Mechanism of Action of High-Dose IL-2 (Aldesleukin) in Metastatic Melanoma and Kidney Cancer
| Status: | Completed |
|---|---|
| Conditions: | Colorectal Cancer, Skin Cancer, Cancer, Cancer |
| Therapuetic Areas: | Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 3/27/2019 |
| Start Date: | March 13, 2006 |
| End Date: | February 27, 2014 |
Studies on the Mechanism of Action of High-Dose IL-2 in Metastatic Melanoma and Renal Cell Cancer
Background:
-Although IL-2 can shrink tumors in about 20 percent of patients with metastatic kidney
cancer and in 15 percent of patients with metastatic melanoma, it is not fully known how the
drug works.
Objectives:
-To better understand how IL-2 causes tumors to shrink.
Eligibility:
-Patients 18 years of age or older with metastatic kidney cancer or metastatic melanoma
Design:
- 135 patients with melanoma and 110 patients with kidney cancer may be enrolled.
- Patients are hospitalized for about 7 days for each treatment. They receive IL-2
intravenously (through a vein) over 15 minutes every 8 hours for up to 4 days or 12
doses. This constitutes one treatment cycle.
- Research blood samples are collected daily during the first treatment cycle and for one
or two days following the last dose.
- Patients may be asked to undergo leukapheresis, a procedure for collecting large
quantities of white blood cells. This involves collecting blood through a needle in an
arm vein. The blood is directed through a cell separator where the white cells are
extracted. The rest of the blood (red cells, platelets, and plasma) is returned to the
patient through the same needle or through a needle in the other arm.
- About 7-10 days after discharge from the hospital, patients return for a second
treatment cycle but without research blood sampling.
- 2 months after therapy, patients are evaluated with scans, and x-rays, and blood tests
to evaluate the tumor and the effects of the treatment on immune cells.
- Patients whose tumors shrink or remain stable may continue treatment (without repeating
the full set of research blood samples) as long as they benefit from the treatment and
do not develop unacceptable side effects. Patients who continue treatment are evaluated
every 2 months for 3 to 4 times and then every 3 to 6 months.
-Although IL-2 can shrink tumors in about 20 percent of patients with metastatic kidney
cancer and in 15 percent of patients with metastatic melanoma, it is not fully known how the
drug works.
Objectives:
-To better understand how IL-2 causes tumors to shrink.
Eligibility:
-Patients 18 years of age or older with metastatic kidney cancer or metastatic melanoma
Design:
- 135 patients with melanoma and 110 patients with kidney cancer may be enrolled.
- Patients are hospitalized for about 7 days for each treatment. They receive IL-2
intravenously (through a vein) over 15 minutes every 8 hours for up to 4 days or 12
doses. This constitutes one treatment cycle.
- Research blood samples are collected daily during the first treatment cycle and for one
or two days following the last dose.
- Patients may be asked to undergo leukapheresis, a procedure for collecting large
quantities of white blood cells. This involves collecting blood through a needle in an
arm vein. The blood is directed through a cell separator where the white cells are
extracted. The rest of the blood (red cells, platelets, and plasma) is returned to the
patient through the same needle or through a needle in the other arm.
- About 7-10 days after discharge from the hospital, patients return for a second
treatment cycle but without research blood sampling.
- 2 months after therapy, patients are evaluated with scans, and x-rays, and blood tests
to evaluate the tumor and the effects of the treatment on immune cells.
- Patients whose tumors shrink or remain stable may continue treatment (without repeating
the full set of research blood samples) as long as they benefit from the treatment and
do not develop unacceptable side effects. Patients who continue treatment are evaluated
every 2 months for 3 to 4 times and then every 3 to 6 months.
Background:
- Although interleukin-2 (IL-2) was approved as standard therapy by the US Food and Drug
Administration for metastasis melanoma and renal cell carcinoma, the mechanism of action
in these patient populations is still not completely understood.
- Methods for studying regulatory T-cells and measuring recently discovered cytokines were
not available during earlier studies of IL-2 administration.
Objectives:
- Explore peripheral blood samples of patients with metastatic renal cell cancer or melanoma
receiving high-dose IL-2 to identify serum protein levels and lymphocyte phenotypes that may
be associated with or predictive of tumor regression.
