Aldesleukin

Aldesleukin
Black Box Warning
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aparna Vuppala, M.B.B.S. [2]

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Black Box Warning

WARNINGS See full prescribing information for complete Boxed Warning. Therapy with aldesleukin for injection should be restricted to patients with normal cardiac and pulmonary functions as defined by thallium stress testing and formal pulmonary function testing. Extreme caution should be used in patients with a normal thallium stress test and a normal pulmonary function test who have a history of cardiac or pulmonary disease. Aldesleukin should be administered in a hospital setting under the supervision of a qualified physician experienced in the use of anticancer agents. An intensive care facility and specialists skilled in cardiopulmonary or intensive care medicine must be available. Aldesleukin administration has been associated with capillary leak syndrome (CLS) which is characterized by a loss of vascular tone and extravasation of plasma proteins and fluid into the extravascular space. CLS results in hypotension and reduced organ perfusion which may be severe and can result in death. CLS may be associated with cardiac arrhythmias (supraventricular and ventricular), angina, myocardial infarction, respiratory insufficiency requiring intubation, gastrointestinal bleeding or infarction, renal insufficiency, edema, and mental status changes. Aldesleukin treatment is associated with impaired neutrophil function (reduced chemotaxis) and with an increased risk of disseminated infection, including sepsis and bacterial endocarditis. Consequently, preexisting bacterial infections should be adequately treated prior to initiation of Aldesleukin therapy. Patients with indwelling central lines are particularly at risk for infection with gram positive microorganisms. Antibiotic prophylaxis with oxacillin, nafcillin, ciprofloxacin, or vancomycin has been associated with a reduced incidence of staphylococcal infections. Aldesleukin administration should be withheld in patients developing moderate to severe lethargy or somnolence, continued administration may result in coma.

Overview

Aldesleukin is an interleukin-2 that is FDA approved for the treatment of adults with metastatic renal cell carcinoma (metastatic RCC) and metastatic melanoma.. There is a Black Box Warning for this drug as shown here. Common adverse reactions include anaphylaxis, cellulitis, injection site necrosis, retroperitoneal hemorrhage, cardiomyopathy, cerebral hemorrhage, fatal endocarditis , hypertension, cholecystitis, colitis, gastritis, hepatitis, hepatosplenomegaly, intestinal obstruction, hyperthyroidism, neutropenia, myopathy, myositis, rhabdomyolysis, cerebral lesions, encephalopathy.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

• Aldesleukin is indicated for the treatment of adults with metastatic renal cell carcinoma (metastatic RCC).
• Aldesleukin is indicated for the treatment of adults with metastatic melanoma.
• Careful patient selection is mandatory prior to the administration of Aldesleukin.
• Evaluation of clinical studies to date reveals that patients with more favorable ECOG performance status (ECOG PS 0) at treatment initiation respond better to Aldesleukin, with a higher response rate and lower toxicity . Therefore, selection of patients for treatment should include assessment of performance status.
• Experience in patients with ECOG PS >1 is extremely limited.

Dosage

• The recommended PROLEUKIN® (aldesleukin) for injection treatment regimen is administered by a 15-minute IV infusion every 8 hours. The following schedule has been used to treat adult patients with metastatic renal cell carcinoma (metastatic RCC) or metastatic melanoma. Each course of treatment consists of two 5-day treatment cycles separated by a rest period.
• 400,000 IU/kg (0.037 mg/kg) dose administered every 8 hours by a 15-minute IV infusion for a maximum of 14 doses. Following 9 days of rest, the schedule is repeated for another 14 doses, for a maximum of 28 doses per course, as tolerated.
• During clinical trials, doses were frequently withheld for toxicity. Metastatic RCC patients treated with this schedule received a median of 20 of the 28 doses during the first course of therapy. Metastatic melanoma patients received a median of 18 doses during the first course of therapy.

Retreatment

• Patients should be evaluated for response approximately 4 weeks after completion of a course of therapy and again immediately prior to the scheduled start of the next treatment course. Additional courses of treatment should be given to patients only if there is some tumor shrinkage following the last (course and retreatment is not contraindicated ). Each treatment course should be separated by a rest period of at least 7 weeks from the date of hospital discharge.

Dose Modifications

• Dose modification for toxicity should be accomplished by withholding or interrupting a dose rather than reducing the dose to be given. Decisions to stop, hold, or restart Aldesleukin therapy must be made after a global assessment of the patient. With this in mind, the following guidelines should be used:

This image is provided by the National Library of Medicine.

Reconstitution and Dilution Directions: Reconstitution and dilution procedures other than those recommended may alter the delivery and/or pharmacology of Aldesleukin and thus should be avoided.

