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Peripheral Stem Cell Transplantation in Treating Patients With Metastatic or Recurrent Kidney Cancer
This study is ongoing, but not recruiting participants.
Sponsors and Collaborators: Fox Chase Cancer Center
National Cancer Institute (NCI)
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT00025519
  Purpose

RATIONALE: Peripheral stem cell transplantation may be able to replace immune cells that were destroyed by chemotherapy and radiation therapy used to kill cancer cells. Sometimes the transplanted cells can be rejected by the body's tissues. Mycophenolate mofetil, tacrolimus, and donor white blood cells may prevent this from happening.

PURPOSE: Phase II trial to study the effectiveness of chemotherapy followed by peripheral stem cell transplantation in treating patients who have metastatic or recurrent kidney cancer.


Condition Intervention Phase
Kidney Cancer
Drug: fludarabine phosphate
Drug: mycophenolate mofetil
Drug: tacrolimus
Drug: thalidomide
Drug: therapeutic allogeneic lymphocytes
Procedure: peripheral blood stem cell transplantation
Procedure: radiation therapy
Phase II

MedlinePlus related topics: Cancer Kidney Cancer
Drug Information available for: Thalidomide Fludarabine Fludarabine monophosphate Tacrolimus Mycophenolate Mofetil Mycophenolate mofetil hydrochloride Tacrolimus anhydrous
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Open Label
Official Title: Submyeloablative Allogeneic Blood Stem Cell Transplantation With HLA Identical Donor Lymphocyte Infusions From Matched Related and Matched Unrelated Donors for Treatment of Metastatic Renal Cell Carcinoma

Further study details as provided by National Cancer Institute (NCI):

Study Start Date: June 2001
Detailed Description:

OBJECTIVES:

  • Determine the feasibility of submyeloablative HLA-identical allogeneic peripheral blood stem cell transplantation in patients with metastatic or recurrent renal cell carcinoma.
  • Determine the toxicity of this regimen, in terms of incidence and severity of graft rejection, acute graft-vs-host disease (GVHD), chronic GVHD, adverse effects from the preparative regimen and thalidomide, and infection and bleeding, in these patients.
  • Determine the efficacy of this regimen, in terms of objective partial and complete response rates, in these patients.
  • Determine the engraftment rates and extent of chimerism in patients treated with this regimen.
  • Determine the overall survival and time to treatment failure rate in patients treated with this regimen.
  • Determine the impact of thalidomide on the treatment of chronic GVHD in patients treated with this regimen.

OUTLINE: Patients are stratified according to risk (low vs high).

Patients receive fludarabine IV over 30 minutes once daily on days -4 to -2 followed by total body irradiation on day -1. Patients receive tacrolimus IV over 24 hours or orally daily on days -3 to 35 and oral mycophenolate mofetil twice daily on days -3 to 28 as graft-vs-host disease (GVHD) prophylaxis. Patients undergo allogeneic peripheral blood stem cell transplantation over 1-2 hours on day 0.

Patients maintaining a mixed chimerism with no evidence of grade III or IV GVHD receive donor lymphocyte infusions (DLI) on days 60, 90, and 120. Patients may receive additional DLI as needed. Patients with limited chronic GVHD receive oral thalidomide daily beginning after day 80 and continuing for 1 year or until disease progression or resolution of chronic GVHD.

Patients are followed at 1, 3, 6, and 12 months and then every 6 months thereafter.

PROJECTED ACCRUAL: A maximum of 20-40 patients (10-20 per stratum) will be accrued for this study.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed renal cell carcinoma (RCC)

    • Histology demonstrates major clear cell component
    • Metastatic (stage IV) or recurrent disease
  • Prior debulking nephrectomy required

    • Disease not amenable to complete surgical resection
  • Must have HLA-identical donor

    • Matched related sibling donors must have 6/6 serologic HLA A, B, and DR match with molecular confirmation at DRB1

      • A 5/6 serologic mismatch with one antigen mismatch at locus A or B (not DR) with molecular confirmation at locus A, B, and DRB1 allowed
    • Matched unrelated donors must have a minimum of 8 out of 10 molecular matches at loci A, B, C, DRB1, and DQB1
  • No brain metastases

