Please use this identifier to cite or link to this item:
https://doi.org/10.1186/1471-2407-14-592
DC Field | Value | |
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dc.title | 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 | |
dc.contributor.author | Haaland, B | |
dc.contributor.author | Chopra, A | |
dc.contributor.author | Acharyya, S | |
dc.contributor.author | Fay, A.P | |
dc.contributor.author | Lopes, G.L | |
dc.date.accessioned | 2020-10-27T11:11:13Z | |
dc.date.available | 2020-10-27T11:11:13Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Haaland, 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.issn | 14712407 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/181520 | |
dc.description.abstract | Background: 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.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | bevacizumab | |
dc.subject | interferon | |
dc.subject | pazopanib | |
dc.subject | sunitinib | |
dc.subject | angiogenesis inhibitor | |
dc.subject | antineoplastic agent | |
dc.subject | bevacizumab | |
dc.subject | indole derivative | |
dc.subject | interferon | |
dc.subject | monoclonal antibody | |
dc.subject | pazopanib | |
dc.subject | pyrimidine derivative | |
dc.subject | pyrrole derivative | |
dc.subject | sulfonamide | |
dc.subject | sunitinib | |
dc.subject | anemia | |
dc.subject | anorexia | |
dc.subject | Article | |
dc.subject | asthenia | |
dc.subject | cancer risk | |
dc.subject | comparative study | |
dc.subject | diarrhea | |
dc.subject | drug efficacy | |
dc.subject | drug safety | |
dc.subject | drug withdrawal | |
dc.subject | dyspnea | |
dc.subject | fatigue | |
dc.subject | fever | |
dc.subject | headache | |
dc.subject | human | |
dc.subject | hypertension | |
dc.subject | kidney carcinoma | |
dc.subject | loss of appetite | |
dc.subject | metastatic clear cell renal cell carcinoma | |
dc.subject | metastatic clear cell renal cell carcinoma | |
dc.subject | nausea | |
dc.subject | neutropenia | |
dc.subject | overall survival | |
dc.subject | progression free survival | |
dc.subject | proteinuria | |
dc.subject | randomized controlled trial (topic) | |
dc.subject | side effect | |
dc.subject | systematic review | |
dc.subject | thrombocytopenia | |
dc.subject | thyroid disease | |
dc.subject | treatment outcome | |
dc.subject | treatment response | |
dc.subject | Carcinoma, Renal Cell | |
dc.subject | Kidney Neoplasms | |
dc.subject | meta analysis | |
dc.subject | molecularly targeted therapy | |
dc.subject | Neoplasm Metastasis | |
dc.subject | survival | |
dc.subject | Angiogenesis Inhibitors | |
dc.subject | Antibodies, Monoclonal, Humanized | |
dc.subject | Antineoplastic Agents | |
dc.subject | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject | Carcinoma, Renal Cell | |
dc.subject | Humans | |
dc.subject | Indoles | |
dc.subject | Interferons | |
dc.subject | Kidney Neoplasms | |
dc.subject | Molecular Targeted Therapy | |
dc.subject | Neoplasm Metastasis | |
dc.subject | Pyrimidines | |
dc.subject | Pyrroles | |
dc.subject | Randomized Controlled Trials as Topic | |
dc.subject | Sulfonamides | |
dc.subject | Survival Analysis | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1186/1471-2407-14-592 | |
dc.description.sourcetitle | BMC Cancer | |
dc.description.volume | 14 | |
dc.description.issue | 1 | |
dc.description.page | 592 | |
Appears in Collections: | Elements Staff Publications |
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