• Aldesleukin is a sterile, white to off-white, preservative-free, lyophilized powder suitable for IV infusion upon reconstitution and dilution. EACH VIAL CONTAINS 22 MILLION IU (1.3 MG) OF Aldesleukin AND SHOULD BE RECONSTITUTED ASEPTICALLY WITH 1.2 ML OF STERILE WATER FOR INJECTION, USP. WHEN RECONSTITUTED AS DIRECTED, EACH ML CONTAINS 18 MILLION IU (1.1 MG) OF PROLEUKIN. The resulting solution should be a clear, colorless to slightly yellow liquid. The vial is for single-use only and any unused portion should be discarded.
• During reconstitution, the Sterile Water for Injection, USP should be directed at the side of the vial and the contents gently swirled to avoid excess foaming. DO NOT SHAKE.
• The dose of Aldesleukin, reconstituted with Sterile Water for Injection, USP (without preservative) should be diluted aseptically in 50 mL of 5% Dextrose Injection, USP (D5W) and infused over a 15-minute period.
• In cases where the total dose of Aldesleukin is 1.5 mg or less (e.g., a patient with a body weight of less than 40 kilograms), the dose of Aldesleukin should be diluted in a smaller volume of D5W. Concentrations of Aldesleukin below 30 µg/mL and above 70 µg/mL have shown increased variability in drug delivery. Dilution and delivery of Aldesleukin outside of this concentration range should be avoided.
• Glass bottles and plastic (polyvinyl chloride) bags have been used in clinical trials with comparable results. It is recommended that plastic bags be used as the dilution container since experimental studies suggest that use of plastic containers results in more consistent drug delivery. In-line filters should not be used when administering Aldesleukin.
• Before and after reconstitution and dilution, store in a refrigerator at 2° to 8°C (36° to 46°F). Do not freeze. Administer Aldesleukin within 48 hours of reconstitution. The solution should be brought to room temperature prior to infusion in the patient.
• Reconstitution or dilution with Bacteriostatic Water for Injection, USP, or 0.9% Sodium Chloride Injection, USP should be avoided because of increased aggregation. Aldesleukin should not be coadministered with other drugs in the same container.
• Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Aldesleukin in adult patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Aldesleukin in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

Safety and effectiveness in children under 18 years of age have not been established.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

Safety and effectiveness in children under 18 years of age have not been established..

Non–Guideline-Supported Use

Safety and effectiveness in children under 18 years of age have not been established.

Contraindications

• Aldesleukin is contraindicated in patients with a known history of hypersensitivity to interleukin-2 or any component of the Aldesleukin formulation.
• Aldesleukin is contraindicated in patients with an abnormal thallium stress test or abnormal pulmonary function tests and those with organ allografts. Retreatment with Aldesleukin is contraindicated in patients who have experienced the following drug-related toxicities while receiving an earlier course of therapy:

• Sustained ventricular tachycardia (≥5 beats)
• Cardiac arrhythmias not controlled or unresponsive to management
• Chest pain with ECG changes, consistent with angina or myocardial infarction
• Cardiac tamponade
• Intubation for >72 hours
• Renal failure requiring dialysis >72 hours
• Coma or toxic psychosis lasting >48 hours
• Repetitive or difficult to control seizures
• Bowel ischemia/perforation
• GI bleeding requiring surgery

Warnings

WARNINGS See full prescribing information for complete Boxed Warning. Therapy with aldesleukin for injection should be restricted to patients with normal cardiac and pulmonary functions as defined by thallium stress testing and formal pulmonary function testing. Extreme caution should be used in patients with a normal thallium stress test and a normal pulmonary function test who have a history of cardiac or pulmonary disease. Aldesleukin should be administered in a hospital setting under the supervision of a qualified physician experienced in the use of anticancer agents. An intensive care facility and specialists skilled in cardiopulmonary or intensive care medicine must be available. Aldesleukin administration has been associated with capillary leak syndrome (CLS) which is characterized by a loss of vascular tone and extravasation of plasma proteins and fluid into the extravascular space. CLS results in hypotension and reduced organ perfusion which may be severe and can result in death. CLS may be associated with cardiac arrhythmias (supraventricular and ventricular), angina, myocardial infarction, respiratory insufficiency requiring intubation, gastrointestinal bleeding or infarction, renal insufficiency, edema, and mental status changes. Aldesleukin treatment is associated with impaired neutrophil function (reduced chemotaxis) and with an increased risk of disseminated infection, including sepsis and bacterial endocarditis. Consequently, preexisting bacterial infections should be adequately treated prior to initiation of Aldesleukin therapy. Patients with indwelling central lines are particularly at risk for infection with gram positive microorganisms. Antibiotic prophylaxis with oxacillin, nafcillin, ciprofloxacin, or vancomycin has been associated with a reduced incidence of staphylococcal infections. Aldesleukin administration should be withheld in patients developing moderate to severe lethargy or somnolence, continued administration may result in coma.

