Journal of Clinical Oncology, Vol 11, 1618-1623, Copyright © 1993 by American Society of Clinical Oncology
Dose-response study of alendronate sodium for the treatment of cancer- associated hypercalcemia
SR Nussbaum, RP Warrell Jr, R Rude, J Glusman, JP Bilezikian, AF Stewart, M Stepanavage, JF Sacco, SD Averbuch and BJ Gertz
Harvard Medical School, Boston, MA.
PURPOSE: A randomized, double-blind, dose-ranging study of single-dose
intravenous (IV) therapy with alendronate sodium (aminohydroxybutylidene
bisphosphonate) was performed in patients with cancer-associated
hypercalcemia. PATIENTS AND METHODS: Patients with hypercalcemia who had
not received antitumor therapy in the preceding 7 days were treated with 48
hours of IV hydration. Patients with persistent hypercalcemia
(albumin-corrected serum calcium concentration [CSCC] > or = 11.5 mg/dL)
were randomly assigned to receive 2.5, 5, 10, or 15 mg of alendronate
infused over 2 hours, or 10 mg of alendronate infused over 24 hours.
Fifty-nine patients were treated and 50 patients were assessable for the
dose-response relationship. RESULTS: Normalization of CSCC (< or = 10.5
mg/dL) was achieved in 22%, 82%, 75%, and 90% of assessable patients in the
2.5-, 5-, 10- (2- and 24- hour groups pooled), and 15-mg dose groups,
respectively, within 8 days of therapy. Doses > or = 5 mg were
significantly superior to the 2.5-mg dose level (P < .05). There was no
significant difference in the minimum CSCC achieved between the 2- and
24-hour infusions of the 10-mg dose. Based on an intent-to-treat analysis
of all randomized patients, the overall complete response rate was 74% for
dose levels greater than 2.5 mg. For assessable patients who responded to
> or = 5 mg of alendronate, the estimated median duration of
normocalcemia was 10 days (range, 1 to 25). The estimated median time to
relapse (CSCC > 11.5 mg/dL) was 15 days from initial treatment and 12
days from initial response, respectively. Adverse events included a
transient febrile response in 34% of patients and eight episodes of
reversible elevations in serum transaminase levels among treated patients.
CONCLUSION: While a statistically significant dose-response relationship
was not clearly evident at doses greater than 5 mg, single doses of > or
= 5 mg alendronate sodium effectively lowered serum calcium concentrations
and were well tolerated in the treatment of cancer-associated
hypercalcemia.