Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2407-14-592
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dc.titleComparative effectiveness of approved first-line anti-angiogenic and molecularly targeted therapeutic agents in the treatment of good and intermediate risk metastatic clear cell renal cell carcinoma
dc.contributor.authorHaaland, B
dc.contributor.authorChopra, A
dc.contributor.authorAcharyya, S
dc.contributor.authorFay, A.P
dc.contributor.authorLopes, G.L
dc.date.accessioned2020-10-27T11:11:13Z
dc.date.available2020-10-27T11:11:13Z
dc.date.issued2014
dc.identifier.citationHaaland, B, Chopra, A, Acharyya, S, Fay, A.P, Lopes, G.L (2014). Comparative effectiveness of approved first-line anti-angiogenic and molecularly targeted therapeutic agents in the treatment of good and intermediate risk metastatic clear cell renal cell carcinoma. BMC Cancer 14 (1) : 592. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2407-14-592
dc.identifier.issn14712407
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181520
dc.description.abstractBackground: Based on improved clinical outcomes in randomized controlled clinical trials (RCTs) the FDA and EMA have approved bevacizumab with interferon, sunitinib, and pazopanib in the first-line treatment of low to intermediate risk metastatic clear cell renal cell carcinoma (mRCC). However, there is little comparative data to help in choosing the most effective drug among these agents. Methods: We performed an indirect comparative effectiveness analysis of the pivotal RCTs of bevacizumab with interferon, sunitinib, or pazopanib compared to one another or interferon alone in first-line treatment of metastatic or advanced RCC. Endpoints of interest were overall survival (OS), progression free survival (PFS), and response rate (RR). Adverse events were also examined. Results: The meta-estimate of the hazard ratio (95% confidence interval) for OS for bevacizumab with interferon vs. interferon alone was 0.86 (0.76-0.97), for sunitinib vs. interferon alone was 0.82 (0.67-1.00), for pazopanib vs. interferon alone was 0.74 (0.57-0.97), for sunitinib vs. bevacizumab with interferon was 0.95 (0.75-1.20), for pazopanib vs. bevacizumab with interferon was 0.86 (0.64-1.16), and for pazopanib vs. sunitinib was 0.91 (0.76-1.08). Similarly, bevacizumab with interferon, sunitinib, or pazopanib had better PFS and RR than interferon alone. Sunitinib and pazopanib had better RR than bevacizumab with interferon and there was suggestive evidence pazopanib may outperform sunitinib in terms of RR. Conclusions: Bevacizumab with interferon, sunitinib, and pazopanib are adequate first-line options in treatment of mRCC. Interferon alone should not be considered an optimal first-line treatment. © 2014 Haaland et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectbevacizumab
dc.subjectinterferon
dc.subjectpazopanib
dc.subjectsunitinib
dc.subjectangiogenesis inhibitor
dc.subjectantineoplastic agent
dc.subjectbevacizumab
dc.subjectindole derivative
dc.subjectinterferon
dc.subjectmonoclonal antibody
dc.subjectpazopanib
dc.subjectpyrimidine derivative
dc.subjectpyrrole derivative
dc.subjectsulfonamide
dc.subjectsunitinib
dc.subjectanemia
dc.subjectanorexia
dc.subjectArticle
dc.subjectasthenia
dc.subjectcancer risk
dc.subjectcomparative study
dc.subjectdiarrhea
dc.subjectdrug efficacy
dc.subjectdrug safety
dc.subjectdrug withdrawal
dc.subjectdyspnea
dc.subjectfatigue
dc.subjectfever
dc.subjectheadache
dc.subjecthuman
dc.subjecthypertension
dc.subjectkidney carcinoma
dc.subjectloss of appetite
dc.subjectmetastatic clear cell renal cell carcinoma
dc.subjectmetastatic clear cell renal cell carcinoma
dc.subjectnausea
dc.subjectneutropenia
dc.subjectoverall survival
dc.subjectprogression free survival
dc.subjectproteinuria
dc.subjectrandomized controlled trial (topic)
dc.subjectside effect
dc.subjectsystematic review
dc.subjectthrombocytopenia
dc.subjectthyroid disease
dc.subjecttreatment outcome
dc.subjecttreatment response
dc.subjectCarcinoma, Renal Cell
dc.subjectKidney Neoplasms
dc.subjectmeta analysis
dc.subjectmolecularly targeted therapy
dc.subjectNeoplasm Metastasis
dc.subjectsurvival
dc.subjectAngiogenesis Inhibitors
dc.subjectAntibodies, Monoclonal, Humanized
dc.subjectAntineoplastic Agents
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectCarcinoma, Renal Cell
dc.subjectHumans
dc.subjectIndoles
dc.subjectInterferons
dc.subjectKidney Neoplasms
dc.subjectMolecular Targeted Therapy
dc.subjectNeoplasm Metastasis
dc.subjectPyrimidines
dc.subjectPyrroles
dc.subjectRandomized Controlled Trials as Topic
dc.subjectSulfonamides
dc.subjectSurvival Analysis
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1186/1471-2407-14-592
dc.description.sourcetitleBMC Cancer
dc.description.volume14
dc.description.issue1
dc.description.page592
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