Reduces morbidity from skeletal metastases in breast cancer patients during long-term bisphosphonate (apd) treatment

Publication date

1987-10-31

Authors

Holten-Verzantvoort, A.Th. van
Bijvoet, O.L.M.
Hermans, J.
Harinck, H.I.J.
Elte, J.W.F.
Beex, L.V.A.M.
Cleton, F.J.
Kroon, H.M.
Vermey, P.
Neijt, J.P.

Editors

Advisors

Supervisors

DOI

Document Type

Article
Open Access logo

License

Abstract

131 patients with osteolytic metastases from breast cancer were randomised to receive long-term oral treatment with aminohydroxy-propylidene-bisphosphonate (APD), 300 mg daily (n = 70), or to act as controls (n = 61) in a multicentre trial. Specific antitumour therapy was at the discretion of the clinician and variable. An interim analysis was made after a median follow-up of 13 months in the APD group and 14 months in the controls. There was a significant reduction in pathological fractures and severe bone pain in the APD group, and hypercalcaemia was prevented. Consequently the necessity for radiotherapy for skeletal complications was more than halved; the number of systemic therapy changes was also reduced. Gastrointestinal side-effects of APD led to a drop-out of 8% of patients. Oral supportive APD therapy is simple and convenient, and significantly reduces skeletal morbidity in advanced breast cancer.

Keywords

Citation