Literature DB >> 30345423

Adjuvant Antiangiogenic Agents in Post-nephrectomy Renal Cell Carcinoma: A Systematic Review and Meta-analysis.

Mohamad B Sonbol1, Belal Firwana2, Talal Hilal1, Zhen Wang3, Diana Almader-Douglas4, Richard W Joseph5, Thai H Ho1.   

Abstract

CONTEXT: The role of antiangiogenic agents in advanced renal cell carcinoma (RCC) is well established. However, it is still not clear whether this benefit can be extrapolated to the adjuvant setting.
OBJECTIVE: To determine the efficacy and safety of antiangiogenic agents in patients with RCC and a high risk of relapse after nephrectomy. EVIDENCE ACQUISITION: We searched PubMed, Embase, and the Cochrane Central Register of Controlled Trials for randomized controlled trials (RCTs) evaluating the use of any oral antiangiogenic agent compared to placebo in post-nephrectomy RCC patients. Prespecified data elements were extracted from each trial. Outcomes of interest included overall survival (OS) and disease-free survival (DFS). The overall effect was pooled using the DerSimonian and Laird random-effects models. EVIDENCE SYNTHESIS: Three RCTs comparing antiangiogenics to placebo among 3693 patients met our inclusion criteria and were used in meta-analyses. Overall, antiangiogenics did not improve DFS (hazard ratio [HR] 0.92, 95% confidence interval [CI] 0.78-1.07) or OS (HR 0.99, 95% CI 0.79-1.25). These results persisted when restricting the analysis to patients with clear cell carcinoma and patients with highest risk of relapse. Similarly, sunitinib did not show any improvement in the entire cohort for either DFS (HR 0.89, 95% CI 0.67-1.19) or OS (HR 1.11, 95% CI 0.90-1.37).
CONCLUSIONS: In this meta-analysis, antiangiogenics did not improve OS and DFS over placebo in high-risk RCC after nephrectomy. Further studies are needed to identify the patient population that might derive a benefit from antiangiogenics in the adjuvant setting. PATIENT
SUMMARY: In this article, we found that there is currently insufficient evidence to support the use of oral antiangiogenics in nonmetastatic renal cell carcinoma after nephrectomy. In addition, the use of oral antiangiogenics was associated with a 2.7-fold higher rate of significant side effects compared to placebo.

Entities:  

Keywords:  Adjuvant chemotherapy; Pazopanib; Renal cell carcinoma; Sorafenib; Sunitinib; Tyrosine kinase inhibitors

Year:  2018        PMID: 30345423      PMCID: PMC6192050          DOI: 10.1016/j.euo.2018.03.012

Source DB:  PubMed          Journal:  Eur Urol Oncol        ISSN: 2588-9311


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Authors:  Fausto Petrelli; Gianluca Tomasello; Michele Ghidini; Veronica Lonati; Rodolfo Passalacqua; Sandro Barni
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3.  Evaluation of the National Comprehensive Cancer Network and American Urological Association renal cell carcinoma surveillance guidelines.

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4.  Cancer Statistics, 2017.

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5.  Adjuvant Sunitinib in High-Risk Renal-Cell Carcinoma after Nephrectomy.

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Journal:  N Engl J Med       Date:  2016-10-09       Impact factor: 91.245

6.  Randomized Phase III Trial of Adjuvant Pazopanib Versus Placebo After Nephrectomy in Patients With Localized or Locally Advanced Renal Cell Carcinoma.

Authors:  Robert J Motzer; Naomi B Haas; Frede Donskov; Marine Gross-Goupil; Sergei Varlamov; Evgeny Kopyltsov; Jae Lyun Lee; Bohuslav Melichar; Brian I Rini; Toni K Choueiri; Milada Zemanova; Lori A Wood; M Neil Reaume; Arnulf Stenzl; Simon Chowdhury; Ho Yeong Lim; Ray McDermott; Agnieszka Michael; Weichao Bao; Marlene J Carrasco-Alfonso; Paola Aimone; Maurizio Voi; Christian Doehn; Paul Russo; Cora N Sternberg
Journal:  J Clin Oncol       Date:  2017-09-13       Impact factor: 44.544

Review 7.  Adjuvant therapy for locally advanced renal cell carcinoma: A meta-analysis and systematic review.

Authors:  Yangyang Bai; Songchao Li; Zhankui Jia; Yinghui Ding; Chaohui Gu; Jinjian Yang
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8.  The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate healthcare interventions: explanation and elaboration.

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9.  Adjuvant sunitinib or sorafenib for high-risk, non-metastatic renal-cell carcinoma (ECOG-ACRIN E2805): a double-blind, placebo-controlled, randomised, phase 3 trial.

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Journal:  Lancet       Date:  2016-03-09       Impact factor: 79.321

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  2 in total

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