Version May 2024
Essential thrombocythemia (alternative agent): Oral: Initial: 0.5 mg 4 times daily or 1 mg twice daily (most patients will experience adequate response at dose ranges of 1.5 to 3 mg per day).
Dose titration: Maintain initial dose for at least 1 week, then titrate to reduce and maintain platelet count <600,000/mm3 and ideally between 150,000/mm3 and 400,000/mm3; the dose must not be increased by >0.5 mg per day in any 1 week; maximum single dose: 2.5 mg; maximum daily dose: 10 mg
Off-label dosing: Oral: 0.5 mg twice daily for 1 week, then adjust dose to maintain platelet counts at normal (≤450,000/mm3) or near normal (450,000/mm3 to 600,000/mm3) levels (Ref).
Dosage adjustment for concomitant therapy: Significant drug interactions exist, requiring dose/frequency adjustment or avoidance. Consult drug interactions database for more information.
There are no dosage adjustments provided in the manufacturer's labeling; however, CrCl <30 mL/minute had no significant effect on anagrelide pharmacokinetics.
Hemodialysis: Not dialyzable (Ref)
Moderate impairment (Child-Pugh score 7 to 9): Initial: 0.5 mg once daily; maintain for at least 1 week with careful monitoring of cardiovascular status; if tolerated, may increase dose; the dose must not be increased by >0.5 mg per day in any 1 week.
Severe impairment (Child-Pugh score ≥10): Avoid use.
Refer to adult dosing.
(For additional information see "Anagrelide: Pediatric drug information")
Essential thrombocythemia: Very limited data available; several small case series: Children ≥6 years and Adolescents: Oral: Initial: 0.5 mg 2-3 times daily; increase at weekly intervals in 0.5 mg increments until platelet count begins to decrease; usual reported maintenance dose range: 1-2.5 mg/day; maximum daily dose: 10 mg/day (per manufacturer) although the maximum reported dose for essential thrombocythemia: 4 mg/day; once platelet count normalizes, further adjust dose to lowest effective dose; in some cases, discontinuation of therapy has been accomplished (Ref); Note: Essential thrombocytopenia is also considered a type myeloproliferative disorder.
Secondary thrombocythemia (associated with myeloproliferative disorders): Children >6 years and Adolescents: Oral: Initial: 0.5 mg once daily; usual range: 0.5 mg 1-4 times daily; median maintenance daily dose: Patient age 7-11 years: 1.75 mg/day; patient age: 11-14 years: 2 mg; Note: Maintain initial dose for ≥1 week, then adjust to the lowest effective dose to reduce and maintain platelet count <600,000/mm3 ideally to the normal range; the dose must not be increased by >0.5 mg per day in any 1 week; maximum single dose: 2.5 mg; maximum daily dose: 10 mg/day
Dosage adjustment for concomitant therapy: Significant drug interactions exist, requiring dose/frequency adjustment or avoidance. Consult drug interactions database for more information.
Children and Adolescents: No adjustment required in renal insufficiency; monitor closely.
The following adverse drug reactions and incidences are derived from product labeling unless otherwise specified. Frequency of adverse reactions is similar in adult and pediatric patients. Listed incidences are for adults unless otherwise specified.
