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Sirolimus in Kidney Transplant Patients With Squamous Cell Skin Carcinoma

A Phase II Study of Sirolimus in Renal Transplant Patients Diagnosed With New or Recurrent Squamous Cell Skin Carcinoma Currently on Calcineurin-based Immunosuppression.

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01764607
Enrollment
1
Registered
2013-01-09
Start date
2013-04-30
Completion date
2014-06-30
Last updated
2018-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Squamous Cell Skin Carcinoma

Keywords

Squamous, Renal, Transplant

Brief summary

Solid organ transplant recipients (SOTR) have a 3-5x increased occurrence of cancer in contrast to the general population with basal and squamous cell skin cancer. The use of immunosuppressant or anti-rejection drugs that are needed after SOTR is known to increase the risk of developing certain kinds of cancer. The purpose of this study is to find out how well Sirolimus (also known as Rapamune) works at treating squamous cell carcinoma in renal transplant patients.

Detailed description

This is a Phase II randomized study to evaluate the effectiveness of Sirolimus in treating and preventing squamous cell skin cancer carcinoma using a Simon's 2-stage design. As part of the study, after the biopsy results of the skin cancer show squamous cell carcinoma and consent had been obtain, the participant will begin taking Sirolimus. The calcineurin inhibitor (tacrolimus or cyclosporine) will be discontinued once the transplant doctors find that the participants Sirolimus is therapeutic by checking blood tests once a week x 3 weeks. Approximately 5 weeks after starting Sirolimus, the squamous cell skin cancer will be removed by a surgeon. Participant next follow up visit for the study is scheduled one year post-operatively. .The study will look at your squamous cell skin cancer under the microscope to see if sirolimus had any effect at treating your squamous cell skin cancer.

Interventions

DRUGSirolimus

Patients randomized to this arm of the study will receive sirolimus from the time of randomization at least until 5 weeks or the removal of the skin tumor. Nephrology will determine/manage the immunosuppressant therapy.

Sponsors

University of Florida
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologically or cytologically proven squamous cell skin carcinoma * Recipient of a renal organ transplant at least one year prior to study enrollment * Receiving a CNI for at least 6 months prior to diagnosis of skin cancer * No current evidence of graft rejection, except low-grade, chronic graft rejection * Measurable disease by caliper measurement * Life expectancy \> 6 months * Age of at least 18 years * Adequate organ and marrow function as determined by ANC, HGB, PLT, Total Bili, AST, and creatinine clearance * Ability to understand/willingness to sign a written informed consent form

Exclusion criteria

* Inability to give informed consent * Major surgery within 4 week prior to starting study drug * Chronic or non-healing open wounds * Pregnant and nursing women * Women and men of child-bearing potential must agree to use adequate contraception prior to study entry and for the study duration * Prior use of an mTOR inhibitor * Pre-existing clinically significant cardiac, hepatic, pulmonary, or renal dysfunction * HIV-positive patients * Proteinuria (\> 1 gram) * Prior or current history of uncontrolled hyperlipidemia (cholesterol \> 302 mg/dl or triglycerides 354 mg/dl * Currently receiving any investigational agents * History of allergic reactions attributed to compounds of similar chemical or biologic composition to sirolimus (mTOR inhibitors) * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrythmia, or psychiatric illness/social situations that would limit compliance with study requirements

Design outcomes

Primary

MeasureTime frameDescription
Measure of Squamous Cell Skin Carcinoma in PatientsBaseline, time of surgical removal (5 weeks) and 1 year.Baseline: Measuring of squamous cell skin carcinoma, Week 5: Measuring and surgical removal of squamous cell skin cancer with microscopic evaluation, and in 1 year.

Secondary

MeasureTime frameDescription
Evaluation of Skin Tumor for Squamous Cell Skin CarcinomaAt baseline and time of surgical removal (5 weeks).Tumor will be analyzed at baseline and time of surgical removal by both laboratory and microscopic testing.

Countries

United States

Participant flow

Participants by arm

ArmCount
Sirolimus Treatment
Patients will receive sirolimus 5 weeks prior to removal of squamous cell skin carcinoma. After the 5 weeks of treatment, nephrology will determine/manage each patient's immunosuppressant therapy. Sirolimus: Patients randomized to this arm of the study will receive sirolimus from the time of randomization at least until 5 weeks or the removal of the skin tumor. Nephrology will determine/manage the immunosuppressant therapy.
1
Total1

Baseline characteristics

CharacteristicSirolimus Treatment
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
1 Participants
Region of Enrollment
United States
1 participants
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
1 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
1 / 1
serious
Total, serious adverse events
0 / 1

Outcome results

Primary

Measure of Squamous Cell Skin Carcinoma in Patients

Baseline: Measuring of squamous cell skin carcinoma, Week 5: Measuring and surgical removal of squamous cell skin cancer with microscopic evaluation, and in 1 year.

Time frame: Baseline, time of surgical removal (5 weeks) and 1 year.

ArmMeasureGroupValue (NUMBER)
Sirolimus TreatmentMeasure of Squamous Cell Skin Carcinoma in PatientsMeasurement at Baseline15 mm
Sirolimus TreatmentMeasure of Squamous Cell Skin Carcinoma in PatientsMeasurement at 5 Weeks12 mm
Sirolimus TreatmentMeasure of Squamous Cell Skin Carcinoma in PatientsMeasurement at 1 Year0 mm
Secondary

Evaluation of Skin Tumor for Squamous Cell Skin Carcinoma

Tumor will be analyzed at baseline and time of surgical removal by both laboratory and microscopic testing.

Time frame: At baseline and time of surgical removal (5 weeks).

ArmMeasureValue (NUMBER)
Sirolimus TreatmentEvaluation of Skin Tumor for Squamous Cell Skin Carcinoma80 percentage of baseline size

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026