TY - JOUR
T1 - Treatment persistence with monthly zoledronic acid is associated with lower risk and frequency of skeletal complications in patients with breast cancer and bone metastasis
AU - Hatoum, Hind T.
AU - Lin, Swu Jane
AU - Smith, Matthew R.
AU - Guo, Amy
AU - Lipton, Allan
N1 - Funding Information:
The study was supported by Novartis Pharmaceuticals Corporation. H.T. Hatoum is a paid consultant to Novartis Pharmaceuticals Corporation, the marketer of ZA. S. Lin is a consultant to H.T. Hatoum & Company. M.R. Smith and A. Lipton act in an advisory capacity to Novartis, and A. Lipton has received laboratory research funding and provided expert testimony for Novartis. A. Guo is an employee of Novartis. The authors had full control of the findings and results presented without any oversight or interference from the sponsor of the work.
PY - 2011/6
Y1 - 2011/6
N2 - Background: Zoledronic acid (ZA) reduces skeletal complications in breast cancer patients with bone metastases. This study explored relationships between ZA treatment persistence and patient outcomes. Methods: Two thousand three hundred ninety-four female patients with breast cancer and bone metastasis were identified from the PharMetrics® Integrated Database between January 2003 and October 2006. Of these women, 714 (29.7%) received ZA; the remainder received no intravenous (IV) bisphosphonate (untreated). ZA treatment persistence was measured from first treatment to the first treatment gap > 45 days. Treatment persistence was categorized as short ( ≤ 90 days, n = 230), medium (91-180 days, n = 171), or long ( > 180 days, n = 313). Relationships between ZA treatment and persistence on outcomes were assessed in regression models adjusted for age, comorbidities, and propensity to receive treatment. Results: Compared with untreated patients, after multivariate adjustment, ZA-treated patients experienced a 25% lower rate of skeletal complications (P < .05), were at lower risk for skeletal complications or loss to follow-up (hazard ratio [HR] = 0.67; P < .001), and had 41% longer follow-up time (P < .001). The skeletal complication risk was lower in the long-persistence group than in the short-persistence group (HR = 0.576; P < .05). In patients with ≤ 1 skeletal complication, the long-persistence group had 39% fewer skeletal complications than the short-persistence group (P < .01). The mediumand long-persistence groups had 40% and 139% longer follow-up than the short-persistence group (both P < .001). Conclusions: ZA treatment was associated with lower risk and frequency of skeletal complications and longer follow-up time. Greater persistence with ZA treatment was associated with better outcomes.
AB - Background: Zoledronic acid (ZA) reduces skeletal complications in breast cancer patients with bone metastases. This study explored relationships between ZA treatment persistence and patient outcomes. Methods: Two thousand three hundred ninety-four female patients with breast cancer and bone metastasis were identified from the PharMetrics® Integrated Database between January 2003 and October 2006. Of these women, 714 (29.7%) received ZA; the remainder received no intravenous (IV) bisphosphonate (untreated). ZA treatment persistence was measured from first treatment to the first treatment gap > 45 days. Treatment persistence was categorized as short ( ≤ 90 days, n = 230), medium (91-180 days, n = 171), or long ( > 180 days, n = 313). Relationships between ZA treatment and persistence on outcomes were assessed in regression models adjusted for age, comorbidities, and propensity to receive treatment. Results: Compared with untreated patients, after multivariate adjustment, ZA-treated patients experienced a 25% lower rate of skeletal complications (P < .05), were at lower risk for skeletal complications or loss to follow-up (hazard ratio [HR] = 0.67; P < .001), and had 41% longer follow-up time (P < .001). The skeletal complication risk was lower in the long-persistence group than in the short-persistence group (HR = 0.576; P < .05). In patients with ≤ 1 skeletal complication, the long-persistence group had 39% fewer skeletal complications than the short-persistence group (P < .01). The mediumand long-persistence groups had 40% and 139% longer follow-up than the short-persistence group (both P < .001). Conclusions: ZA treatment was associated with lower risk and frequency of skeletal complications and longer follow-up time. Greater persistence with ZA treatment was associated with better outcomes.
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U2 - 10.1016/j.clbc.2011.03.015
DO - 10.1016/j.clbc.2011.03.015
M3 - Article
C2 - 21665138
AN - SCOPUS:80053402464
SN - 1526-8209
VL - 11
SP - 177
EP - 183
JO - Clinical Breast Cancer
JF - Clinical Breast Cancer
IS - 3
ER -