    • Negative MRI required

PATIENT CHARACTERISTICS:

Age:

  • 18 to 65

Performance status:

  • Karnofsky 80-100% OR
  • ECOG 0-1

Life expectancy:

  • Not specified

Hematopoietic:

  • Not specified

Hepatic:

  • Bilirubin less than 2 times upper limit of normal (ULN)
  • ALT/AST less than 2 times ULN
  • Alkaline phosphatase less than 2 times ULN
  • Hepatitis A, B, and C negative

Renal:

  • Creatinine clearance greater than 50 mL/min
  • Calcium less than 10.5 mg/dL (bisphosphonates allowed)

Cardiovascular:

  • LVEF no less than 10% below lower limit of normal

Pulmonary:

  • FEV_1 and DLCO greater than 50%

Other:

  • HIV negative
  • No active bacterial, fungal, or viral (including cytomegalovirus) infections
  • No intolerance or allergy to tacrolimus, mycophenolate mofetil, or fludarabine
  • No intolerance to 200 cGy of total body irradiation
  • No other serious comorbid disease, neurologic condition, or psychosocial condition that would preclude study follow-up
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception for at least 1 month before, during, and for at least 3 months after study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Prior interleukin-2 allowed
  • Prior interferon alfa allowed

Chemotherapy:

  • Prior chemotherapy allowed
  • No other concurrent chemotherapy for RCC

Endocrine therapy:

  • No concurrent corticosteroids for other comorbid disease

Radiotherapy:

  • No prior extensive radiotherapy to marrow microenvironment greater than 20% of total marrow mass
  • No prior radiotherapy that has reached tissue tolerance for heart, lung, liver, kidney, or spinal cord

Surgery:

  • See Disease Characteristics

Other:

  • No other concurrent therapy for RCC
  • No concurrent enrollment on another investigational protocol for treatment of RCC
  • No other concurrent immunosuppressive medications
  • No other concurrent investigational drugs
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00025519

Locations
United States, Pennsylvania
Fox Chase - Temple Cancer Center
Philadelphia, Pennsylvania, United States, 19111-2442
Fox Chase Cancer Center
Philadelphia, Pennsylvania, United States, 19111-2497
Sponsors and Collaborators
Fox Chase Cancer Center
Investigators
Study Chair: Gary R. Hudes, MD Fox Chase Cancer Center
  More Information

Clinical trial summary from the National Cancer Institute's PDQ® database  This link exits the ClinicalTrials.gov site

Study ID Numbers: CDR0000068970, FCCC-01006, TUHSC-3721, NCI-G01-2021
Study First Received: October 11, 2001
Last Updated: October 12, 2008
ClinicalTrials.gov Identifier: NCT00025519  
Health Authority: United States: Federal Government

Keywords provided by National Cancer Institute (NCI):
stage IV renal cell cancer
recurrent renal cell cancer
clear cell renal cell carcinoma

Study placed in the following topic categories:
Thalidomide
Urogenital Neoplasms
Tacrolimus
Fludarabine monophosphate
Renal cancer
Urologic Neoplasms
Kidney cancer
Recurrence
Carcinoma
Urologic Diseases
Kidney Neoplasms
Mycophenolate mofetil
Carcinoma, Renal Cell
Fludarabine
Kidney Diseases
Adenocarcinoma
Clear cell renal cell carcinoma
Urinary tract neoplasm
Neoplasms, Glandular and Epithelial

Additional relevant MeSH terms:
Antimetabolites
Anti-Infective Agents
Antimetabolites, Antineoplastic
Neoplasms by Histologic Type
Molecular Mechanisms of Pharmacological Action
Immunologic Factors
Antineoplastic Agents
Growth Substances
Physiological Effects of Drugs
Immunosuppressive Agents
Angiogenesis Inhibitors
Pharmacologic Actions
Anti-Bacterial Agents
Neoplasms
Neoplasms by Site
Therapeutic Uses
Growth Inhibitors
Angiogenesis Modulating Agents
Leprostatic Agents

ClinicalTrials.gov processed this record on January 16, 2009