>10%:
Cardiovascular: Edema (21%), palpitations (26%)
Gastrointestinal: Abdominal pain (16%), diarrhea (26%), nausea (17%)
Nervous system: Dizziness (15%), headache (44%), pain (15%)
Neuromuscular & skeletal: Asthenia (23%)
Respiratory: Dyspnea (12%)
1% to 10%:
Cardiovascular: Angina pectoris (1% to 5%), cardiac arrhythmia (1% to 5%), chest pain (8%), heart failure (1% to 5%), hypertension (1% to 5%), orthostatic hypotension (1% to 5%), peripheral edema (9%), syncope (1% to 5%), tachycardia (8%), vasodilation (1% to 5%)
Dermatologic: Alopecia (1% to 5%), ecchymoses (1% to 5%), pruritus (6%), skin rash (8%)
Gastrointestinal: Anorexia (8%), constipation (1% to 5%), dyspepsia (5%), flatulence (10%), gastritis (1% to 5%), gastrointestinal hemorrhage (1% to 5%), vomiting (10%)
Genitourinary: Hematuria (1% to 5%)
Hematologic & oncologic: Anemia (1% to 5%), hemorrhage (1% to 5%), thrombocytopenia (1% to 5%)
Hepatic: Increased liver enzymes (1% to 5%)
Nervous system: Amnesia (1% to 5%), chills (1% to 5%), confusion (1% to 5%), depression (1% to 5%), drowsiness (1% to 5%), insomnia (1% to 5%), malaise (6%), migraine (1% to 5%), nervousness (1% to 5%), paresthesia (6%)
Neuromuscular & skeletal: Arthralgia (1% to 5%), back pain (6%), myalgia (1% to 5%)
Ophthalmic: Diplopia (1% to 5%), visual disturbance (1% to 5%)
Otic: Tinnitus (1% to 5%)
Renal: Renal failure syndrome (1% to 5%)
Respiratory: Cough (6%), epistaxis (1% to <5%), flu-like symptoms (1% to 5%), pneumonia (1% to 5%)
Miscellaneous: Fever (9%)
<1%:
Cardiovascular: Supraventricular tachycardia, ventricular tachycardia
Nervous system: Hypoesthesia
Frequency not defined:
Cardiovascular: Acute myocardial infarction, atrial fibrillation, cardiomegaly, cardiomyopathy, cerebrovascular accident, complete atrioventricular block, pericardial effusion, prolonged QT interval on ECG
Gastrointestinal: Pancreatitis
Nervous system: Fatigue (pediatric patients)
Neuromuscular & skeletal: Muscle cramps (pediatric patients)
Respiratory: Pleural effusion, pulmonary fibrosis, pulmonary hypertension, pulmonary infiltrates
Postmarketing:
Cardiovascular: Cerebral infarction, Prinzmetal angina, torsades de pointes
Dermatologic: Skin photosensitivity (pediatric patients)
Hematologic & oncologic: Leukocytosis (pediatric patients)
Hepatic: Hepatotoxicity (including increased serum alanine aminotransferase [>3 x ULN], increased serum aspartate aminotransferase [>3 x ULN])
Renal: Interstitial nephritis
Respiratory: Interstitial pulmonary disease (including eosinophilic pneumonitis, hypersensitivity pneumonitis, interstitial pneumonitis)
There are no contraindications listed in the US manufacturer's labeling.
Canadian labeling: Hypersensitivity to anagrelide or any component of the formulation; severe hepatic impairment; rare heredity condition of galactose intolerance, glucose-galactose malabsorption, or congenital lactase deficiency.
Concerns related to adverse effects:
• Bleeding risk: The risk for major hemorrhagic events is increased when anagrelide is used concomitantly with aspirin; assess risks versus benefits if using anagrelide in combination with aspirin. Monitor for bleeding, particularly when used concurrently with other agents known to increase bleeding risk (eg, anticoagulants, nonsteroidal anti-inflammatory drugs, antiplatelet agents, other phosphodiesterase 3 [PDE3] inhibitors, selective serotonin reuptake inhibitors).
• Cardiovascular adverse events: Ventricular tachycardia and torsades de pointes have been reported with anagrelide. As with other PDE3 inhibitors, anagrelide may cause vasodilation, tachycardia, palpitations and heart failure. PDE3 inhibitors are associated with decreased survival (compared to placebo) in patients with class III or IV heart failure. In a scientific statement from the American Heart Association, anagrelide has been determined to be an agent that may cause direct myocardial toxicity (magnitude: major) (AHA [Page 2016]). Dose-related increases in heart rate and mean QTc interval have been observed in a clinical trial. The maximum change in mean heart rate was ~8 beats per minute (bpm) at a dose of 0.5 mg and ~29 bpm with a 2.5 mg dose. The maximum mean change in QTc I (individual subject correlation) from placebo was 7 msec and 13 msec with doses of 0.5 and 2.5 mg, respectively. Do not use in patients with hypokalemia, congenital long QT syndrome, a known history of acquired QTc prolongation, or when using concomitant therapy that may prolong the QTc interval. Hypotension accompanied by dizziness may occur, particularly with higher doses. Consider periodic ECG monitoring in patients with heart failure, bradyarrhythmias, or electrolyte abnormalities. The benefits of anagrelide therapy should outweigh risks in patients with cardiovascular disease. Pretreatment cardiovascular evaluation (including ECG) and careful monitoring during treatment is recommended.
• Pulmonary hypertension: Pulmonary hypertension has been reported with anagrelide; evaluate for signs and symptoms of underlying cardiopulmonary disease prior to and during anagrelide therapy.