• Because of the severe adverse events which generally accompany Aldesleukin therapy at the recommended dosages, thorough clinical evaluation should be performed to identify patients with significant cardiac, pulmonary, renal, hepatic, or CNS impairment in whom Aldesleukin is contraindicated. Patients with normal cardiovascular, pulmonary, hepatic, and CNS function may experience serious, life threatening or fatal adverse events. Adverse events are frequent, often serious, and sometimes fatal.
• Should adverse events, which require dose modification occur, dosage should be withheld rather than reduced .
• Aldesleukin has been associated with exacerbation of pre-existing or initial presentation of autoimmune disease and inflammatory disorders. Exacerbation of Crohn’s disease, scleroderma, thyroiditis, inflammatory arthritis, diabetes mellitus, oculo-bulbar myasthenia gravis, crescentic IgA glomerulonephritis, cholecystitis, cerebral vasculitis, Stevens-Johnson syndrome and bullous pemphigoid, has been reported following treatment with IL-2.
• All patients should have thorough evaluation and treatment of CNS metastases and have a negative scan prior to receiving Aldesleukin therapy. New neurologic signs, symptoms, and anatomic lesions following Aldesleukin therapy have been reported in patients without evidence of CNS metastases. Clinical manifestations included changes in mental status, speech difficulties, cortical blindness, limb or gait ataxia, hallucinations, agitation, obtundation, and coma. Radiological findings included multiple and, less commonly, single cortical lesions on MRI and evidence of demyelination. Neurologic signs and symptoms associated with Aldesleukin therapy usually improve after discontinuation of Aldesleukin therapy, however, there are reports of permanent neurologic defects. One case of possible cerebral vasculitis, responsive to dexamethasone, has been reported. In patients with known seizure disorders, extreme caution should be exercised as Aldesleukin may cause seizures.

PRECAUTIONS

General

• Patients should have normal cardiac, pulmonary, hepatic, and CNS function at the start of therapy . Capillary leak syndrome (CLS) begins immediately after aldesleukin treatment starts and is marked by increased capillary permeability to protein and fluids and reduced vascular tone. In most patients, this results in a concomitant drop in mean arterial blood pressure within 2 to 12 hours after the start of treatment. With continued therapy, clinically significant hypotension (defined as systolic blood pressure below 90 mm Hg or a 20 mm Hg drop from baseline systolic pressure) and hypoperfusion will occur. In addition, extravasation of protein and fluids into the extravascular space will lead to the formation of edema and creation of new effusions.
• Medical management of CLS begins with careful monitoring of the patient’s fluid and organ perfusion status. This is achieved by frequent determination of blood pressure and pulse, and by monitoring organ function, which includes assessment of mental status and urine output. Hypovolemia is assessed by catheterization and central pressure monitoring.
• Flexibility in fluid and pressor management is essential for maintaining organ perfusion and blood pressure. Consequently, extreme caution should be used in treating patients with fixed requirements for large volumes of fluid (e.g., patients with hypercalcemia). Administration of IV fluids, either colloids or crystalloids is recommended for treatment of hypovolemia. Correction of hypovolemia may require large volumes of IV fluids but caution is required because unrestrained fluid administration may exacerbate problems associated with edema formation or effusions. With extravascular fluid accumulation, edema is common and ascites, pleural or pericardial effusions may develop. Management of these events depends on a careful balancing of the effects of fluid shifts so that neither the consequences of hypovolemia (e.g., impaired organ perfusion) nor the consequences of fluid accumulations (e.g., pulmonary edema) exceed the patient’s tolerance.
• Clinical experience has shown that early administration of dopamine (1 to 5 µg/kg/min) to patients manifesting capillary leak syndrome, before the onset of hypotension, can help to maintain organ perfusion particularly to the kidney and thus preserve urine output. Weight and urine output should be carefully monitored. If organ perfusion and blood pressure are not sustained by dopamine therapy, clinical investigators have increased the dose of dopamine to 6 to 10 µg/kg/min or have added phenylephrine hydrochloride (1 to 5 µg/kg/min) to low dose dopamine . Prolonged use of pressors, either in combination or as individual agents, at relatively high doses, may be associated with cardiac rhythm disturbances. If there has been excessive weight gain or edema formation, particularly if associated with shortness of breath from pulmonary congestion, use of diuretics, once blood pressure has normalized, has been shown to hasten recovery. NOTE: Prior to the use of any product mentioned, the physician should refer to the package insert for the respective product.
• Aldesleukin treatment should be withheld for failure to maintain organ perfusion as demonstrated by altered mental status, reduced urine output, a fall in the systolic blood pressure below 90 mm Hg or onset of cardiac arrhythmias . Recovery from CLS begins soon after cessation of Aldesleukin therapy. Usually, within a few hours, the blood pressure rises, organ perfusion is restored and reabsorption of extravasated fluid and protein begins.
• Kidney and liver function are impaired during Aldesleukin treatment. Use of concomitant nephrotoxic or hepatotoxic medications may further increase toxicity to the kidney or liver.
• Mental status changes including irritability, confusion, or depression which occur while receiving Aldesleukin may be indicators of bacteremia or early bacterial sepsis, hypoperfusion, occult CNS malignancy, or direct Aldesleukin-induced CNS toxicity. Alterations in mental status due solely to Aldesleukin therapy may progress for several days before recovery begins. Rarely, patients have sustained permanent neurologic deficits .
• Exacerbation of pre-existing autoimmune disease or initial presentation of autoimmune and inflammatory disorders has been reported following Aldesleukin alone or in combination with interferon . Hypothyroidism, sometimes preceded by hyperthyroidism, has been reported following Aldesleukin treatment. Some of these patients required thyroid replacement therapy. Changes in thyroid function may be a manifestation of autoimmunity. Onset of symptomatic hyperglycemia and/or diabetes mellitus has been reported during Aldesleukin therapy.
• Aldesleukin enhancement of cellular immune function may increase the risk of allograft rejection in transplant patients.

