Laboratory-Treated Autologous Lymphocytes and Aldesleukin After Cyclophosphamide and Fludarabine in Treating Patients With Metastatic Melanoma

NCT ID: NCT00863330

Last Updated: 2024-10-03

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-02-28
• Study Completion Date: 2012-07-31

Brief Summary

RATIONALE: Treating lymphocytes in the laboratory may help the lymphocytes kill more tumor cells when they are put back in the body. Aldesleukin may stimulate the lymphocytes to kill tumor cells. Drugs used in chemotherapy, such as cyclophosphamide and fludarabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving laboratory-treated lymphocytes and aldesleukin together with cyclophosphamide and fludarabine may kill more tumor cells.

PURPOSE: This phase II trial is studying how well laboratory-treated autologous lymphocytes and aldesleukin work when given after cyclophosphamide and fludarabine in treating patients with metastatic melanoma.

Detailed Description

OBJECTIVES:

Primary

• Determine the ability of treatment with short-term cultured autologous tumor-infiltrating lymphocytes (TIL) in combination with high-dose aldesleukin after a nonmyeloablative lymphocyte-depleting preparative regimen comprising cyclophosphamide and fludarabine phosphate to mediate tumor regression in patients with metastatic melanoma.
• Determine the toxicity of this treatment regimen.

Secondary

• Determine the rate of repopulation of the young TIL cells.
• Establish in vitro immunological correlates that predict in vivo persistence and clinical response.

OUTLINE:

• Conditioning regimen: Patients receive cyclophosphamide IV over 1 hour on days -7 and -6 and fludarabine phosphate IV over 30 minutes on days -5 to -1.
• Tumor-infiltrating lymphocyte (TIL) infusion and high-dose aldesleukin: Patients receive short-term cultured autologous TIL IV over 20-30 minutes on day 0. Patients also receive high-dose aldesleukin IV over 15 minutes every 8 hours on days 0-4.

Patients with stable disease, partial response, or recurrent disease after initial response may receive 1 additional course of treatment (as above) beginning 8 weeks after completion of aldesleukin.

Blood samples are collected at baseline, at 1 week and 1 month after TIL infusion, and then periodically thereafter for research studies. Samples are analyzed for differences in function and phenotype prior to and after TIL infusion. The immunological correlates of treatment are also evaluated using FACS, cytokine release assays, ELISPOT assays, flow cytometry, and PCR. TIL that are cryopreserved at the time of infusion are analyzed to determine cell phenotype and function; correlation of in vitro characteristics of the infused cells with in vivo antitumor activity; and the activity, specificity, and telomere length using flow FISH.

After completion of study treatment, patients are followed at 4-6 weeks, every 3 months for 1 year, every 6 months for 2 years, and then annually for 2 years.

Conditions

Melanoma (Skin)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Determine toxicity of treatment regimen.

Group Type: EXPERIMENTAL

Tumor Infiltrating Lymphocytes (TIL)

Intervention Type: BIOLOGICAL

Tumor harvest process tumor infiltrating lymphocytes. Non myeloblative chemotherapy consisting of cyclophosphamide and fludarabine. Infusion of TIL cells followed by high dose IL-2.

Interventions

Tumor Infiltrating Lymphocytes (TIL)

Tumor harvest process tumor infiltrating lymphocytes. Non myeloblative chemotherapy consisting of cyclophosphamide and fludarabine. Infusion of TIL cells followed by high dose IL-2.

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Measurable disease with ≥ 1 lesion that is resectable for tumor-infiltrating lymphocyte generation
• Patients with ≥ 1 brain metastases < 1 cm each, or 1-2 brain metastases > 1 cm are eligible provided they have been treated and stable for ≥ 3 months

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1
• Life expectancy > 3 months
• ANC > 1,000/mm^3 (without filgrastim support)
• WBC > 3,000/mm^3
• Hemoglobin > 8.0 g/dL
• Platelet count > 100,000/mm^3
• Serum ALT/AST < 3 times upper limit of normal
• Total bilirubin ≤ 2 mg/dL (< 3 mg/dL in patients with Gilbert's syndrome)
• Serum creatinine ≤ 1.6 mg/dL
• LVEF > 45% in patients meeting the following criteria:

• Clinically significant atrial and/or ventricular arrhythmias, including, but not limited to, atrial fibrillation, ventricular tachycardia, or second- or third-degree heart block
• At least 60 years of age
• FEV_1 > 60% in patients meeting the following criteria:

• Prolonged history of cigarette smoking
• Symptoms of respiratory dysfunction
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for 4 months after completion of study treatment
• No HIV or hepatitis B or C positivity
• No form of primary immunodeficiency (e.g., severe combined immunodeficiency disease or AIDS)
• No opportunistic infections
• No active systemic infections
• No history of severe immediate hypersensitivity reaction to any of the agents used in this study
• No coagulation disorders
• No myocardial infarction, cardiac arrhythmias, or positive stress thallium or comparable test
• No history of coronary revascularization or ischemic symptoms
• No obstructive or restrictive pulmonary disease
• No other active major medical illness of the cardiovascular, respiratory, or immune system

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• Recovered from prior therapy (alopecia or vitiligo allowed)
• At least 6 weeks since prior ipilimumab

• Must have normal colonoscopy with normal colonic biopsies
• At least 4 weeks since prior systemic therapy
• Minor surgical procedures within the past 3 weeks allowed provided all toxicities have recovered to ≤ grade 1
• No concurrent systemic steroids
• No other concurrent experimental agents

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Wake Forest University Health Sciences

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

John P. Hanson, MD

Role: PRINCIPAL_INVESTIGATOR

St. Luke's Medical Center

Jonathan S. Treisman, MD

Role: PRINCIPAL_INVESTIGATOR

St. Luke's Medical Center

Locations

Aurora St. Luke's Medical Center

Milwaukee, Wisconsin, United States

Countries

United States

Other Identifiers

STLMC-L-0839

Identifier Type: -

Identifier Source: secondary_id

CDR0000636885

Identifier Type: -

Identifier Source: org_study_id