dabrafenib
General
High Alert Medication: This medication bears a heightened risk of causing significant patient harm when it is used in error.
Genetic Implications:
Pronunciation:
da-braf-e-nib
Trade Name(s)
- Tafinlar
Ther. Class.
Pharm. Class.
kinase inhibitors
Indications
Metastatic or unresectable melanoma in patients with the BRAF V600E mutation (as monotherapy).
Metastatic or unresectable melanoma in patients with the BRAF V600E or V600K mutation (in combination with trametinib).
Adjuvant treatment of melanoma in patients with the BRAF V600E or V600K mutation and lymph node involvement following complete resection (in combination with trametinib).
Metastatic non-small cell lung cancer (NSCLC) in patients with the BRAF V600E mutation (in combination with trametinib).
Locally advanced or metastatic anaplastic thyroid cancer in patients with the BRAF V600E mutation and no satisfactory locoregional treatment options (in combination with trametinib).
Unresectable or metastatic solid tumors with the BRAF V600E mutation in patients who have progressed following prior treatment and have no satisfactory alternative treatment options (in combination with trametinib).
Low-grade glioma with a BRAF V600E mutation in patients who require systemic therapy (in combination with trametinib).
Action
Inhibits kinase, an enzyme that promotes cell proliferation.
Therapeutic Effect(s):
Decreased spread/progression of melanoma, NSCLC, anaplastic thyroid cancer, low-grade gliomas, and other solid tumors.
Pharmacokinetics
Absorption: Well absorbed (95%) following oral administration.
Distribution: Unknown.
Protein Binding: 99.7%.
Metabolism and Excretion: Mostly metabolized by the CYP2C8 and CYP3A4 isoenzymes; two metabolites (hydroxy-dabrafenib and desmethyl-1–dabrafenib) have antineoplastic activity. Excreted as metabolites in feces (72%) and urine (23%).
Half-life: Dabrafenib: 8 hr; hydroxy-dabrafenib: 10 hr, desmethyl-1–dabrafenib: 21–22 hr.
TIME/ACTION PROFILE (progression-free survival)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
PO | within 1 mo | 1–2 mo | 8 mo |
Contraindication/Precautions
Contraindicated in:
- BRAF wild-type solid tumors (may ↑ proliferation);
- OB: Pregnancy;
- Lactation: Lactation.
Use Cautiously in:
History of glucose-6-phosphate dehydrogenase (G6PD) deficiency (may cause hemolytic anemia);
- Diabetes;
- Moderate or severe hepatic impairment;
- Moderate or severe renal impairment;
- Rep: Women of reproductive potential and men with female partners of reproductive potential;
- Pedi: Safety and effectiveness not established in children <18 yr (as monotherapy) or <1 yr (in combination with trametinib for unresectable or metastatic solid tumors or low-grade gliomas with BRAF V600E mutation).
Adverse Reactions/Side Effects
CV: HF, THROMBOEMBOLISM
Derm: alopecia, hyperkeratosis, palmar-plantar erythrodysesthesia, papilloma, cutaneous squamous cell carcinoma, DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS (DRESS), photosensitivity, STEVENS-JOHNSON SYNDROME
EENT: iritis, retinal detachment, uveitis
Endo: hyperglycemia
F and E: hypophosphatemia, hyponatremia
GI: constipation, PANCREATITIS
Hemat: BLEEDING, hemophagocytic lymphohistiocytosis
MS: arthralgia, back pain, myalgia
Neuro: headache, fatigue, peripheral neuropathy
Resp: cough, nasopharyngitis
Misc: fever (including serious febrile reactions), chills, MALIGNANCY
* CAPITALS indicate life-threatening.
Underline indicate most frequent.
Interactions
Drug-Drug
- Concurrent use of strong CYP3A4 inhibitors or strong CYP2C8 inhibitors, including ketoconazole, nefazodone, clarithromycin, and gemfibrozil, may ↑ levels and ↑ the risk of toxicity and should be avoided.
- Concurrent use of strong CYP3A4 inducers or strong CYP2C8 inducers, including carbamazepine, phenobarbital, phenytoin, and rifampin, may ↓ levels and ↓ effectiveness.
- Drugs that ↑ gastric pH, including antacids, H2 -receptor antagonists, and proton pump inhibitors, may ↓ levels and effectiveness.