Laboratory Tests

• The following clinical evaluations are recommended for all patients, prior to beginning treatment and then daily during drug administration.

• Standard hematologic tests-including CBC, differential and platelet counts
• Blood chemistries-including electrolytes, renal and hepatic function tests
• Chest x-rays

• Serum creatinine should be ≤1.5 mg/dL prior to initiation of Aldesleukin treatment.
• All patients should have baseline pulmonary function tests with arterial blood gases. Adequate pulmonary function should be documented (FEV1 >2 liters or ≥75% of predicted for height and age) prior to initiating therapy.
• All patients should be screened with a stress thallium study. Normal ejection fraction and unimpaired wall motion should be documented. If a thallium stress test suggests minor wall motion abnormalities further testing is suggested to exclude significant coronary artery disease.
• Daily monitoring during therapy with Aldesleukin should include vital signs (temperature, pulse, blood pressure, and respiration rate), weight, and fluid intake and output. In a patient with a decreased systolic blood pressure, especially less than 90 mm Hg, constant cardiac rhythm monitoring should be conducted. If an abnormal complex or rhythm is seen, an ECG should be performed. Vital signs in these hypotensive patients should be taken hourly.
• During treatment, pulmonary function should be monitored on a regular basis by clinical examination, assessment of vital signs and pulse oximetry. Patients with dyspnea or clinical signs of respiratory impairment (tachypnea or rales) should be further assessed with arterial blood gas determination. These tests are to be repeated as often as clinically indicated.
• Cardiac function should be assessed daily by clinical examination and assessment of vital signs. Patients with signs or symptoms of chest pain, murmurs, gallops, irregular rhythm or palpitations should be further assessed with an ECG examination and cardiac enzyme evaluation. Evidence of myocardial injury, including findings compatible with myocardial infarction or myocarditis, has been reported. Ventricular hypokinesia due to myocarditis may be persistent for several months. If there is evidence of cardiac ischemia or congestive heart failure, Aldesleukin therapy should be held, and a repeat thallium study should be done.

Delayed Adverse Reactions to Iodinated Contrast Media

• A review of the literature revealed that 12.6% (range 11-28%) of 501 patients treated with various interleukin-2 containing regimens who were subsequently administered radiographic iodinated contrast media experienced acute, atypical adverse reactions. The onset of symptoms usually occurred within hours (most commonly 1 to 4 hours) following the administration of contrast media. These reactions include fever, chills, nausea, vomiting, pruritus, rash, diarrhea, hypotension, edema, and oliguria. Some clinicians have noted that these reactions resemble the immediate side effects caused by interleukin-2 administration, however the cause of contrast reactions after interleukin-2 therapy is unknown. Most events were reported to occur when contrast media was given within 4 weeks after the last dose of interleukin-2. These events were also reported to occur when contrast media was given several months after interleukin-2 treatment.13

Adverse Reactions

Clinical Trials Experience

• The rate of drug-related deaths in the 255 metastatic RCC patients who received single-agent aldesleukin was 4% (11/255), the rate of drug-related deaths in the 270 metastatic melanoma patients who received single-agent Aldesleukin was 2% (6/270).
• The following data on common adverse events (reported in greater than 10% of patients, any grade), presented by body system, decreasing frequency and by preferred term (COSTART) are based on 525 patients (255 with renal cell cancer and 270 with metastatic melanoma) treated with the recommended infusion dosing regimen.