Eligibility:
- Patients with metastatic renal cell cancer or melanoma who are greater than or equal to
18 years of age, with an ECOG of 0 or 1 who have an expected survival greater than three
months.
- Patients with systemic infections, coagulation disorders, or major medical illnesses of
the cardiovascular, respiratory or immune system will be excluded, including patients
with ejection fractions less than 45% or FEV1 or VC less than or equal to 60% predicted.
- Patients must not have had prior therapy within 28 days, previous IL-2 therapy, be
pregnant, have untreated or clinically significant tumor involvement of the CNS or major
nerve compression, or have greater than 25% estimated hepatic replacement.
Design:
- Aldesleukin 720,000 IU/kg intravenous bolus over 15 minutes every eight hours for up to
12 doses will be administered as a cycle of treatment.
- Seven to 10 days after discharge, a second cycle of treatment will be administered.
- 20 mLs of blood for serum and 20 mLs of blood for peripheral blood cells will be
collected daily during the first cycle of aldesleukin administration and the day
following the last dose. 20 mLs of blood for serum and 50 mLs of blood for cell
separation will be obtained on days 2 through 4 following completion of IL-2
administration. On one of these days, an additional 50 mLs of blood for cell separation
or a 2 hour apheresis may be substituted.
- Approximately two months from the beginning of therapy, a response assessment will be
performed.
- Patients with stable or regressing disease will receive a second complete treatment
course. Subsequent courses may be administered if there is evidence of on-going tumor
regression without long-term or irreversible toxicity.
- In the first 5 patients of each diagnosis (metastatic renal cell cancer and melanoma)
the following cytokine levels will be assayed: VEGF, CD40L, FASL, TRAIL, GRO-alpha,
IP10, GM-CSF, IFN-gamma, IFN-alpha, IL-1, IL-5, IL-6, IL-8, IL-10, IL-12, IL-13, IL-15,
TNF-alpha, TNF-beta; and the following phenotypic markers will be studied: CD3, CD4,
CD8, CD16, CD25, CD27, CD28, CD56, CD80, CD95, CD107a, CD152, FoxP3, annexin V.
- After the first 10 patients have been analyzed, the scope of the tests will be narrowed
to those which show a response to IL-2.
- Initially, a total of 127 evaluable patients with melanoma will be enrolled, with a
presumed 15% response rate. With the approval of amendment F, a new accrual ceiling of
200 patients with metastatic melanoma will be established to complete the proposed
analysis.
- A total of 100 evaluable patients with renal cell carcinoma will be enrolled with a
presumed 20% response rate.
- Allowing for a small number of inevaluable patients, a total of 200 patients with
melanoma and 110 patients with renal cell carcinoma may be enrolled.
- Although interleukin-2 (IL-2) was approved as standard therapy by the US Food and Drug
Administration for metastasis melanoma and renal cell carcinoma, the mechanism of action
in these patient populations is still not completely understood.
- Methods for studying regulatory T-cells and measuring recently discovered cytokines were
not available during earlier studies of IL-2 administration.
Objectives:
- Explore peripheral blood samples of patients with metastatic renal cell cancer or melanoma
receiving high-dose IL-2 to identify serum protein levels and lymphocyte phenotypes that may
be associated with or predictive of tumor regression.
Eligibility:
- Patients with metastatic renal cell cancer or melanoma who are greater than or equal to
18 years of age, with an ECOG of 0 or 1 who have an expected survival greater than three
months.
- Patients with systemic infections, coagulation disorders, or major medical illnesses of
the cardiovascular, respiratory or immune system will be excluded, including patients
with ejection fractions less than 45% or FEV1 or VC less than or equal to 60% predicted.
- Patients must not have had prior therapy within 28 days, previous IL-2 therapy, be
pregnant, have untreated or clinically significant tumor involvement of the CNS or major
nerve compression, or have greater than 25% estimated hepatic replacement.
Design:
- Aldesleukin 720,000 IU/kg intravenous bolus over 15 minutes every eight hours for up to
12 doses will be administered as a cycle of treatment.
