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[Prognostic factors for metastatic renal cell carcinoma treated with second-line targeted therapies]. | LitMetric

[Prognostic factors for metastatic renal cell carcinoma treated with second-line targeted therapies].

Prog Urol

Service d'urologie et transplantation, centre hospitalier et universitaire de Rouen, 1, rue de Germont, 76031 Rouen cedex, France; Équipe de recherche d'oncologie normande (IRON), centre hospitalier et universitaire de Rouen, 1, rue de Germont, 76031 Rouen cedex, France; Unité d'oncologie urologique et digestive, centre hospitalier et universitaire de Rouen, 1, rue de Germont, 76031 Rouen cedex, France. Electronic address:

Published: January 2016

Objective: To assess the prognostic value of clinical and biological features in patients treated with second-line targeted therapies (TT) for a metastatic renal cell carcinoma (mRCC).

Material And Methods: A retrospective study was performed including 60 patients treated with second-line TT from 2006 to 2013. Clinical and biological features were collected, including TT-induced toxicities, Heng and MSKCC prognostic scores, and renal function. Overall survival (OS) and progression-free survival (PFS) were assessed using univariate and multivariate analysis.

Results: The median age was 61 years [39-81]. MSKCC and Heng scores were significantly prognostic for OS and PFS (P<0.05). Hypo-albuminemia, anemia and brain metastasis were associated with poorer OS and PFS (P<0.05). Severe induced toxicities had a prognostic impact with higher OS (26 months vs 10 months, P=0.003) and PFS (5 months vs 4 months, P=0.047). Renal function impairment at the initiation of the second line was also associated with higher survival (OS=24 months vs 9 months, P=0.035 and PFS=7 months vs 4 months, P=0.043). On multivariate analysis, induced toxicity was found as an independent factor of good prognosis for OS (HR=0.36; P=0.01).

Conclusion: Our results suggested that renal function impairment and TT-induced toxicities in the second line of treatment for mRCC have a potential prognostic interest as it had previously been reported for the first line of TT.

Level Of Evidence: 5.

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Source
http://dx.doi.org/10.1016/j.purol.2015.09.007DOI Listing

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