This image is provided by the National Library of Medicine.

• The following life-threatening (grade 4) events were reported by <1% of the 525 patients: hypothermia, shock, bradycardia, ventricular extrasystoles, myocardial ischemia, syncope, hemorrhage, atrial arrhythmia, phlebitis, AV block second degree, endocarditis, pericardial effusion, peripheral gangrene, thrombosis, coronary artery disorder, stomatitis, nausea and vomiting, liver function tests abnormal, gastrointestinal hemorrhage, hematemesis, bloody diarrhea, gastrointestinal disorder, intestinal perforation, pancreatitis, anemia, leukopenia, leukocytosis, hypocalcemia, alkaline phosphatase increase, BUN increase, hyperuricemia, NPN increase, respiratory acidosis, somnolence, agitation, neuropathy, paranoid reaction, convulsion, grand mal convulsion, delirium, asthma, lung edema, hyperventilation, hypoxia, hemoptysis, hypoventilation, pneumothorax, mydriasis, pupillary disorder, kidney function abnormal, kidney failure, acute tubular necrosis.
• In an additional population of greater than 1,800 patients treated with Aldesleukin-based regimens using a variety of doses and schedules (e.g., subcutaneous, continuous infusion, administration with LAK cells) the following serious adverse events were reported: duodenal ulceration, bowel necrosis, myocarditis, supraventricular tachycardia, permanent or transient blindness secondary to optic neuritis, transient ischemic attacks, meningitis, cerebral edema, pericarditis, allergic interstitial nephritis, tracheo-esophageal fistula.
• In the same clinical population, the following fatal events each occurred with a frequency of <1%: malignant hyperthermia, cardiac arrest, myocardial infarction, pulmonary emboli, stroke, intestinal perforation, liver or renal failure, severe depression leading to suicide, pulmonary edema, respiratory arrest, respiratory failure. In patients with both metastatic RCC and metastatic melanoma, those with ECOG PS of 1 or higher had a higher treatment-related mortality and serious adverse events.
• Most adverse reactions are self-limiting and, usually, but not invariably, reverse or improve within 2 or 3 days of discontinuation of therapy. Examples of adverse reactions with permanent sequelae include: myocardial infarction, bowel perforation/infarction, and gangrene.

Postmarketing Experience

• In post-marketing experience, the following serious adverse events have been reported in a variety of treatment regimens that include interleukin-2: anaphylaxis, cellulitis, injection site necrosis, retroperitoneal hemorrhage, cardiomyopathy, cerebral hemorrhage, fatal endocarditis , hypertension, cholecystitis, colitis, gastritis, hepatitis, hepatosplenomegaly, intestinal obstruction, hyperthyroidism, neutropenia, myopathy, myositis, rhabdomyolysis, cerebral lesions, encephalopathy, extrapyramidal syndrome, insomnia, neuralgia, neuritis, neuropathy (demyelination), urticaria, pneumonia (bacterial, fungal, viral).
• Exacerbation or initial presentation of a number of autoimmune and inflammatory disorders have been reported. Persistent but nonprogressive vitiligo has been observed in malignant melanoma patients treated with interleukin-2. Synergistic, additive and novel toxicities have been reported with Aldesleukin used in combination with other drugs. Novel toxicities include delayed adverse reactions to iodinated contrast media and hypersensitivity reactions to antineoplastic agents.
• Experience has shown the following concomitant medications to be useful in the management of patients on Aldesleukin therapy: a) standard antipyretic therapy, including nonsteroidal anti-inflammatories (NSAIDs), started immediately prior to Aldesleukin to reduce fever. Renal function should be monitored as some NSAIDs may cause synergistic nephrotoxicity, b) meperidine used to control the rigors associated with fever, c) H2 antagonists given for prophylaxis of gastrointestinal irritation and bleeding, d) antiemetics and antidiarrheals used as needed to treat other gastrointestinal side effects. Generally these medications were discontinued 12 hours after the last dose of PROLEUKIN.
• Patients with indwelling central lines have a higher risk of infection with gram positive organism]s.9-11 A reduced incidence of staphylococcal infections in Aldesleukin studies has been associated with the use of antibiotic prophylaxis which includes the use of oxacillin, nafcillin, ciprofloxacin, or vancomycin. Hydroxyzine or diphenhydramine has been used to control symptoms from pruritic rashes and continued until resolution of pruritus. Topical creams and ointments should be applied as needed for skin manifestations. Preparations containing a steroid (e.g., hydrocortisone) should be avoided. NOTE: Prior to the use of any product mentioned, the physician should refer to the package insert for the respective product.