• Pulmonary toxicity: Interstitial lung disease (including allergic alveolitis, eosinophilic pneumonia, and interstitial pneumonitis) has been associated with anagrelide. The onset is from 1 week to several years after anagrelide initiation, usually presenting with progressive dyspnea with lung infiltrations; symptoms usually improve after discontinuation.
• Renal abnormalities: Renal abnormalities (including hematuria and renal failure) have been observed with anagrelide.
Disease-related concerns:
• Hepatic impairment: Hepatic impairment increases anagrelide exposure and may increase the risk of QTc prolongation. Assess risks versus benefits of anagrelide treatment in patients with mild to moderate hepatic impairment; dosage reduction and careful cardiovascular monitoring are required for moderate impairment. Avoid use in patients with severe impairment. Monitor liver function prior to and during treatment.
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.
Capsule, Oral:
Agrylin: 0.5 mg
Generic: 0.5 mg, 1 mg
Yes
Capsules (Agrylin Oral)
0.5 mg (per each): $9.92
Capsules (Anagrelide HCl Oral)
0.5 mg (per each): $11.16
1 mg (per each): $24.07
Disclaimer: A representative AWP (Average Wholesale Price) price or price range is provided as reference price only. A range is provided when more than one manufacturer's AWP price is available and uses the low and high price reported by the manufacturers to determine the range. The pricing data should be used for benchmarking purposes only, and as such should not be used alone to set or adjudicate any prices for reimbursement or purchasing functions or considered to be an exact price for a single product and/or manufacturer. Medi-Span expressly disclaims all warranties of any kind or nature, whether express or implied, and assumes no liability with respect to accuracy of price or price range data published in its solutions. In no event shall Medi-Span be liable for special, indirect, incidental, or consequential damages arising from use of price or price range data. Pricing data is updated monthly.
Excipient information presented when available (limited, particularly for generics); consult specific product labeling.
Capsule, Oral:
Agrylin: 0.5 mg
Generic: 0.5 mg, 1 mg
Oral: May be administered without regard to food.
May be administered without regard to food.
Essential thrombocythemia: Treatment of thrombocythemia secondary to myeloproliferative neoplasms to reduce elevated platelets and the risk of thrombosis and to reduce associated symptoms (including thrombo-hemorrhagic events).
Note: The use of hydroxyurea and low-dose aspirin may be preferred over anagrelide for the initial treatment of essential thrombocythemia; however, anagrelide may be appropriate in patients who are resistant or intolerant to hydroxyurea (ESMO [Vannucchi 2015]).
Anagrelide may be confused with anastrozole
Substrate of CYP1A2 (major); Note: Assignment of Major/Minor substrate status based on clinically relevant drug interaction potential
Note: Interacting drugs may not be individually listed below if they are part of a group interaction (eg, individual drugs within “CYP3A4 Inducers [Strong]” are NOT listed). For a complete list of drug interactions by individual drug name and detailed management recommendations, use the Lexicomp drug interactions program by clicking on the “Launch drug interactions program” link above.
Agents with Antiplatelet Properties (e.g., P2Y12 inhibitors, NSAIDs, SSRIs, etc.): Anagrelide may enhance the antiplatelet effect of Agents with Antiplatelet Properties. Risk C: Monitor therapy
Anticoagulants: Anagrelide may enhance the anticoagulant effect of Anticoagulants. Risk C: Monitor therapy
Aspirin: Anagrelide may enhance the antiplatelet effect of Aspirin. Risk C: Monitor therapy
Broccoli: May decrease the serum concentration of CYP1A2 Substrates (High risk with Inducers). Risk C: Monitor therapy
Cannabis: May decrease the serum concentration of CYP1A2 Substrates (High risk with Inducers). Risk C: Monitor therapy
Cilostazol: Anagrelide may enhance the adverse/toxic effect of Cilostazol. Risk X: Avoid combination
CYP1A2 Inducers (Moderate): May decrease serum concentrations of the active metabolite(s) of Anagrelide. CYP1A2 Inducers (Moderate) may decrease the serum concentration of Anagrelide. Risk C: Monitor therapy
CYP1A2 Inhibitors (Moderate): May increase serum concentrations of the active metabolite(s) of Anagrelide. CYP1A2 Inhibitors (Moderate) may increase the serum concentration of Anagrelide. Risk C: Monitor therapy
