Journal of Clinical Oncology, Vol 11, 491-498, Copyright © 1993 by American Society of Clinical Oncology
Palliative pamidronate treatment in patients with bone metastases from breast cancer
AT van Holten-Verzantvoort, HM Kroon, OL Bijvoet, FJ Cleton, LV Beex, G Blijham, J Hermans, JP Neijt, SE Papapoulos and HP Sleeboom
Department of Clinical Oncology, Leiden University Hospital, The Netherlands.
PURPOSE: An open, randomized study was performed to assess the effects of
supportive pamidronate treatment on morbidity from bone metastases in
breast cancer patients. PATIENTS AND METHODS: Eighty-one pamidronate
patients and 80 control patients were monitored for a median of 18 and 21
months, respectively, for events of skeletal morbidity and the radiologic
course of metastatic bone disease. The oral pamidronate dose was 600 mg/d
(high dose [HD]) during the earliest study years, then changed to 300 mg/d
(low dose [LD]) because of gastrointestinal toxicity. Twenty-nine of 81
pamidronate (HD/LD) patients first received 600 mg/d and were then changed
to 300 mg/d; 52 of 81 pamidronate LD patients received 300 mg/d throughout
the study. Tumor treatment was unrestricted. RESULTS: An overall
intent-to-treat analysis was performed. In the pamidronate group, the
occurrence of hypercalcemia, severe bone pain, and symptomatic impending
fractures decreased by 65%, 30%, and 50%, respectively; event-rates of
systemic treatment and radiotherapy decreased by 35% (P < or = .02). The
event-free period (EFP), radiologic course of disease, and survival did not
improve. Subgroup analyses suggested a dose-dependent treatment effect.
Compared with their controls, in pamidronate HD/LD patients, events
occurred 60% to 90% less frequently (P < or = .03) and the EFP was
prolonged (P = .002). In pamidronate LD patients, event-rates decreased by
15% to 45% (P < or = .04). Gastrointestinal toxicity of pamidronate
caused a 23% drop-out rate, but other cancer-associated factors seemed to
contribute to this toxicity. CONCLUSION: Pamidronate treatment of breast
cancer patients efficaciously reduced skeletal morbidity. The effect
appeared to be dose-dependent. Further research on dose and mode of
treatment is mandatory.

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