Drug Interactions

• Aldesleukin may affect central nervous function. Therefore, interactions could occur following concomitant administration of psychotropic drugs (e.g., narcotics, analgesics, antiemetics, sedatives, tranquilizers).
• Concurrent administration of drugs possessing nephrotoxic (e.g., aminoglycosides, indomethacin), myelotoxic (e.g., cytotoxic chemotherapy), cardiotoxic (e.g., doxorubicin) or hepatotoxic (e.g., methotrexate, asparaginase) effects with Aldesleukin may increase toxicity in these organ systems. The safety and efficacy of Aldesleukin in combination with any antineoplastic agents have not been established.
• In addition, reduced kidney and liver function secondary to Aldesleukin treatment may delay elimination of concomitant medications and increase the risk of adverse events from those drugs.
• Hypersensitivity reactions have been reported in patients receiving combination regimens containing sequential high dose Aldesleukin and antineoplastic agents, specifically, dacarbazine, cis-platinum, tamoxifen and interferon-alfa. These reactions consisted of erythema, pruritus, and hypotension and occurred within hours of administration of chemotherapy. These events required medical intervention in some patients.
• Myocardial injury, including myocardial infarction, myocarditis, ventricular hypokinesia, and severe rhabdomyolysis appear to be increased in patients receiving Aldesleukin and interferon-alfa concurrently.
• Exacerbation or the initial presentation of a number of autoimmune and inflammatory disorders has been observed following concurrent use of interferon-alfa and PROLEUKIN, including crescentic IgA glomerulonephritis, oculo-bulbar myasthenia gravis, inflammatory arthritis, thyroiditis, bullous pemphigoid, and Stevens-Johnson syndrome.
• Although glucocorticoids have been shown to reduce PROLEUKIN-induced side effects including fever, renal insufficiency, hyperbilirubinemia, confusion, and dyspnea, concomitant administration of these agents with Aldesleukin may reduce the antitumor effectiveness of Aldesleukin and thus should be avoided.
• Beta-blockers and other antihypertensives may potentiate the hypotension seen with Aldesleukin.

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA): C

• Aldesleukin has been shown to have embryolethal effects in rats when given in doses at 27 to 36 times the human dose (scaled by body weight). Significant maternal toxicities were observed in pregnant rats administered Aldesleukin by IV injection at doses 2.1 to 36 times higher than the human dose during critical period of organogenesis. No evidence of teratogenicity was observed other than that attributed to maternal toxicity. There are no adequate well-controlled studies of Aldesleukin in pregnant women. Aldesleukin should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Pregnancy Category (AUS): There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Aldesleukin in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Aldesleukin during labor and delivery.

Nursing Mothers

• It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from Aldesleukin, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use

Safety and effectiveness in children under 18 years of age have not been established.

Geriatic Use

• There were a small number of patients aged 65 and over in clinical trials of Aldesleukin, experience is limited to 27 patients, eight with metastatic melanoma and nineteen with metastatic renal cell carcinoma. The response rates were similar in patients 65 years and over as compared to those less than 65 years of age. The median number of courses and the median number of doses per course were similar between older and younger patients.
• Aldesleukin is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. The pattern of organ system toxicity and the proportion of patients with severe toxicities by organ system were generally similar in patients 65 and older and younger patients. There was a trend, however, towards an increased incidence of severe urogenital toxicities and dyspnea in the older patients.

Gender

There is no FDA guidance on the use of Aldesleukin with respect to specific gender populations.

Race

There is no FDA guidance on the use of Aldesleukin with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Aldesleukin in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Aldesleukin in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Aldesleukin in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Aldesleukin in patients who are immunocompromised.

Administration and Monitoring

Administration

• Intravenous

Monitoring

• Daily monitoring during therapy with Aldesleukin should include vital signs (temperature, pulse, blood pressure, and respiration rate), weight, and fluid intake and output. In a patient with a decreased systolic blood pressure, especially less than 90 mm Hg, constant cardiac rhythm monitoring should be conducted. If an abnormal complex or rhythm is seen, an ECG should be performed. Vital signs in these hypotensive patients should be taken hourly.
• During treatment, pulmonary function should be monitored on a regular basis by clinical examination, assessment of vital signs and pulse oximetry.

IV Compatibility

There is limited information regarding the compatibility of Aldesleukin and IV administrations.

Overdosage

• Side effects following the use of aldesleukin appear to be dose-related. Exceeding the recommended dose has been associated with a more rapid onset of expected dose-limiting toxicities. Symptoms which persist after cessation of Aldesleukin should be monitored and treated supportively. Life-threatening toxicities may be ameliorated by the intravenous administration of dexamethasone, which may also result in loss of the therapeutic effects of Aldesleukin.

