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CompletedNCT00403169Updated Jul 2, 2026Results posted

Lenalidomide in Treating Patients With Advanced or Unresectable Kidney Cancer

A Phase 2 interventional study of lenalidomide in Kidney Cancer, sponsored by The Cleveland Clinic. Completed at 1 site in United States. Open to participants aged 18 Years to 120 Years. Per ClinicalTrials.gov, last updated 2026-07-02.

Sponsored by The Cleveland Clinic · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
28
Allocation
Not applicable
Ages
18 Years to 120 Years
Sex
All
01

Study summary

RATIONALE: Lenalidomide may stop the growth of kidney cancer by blocking blood flow to the tumor.

PURPOSE: This phase II trial is studying how well lenalidomide works in treating patients with advanced or unresectable kidney cancer.

Read the detailed description

OBJECTIVES:

  • Evaluate the best response in patients with advanced or unresectable renal cell carcinoma (RCC) treated with lenalidomide.
  • Evaluate the response duration, time to tumor progression, and survival of patients with advanced RCC treated with lenalidomide.
  • Evaluate the safety of this drug in these patients.

OUTLINE: This is an open-label study.

Patients receive oral lenalidomide daily on days 1-21. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression.

After completion of study treatment, patients are followed every 3 months.

PROJECTED ACCRUAL: A total of 26 patients will be accrued for this study.

02

Conditions studied

  • Kidney Cancer

Keywords

  • stage III renal cell cancer
  • stage IV renal cell cancer
  • recurrent renal cell cancer
03

In context

Kidney Neoplasms

956 studies on the registry are indexed under Kidney Neoplasms; 210 are open to participants now.

This study's enrollment of 28 is below the median of 43 across 650 interventional studies indexed under Kidney Neoplasms.

Browse Kidney Neoplasms studies →

Lead sponsor

The Cleveland Clinic is the lead sponsor of 818 studies on the registry; 118 are open to participants now.

Of its 89 completed or terminated interventional studies of FDA-regulated products, 72 (81%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 120 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed renal cell carcinoma (RCC)

    • Advanced or unresectable RCC
  • Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 20 mm with conventional techniques OR ≥ 10 mm with spiral CT scan
  • No brain metastases

    • Brain metastases that have been treated with either radiotherapy or surgery and remain asymptomatic, with no active brain metastases, as shown by CT scan or MRI, for ≥ 6 months are allowed

PATIENT CHARACTERISTICS:

  • ECOG performance status (PS) 0-1 OR Karnofsky PS 70-100%
  • Absolute neutrophil count ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Creatinine ≤ 2.0 mg/dL
  • Bilirubin ≤ 1.5 mg/dL
  • AST and ALT ≤ 2.5 times upper limit of normal (ULN) (5 times ULN if hepatic metastases are present)
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No other malignancies within the past 5 years, except for treated basal cell or squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, localized prostate cancer, or superficial bladder cancer
  • No history of allergic reactions attributed to compounds of similar chemical or biological composition to lenalidomide or thalidomide
  • No uncontrolled intercurrent illness including, but not limited to, any of the following:

    • Ongoing or active infection
    • Symptomatic congestive heart failure
    • Unstable angina pectoris
    • Cardiac arrhythmia
    • Psychiatric illness or social situation that would limit study compliance
  • No hepatitis A, B, or C positivity
  • No HIV positivity

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No more than 1 prior systemic therapy for RCC (e.g., chemotherapy, hormonal therapy, immunotherapy)
  • At least 4 weeks since prior surgery, radiotherapy, hormonal therapy, chemotherapy, or immunotherapy and recovered
  • No prior lenalidomide
  • No other concurrent anticancer agents or treatments
  • No other concurrent investigational agents
  • No concurrent sargramostim (GM-CSF), radiotherapy, or thalidomide
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    Lenalidomide for Advanced RCC

    25 mg/day Lenalidomide for 21 days per cycle.

    Drug: lenalidomide

Interventions

  • Druglenalidomide

    drug

    Also known as: CC-5013

06

What researchers measure

Primary outcomes

  1. Objective Response Rate

    The objective response rate was defined by RECIST.

    Time frame: Baseline and every 2 weeks until study completion, up to 1.5 years

Secondary outcomes

  1. Toxicity--Most Common AEs

    Most commonly reported Serious Adverse Events

    Time frame: Baseline and every 2 weeks until study completion. Number of cycles is open ended.

  2. Overall Survival

    Time frame: 1 to 16 cycles, until patient expires, is lost to follow up or withdraws consent

07

Results

Posted Jul 2, 2026

Participant flow

Participant flow — Overall Study
MilestoneLenalidomide for Advanced RCC
Started28
Completed28
Not completed0

Outcome measures

PrimaryObjective Response Rate

The objective response rate was defined by RECIST.

Time frame:
Baseline and every 2 weeks until study completion, up to 1.5 years
Reported as:
Count of participants · Participants
Objective Response Rate
ParticipantsLenalidomide for Advanced RCC
Objective Response Rate3
SecondaryToxicity--Most Common AEs

Most commonly reported Serious Adverse Events

Time frame:
Baseline and every 2 weeks until study completion. Number of cycles is open ended.
Reported as:
Number · percentage of participants
Toxicity--Most Common AEs
percentage of participantsLenalidomide for Advanced RCC
Fatigue11
Skin Toxicity11
Neutropenia36
SecondaryOverall Survival
Time frame:
1 to 16 cycles, until patient expires, is lost to follow up or withdraws consent
Reported as:
Count of participants · Participants
Overall Survival
ParticipantsLenalidomide for Advanced RCC
Overall Survival17

Adverse events

Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Lenalidomide for Advanced RCC11/28 (39.3%)16/28 (57.1%)28/28 (100%)
Most frequent serious events
Most frequent serious events
EventLenalidomide for Advanced RCC
NeutropeniaBlood and lymphatic system disorders10/28
FatigueGeneral disorders3/28
Skin ReactionSkin and subcutaneous tissue disorders3/28
Most frequent other events
Most frequent other events
EventLenalidomide for Advanced RCC
FatigueGeneral disorders21/28
Skin ReactionsSkin and subcutaneous tissue disorders16/28
Nausea/EmesisGastrointestinal disorders10/28
ConstipationGastrointestinal disorders8/28
DiarrheaGastrointestinal disorders8/28
EdemaGeneral disorders6/28
Cough/DyspneaRespiratory, thoracic and mediastinal disorders4/28
DizzinessGeneral disorders4/28
NeuropathyNervous system disorders3/28

Baseline characteristics

Age, Continuous
Age, Continuous(years)Lenalidomide for Advanced RCC
Mean63.5 ± 9.3
Sex: Female, Male
Sex: Female, Male(Participants)Lenalidomide for Advanced RCC
Female9
Male19
08

Study locations

1 site
  • Case Comprehensive Cancer Center
    Cleveland, Ohio 44106-5065, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00403169
Lead sponsor
The Cleveland Clinic
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Nov 23, 2006
Start date
Aug 2004
Primary completion
May 2009
Completion
May 2009
Results posted
Jul 2, 2026
Last update
Jul 2, 2026

Study contacts

Robert Dreicer, MD, FACP
study chair · Case Comprehensive Cancer Center
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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