- Seven to 10 days after discharge, a second cycle of treatment will be administered.
- 20 mLs of blood for serum and 20 mLs of blood for peripheral blood cells will be
collected daily during the first cycle of aldesleukin administration and the day
following the last dose. 20 mLs of blood for serum and 50 mLs of blood for cell
separation will be obtained on days 2 through 4 following completion of IL-2
administration. On one of these days, an additional 50 mLs of blood for cell separation
or a 2 hour apheresis may be substituted.
- Approximately two months from the beginning of therapy, a response assessment will be
performed.
- Patients with stable or regressing disease will receive a second complete treatment
course. Subsequent courses may be administered if there is evidence of on-going tumor
regression without long-term or irreversible toxicity.
- In the first 5 patients of each diagnosis (metastatic renal cell cancer and melanoma)
the following cytokine levels will be assayed: VEGF, CD40L, FASL, TRAIL, GRO-alpha,
IP10, GM-CSF, IFN-gamma, IFN-alpha, IL-1, IL-5, IL-6, IL-8, IL-10, IL-12, IL-13, IL-15,
TNF-alpha, TNF-beta; and the following phenotypic markers will be studied: CD3, CD4,
CD8, CD16, CD25, CD27, CD28, CD56, CD80, CD95, CD107a, CD152, FoxP3, annexin V.
- After the first 10 patients have been analyzed, the scope of the tests will be narrowed
to those which show a response to IL-2.
- Initially, a total of 127 evaluable patients with melanoma will be enrolled, with a
presumed 15% response rate. With the approval of amendment F, a new accrual ceiling of
200 patients with metastatic melanoma will be established to complete the proposed
analysis.
- A total of 100 evaluable patients with renal cell carcinoma will be enrolled with a
presumed 20% response rate.
- Allowing for a small number of inevaluable patients, a total of 200 patients with
melanoma and 110 patients with renal cell carcinoma may be enrolled.
- INCLUSION CRITERIA:
- Any patient with metastatic, measurable, histologically-proven RCC or melanoma who is
a candidate for high-dose IL-2 therapy.
- Expected survival greater than three months.
- Age greater than or equal to18 years old.
- ECOG less than 2.
- Serum creatinine less than or equal to 1.4 mg/dl or creatinine clearance greater than
or equal to 90 mL/min, and total bilirubin less than or equal to 2.0 mg/dl, except in
patients with Gilbert's Syndrome who must have a total bilirubin less than 3.0 mg/dl.
- Platelet count greater than 100,000/mm(3).
- Absolute neutrophil count greater than 1000/mm(3).
- Serum ALT/AST less than three times the upper limit of normal.
- Must be willing to sign a durable power of attorney.
- Must be willing to practice effective contraception (regardless of gender).
- Must be willing to sign the informed consent document.
EXCLUSION CRITERIA:
- Significant second malignancy within 3 years of protocol entry or likely to require
intervention in the year following protocol entry.
- Significant psychiatric disease which in the opinion of the Principal Investigator
would prevent adequate informed consent or render immunotherapy unsafe or
contraindicated.
- Requirement for systemic or inhaled steroid administration (topical therapy is
acceptable).
- Prior therapy within 28 days (except focal radiation for bone lesion).
- Systemic infections, coagulation disorders or evidence of active bleeding, or other
major medical illnesses of the cardiovascular, respiratory or immune system.
- ECOG performance status greater than 2.
- Pregnancy.
- Previous IL-2 therapy.
- Positive HIV antibody titer, Seropositive for hepatitis B or C antigen.
- FEV1 or VC less than or equal to 65% of predicted (pulmonary function screening to be
done in patients with significant smoking history [greater than 20pk/years] or
suspicion of pulmonary disease by history or examination).
- Abnormal stress cardiac exam (to be done in all patients greater than or equal to 60
years old and others as indicated clinically) or active cardiac ischemia or
significantly abnormal EKG.
- Greater than 25% estimated hepatic replacement by tumor or SGOT or SGPT greater than
3x normal.
- Untreated or clinically significant (i.e. because of size or presence of edema) tumor
involvement of the CNS or major nerve compression.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
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