NOTE: Prior to the use of dexamethasone, the physician should refer to the package insert for this product.

Pharmacology

This image is provided by the National Library of Medicine.

Mechanism of Action

• Aldesleukin has been shown to possess the biological activities of human native interleukin-2.1,2 In vitro studies performed on human cell lines demonstrate the immunoregulatory properties of Aldesleukin , including: a) enhancement of lymphocyte mitogenesis and stimulation of long-term growth of human interleukin-2 dependent cell lines, b) enhancement of lymphocyte cytotoxicity, c) induction of killer cell (lymphokine-activated (LAK) and natural (NK)) activity, and d) induction of interferon-gamma production.
• The in vivo administration of Aldesleukin in animals and humans produces multiple immunological effects in a dose dependent manner. These effects include activation of cellular immunity with profound lymphocytosis, eosinophilia, and thrombocytopenia, and the production of cytokines including tumor necrosis factor, IL-1 and gamma interferon. 3 In vivo experiments in murine tumor models have shown inhibition of tumor growth.4 The exact mechanism by which Aldesleukin mediates its antitumor activity in animals and humans is unknown.

Structure

• Aldesleukin for injection, a human recombinant interleukin-2 product, is a highly purified protein with a molecular weight of approximately 15,300 daltons. The chemical name is des-alanyl-1, serine-125 human interleukin-2. Aldesleukin , a lymphokine, is produced by recombinant DNA technology using a genetically engineered E. coli strain containing an analog of the human interleukin-2 gene. Genetic engineering techniques were used to modify the human IL-2 gene, and the resulting expression clone encodes a modified human interleukin-2. This recombinant form differs from native interleukin-2 in the following ways: a) Aldesleukin is not glycosylated because it is derived from E. coli , b) the molecule has no N-terminal alanine, the codon for this amino acid was deleted during the genetic engineering procedure, c) the molecule has serine substituted for cysteine at amino acid position 125, this was accomplished by site specific manipulation during the genetic engineering procedure, and d) the aggregation state of Aldesleukin is likely to be different from that of native interleukin-2.
• The in vitro biological activities of the native nonrecombinant molecule have been reproduced with Aldesleukin .
• Aldesleukin is supplied as a sterile, white to off-white, lyophilized cake in single-use vials intended for intravenous (IV) administration. When reconstituted with 1.2 mL Sterile Water for Injection, USP, each mL contains 18 million IU (1.1 mg) Aldesleukin , 50 mg mannitol, and 0.18 mg sodium dodecyl sulfate, buffered with approximately 0.17 mg monobasic and 0.89 mg dibasic sodium phosphate to a pH of 7.5 (range 7.2 to 7.8). The manufacturing process for Aldesleukin involves fermentation in a defined medium containing tetracycline hydrochloride. The presence of the antibiotic is not detectable in the final product. Aldesleukin contains no preservatives in the final product.
• Aldesleukin biological potency is determined by a lymphocyte proliferation bioassay and is expressed in International Units (IU) as established by the World Health Organization 1st International Standard for Interleukin-2 (human). The relationship between potency and protein mass is as follows:
• 18 million (18 x 106) IU Aldesleukin = 1.1 mg protein

Pharmacodynamics

There is limited information regarding Aldesleukin Pharmacodynamics in the drug label.

Pharmacokinetics

• Aldesleukin exists as biologically active, non-covalently bound microaggregates with an average size of 27 recombinant interleukin-2 molecules. The solubilizing agent, sodium dodecyl sulfate, may have an effect on the kinetic properties of this product.
• The pharmacokinetic profile of Aldesleukin is characterized by high plasma concentrations following a short IV infusion, rapid distribution into the extravascular space and elimination from the body by metabolism in the kidneys with little or no bioactive protein excreted in the urine. Studies of IV Aldesleukin in sheep and humans indicate that upon completion of infusion, approximately 30% of the administered dose is detectable in plasma. This finding is consistent with studies in rats using radiolabeled Aldesleukin , which demonstrate a rapid (<1 min) uptake of the majority of the label into the lungs, liver, kidney, and spleen.
• The serum half-life (T 1/2) curves of Aldesleukin remaining in the plasma are derived from studies done in 52 cancer patients following a 5-minute IV infusion. These patients were shown to have a distribution and elimination T 1/2 of 13 and 85 minutes, respectively.
• Following the initial rapid organ distribution, the primary route of clearance of circulating Aldesleukin is the kidney. In humans and animals, Aldesleukin is cleared from the circulation by both glomerular filtration and peritubular extraction in the kidney.5-8 This dual mechanism for delivery of Aldesleukin to the proximal tubule may account for the preservation of clearance in patients with rising serum creatinine values. Greater than 80% of the amount of Aldesleukin distributed to plasma, cleared from the circulation and presented to the kidney is metabolized to amino acids in the cells lining the proximal convoluted tubules. In humans, the mean clearance rate in cancer patients is 268 mL/min.
• The relatively rapid clearance of Aldesleukin has led to dosage schedules characterized by frequent, short infusions. Observed serum levels are proportional to the dose of aldesleukin.