- May ↓ effectiveness of other CYP3A4 substrates and CYP2C9 substrates, including midazolam, warfarin, dexamethasone, and hormonal contraceptives.
Drug-Natural Products:
St. John's wort ↓ levels and may ↓ effectiveness; concurrent use should be avoided.
Route/Dosage
Treatment of Unresectable/Metastatic Melanoma, Metastatic Non-Small Cell Lung Cancer, or Locally Advanced/Metastatic Anaplastic Thyroid Cancer
Capsules
PO (Adults): 150 mg twice daily until disease progression or unacceptable toxicity.
Tablets for Oral Suspension
PO (Adults ≥51 kg): 150 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 46–50 kg): 130 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 42–45 kg): 110 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 38–41 kg): 100 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 34–37 kg): 90 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 30–33 kg): 80 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 26–29 kg): 70 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 22–25 kg): 60 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 18–21 kg): 50 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 14–17 kg): 40 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 10–13 kg): 30 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults 8–9 kg): 20 mg twice daily until disease progression or unacceptable toxicity.
Adjuvant Treatment of Unresectable/Metastatic Melanoma
Capsules
PO (Adults): 150 mg twice daily; continue until disease recurrence or unacceptable toxicity for up to 1 yr.
Tablets for Oral Suspension
PO (Adults ≥51 kg): 150 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 46–50 kg): 130 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 42–45 kg): 110 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 38–41 kg): 100 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 34–37 kg): 90 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 30–33 kg): 80 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 26–29 kg): 70 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 22–25 kg): 60 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 18–21 kg): 50 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 14–17 kg): 40 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 10–13 kg): 30 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
PO (Adults 8–9 kg): 20 mg twice daily until disease progression or unacceptable toxicity for up to 1 yr.
Treatment of Unresectable/Metastatic Solid Tumors
Capsules
PO (Adults): 150 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and ≥51 kg): 150 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 38–50 kg): 100 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 26–37 kg): 75 mg twice daily until disease progression or unacceptable toxicity.
Tablets for Oral Suspension
PO (Adults and Children ≥1 yr and ≥51 kg): 150 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 46–50 kg): 130 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 42–45 kg): 110 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 38–41 kg): 100 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 34–37 kg): 90 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 30–33 kg): 80 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 26–29 kg): 70 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 22–25 kg): 60 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 18–21 kg): 50 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 14–17 kg): 40 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 10–13 kg): 30 mg twice daily until disease progression or unacceptable toxicity.
PO (Adults and Children ≥1 yr and 8–9 kg): 20 mg twice daily until disease progression or unacceptable toxicity.
Treatment of Low-Grade Glioma
Capsules
PO (Children ≥1 yr and ≥51 kg): 150 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 38–50 kg): 100 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 26–37 kg): 75 mg twice daily until disease progression or unacceptable toxicity.
Tablets for Oral Suspension
PO (Children ≥1 yr and ≥51 kg): 150 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 46–50 kg): 130 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 42–45 kg): 110 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 38–41 kg): 100 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 34–37 kg): 90 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 30–33 kg): 80 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 26–29 kg): 70 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 22–25 kg): 60 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 18–21 kg): 50 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 14–17 kg): 40 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 10–13 kg): 30 mg twice daily until disease progression or unacceptable toxicity.
PO (Children ≥1 yr and 8–9 kg): 20 mg twice daily until disease progression or unacceptable toxicity.
Availability
Capsules: 50 mg, 75 mg
Tablets for oral suspension: 10 mg
Assessment
- Perform skin examination at baseline, every 2 mo during therapy, and for 6 mo after completion of therapy. If intolerable Grade 2–4 skin toxicity occurs, hold dabrafenib for up to 3 wk. If improved, resume at ↓ dose. If not improved, permanently discontinue dabrafenib.
- Monitor temperature. If temperature is >100.3°F , hold dabrafenib or dabrafenib and trametinib. Evaluate for signs and symptoms of infection and renal dysfunction during and following pyrexia. Restart dabrafenib and trametinib when pyrexia resolved for ≥24 hr, either at the same or ↓ dose. Administer antipyretics as secondary prophylaxis when resuming therapy. Administer prednisone 10 mg daily for ≥5 days for second or subsequent pyrexia if fever does not resolve within 3 days of onset or for pyrexia associated with complications (dehydration, hypotension, renal failure, severe chills/rigors) and with no evidence of active infection.