CYP1A2 Inhibitors (Strong): May increase serum concentrations of the active metabolite(s) of Anagrelide. CYP1A2 Inhibitors (Strong) may increase the serum concentration of Anagrelide. Risk C: Monitor therapy
Enoximone: May enhance the adverse/toxic effect of Anagrelide. Risk X: Avoid combination
Haloperidol: QT-prolonging Agents (Indeterminate Risk - Avoid) may enhance the QTc-prolonging effect of Haloperidol. Risk C: Monitor therapy
Levoketoconazole: QT-prolonging Agents (Indeterminate Risk - Avoid) may enhance the QTc-prolonging effect of Levoketoconazole. Management: Monitor for QTc interval prolongation and ventricular arrhythmias when these agents are combined. Patients with additional risk factors for QTc prolongation may be at even higher risk. Risk C: Monitor therapy
Milrinone: Anagrelide may enhance the adverse/toxic effect of Milrinone. Risk X: Avoid combination
QT-prolonging Agents (Highest Risk): QT-prolonging Agents (Indeterminate Risk - Avoid) may enhance the QTc-prolonging effect of QT-prolonging Agents (Highest Risk). Management: Monitor for QTc interval prolongation and ventricular arrhythmias when these agents are combined. Patients with additional risk factors for QTc prolongation may be at even higher risk. Risk C: Monitor therapy
Riociguat: Anagrelide may enhance the hypotensive effect of Riociguat. Management: Riociguat is contraindicated with nonselective phosphodiesterase (PDE) inhibitors and PDE type 5 inhibitors. Other types of PDE inhibitors are not contraindicated, but caution is advised and patients should be monitored for hypotension. Risk C: Monitor therapy
Data regarding use of anagrelide during pregnancy is limited (Alkindi 2005; Birgegård 2018; Cornet 2017; Doubek 2004; Sobas 2009; Wright 2001).
Thrombocythemia is associated with an increased risk for adverse pregnancy outcomes including miscarriage, stillbirth, and preeclampsia. When treatment for essential thrombocythemia is needed during pregnancy, other agents are currently preferred (Tefferi 2018).
It is not known if anagrelide is present in breast milk.
Due to the potential for serious adverse reactions in the breastfed infant, breastfeeding is not recommended by the manufacturer during therapy and for 1 week after the last anagrelide dose.
Monitor platelet count (every 2 days during the first week of treatment and at least weekly thereafter until the maintenance dose is reached; continue to monitor after cessation of treatment); CBC with differential (monitor closely during first 2 weeks of treatment), liver function (ALT and AST; baseline and during treatment), BUN, and serum creatinine (monitor closely during first weeks of treatment); serum electrolytes; blood pressure; heart rate; cardiovascular exam, including ECG (pretreatment; monitor during therapy). Monitor for signs/symptoms of interstitial lung disease and cardiopulmonary disease; monitor for thrombosis or bleeding. Monitor adherence.
Anagrelide appears to inhibit cyclic nucleotide phosphodiesterase and the release of arachidonic acid from phospholipase, possibly by inhibiting phospholipase A2. Anagrelide also causes a dose-related reduction in platelet production, which results from decreased megakaryocyte hypermaturation (disrupts the postmitotic phase of maturation).
Onset of action: Initial: Within 7 to 14 days; complete response (platelets ≤600,000/mm3): 4 to 12 weeks
Duration: Platelet rebound: Variable; upon discontinuation, platelet count begins to rise within 4 days and returns to baseline in 1 to 2 weeks (may rebound above baseline)
Metabolism: Hepatic; primarily via CYP1A2 to two major metabolites, 3-hydroxy anagrelide (active) and RL603 (inactive)
Half-life elimination: Anagrelide: ~1.5 hours, similar data reported in pediatric patients 7 to 14 years of age; 3-hydroxy anagrelide: ~2.5 hours
Time to peak, serum: ~1 hour (in fasted state), similar data reported in pediatric patients 7 to 14 years of age
Excretion: Urine (<1% as unchanged drug; ~3% as 3-hydroxy anagrelide [active metabolite]; 16% to 20% as RL603 [inactive metabolite])
Hepatic function impairment: AUC increased 8-fold in patients with moderate hepatic function impairment.
Older adult: AUC and Cmax of anagrelide were 61% and 36% higher, respectively, in patients ages 65 to 75 years compared to patients ages 22 to 50 years, but the AUC and Cmax of the active metabolite, 3-hydroxy anagrelide, were 37% and 42% lower, respectively, in the older adult population.
Pediatric: In pediatric patients 7 to 14 years of age; data have shown a decreased maximum serum concentration (48%) and AUC (55%) compared to adults when normalized to dose and bodyweight.
آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟
