| Psychiatric disorders | ||||
| Anxiety | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Depression | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Renal and urinary disorders | ||||
| Hematuria | 7/15 (46.7%) | 9 | 0/2 (0%) | 0 |
| Urinary frequency | 3/15 (20%) | 5 | 0/2 (0%) | 0 |
| Urinary urgency | 3/15 (20%) | 3 | 0/2 (0%) | 0 |
| Urinary tract pain | 2/15 (13.3%) | 3 | 0/2 (0%) | 0 |
| Bladder spasm | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Urinary incontinence | 0/15 (0%) | 0 | 1/2 (50%) | 1 |
| Respiratory, thoracic and mediastinal disorders | ||||
| Cough | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Dyspnea | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Epistaxis | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Skin and subcutaneous tissue disorders | ||||
| Erythroderma | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Pruritus | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Rash acneiform | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
| Rash maculo-papular | 1/15 (6.7%) | 1 | 0/2 (0%) | 0 |
Limitations/Caveats
More Information
Certain Agreements
All Principal Investigators ARE employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
Results Point of Contact
| Name/Title | Dr. Mayer Fishman |
|---|---|
| Organization | H. Lee Moffitt Cancer Center and Research Institute |
| Phone | 813-745-8311 |
| mayer.fishman@moffitt.org |
- MCC-16295
- RV-BLD-PI-0330