A Systematic Review and Meta-analysis Comparing the Effectiveness and Adverse Effects of Different Systemic Treatments for Non-clear Cell Renal Cell Carcinoma
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, metaanalýza, přehledy, systematický přehled
PubMed
27939075
DOI
10.1016/j.eururo.2016.11.020
PII: S0302-2838(16)30853-3
Knihovny.cz E-zdroje
- Klíčová slova
- Chromophobe, Everolimus, Non-clear cell renal cell carcinoma, Papillary, Sunitinib, Systematic review,
- MeSH
- anilidy terapeutické užití MeSH
- axitinib MeSH
- benzimidazoly terapeutické užití MeSH
- bevacizumab terapeutické užití MeSH
- chinoliny terapeutické užití MeSH
- chinolony terapeutické užití MeSH
- erlotinib terapeutické užití MeSH
- everolimus terapeutické užití MeSH
- fenylmočovinové sloučeniny terapeutické užití MeSH
- imidazoly terapeutické užití MeSH
- indazoly terapeutické užití MeSH
- indoly terapeutické užití MeSH
- interferony terapeutické užití MeSH
- interleukin-2 terapeutické užití MeSH
- karcinom z renálních buněk farmakoterapie patologie MeSH
- lidé MeSH
- nádory ledvin farmakoterapie patologie MeSH
- niacinamid analogy a deriváty terapeutické užití MeSH
- přežití bez známek nemoci MeSH
- protinádorové látky terapeutické užití MeSH
- pyridiny terapeutické užití MeSH
- pyrimidiny terapeutické užití MeSH
- pyrrolidinony terapeutické užití MeSH
- pyrroly terapeutické užití MeSH
- sirolimus analogy a deriváty terapeutické užití MeSH
- sorafenib MeSH
- srovnávací výzkum účinnosti MeSH
- sulfonamidy terapeutické užití MeSH
- sunitinib MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- přehledy MeSH
- systematický přehled MeSH
- Názvy látek
- 4-amino-5-fluoro-3-(5-(4-methylpiperazin-1-yl)-1H-benzimidazol-2-yl)quinolin-2(1H)-one MeSH Prohlížeč
- anilidy MeSH
- ARQ 197 MeSH Prohlížeč
- axitinib MeSH
- benzimidazoly MeSH
- bevacizumab MeSH
- cabozantinib MeSH Prohlížeč
- chinoliny MeSH
- chinolony MeSH
- erlotinib MeSH
- everolimus MeSH
- fenylmočovinové sloučeniny MeSH
- imidazoly MeSH
- indazoly MeSH
- indoly MeSH
- interferony MeSH
- interleukin-2 MeSH
- niacinamid MeSH
- pazopanib MeSH Prohlížeč
- protinádorové látky MeSH
- pyridiny MeSH
- pyrimidiny MeSH
- pyrrolidinony MeSH
- pyrroly MeSH
- sirolimus MeSH
- sorafenib MeSH
- sulfonamidy MeSH
- sunitinib MeSH
- temsirolimus MeSH Prohlížeč
- tivozanib MeSH Prohlížeč
CONTEXT: While vascular endothelial growth factor-targeted therapy and mammalian target of rapamycin inhibition are effective strategies in treating clear cell renal cell carcinoma (ccRCC), the most effective therapeutic approach for patients with non-clear cell RCC (non-ccRCC) is unknown. OBJECTIVE: To systematically review relevant literature comparing the oncological outcomes and adverse events of different systemic therapies for patients with metastatic non-ccRCC. EVIDENCE ACQUISITION: Relevant databases including MEDLINE, Embase, and the Cochrane Library were searched up to March 24, 2016. Only comparative studies were included. Risk of bias and confounding assessments were performed. A meta-analysis was planned for and only performed if methodologically appropriate; otherwise, a narrative synthesis was undertaken. EVIDENCE SYNTHESIS: The literature search identified 812 potential titles and abstracts. Five randomized controlled trials, recruiting a total of 365 patients, were included. Three studies compared sunitinib against everolimus, one of which reported the results for non-ccRCC as a subgroup rather than as an entire randomized cohort. Individually, the studies showed a trend towards favoring sunitinib in terms of overall survival and progression-free survival (PFS; Everolimus versus Sunitinib in Patients with Metastatic Non-clear Cell Renal Cell Carcinoma hazard ratio [HR]: 1.41, 80% confidence interval [CI] 1.03-1.92 and 1.41, 95% CI: 0.88-2.27, Evaluation in Metastatic Non-clear Cell Renal Cell Carcinoma HR: 1.16, 95% CI: 0.67-2.01, Efficacy and Safety Comparison of RAD001 Versus Sunitinib in the First-line and Second-line Treatment of Patients with Metastatic Renal Cell Carcinoma HR: 1.5, 95% CI: 0.9-2.8), but this trend did not reach statistical significance in any study. Meta-analysis was performed on two studies which solely recruited patients with non-ccRCC reporting on PFS, the results of which were inconclusive (HR: 1.30, 95% CI: 0.91-1.86). Sunitinib was associated with more Grade 3-4 adverse events than everolimus, although this was not statistically significant. CONCLUSIONS: This systematic review and meta-analysis represent a robust summary of the evidence base for systemic treatment of metastatic non-ccRCC. The results show a trend towards favoring vascular endothelial growth factor-targeted therapy for PFS and overall survival compared with mammalian target of rapamycin inhibitors, although statistical significance was not reached. The relative benefits and harms of these treatments remain uncertain. Further research, either in the form of an individual patient data meta-analysis involving all relevant trials, or a randomized controlled trial with sufficient power to detect potential differences between treatments, is needed. PATIENT SUMMARY: We examined the literature to determine the most effective treatments for advanced kidney cancer patients whose tumors are not of the clear cell subtype. The results suggest that a drug called sunitinib might be more effective than everolimus, but the statistics supporting this statement are not yet entirely reliable. Further research is required to clarify this unmet medical need.
Department of Cancer Medicine Institut Gustave Roussy Villejuif France
Department of Surgical and Perioperative Sciences Urology and Andrology Umeå University Umeå Sweden
Department of Urology and Urologic Oncology Hannover Medical School Hannover Germany
Department of Urology Cabueñes Hospital Gijón Spain
Department of Urology Coimbra University Hospital Coimbra Portugal
Department of Urology Ludwig Maximilians University Munich Germany
Department of Urology Skåne University Hospital Malmö Sweden
Department of Urology Sunderby Hospital Sunderby Sweden
Department of Urology University Hospital Hamburg Eppendorf Hamburg Germany
Department of Urology University Hospital Schleswig Holstein Lübeck Germany
Department of Urology University of Rennes Rennes France
Division of Urology Maggiore della Carità Hospital University of Eastern Piedmont Novara Italy
Division of Urology University of Texas Medical School at Houston Houston TX USA
The Royal Free NHS Trust and Barts Cancer Institute Queen Mary University of London London UK
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