TY - JOUR
T1 - Long-term prevention of skeletal complications of metastatic breast cancer with pamidronate
AU - Hortobagyi, Gabriel N.
AU - Theriault, Richard L.
AU - Lipton, Allan
AU - Porter, Lester
AU - Blayney, Douglas
AU - Sinoff, Clive
AU - Wheeler, Helen
AU - Simeone, Joseph F.
AU - Seaman, John J.
AU - Knight, Robert D.
AU - Heffernan, Maika
AU - Mellars, Kathleen
AU - Reitsma, Dirk J.
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1998/6
Y1 - 1998/6
N2 - Purpose Pamidronate, an aminobisphosphonate, has been shown to lower the risk of skeletal complications associated with lytic bone lesions for up to 1 year in women with stage IV breast cancer who received chemotherapy. We studied the long-term effectiveness and safety of continued treatment with intravenous pamidronate infusions for up to 2 years. Patients and Methods: Three hundred eight-two women with metastatic breast cancer and lytic bone lesions who received chemotherapy were randomly assigned to receive either 90 mg of pamidronate or placebo intravenously every 3 to 4 weeks in this double- blind, multicenter, parallel-group trial. Patients were evaluated monthly for 2 years for skeletal complications, which included pathologic fractures, need for radiation or surgery to treat bone complications, spinal cord compression, and hypercalcemia. Bone pain, analgesic use, bone biochemical markers, performance status, quality of life, radiologic response in bone, and survival were also evaluated. Results: As in the first, year of treatment, the proportion of patients with any skeletal complications was significantly less for the pamidronate than the placebo group of 15, 18, 21, and 24 months (P<.001). The proportions of patients with any pathologic fracture (ie, vertebral and nonvertebral fractures), need for radiation or surgery to treat bone complications, and hypercalcemia were also statistically less for the pamidronate than the placebo group. The median time to the first skeletal complication was 13.9 months in the pamidronate- treated women and 7.0 months in the placebo group (P<.001). Long-term treatment did not result in any unexpected adverse events. Survival did not differ between the two groups. Conclusion: The risk for osteolytic bone lesion complications in metastatic breast cancer was significantly decreased with monthly infusions of 90 mg of pamidronate, and this effect was maintained for at least 2 years. Pamidronate is a useful adjunct to standard chemotherapy in the palliative treatment of metastatic breast cancer.
AB - Purpose Pamidronate, an aminobisphosphonate, has been shown to lower the risk of skeletal complications associated with lytic bone lesions for up to 1 year in women with stage IV breast cancer who received chemotherapy. We studied the long-term effectiveness and safety of continued treatment with intravenous pamidronate infusions for up to 2 years. Patients and Methods: Three hundred eight-two women with metastatic breast cancer and lytic bone lesions who received chemotherapy were randomly assigned to receive either 90 mg of pamidronate or placebo intravenously every 3 to 4 weeks in this double- blind, multicenter, parallel-group trial. Patients were evaluated monthly for 2 years for skeletal complications, which included pathologic fractures, need for radiation or surgery to treat bone complications, spinal cord compression, and hypercalcemia. Bone pain, analgesic use, bone biochemical markers, performance status, quality of life, radiologic response in bone, and survival were also evaluated. Results: As in the first, year of treatment, the proportion of patients with any skeletal complications was significantly less for the pamidronate than the placebo group of 15, 18, 21, and 24 months (P<.001). The proportions of patients with any pathologic fracture (ie, vertebral and nonvertebral fractures), need for radiation or surgery to treat bone complications, and hypercalcemia were also statistically less for the pamidronate than the placebo group. The median time to the first skeletal complication was 13.9 months in the pamidronate- treated women and 7.0 months in the placebo group (P<.001). Long-term treatment did not result in any unexpected adverse events. Survival did not differ between the two groups. Conclusion: The risk for osteolytic bone lesion complications in metastatic breast cancer was significantly decreased with monthly infusions of 90 mg of pamidronate, and this effect was maintained for at least 2 years. Pamidronate is a useful adjunct to standard chemotherapy in the palliative treatment of metastatic breast cancer.
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U2 - 10.1200/JCO.1998.16.6.2038
DO - 10.1200/JCO.1998.16.6.2038
M3 - Article
C2 - 9626201
AN - SCOPUS:7144223389
SN - 0732-183X
VL - 16
SP - 2038
EP - 2044
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 6
ER -