Status:

TERMINATED

Prevention of Skin Cancer in High Risk Patients After Conversion to a Sirolimus-based Immunosuppressive Protocol

Lead Sponsor:

University Hospital of Berlin

Conditions:

Renal Transplant Patients at High-risk for Skin Cancer

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

Transplant recipients have a high risk to develop skin malignancies. This effect depends on the one hand on the immunosuppressive drugs themselves and relates on the other hand on the dosage. Based on...

Eligibility Criteria

Inclusion

  • Recipients of renal allograft with current actinic keratosis I or II or successfully treated actinic keratosis III (inclusion possible immediately after completed wound healing from surgical excision), invasive squamous cell carcinoma (SCC), basal cell carcinoma
  • age 18 years and older
  • minimum period of 6 month after renal transplantation
  • stable renal function and a calculated creatinine clearance of at least 40 ml/min
  • written informed consent
  • proteinuria ≤ 800 mg/d at time of enrolment
  • successfully treated solid tumor (no recurrence or metastasis in the last 2 years)

Exclusion

  • Current Sirolimus- or Everolimus- intake
  • Instable graft function (creatinine clearance \< 40 ml/min)
  • Graft rejection within the 3 previous months
  • Proteinuria \> 800 mg/d
  • Non-controlled hyperlipidemia (Cholesterol \>7,8 mmol/l (300 mg/dl), Triglycerides \> 4 mmol/l (350 mg/dl)
  • Leucopenia \< 2500/nl
  • Thrombocytopenia \< 90/nl
  • Pregnancy or breastfeeding
  • Women of childbearing age without highly effective contraception
  • Known allergy to macrolides
  • Current participation in other studies
  • Refusal to sign informed consent form
  • Neoplasm other than defined as inclusion criteria
  • All contraindications to SRL (see package insert, appendix)
  • Persons who are detained officially or legally to an official institute
  • Acute infections (mycotic, viral or bacterial)
  • Current intake of other substances with known nephrotoxicity
  • Severe liver dysfunction
  • Current intake of CY3A4-inhibitors (e.g. ketoconazole, voriconazole, itraconazole, telithromycin or clarithromycin) or CY3A4-inductors (rifampicin, rifabutin)
  • sucrose-isomaltase deficiency, fructose intolerance, glucose-galactose intolerance
  • azathioprine: known allergy to azathioprine or 6-mercaptopurine, severe bone marrow dysfunction, pancreatitis, vaccination with live vaccine
  • tacrolimus: known allergy to tacrolimus
  • mycophenolatmofetil: known allergy to mycophenolatmofetil, neutropenia, severe active gastrointestinal tract disease, Lesch-Nyhan syndrome or Kelley-Seegmiller syndrome, current intake of azathioprine
  • cyclosporine: known allergy to cyclosporine, increased intracranial pressure

Key Trial Info

Start Date :

March 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2013

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT01797315

Start Date

March 1 2007

End Date

June 1 2013

Last Update

May 4 2017

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