- Monitor for signs and symptoms of ocular toxicity (blurred or ↓ vision, seeing colored dots or halos, swelling, redness, photophobia, eye pain). May require steroid and mydriatic ophthalmic drops. If iritis occurs, do not modify dose. If severe uveitis or mild to moderate uveitis that does not respond to ocular therapy occurs, hold for ≤6 wk. If improved to Grade 0–1, resume at same or ↓ dose. If not improved, permanently discontinue dabrafenib.
- Monitor left ventricular ejection fraction (LVEF) by ECG or multigated acquisition (MUGA) scan before starting therapy with dabrafenib and trametinib, 1 mo after initiation, and then at 2- to 3-mo intervals during therapy. If symptomatic HF occurs with absolute ↓ in LVEF >20% from baseline that is below lower limit of normal (LLN), hold dabrafenib until improved to LLN and absolute ↓ to ≤10% of baseline; then resume at same dose.
- Monitor for signs and symptoms of venous thromboembolism (shortness of breath; chest pain; cool, pale, swollen extremity) during therapy. If uncomplicated deep vein thrombosis or pulmonary embolus (PE) occurs, do not modify dabrafenib dose; hold trametinib ≤3 wk. If improved to Grade 0–1, resume at ↓ dose. If not improved, permanently discontinue. If life-threatening PE occurs, permanently discontinue dabrafenib and trametinib.
- Monitor for signs and symptoms of interstitial lung disease or pneumonitis (cough, dyspnea, hypoxia, pleural effusion, infiltrates) during therapy. If signs and symptoms occur, do not modify dabrafenib dose; permanently discontinue trametinib.
- Assess for bleeding (headache, dizziness, weakness, hemoptysis, hematemesis, red or black tarry stool) during therapy. If Grade 3 hemorrhagic event occurs, hold dabrafenib and trametinib ≤3 wk; if improved, resume at ↓ dose. If Grade 4 hemorrhagic event occurs, permanently discontinue dabrafenib and trametinib.
Lab Test Considerations:
Verify negative pregnancy test prior to initiation.
Confirm presence of BRAF V600E mutation in tumor specimens prior to therapy with dabrafenib, and confirm BRAF V600E or V600K mutation in tumor specimens prior to therapy with dabrafenib and trametinib. Information on FDA-approved tests for the detection of BRAF V600E mutations in ATC, melanoma, and NSCLC is available at http://www.fda.gov/CompanionDiagnostics.
May cause hyperglycemia, requiring ↑ dose of or initiation of insulin or oral hypoglycemic. Monitor serum glucose in patients with pre-existing diabetes or hyperglycemia.
- May cause hypophosphatemia, ↑ alkaline phosphatase, and hyponatremia.
- Monitor for hemolytic anemia in patients with G6PD deficiency.
Implementation
- Dose reduction recommendations: Adults: If taking 75 mg twice daily, 1st dose reduction, 50 mg PO twice daily. Permanently discontinue if unable to tolerate 50 mg twice daily. If taking 100 mg twice daily, 1st dose reduction, 75 mg PO twice daily; 2nd dose reduction, 50 mg PO twice daily. Permanently discontinue if unable to tolerate 50 mg twice daily. If taking 150 mg twice daily, 1st dose reduction, 100 mg PO twice daily; 2nd, 75 mg PO twice daily; 3rd, 50 mg PO twice daily. If 50 mg twice daily is intolerable, permanently discontinue dabrafenib. Pediatric Patients: If 8–9 kg, taking 20 mg twice daily, discontinue dabrafenib if unable to tolerate 10 mg PO twice daily. If 10–13 kg, taking 30 mg twice daily, 1st dose reduction, 20 mg PO twice daily; 2nd, 10 mg PO twice daily. If 14–17 kg, taking 40 mg twice daily, 1st dose reduction, 30 mg PO twice daily; 2nd, 20 mg PO twice daily; 3rd, 10 mg PO twice daily. If 18–21 kg, taking 50 mg twice daily, 1st dose reduction, 30 mg PO twice daily; 2nd, 20 mg PO twice daily; 3rd, 10 mg PO twice daily. If 22–25 kg, taking 60 mg twice daily, 1st dose reduction, 40 mg PO twice daily; 2nd, 30 mg PO twice daily; 3rd, 20 mg PO twice daily. If 26–29 kg, taking 70 mg twice daily, 1st dose reduction, 50 mg PO twice daily; 2nd, 40 mg PO twice daily; 3rd, 20 mg PO twice daily. If 30–33 kg, taking 80 mg twice daily, 1st dose reduction, 50 mg PO twice daily; 2nd, 40 mg PO twice daily; 3rd, 30 mg PO twice daily. If 34–37 kg, taking 90 mg twice daily, 1st dose reduction, 60 mg PO twice daily; 2nd, 50 mg PO twice daily; 3rd, 30 mg PO twice daily. If 38–41 kg, taking 100 mg twice daily, 1st dose reduction, 70 mg PO twice daily; 2nd, 50 mg PO twice daily; 3rd, 30 mg PO twice daily. If 42–45 kg, taking 110 mg twice daily, 1st dose reduction, 70 mg PO twice daily; 2nd, 60 mg PO twice daily; 3rd, 40 mg PO twice daily. If 46–50 kg, taking 130 mg twice daily, 1st dose reduction, 90 mg PO twice daily; 2nd, 70 mg PO twice daily; 3rd, 40 mg PO twice daily. If ≥51 kg, taking 150 mg twice daily, 1st dose reduction, 100 mg PO twice daily; 2nd, 80 mg PO twice daily; 3rd, 50 mg PO twice daily.
