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CINACALCET TAB

Clinical Criteria Summary

Exclusion Criteria

  • Serum calcium less than the lower limit normal (e.g., < 8.4 mg/dL, corrected for serum albumin)

Inclusion Criteria

  • Secondary hyperparathyroidism in a patient with chronic kidney disease (CKD) on chronic dialysis with elevated intact plasma parathyroid hormone (iPTH) level (e.g., greater than 400 pg/ml or significant trend upwards within two to nine times the upper limit normal for the assay) despite management with standard therapy as appropriate (e.g., dietary phosphate restriction, phosphate binders [calcium-based or non-calcium based], calcitriol or vitamin D analogs)
  • Hypercalcemia (e.g., > 12.5 mg/dl, or symptomatic and > 11.3 mg/dl; corrected for serum albumin) in a patient with primary hyperparathyroidism who is not a surgical candidate or with recurrence despite surgical intervention
  • Hypercalcemia (e.g., > 12.5 mg/dl, corrected for serum albumin) in a patient with parathyroid carcinoma despite standard therapy to control hypercalcemia prior to surgical intervention, or who is not a surgical candidate, or who has recurrence despite surgical intervention

FDA Indications & Limitations

  • Secondary hyperparathyroidism in adult patients with CKD on dialysis (Limitation: Not indicated for use in patients with CKD not on dialysis)
  • Hypercalcemia in adult patients with parathyroid carcinoma
  • Hypercalcemia in adult patients with primary hyperparathyroidism for whom parathyroidectomy would be indicated on the basis of serum calcium levels, but who are unable to undergo parathyroidectomy

Hypocalcemia Management & Monitoring

  • Both agents lower serum calcium, leading to potentially severe hypocalcemia (can cause paresthesias, myalgias, muscle spasms, seizures, QT interval prolongation and ventricular arrhythmia); patients predisposed to QT interval prolongation, ventricular arrhythmias, or seizures are at increased risk
  • Close monitoring recommended for development of hypocalcemia, with adjustment of other therapies (e.g., phosphate binders, calcitriol or vitamin D analogs) as indicated
  • For secondary hyperparathyroidism with CKD on dialysis: Monitor serum calcium approximately monthly if receiving maintenance dose
  • For parathyroid carcinoma or primary hyperparathyroidism: Monitor corrected serum calcium every 2 months
  • If calcium is between 8.4 mg/dL and 7.5 mg/dL: Calcium-based phosphate binders and/or vitamin D sterols can be used to increase calcium
  • If calcium is below 7.5 mg/dL or patient has symptoms of hypocalcemia: Hold cinacalcet dose until calcium is 8.0 mg/dL; may resume at a lower dose once calcium is corrected

Dosing & Administration Considerations

  • Refer to Product Information for detailed prescribing information
  • Selection between oral cinacalcet and IV etelcalcetide should depend on treatment response, tolerability, adherence, and cost
  • Patients adequately controlled on cinacalcet, who are tolerating therapy and adherent to the oral once daily treatment regimen, should remain on cinacalcet
  • Concurrent use of calcimimetics could result in severe, life-threatening hypocalcemia; cinacalcet and etelcalcetide should not be used as concomitant therapy

Off-Label Use

  • Long-term safety and efficacy in patients with CKD not on dialysis has not been established; however, individual cases treating a non-dialysis patient with markedly elevated iPTH might be considered
  • Patients treated with cinacalcet who are not on dialysis may be at increased risk for the development of hypocalcemia
  • Limited data show reduction in hypercalcemia and iPTH with cinacalcet in patients with hyperparathyroidism after kidney transplantation; appropriate treatment should be determined on a case by case basis

Pregnancy & Reproductive Safety

  • Refer to prescribing information for animal reproduction studies data to determine use in patients of child-bearing potential, and the need for contraceptive counseling and education on potential risk vs. benefit if patient were to become pregnant

Source Documents