Prognostic factors of metastatic renal cell carcinoma after failure of immunotherapy:: New paradigm from a large phase III trial with shark cartilage extract AE 941

被引:52
作者
Escudier, Bernard
Choueiri, Toni K.
Oudard, Stephane
Szczylik, Cezary
Negrier, Sylvie
Ravaud, Alain
Chevreau, Christine
Venner, Peter
Champagne, Pierre
Croteau, Daniel
Dupont, Eric
Hariton, Claude
Bukowski, Ronald M.
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Inst Gustave Roussy, Villejuif, France
[3] Hop Europeen Georges Pompidou, Paris, France
[4] Ctr Leon Berard, F-69373 Lyon, France
[5] Ctr Hosp Univ Bordeaux, Toulouse, France
[6] Ctr Claudius Regaud, Toulouse, France
[7] Cleveland Clin Taussig Canc Ctr, Cleveland, OH USA
[8] Wojskowy Instytut Medyczny, Warsaw, Poland
[9] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[10] Eterna Labs Inc, Quebec City, PQ, Canada
关键词
kidney; neoplasm metastasis; carcinoma; renal cell; prognosis; shark cartilage extract AE 941;
D O I
10.1016/j.juro.2007.07.035
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: We analyzed prognostic factors, described survival and generated a prognostic model in patients with metastatic renal cell carcinoma in whom immunotherapy failed and who were potentially eligible for novel agents. Materials and Methods: An analysis of the relationship between clinical features and survival was performed in 300 patients with advanced renal cell carcinoma in whom immunotherapy had failed and who were subsequently treated as part of a single, phase III clinical trial with the anti-angiogenic agent Neovastat (shark cartilage extract AE 941). Clinical features were first examined univariately and a stepwise modeling approach based on Cox proportional hazard regression was then performed to generate a multivariate model. Results: Median and progression-free survival (prognostic factors) for the whole cohort was 12.6 and 2 months, respectively. Prognostic features associated with shorter survival on multivariate analysis were the number of metastatic sites (greater than 1), time from nephrectomy to metastatic disease (less than 2 years), high alkaline phosphatase, abnormal corrected serum Ca and high lactate dehydrogenase (greater than 1.5 X the upper limit of normal). Four prognostic subgroups were identified by counting the number of adverse prognostic factors. Median survival in patients with zero adverse prognostic factors was 15.6 months compared to 11.7 months in patients with 1,8.5 months in patients with 2 and 3.5 months in patients with 3 or more. Conclusions: We identified 4 risk groups to predict survival in previously treated patients with renal cell carcinoma. This model was based on data from what is to our knowledge the largest experience in this population. It should be used in clinical trial design, risk stratification and patient counseling.
引用
收藏
页码:1901 / 1905
页数:5
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