Literature DB >> 30421088

The Effectiveness of Sorafenib over Other Targeted Agents in the Second-Line Treatment of Metastatic Renal Cell Carcinoma: a Meta-Analysis.

Hou-Feng Huang1, Xin-Rong Fan1, Zhi-Gang Ji2.   

Abstract

The aim of the study was to perform a meta-analysis to compare the therapeutic effects and adverse events (AEs) of sorafenib in second-line treatments of metastatic renal cell carcinoma (mRCC). We searched online electronic databases: Pubmed, Embase, Cochrane library updated on November 2017.Trials of the effectiveness of sorafenib in second-line treatments of advanced RCC were included, of which the main outcomes were objective response rate (ORR), progression-free survival (PFS), overall survival (OS) and grade 3/4 AE. Other TAs significantly reduced the risk of PFS compared to sorafenib with respect to second-line treatment (HR = 0.74; 95% CI, 0.65-0.83; p < 0.00001). No significant differences were, however, found in patients in terms of the ORR (HR = 1.82; 95% CI, 0.98-3.35; p = 0.06). Frequencies of the most common toxicities were overall similar and adverse events differed only in sensitivity analysis in rash with exclusion of other TAs (HR = 0.16; 95% CI, 0.05-0.52; p = 0.002). Overall survival was not debated between groups. In patients with mRCC, second-line sorafenib is associated with similar ORR as other target agents. While, sorafenib did not demonstrate a PFS advantage compared with other target agents, suggests sorafenib may not benefit patients with mRCC. Tolerability due to toxicities is similar compared sorafenib with other target agents. Further characterization of the RCC oncogenic pathway, and the ongoing clinical trials should help optimize the treatment option for second-line therapy of advanced renal cell carcinoma.

Entities:  

Keywords:  Meta-analysis; Metastatic renal cell carcinoma; Second-line therapy; Sorafenib

Mesh:

Substances:

Year:  2018        PMID: 30421088     DOI: 10.1007/s12253-018-0516-3

Source DB:  PubMed          Journal:  Pathol Oncol Res        ISSN: 1219-4956            Impact factor:   3.201


  16 in total

1.  Quantifying heterogeneity in a meta-analysis.

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4.  Diagnosis and management of renal cell carcinoma. A clinical and pathologic study of 309 cases.

Authors:  D G Skinner; R B Colvin; C D Vermillion; R C Pfister; W F Leadbetter
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6.  Randomized phase III trial of temsirolimus versus sorafenib as second-line therapy after sunitinib in patients with metastatic renal cell carcinoma.

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Journal:  J Clin Oncol       Date:  2013-12-02       Impact factor: 44.544

7.  Axitinib versus sorafenib as second-line treatment for advanced renal cell carcinoma: overall survival analysis and updated results from a randomised phase 3 trial.

Authors:  Robert J Motzer; Bernard Escudier; Piotr Tomczak; Thomas E Hutson; M Dror Michaelson; Sylvie Negrier; Stephane Oudard; Martin E Gore; Jamal Tarazi; Subramanian Hariharan; Connie Chen; Brad Rosbrook; Sinil Kim; Brian I Rini
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Review 8.  Progression-free survival is simply a measure of a drug's effect while administered and is not a surrogate for overall survival.

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Review 9.  Is there still a role for sorafenib in metastatic renal cell carcinoma? A systematic review and meta-analysis of the effectiveness of sorafenib over other targeted agents.

Authors:  Roberto Iacovelli; Elena Verri; Maria Cossu Rocca; Gaetano Aurilio; Daniela Cullurà; Matteo Santoni; Ottavio de Cobelli; Franco Nolé
Journal:  Crit Rev Oncol Hematol       Date:  2016-01-19       Impact factor: 6.312

Review 10.  Comparative Effectiveness of Second-Line Targeted Therapies for Metastatic Renal Cell Carcinoma: A Systematic Review and Meta-Analysis of Real-World Observational Studies.

Authors:  Daniel Y Heng; James Signorovitch; Elyse Swallow; Nanxin Li; Yichen Zhong; Paige Qin; Daisy Y Zhuo; Xufang Wang; Jinhee Park; Sotirios Stergiopoulos; Christian Kollmannsberger
Journal:  PLoS One       Date:  2014-12-10       Impact factor: 3.240

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1.  Melatonin combined with sorafenib synergistically inhibit the invasive ability through targeting metastasis-associated protein 2 expression in human renal cancer cells.

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Journal:  Tzu Chi Med J       Date:  2021-10-21
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