Immunogenicity

• Fifty-seven of 77 (74%) metastatic renal cell carcinoma patients treated with an every 8-hour Aldesleukin regimen and 33 of 50 (66%) metastatic melanoma patients treated with a variety of IV regimens developed low titers of non-neutralizing anti-Aldesleukin antibodies. Neutralizing antibodies were not detected in this group of patients, but have been detected in 1/106 (<1%) patients treated with IV Aldesleukin using a wide variety of schedules and doses. The clinical significance of anti-Aldesleukin antibodies is unknown.

Clinical Experience

• Two hundred fifty-five patients with metastatic renal cell cancer (metastatic RCC) were treated with single agent Aldesleukin in 7 clinical studies conducted at 21 institutions. Two hundred seventy patients with metastatic melanoma were treated with single agent Aldesleukin in 8 clinical studies conducted at 22 institutions. Patients enrolled in trials of single agent Aldesleukin were required to have an Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1 and normal organ function as determined by cardiac stress test, pulmonary function tests, and creatinine ≤1.5 mg/dL. Patients with brain metastases, active infections, organ allografts and diseases requiring steroid treatment were excluded.
• Aldesleukin was given by 15 min IV infusion every 8 hours for up to 5 days (maximum of 14 doses). No treatment was given on days 6 to 14 and then dosing was repeated for up to 5 days on days 15 to 19 (maximum of 14 doses). These 2 cycles constituted 1 course of therapy. Patients could receive a maximum of 28 doses during a course of therapy. In practice >90% of patients had doses withheld. Metastatic RCC patients received a median of 20 of 28 scheduled doses of aldesleukin. Metastatic melanoma patients received a median of 18 of 28 scheduled doses of Aldesleukin during the first course of therapy. Doses were withheld for specific toxicities.
• In the renal cell cancer studies (n=255), objective response was seen in 37 (15%) patients, with 17 (7%) complete and 20 (8%) partial responders (see Table I). The 95% confidence interval for objective response was 11% to 20%. Onset of tumor regression was observed as early as 4 weeks after completion of the first course of treatment, and in some cases, tumor regression continued for up to 12 months after the start of treatment. Responses were observed in both lung and non-lung sites (e.g., liver, lymph node, renal bed occurrences, soft tissue). Responses were also observed in patients with individual bulky lesions and high tumor burden.
• In the metastatic melanoma studies (n=270), objective response was seen in 43 (16%) patients, with 17 (6%) complete and 26 (10%) partial responders (see Table I). The 95% confidence interval for objective response was 12% to 21%. Responses in metastatic melanoma patients were observed in both visceral and non-visceral sites (e.g., lung, liver, lymph node, soft tissue, adrenal, subcutaneous). Responses were also observed in patients with individual bulky lesions and large cumulative tumor burden.

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Nonclinical Toxicology

Carcinogenesis, Mutagenesis, Impairment of Fertility

• There have been no studies conducted assessing the carcinogenic or mutagenic potential of Aldesleukin .
• There have been no studies conducted assessing the effect of Aldesleukin on fertility. It is recommended that this drug not be administered to fertile persons of either gender not practicing effective contraception.

Clinical Studies

There is limited information regarding Aldesleukin Clinical Studies in the drug label.

How Supplied

• aldesleukin for injection is supplied in individually boxed single-use vials. Each vial contains 22 x 106 IU of Aldesleukin . Discard unused portion.
• NDC 0078-0495-61 Individually boxed single-use vial

Storage

• Store vials of lyophilized Aldesleukin in a refrigerator at 2° to 8°C (36° to 46°F). PROTECT FROM LIGHT. Store in carton until time of use.
• Reconstituted or diluted Aldesleukin is stable for up to 48 hours at refrigerated and room temperatures, 2° to 25°C (36° to 77°F). However, since this product contains no preservative, the reconstituted and diluted solutions should be stored in the refrigerator.
• Do not use beyond the expiration date printed on the vial. NOTE: This product contains no preservative.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Aldesleukin Patient Counseling Information in the drug label.

Precautions with Alcohol

Alcohol-Aldesleukin interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

• Proleukin

Look-Alike Drug Names

There is limited information regarding Aldesleukin Look-Alike Drug Names in the drug label.

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

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