Adjunctive therapy with 25-hydroxyvitamin D and articles therefor
Methods, compositions, and kits for adjunctive therapy using 25-hydroxyvitamin D are disclosed. The 25-hydroxyvitamin D may be administered with an agent that increases the risk of hypocalcemia, such as cinacalcet or a salt thereof, and/or an anticancer agent. The adjunctive therapy is effective to treat and prevent iatrogenic hypocalcemia and/or secondary hyperparathyroidism, as well as delay cancer progression and the time to a post-treatment skeletal related event.
1. A method of treating or preventing iatrogenic hypocalcemia and/or secondary hyperparathyroidism in a patient treated with an agent that increases the risk of hypocalcemia, comprising administering to the patient a formulation comprising a 25-hydroxyvitamin D compound.
2. The method of claim 1 , wherein the agent that increases the risk of hypocalcemia is an antiresorptive agent.
3. The method of claim 2 , wherein the antiresorptive agent is zoledronic acid or denosumab.
4. The method of claim 1 , wherein the patient is a cancer patient.
5. The method of claim 1 , wherein the formulation comprising a 25-hydroxyvitamin D compound is a modified release pharmaceutical formulation.
6. The method of claim 5 , wherein the modified release pharmaceutical formulation is a controlled release pharmaceutical formulation.
7. The method of claim 5 , wherein the pharmaceutical formulation comprises 25-hydroxyvitamin D in an oral modified release formulation, optionally a controlled release formulation.
8. The method of claim 1 , wherein the pharmaceutical formulation comprises 25-hydroxyvitamin D in an amount effective to safely increase the patient's serum level of 25-hydroxyvitamin D to at least 30 ng/mL, optionally in a range of about 30 ng/mL to about 100 ng/mL.
9. The method of claim 1 , wherein the 25-hydroxyvitamin D comprises 25-hydroxyvitamin D3, 25-hydroxyvitamin D2, or a combination thereof.
10. The method of claim 9 , wherein the 25-hydroxyvitamin D comprises 25-hydroxyvitamin D3.
11. The method of claim 1 , wherein the 25-hydroxyvitamin D is administered in a dosage of 1 mcg to 1000 mcg per day.
12. A method of lowering elevated serum parathyroid hormone levels and/or stabilizing serum calcium levels in a patient having a bone metastasis and treated with an agent that increases the risk of hypocalcemia comprising administering to the patient an effective amount of 25-hydroxyvitamin D.
13. The method of claim 12 , wherein the method lowers the serum parathyroid hormone levels in the cancer patient by at least 30%.
14. The method of claim 12 , wherein the method stabilizes the serum calcium levels in a range of about 8.3 mg/dL and about 11.6 mg/dL, corrected for serum albumin.
15. The method of claim 12 , wherein the agent that increases the risk of hypocalcemia is an antiresorptive agent.
16. The method of claim 12 , wherein the patient is a cancer patient.
17. The method of claim 12 , wherein the pharmaceutical formulation comprising a 25-hydroxyvitamin D compound is a modified release pharmaceutical formulation.
18. The method of claim 17 , wherein the modified release pharmaceutical formulation is a controlled release pharmaceutical formulation, optionally an oral controlled release pharmaceutical formulation.
19. The method of claim 17 , wherein the pharmaceutical formulation comprises 25-hydroxyvitamin D in an oral modified release formulation, optionally a controlled release formulation.
20. The method of claim 12 , wherein the 25-hydroxyvitamin D comprises 25-hydroxyvitamin D3, 25-hydroxyvitamin D2, or a combination thereof.
21. A method of treating a patient at risk for hypocalcemia wherein the patient is treated with an agent that increases the risk of hypocalcemia, comprising administering to the patient 25-hydroxyvitamin D in an amount effective to restore and maintain blood 25(OH)D levels to at least 30 ng/mL.
22. The method of claim 8 , comprising administering the 25-hydroxyvitamin D compound to safely increase the patient's serum total 25-hydroxyvitamin D level to in a range of about 50 ng/mL to about 100 ng/mL.
23. The method of claim 12 , comprising administering the 25-hydroxyvitamin D compound to safely increase the patient's serum total 25-hydroxyvitamin D level to in a range of about 50 ng/mL to about 100 ng/mL.
24. The method of claim 21 , comprising administering the 25-hydroxyvitamin D compound to safely increase the patient's serum total 25-hydroxyvitamin D level to in a range of about 50 ng/mL to about 100 ng/mL.