- PO Administer capsules twice daily about 12 hr apart. Administer on empty stomach ≥1 hr before or 2 hr after food. DNC: Swallow capsules whole; do not open, crush, break, or chew.
- When administered with trametinib, administer once-daily dose of trametinib at same time each day with either morning or evening dose of dabrafenib.
- For tablets for oral suspension, only use dosing cups provided. Add cool drinking water to markings on cup. For 1–4 tablets, use 5 mL water; for 5–15 tablets, use 10 mL water. Put tablets in cup with water and gently stir until tablets break apart; may take 3 min. Suspension is cloudy white and may contain small pieces. Administer suspension within 30 min of preparing; if >30 min, dispose of suspension. To access medicine residue in cup, add 5 mL of drinking water, stir, and drink the water and residual mixture. If 1–4 tablets were used, rinse and drink once; if 5–15 tablets used, repeat rinse procedure twice.
- For tablets for oral suspension for use with oral syringe or feeding tube, use directions for oral suspension above. If dose is 1–3 tablets, use ≥10 French. If dose is 4–15 tablets, use ≥12 French. Flush feeding tube before administering; then draw up all suspension from dosing cup with syringe and administer according to manufacturer's instructions. If using an oral syringe, place the tip pointing toward the inside of the cheek. Slowly push the plunger until full dose administered. Add 5 mL water to dosing cup and stir to loosen medicine residue. Draw up mixture and administer via feeding tube or orally. Repeat procedure 3 times.
Patient/Family Teaching
- Explain purpose and side effects of medication. Advise patient to read Patient Information before starting therapy.
- Take missed dose as soon as remembered unless within 6 hr of next dose; then omit and take regularly scheduled dose. If vomiting occurs after administration, do not take an additional dose.
- Inform patient that dabrafenib ↑ risk of developing new cutaneous malignancies and to notify health care professional immediately if new lesions (wart, skin sore, or reddish bump that bleeds or does not heal) or changes in size or color of existing moles or lesions occur.
- Caution patient to use sunscreen and protective clothing to prevent photosensitivity reactions.
- Advise patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to consult with health care professional before taking other medications, especially St. John's wort.
- Advise patient to notify health care professional if fever; ↑ thirst, appetite, or urination; fruity breath; visual changes; eye pain or swelling; ↑ bleeding; skin blisters, sores, or peeling; high fever; flu-like symptoms; enlarged lymph nodes; thromboembolism; or HF occur.
- Rep: Advise women of reproductive potential and men (including those who have had vasectomies) with female partners of reproductive potential to use a highly effective nonhormonal contraception during and for ≥2 wk after last dose of dabrafenib. Dabrafenib may ↓ effectiveness of hormonal contraceptives. Advise patient to notify health care professional if pregnancy is suspected and to avoid breastfeeding during and for 2 wk after last dose. Advise patients to seek counseling on fertility and family planning before beginning therapy; may permanently impair fertility in both sexes.
Evaluation/Desired Outcomes
Decrease in progression of malignant melanoma, NSCLC, anaplastic thyroid cancer, low-grade gliomas, and other solid tumors.