Gemcitabine, Carboplatin, And Lenalidomide For Treatment Of Advanced/Metastatic Urothelial Cancer And Other Solid Tumors

Study Overview

Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors

Background: - Gemcitabine and carboplatin are chemotherapy drugs used to treat several types of cancer, including cancer of the pancreas, bladder, ovaries, and lung. Lenalidomide, a drug that prevents the growth of new blood vessels in tumors, has been approved for treatment of certain blood cancers, but it has not yet been approved for use in combination with gemcitabine and carboplatin. Researchers are interested in determining the safest and most effective dose of this combined form of chemotherapy for solid tumors, particularly for urothelial cancer (tumors of the bladder, urethra, ureter, or renal pelvis). Objectives: * To evaluate the safety and effectiveness of combined lenalidomide, gemcitabine, and carboplatin as a treatment for solid tumor cancers. * To evaluate the safety and effectiveness of combined lenalidomide, gemcitabine, and carboplatin as a treatment for urothelial (bladder) cancer. Eligibility: * Individuals at least 18 years of age who have been diagnosed with solid tumors that have not responded to standard treatments. * Individuals at least 18 years of age who have been diagnosed with urothelial cancer that has not responded to standard treatments. Design: * Participants will be screened with a physical examination, medical history, blood tests, and tumor imaging studies. * Participants with urothelial cancer will receive lenalidomide alone for the first 14 days of a 21-day cycle before starting the first full treatment cycle. * All participants will receive gemcitabine on days 1 and 8, and carboplatin on day 1 only, of every 21-day treatment cycle. Lenalidomide will be taken daily at home for the first 14 days of each cycle. Participants will be asked to take aspirin or other medications to prevent the possibility of blood clots. * Participants may receive up to six cycles of treatment with this combination. If after six cycles the cancer has not grown or has shrunk, participants may continue to take lenalidomide alone for an additional 6 months (total of 12 months of therapy) or until the cancer recurs. * Participants will be monitored with blood samples, physical examinations, and tumor imaging studies through the cycles of treatment. * After the end of the last treatment cycle, participants will have followup visits every 3 months for the next 18 months, then every 6 months for another 18 months, and then yearly.

BACKGROUND: * Gemcitabine plus carboplatin is an accepted first-line therapy in patients unfit for cisplatin chemotherapy with metastatic urothelial carcinoma or other solid tumor malignancies. * Both non-clinical and clinical data support targeting angiogenesis in urothelial carcinoma and other solid tumors. * Both non-clinical and clinical data support targeting the immune system in urothelial carcinoma and other solid tumors. * Lenalidomide has both anti-angiogenic and potent immunomodulatory properties. * Lenalidomide has been safely coadministered with cytotoxic therapy in patients with solid tumors and non-clinical studies demonstrate possible synergy with gemcitabine. OBJECTIVES: Primary - To establish the dose-limiting toxicity (DLT) and maximum tolerated dose (MTD) of lenalidomide which can be safely combined with gemcitabine and carboplatin in patients with advanced/metastatic UC and other solid tumors that are unfit for cisplatin. Secondary * To preliminarily evaluate the progression free survival, response rate and overall survival in patients with advanced/metastatic UC and other solid tumors treated with the combination of lenalidomide, gemcitabine, and carboplatin. * To determine the effects of treatment on a set of 4 laboratory parameters (including Treg, sIL-2R, VEGF and CTC.) in the expansion cohort of patients with bladder cancer treated at the MTD. ELIGIBILITY: * Adult patients with histologic documentation of an advanced solid tumor with unresectable or metastatic disease. * Urothelial cancer patients should be ineligible for cisplatin based on one or more of the following: * Calculated creatinine clearance of < 60 mL/min (but greater than or equal to 30 mL/min) * Solitary kidney * Karnofsky Performance Status < 80% * No prior combination systemic chemotherapy for metastatic disease allowed for patients with UC, except single agent radiosensitizing chemotherapy (not considered prior systemic therapy), or prior neoadjuvant or adjuvant systemic chemotherapy (including cisplatin-based) is allowed provided if it was completed (Bullet) 6 months prior to diagnosis of metastatic disease; or prior intravesical therapy is permitted. Up to 1 line of chemotherapy in the metastatic setting is permitted for non UC patients. * Laboratory evaluation must meet safety requirements, including a creatinine clearance greater than 30 using the Cockroft-Gault formula; may not be pregnant or breast-feeding. DESIGN: * This is a single-institution phase I study of gemcitabine (1000 mg/m2 on days 1 and 8) and carboplatin (AUC 5 on day 1) plus escalating doses of lenalidomide (GCL) in patients with advanced/metastatic UC and other solid tumors ineligible for cisplatin therapy. Lenalidomide will be administered once daily on days 1 through 14 every 21 days at escalating dose. An expansion cohort at the MTD of an additional 15 patients with bladder cancer will be enrolled in order to determine whether there are differences between pre-treatment and post-treatment levels of the following parameters: Treg, sIL- 2R, VEGF and CTC. * Patients will receive a total of 6 cycles of gemcitabine and carboplatin in combination with lenalidomide unless disease progression or unacceptable toxicity occurs. Patients who achieve stable disease, a partial response, or a complete response after completion of 6 cycles will be eligible to continue lenalidomide alone at the same dose and schedule until disease progression. Restaging evaluations will occur after every 3 cycles of treatment (approximately 9 weeks). * Based on a standard 3+3 design with 4 dose levels per cohort, a maximum of 24 patients, with the potential for an additional 3 patients with CrCl>60 mL/min, may need to be evaluated to determine the dose limiting toxicities (DLTs) and maximum tolerated dose (MTD) of lenalidomide in this combination therapy. With an expansion cohort of 15 patients at MTD, a total of 42 subjects may be enrolled over 1.5 -3 years.

Urethral Neoplasms
Neoplasms, Urethral
Cancer of the Urethra
Urethral Cancer

DRUG: Gemcitabine
DRUG: Carboplatin
DRUG: Lenalidomide

110140
11-C-0140

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 Registration Dates	Results Reporting Dates	Study Record Updates
First Submitted 2011-05-11	Results First Submitted N/A	Last Update Submitted that met QC Criteria 2025-05-02
First Submitted that Met QC Criteria 2011-05-11	Results First Submitted that Met QC Criteria N/A	Last Update Posted (ACTUAL) 2025-05-04
First Posted (ACTUAL) 2011-05-12	Results First Posted N/A	Last Verified 2025-05-01

Study Plan

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

Design Details

Primary Purpose:
Treatment

Allocation:
Non Randomized

Interventional Model:
Sequential

Masking:
None

Arms and Interventions

Participant Group/Arm	Intervention/Treatment
EXPERIMENTAL: Arm 1 Standard of Care plus escalating doses of Lenalidomide	DRUG: Gemcitabine 1,000mg/m2 IVPB over 30 min x 1 DRUG: Carboplatin AUC 5** IVPB over 30 min x 1 DRUG: Lenalidomide Escalating Doses starting at 2.5 po daily up to 25 mg po daily until MTD is reached.
EXPERIMENTAL: Arm 2 Lenalidomide Lead for 14 days + standard of care + lenalidomide MTD	DRUG: Gemcitabine 1,000mg/m2 IVPB over 30 min x 1 DRUG: Carboplatin AUC 5** IVPB over 30 min x 1 DRUG: Lenalidomide Escalating Doses starting at 2.5 po daily up to 25 mg po daily until MTD is reached.

Participant Group/Arm

Intervention/Treatment

EXPERIMENTAL: Arm 1

Standard of Care plus escalating doses of Lenalidomide

DRUG: Gemcitabine

1,000mg/m2 IVPB over 30 min x 1

DRUG: Carboplatin

AUC 5** IVPB over 30 min x 1

DRUG: Lenalidomide

Escalating Doses starting at 2.5 po daily up to 25 mg po daily until MTD is reached.

EXPERIMENTAL: Arm 2

Lenalidomide Lead for 14 days + standard of care + lenalidomide MTD

DRUG: Gemcitabine

1,000mg/m2 IVPB over 30 min x 1

DRUG: Carboplatin

AUC 5** IVPB over 30 min x 1

DRUG: Lenalidomide

Escalating Doses starting at 2.5 po daily up to 25 mg po daily until MTD is reached.

Primary Outcome Measures	Measure Description	Time Frame
dose limiting toxicity (DLT)	any grade 3 or 4 toxicity with exceptions listed in protocol; MTD is one dose level below the dose that induces DLT in more than 1/6 patients	Maximum Tolerated Dose (MTD)

Secondary Outcome Measures	Measure Description	Time Frame
response rate	Percentage of patients whose cancer shrinks or disappears after treatment	every 3 months for the first 18 months, every 6 months for the subsequent 18 months, then yearly
progression free survival	time during which a patient shows no signs or symptoms of the growth or the spreading of a tumor	every 3 months for the first 18 months, every 6 months for the subsequent 18 months, then yearly
overall survival	The length of time from the start of treatment that patients are still alive	every 3 months for the first 18 months, every 6 months for the subsequent 18 months, then yearly
effects of treatment on Treg, sIL-2R, VEGF, CTC and CEC	determine the effects of treatment on a set of 5 laboratory parameters (including Treg, sIL-2R, VEGF, CTC and CEC in the expansion cohort of patients with bladder cancer treated at the MTD	baseline, lead-in day 8, lead-in day 14 and C1D8

Contacts and Locations

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

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.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

INCLUSION CRITERIA:

Unresectable or metastatic disease
Urothelial cancer patients should be ineligible for cisplatin based on one or more of the following:
Calculated creatinine clearance of < 60 mL/min (but greater than or equal to 30 mL/min)
Solitary kidney
Karnofsky Performance Status < 80%
Age greater than or equal to 18 years of age; UC is not a common cancer in children and without proven benefit, this combination of chemotherapy agents presents too great a risk for conducting as a phase I study in children.
Karnofsky Performance Status greater than or equal to 60%
Required Initial Laboratory Values:
Absolute neutrophil count greater than or equal to 1.2 x 10(9)/L
Platelets greater than or equal to 100 x 10(9)/L
Bilirubin less than or equal to 1.5 times the upper limit of normal for the institution or less than or equal to 3 mg/dl in a subject with Gilbert Syndrome
Aspartate transaminase (AST) and alanine transaminase (ALT) less than or equal to 3 times the ULN for the institution (less than or equal to 5 times the ULN is acceptable if liver has tumor involvement).
Serum creatinine < 2 or calculated creatinine clearance (CrCl) greater than or equal to 30 mL/min
Ability to understand and willingness to sign the written informed consent document.
Patients must be able to swallow whole capsules. Capsules must not be crushed or chewed; capsules must not be opened.

For urothelial cancer patients, no prior combination systemic chemotherapy for metastatic disease, except:
Single-agent radiosensitizing chemotherapy is not considered prior systemic therapy
Prior neoadjuvant or adjuvant systemic chemotherapy (including cisplatin-based) is allowed provided it was completed greater than or equal to 6 months prior to the diagnosis of metastatic disease
Prior intravesical therapy is permitted
For non-urothelial cancer patients, no more than 1 prior line of combination systemic chemotherapy for metastatic disease is allowed
Less than or equal to 2 weeks since radiation therapy
Unstable angina
New York Heart Association (NYHA) Grade II or greater congestive heart failure
History of myocardial infarction within 6 months
History of stroke within 6 months
Clinically significant peripheral vascular disease
Evidence of bleeding diathesis or coagulopathy. Patients that are on anticoagulation therapy for DVT will be allowed to enroll and continue on the treatment dose of enoxaparin or other anticoagulation such a warfarin.
Patients with contraindications to anticoagulation therapy for deep venous thrombosis such as:
Patients on full treatment dose of anticoagulation such as those patients being treated for a deep vein thrombosis or pulmonary embolus.
Presence of central nervous system or brain metastases
Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 1
Anticipation of need for major surgical procedure during the course of the study

Females of childbearing potential (FCBP) must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10 14 days and again within 24 hours prior to starting Cycle 1 of lenalidomide. Further, they 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 starting 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. A FCBP is a sexually mature woman who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months). All patients must be counseled at a minimum of every 28 days about pregnancy precautions and risks of fetal exposure.
Inability to comply with study and/or follow-up procedures
Patients may not be receiving any other investigational agents
History of allergic reactions attributed to compounds of similar chemical or biologic composition to lenalidomide, gemcitabine or carboplatin, or other agents used in study.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Due to the possibility of infection reactivation, patients who are known seropositive for or who have active viral infection with human immunodeficiency virus (HIV) are NOT eligible.

Collaborators and Investigators

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

Investigators

PRINCIPAL_INVESTIGATOR: Andrea B Apolo, M.D., National Cancer Institute (NCI)

Publications

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

General Publications

Dredge K, Horsfall R, Robinson SP, Zhang LH, Lu L, Tang Y, Shirley MA, Muller G, Schafer P, Stirling D, Dalgleish AG, Bartlett JB. Orally administered lenalidomide (CC-5013) is anti-angiogenic in vivo and inhibits endothelial cell migration and Akt phosphorylation in vitro. Microvasc Res. 2005 Jan;69(1-2):56-63. doi: 10.1016/j.mvr.2005.01.002.
Corral LG, Haslett PA, Muller GW, Chen R, Wong LM, Ocampo CJ, Patterson RT, Stirling DI, Kaplan G. Differential cytokine modulation and T cell activation by two distinct classes of thalidomide analogues that are potent inhibitors of TNF-alpha. J Immunol. 1999 Jul 1;163(1):380-6.
Schafer PH, Gandhi AK, Loveland MA, Chen RS, Man HW, Schnetkamp PP, Wolbring G, Govinda S, Corral LG, Payvandi F, Muller GW, Stirling DI. Enhancement of cytokine production and AP-1 transcriptional activity in T cells by thalidomide-related immunomodulatory drugs. J Pharmacol Exp Ther. 2003 Jun;305(3):1222-32. doi: 10.1124/jpet.102.048496. Epub 2003 Mar 20.

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