Systematic Literature Review and Network Meta-Analysis Comparing Bone-Targeted Agents for the Prevention of Skeletal-Related Events in Cancer Patients With Bone Metastasis

被引:39
作者
Wang, Zhiyu [1 ]
Qiao, Dan [1 ]
Lu, Yaohong [1 ]
Curtis, Dana [2 ]
Wen, Xiaoting [1 ]
Yao, Yang [1 ]
Zhao, Hui [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Internal Oncol, Shanghai 200233, Peoples R China
[2] Thomas Jefferson Univ, Radiat Oncol, Philadelphia, PA 19107 USA
关键词
Bisphosphonates; Denosumab; Skeletal-related events; Bone metastasis; Network meta-analysis; LONG-TERM EFFICACY; ADVANCED BREAST-CANCER; QUALITY-OF-LIFE; ZOLEDRONIC ACID; DOUBLE-BLIND; PROSTATE-CANCER; PHASE-III; PAMIDRONATE DISODIUM; MULTIPLE-MYELOMA; SOLID TUMORS;
D O I
10.1634/theoncologist.2014-0328
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Complications from skeletal-related events (SREs) constitute a challenge in the care of cancer patients with bone metastasis (BM). Objectives. This study evaluated the comparative effectiveness of pamidronate, ibandronate, zoledronate, and denosumab in reducing the morbidity of SREs in cancer patients with BM. Methods. Medline (1948 to January 2014), Embase (1980 to January 2014), the Cochrane Library (2014 issue 1), and Web of Science with Conference Proceedings (1970 to January 2014) were searched. Only randomized controlled trials assessing denosumab, bisphosphonates, or placebo in cancer patients with BM were included. The primary outcomes were SREs and SREs by type. The network meta-analysis (NMA) was performed with a random-effects Bayesian model. Results. The NMA included 14 trials with 10,192 patients. Denosumab was superior to placebo in reducing the risk of SREs (odds ratio [OR]: 0.49; 95% confidence interval [CI]: 0.31-0.75), followed by zoledronate (OR: 0.57; 95% CI: 0.41-0.77) and pamidronate (OR: 0.55; 95% CI: 0.41-0.72). lbandronate compared with placebo could not reduce the risk of SREs. Denosumab was superior to placebo in reducing the risk of pathologic fractures (OR: 0.50; 95% CI: 0.32-0.79), followed by zoledronate (OR: 0.61; 95% CI: 0.43-0.86). Denosumab was superior to placebo in reducing the risk of radiation (OR: 0.51; 95% CI: 0.35-0.75), followed by pamidronate (OR: 0.67; 95% CI: 0.52-0.86) and zoledronate (OR: 0.70; 95% CI: 0.52-0.96). Conclusion. This NMA showed that denosumab, zoledronate, and pamidronate were generally effective in preventing SREs in cancer patients with BM. Denosumab and zoledronate were also associated with reductions in the risk of pathologic fractures and radiation compared with placebo. Denosumab was shown to be the most effective of the bone-targeted agents.
引用
收藏
页码:440 / 449
页数:10
相关论文
共 62 条
  • [1] Bayesian methods for evidence synthesis in cost-effectiveness analysis
    Ades, AE
    Sculpher, M
    Sutton, A
    Abrams, K
    Cooper, N
    Welton, N
    Lu, GB
    [J]. PHARMACOECONOMICS, 2006, 24 (01) : 1 - 19
  • [2] Efficacy and safety of 12-weekly versus 4-weekly zoledronic acid for prolonged treatment of patients with bone metastases from breast cancer (ZOOM): a phase 3, open-label, randomised, non-inferiority trial
    Amadori, Dino
    Aglietta, Massimo
    Alessi, Barbara
    Gianni, Lorenzo
    Ibrahim, Toni
    Farina, Gabriella
    Gaion, Fernando
    Bertoldo, Francesco
    Santini, Daniele
    Rondena, Roberta
    Bogani, Paola
    Ripamonti, Carla I.
    [J]. LANCET ONCOLOGY, 2013, 14 (07) : 663 - 670
  • [3] Understanding heterogeneity in meta-analysis: the role of meta-regression
    Baker, W. L.
    White, C. Michael
    Cappelleri, J. C.
    Kluger, J.
    Coleman, C. I.
    [J]. INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2009, 63 (10) : 1426 - 1434
  • [4] Oral ibandronic acid versus intravenous zoledronic acid in treatment of bone metastases from breast cancer: a randomised, open label, non-inferiority phase 3 trial
    Barrett-Lee, Peter
    Casbard, Angela
    Abraham, Jacinta
    Hood, Kerenza
    Coleman, Robert
    Simmonds, Peter
    Timmins, Hayley
    Wheatley, Duncan
    Grieve, Robert
    Griffithst, Gareth
    Murray, Nick
    [J]. LANCET ONCOLOGY, 2014, 15 (01) : 114 - 122
  • [5] Berenson JR, 2001, CANCER, V91, P1191, DOI 10.1002/1097-0142(20010401)91:7<1191::AID-CNCR1119>3.0.CO
  • [6] 2-0
  • [7] A study of the biological receptor activator of nuclear factor-κB ligand inhibitor, denosumab, in patients with multiple myeloma or bone metastases from breast cancer
    Body, JJ
    Facon, T
    Coleman, RE
    Lipton, A
    Geurs, F
    Fan, M
    Holloway, D
    Peterson, MC
    Bekker, P
    [J]. CLINICAL CANCER RESEARCH, 2006, 12 (04) : 1221 - 1228
  • [8] Oral ibandronate reduces the risk of skeletal complications in breast cancer patients with metastatic bone disease: results from two randomised, placebo-controlled phase III studies
    Body, JJ
    Diel, IJ
    Lichinitzer, M
    Lazarev, A
    Pecherstorfer, M
    Bell, R
    Tripathy, D
    Bergstronn, B
    [J]. BRITISH JOURNAL OF CANCER, 2004, 90 (06) : 1133 - 1137
  • [9] Intravenous ibandronate reduces the incidence of skeletal complications in patients with breast cancer and bone metastases
    Body, JJ
    Diel, IJ
    Lichinitser, MR
    Kreuser, ED
    Dornoff, W
    Gorbunova, VA
    Budde, M
    Bergström, B
    [J]. ANNALS OF ONCOLOGY, 2003, 14 (09) : 1399 - 1405
  • [10] The results of direct and indirect treatment comparisons in meta-analysis of randomized controlled trials
    Bucher, HC
    Guyatt, GH
    Griffith, LE
    Walter, SD
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 1997, 50 (06) : 683 - 691