Pain Outcomes in Patients With Advanced Breast Cancer and Bone Metastases Results From a Randomized, Double-Blind Study of Denosumab and Zoledronic Acid

被引:105
|
作者
Cleeland, Charles S. [1 ]
Body, Jean-Jacques [2 ]
Stopeck, Alison [3 ]
von Moos, Roger [4 ]
Fallowfield, Lesley [5 ]
Mathias, Susan D. [6 ]
Patrick, Donald L. [7 ]
Clemons, Mark [8 ]
Tonkin, Katia [9 ]
Masuda, Norikazu [10 ]
Lipton, Allan [11 ]
de Boer, Richard [12 ]
Salvagni, Stefania [13 ]
Oliveira, Celia Tosello [14 ]
Qian, Yi [15 ]
Jiang, Qi [15 ]
Dansey, Roger [16 ]
Braun, Ada [16 ]
Chung, Karen [17 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Symptom Res, Houston, TX 77030 USA
[2] Brugmann Univ Hosp, Dept Med, Brussels, Belgium
[3] Univ Arizona, Arizona Canc Ctr, Dept Hematol & Oncol, Tucson, AZ USA
[4] Cantonal Hosp Graubunden, Dept Hematol & Oncol, Chur, Switzerland
[5] Univ Sussex, Sussex Hlth Outcomes Res & Educ Canc SHORE C, Brighton, E Sussex, England
[6] Hlth Outcomes Solut, Winter Pk, FL USA
[7] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA
[8] Ottawa Hosp Canc Ctr, Div Med Oncol, Ottawa, ON, Canada
[9] Cross Canc Inst, Div Med Oncol, Edmonton, AB T6G 1Z2, Canada
[10] Osaka Natl Hosp, Dept Surg, Breast Oncol Unit, Osaka, Japan
[11] Penn State Milton S Hershey Med Ctr, Dept Hematol & Oncol, Hershey, PA USA
[12] Western & Royal Melbourne Hosp, Dept Med Oncol, Melbourne, Vic, Australia
[13] Univ Hosp Parma, Div Med Oncol, Parma, Italy
[14] Brazilian Inst Canc Control, Dept Clin Oncol, Sao Paulo, Brazil
[15] Amgen Inc, Dept Biostat & Epidemiol, Thousand Oaks, CA 91320 USA
[16] Amgen Inc, Dept Hematol Oncol, Thousand Oaks, CA 91320 USA
[17] Amgen Inc, Dept Global Hlth Econ, Thousand Oaks, CA 91320 USA
关键词
RANK ligand; denosumab; clinical trial; zoledronic acid; breast neoplasms; pain; analgesics; QUALITY-OF-LIFE; SKELETAL METASTASES; MULTIPLE-MYELOMA; PHASE-III; SEVERITY; SAFETY;
D O I
10.1002/cncr.27789
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: In this study, the authors evaluated the effect of denosumab versus zoledronic acid (ZA) on pain in patients with advanced breast cancer and bone metastases. METHODS: The prevention of pain, reduction in pain interference with daily life activities, and the proportion of patients requiring strong opioid analgesics were assessed in a randomized, double-blind, double-dummy phase 3 study comparing denosumab with ZA for preventing skeletal-related events in 2046 patients who had breast cancer and bone metastases. Patients completed the Brief Pain Inventory-Short Form at baseline and monthly thereafter. RESULTS: Fewer patients who received denosumab reported a clinically meaningful worsening of pain severity (2-point increase) from baseline compared with patients who received ZA, and a trend was observed toward delayed time to pain worsening with denosumab versus ZA (denosumab, 8.5 months; ZA, 7.4 months; P = .08). In patients who had no/mild pain at baseline, a 4-month delay in progression to moderate/severe pain was observed with denosumab compared with ZA (9.7 months vs 5.8 months; P = .002). Denosumab delayed the time to increased pain interference by approximately 1 month compared with ZA (denosumab, 16.0 months; ZA, 14.9 months; P = .09). The time to pain improvement (P = .72) and the time to decreased pain interference (P = .92) were similar between the groups. Fewer denosumab-treated patients reported increased analgesic use from no/low use at baseline to strong opioid use. CONCLUSIONS: Denosumab demonstrated improved pain prevention and comparable pain palliation compared with ZA. In addition, fewer denosumab-treated patients shifted to strong opioid analgesic use. Cancer 2013. (c) 2012 American Cancer Society.
引用
收藏
页码:832 / 838
页数:7
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