Adoptive Immunotherapy, Aldesleukin, and Zoledronate in Treating Patients With Stage IV Kidney Cancer and Lung Metastases

Metastatic Cancer Clinical Trial

Official title:

Phase I/II Study of Adoptive Immunotherapy Comprising Pyrophosphomonoester Antigen-stimulated T Cells, IL-2, and Nitrogen-containing Bisphosphonates in Patients With Stage IV Renal Cell Carcinoma

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00588913
• Other study ID #: TRIC-CTR-GU-05-01
• Secondary ID: CDR0000581156
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: December 20, 2007
• Last updated: July 9, 2013
• Start date: January 2006
• Est. completion date: August 2009

Study information

• Verified date: August 2009
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Cellular adoptive immunotherapy uses a person's white blood cells that are treated in the laboratory to stimulate the immune system in different ways and stop tumor cells from growing. Aldesleukin may help the laboratory-treated white blood cells stay in the body longer. Drugs used in chemotherapy, such as zoledronic acid, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving cellular adoptive immunotherapy together with interleukin-2 and zoledronic acid may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects of giving cellular adoptive immunotherapy together with aldesleukin and zoledronic acid and to see how well it works in treating patients with stage IV kidney cancer and lung metastases.

Description:

OBJECTIVES:

• Determine the safety of adoptive immunotherapy comprising 2-methyl-3-butenyl-1-pyrophosphate-stimulated gamma delta (gd) T cells, zoledronate, and IL-2 after nephrectomy, especially with regard to the incidence and frequency of adverse events.

• Determine the duration of in vivo persistence of the transferred gd T cells in patients.

• Determine the doubling time of tumor growth before and after adoptive immunotherapy.

• Determine the tumor-size reducing effect of adoptive immunotherapy based on the Best Overall Response Chart.

OUTLINE: Patients undergo leukapheresis for the harvest of peripheral blood mononuclear cells (PBMCs). PBMCs are stimulated with 2-methyl-3-butenyl-1-pyrophosphate and aldesleukin for 11 days. Patients then receive the expanded Gamma Delta T cells, aldesleukin, and zoledronic acid once a month for 6 months.

After completion of study treatment, patients are followed for up to 1 month.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: August 2009
• Est. primary completion date: March 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 80 Years

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed renal carcinoma

• Stage IV disease with lung metastases

• Bidimensionally measurable lung metastases by CT scan

• Meets 1 or more of the following criteria:

• No change in disease status or progressive disease after prior aldesleukin administration for 3 months or more

• Lung metastases after treatment with prior nephrectomy

• Patients with clear cell renal carcinoma must have undergone nephrectomy prior to study entry

• Patients with progression of metastatic lung cancer after nephrectomy also must have received interferon alfa for 3 months or more (prior to study entry)

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1

• Life expectancy > 6 months

• Leukocyte count = 3,000/mm³

• ANC = 1,500/mm³

• Platelet count = 100,000/mm³

• Serum bilirubin = 1.5 mg/dL

• AST/ALT = 2.5 times normal

• Serum creatinine = 1.7 mg/dL

• LDH = 1.5 times normal

• Not pregnant nor nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No active infection with hepatitis virus or HIV

• No poorly controlled heart failure or arrhythmia

• No hypercalcemia that require medication

• No C-reactive protein with an infectious disease that requires medication

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics

• At least 3 weeks since prior chemotherapy, radiation therapy, or biologic therapy

• No prior bone marrow transplantation or organ transplantation

• No concurrent steroid therapy

• No concurrent antidepressant therapy

Study Design

Allocation: Non-Randomized, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma, Renal Cell
• Kidney Cancer
• Kidney Neoplasms
• Metastatic Cancer
• Neoplasm Metastasis

Intervention

Biological:
• aldesleukin

• therapeutic autologous lymphocytes

Drug:
• zoledronic acid

Locations

Country	Name	City	State
Japan	Kyoto University Hospital	Kyoto
Japan	Tokyo Women's Medical University	Tokyo

Sponsors (1)

Lead Sponsor	Collaborator
Tokyo Women's Medical University

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency and severity of adverse events based on NCI-CTCAE version 3.0			Yes
Primary	Proportion of gd T-cells in peripheral blood			No
Secondary	Secondary doubling time of tumor growth			No
Secondary	Overall response			No