2015
DOI: 10.3111/13696998.2015.1105230
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Comparative net cost impact of the utilization of panitumumab versus cetuximab for the treatment of patients with metastatic colorectal cancer in Canada

Abstract: Treating chemorefractory mCRC patients with panitumumab rather than cetuximab reduced healthcare resource costs. Provincial healthcare savings achieved with the use of panitumumab could potentially be re-allocated to other cancer treatments, although further study would be needed to validate this assumption.

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Cited by 6 publications
(3 citation statements)
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“…Other targeted molecular therapies include the use of drugs that inhibit the endothelial growth factor receptor (EGFR)-related factors to control tumour cell proliferation and differentiation. These drugs include cetuximab and panitumumab [117,118].…”
Section: Monoclonal Antibodies and Avastinmentioning
confidence: 99%
“…Other targeted molecular therapies include the use of drugs that inhibit the endothelial growth factor receptor (EGFR)-related factors to control tumour cell proliferation and differentiation. These drugs include cetuximab and panitumumab [117,118].…”
Section: Monoclonal Antibodies and Avastinmentioning
confidence: 99%
“…This kind of analysis is performed when the health-related quality of life (HRQOL) is considered an important outcome. 24 Some studies addressed and compared the costs [25][26][27][28] or effectiveness [29][30][31][32] of the drugs investigated in this study separately. Some others investigated the cost-effectiveness of various drug combinations used in the treatment of stage IV colorectal cancer (not the drug combinations examined in the present study).…”
Section: Introductionmentioning
confidence: 99%
“…Current targeted drugs can be roughly divided into the following categories: (1) drugs that inhibit VEGF-related factors to reduce angiopoiesis, including bevacizumab [6], cediranib [7], axitinib [8], and sorafenib [9]; (2) drugs that inhibit EGFR-related factors to control tumor cell proliferation and differentiation, including cetuximab [10], panitumumab [11], and gefitinib [12]; (3) drugs that inhibit angiopoietin, including sunitinib [13], celecoxib [14], and trebananib [15]; and (4) drugs that inhibit tumor proliferation though other relevant pathways, e.g. conatumumab causes apoptosis of cancer cells by targeting DR5 [16] and ganitumab inhibits tumor cell proliferation by inhibiting IGF signaling [17].…”
Section: Introductionmentioning
confidence: 99%