Prognostic impact of baseline serum C-reactive protein in patients with metastatic renal cell carcinoma (RCC) treated with sunitinib

被引:71
作者
Beuselinck, Benoit [1 ,2 ,3 ]
Vano, Yann-Alexandre [4 ]
Oudard, Stephane [4 ]
Wolter, Pascal [1 ,2 ]
De Smet, Robert [1 ,2 ]
Depoorter, Lore [1 ,2 ]
Teghom, Corine [4 ]
Karadimou, Alexandra [3 ]
Zucman-Rossi, Jessica [3 ]
Debruyne, Philip R. [5 ]
Van Poppel, Hendrik [6 ]
Joniau, Steven [6 ]
Lerut, Evelyne [7 ]
Strijbos, Michiel [1 ,2 ]
Dumez, Herlinde [1 ,2 ]
Paridaens, Robert [1 ,2 ]
Van Calster, Ben [8 ]
Schoffski, Patrick [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Univ Hosp Leuven, Dept Gen Med Oncol, Leuven Canc Inst, Leuven, Belgium
[2] Katholieke Univ Leuven, Univ Hosp Leuven, Expt Oncol Lab, Leuven Canc Inst, Leuven, Belgium
[3] Univ Paris 05, INSERM, Genom Fonct Tumeurs Solides U674, Paris, France
[4] Univ Paris 05, Georges Pompidou European Hosp, Dept Med Oncol, Paris, France
[5] AZ Groeninge, Dept Med Oncol, Kortrijk, Belgium
[6] Katholieke Univ Leuven, Dept Urol, Leuven, Belgium
[7] Katholieke Univ Leuven, Dept Pathol, Leuven, Belgium
[8] Katholieke Univ Leuven, Biostat Sect, Dept Dev & Regenerat, Leuven, Belgium
关键词
renal cell carcinoma; RCC; sunitinib; prognostic markers; C-reactive protein; INTERFERON-ALPHA; CANCER STATISTICS; TARGETED THERAPY; DOUBLE-BLIND; INTERLEUKIN-6; SURVIVAL; REGRESSION; LEVEL;
D O I
10.1111/bju.12494
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
100201 [内科学]; 100221 [泌尿外科学];
摘要
Objective To evaluate the impact of baseline serum C-reactive protein (CRP) level on outcome in patients with metastatic renal cell carcinoma (mRCC) treated with sunitinib. Patients and Methods We reviewed the charts of patients with mRCC who started sunitinib as a first targeted treatment between 2005 and 2012 in three hospitals in Belgium and France. Collected data included known prognostic factors for mRCC, anatomical location of metastatic sites, response rate (RR), progression-free survival (PFS) and overall survival (OS). Results A total of 200 eligible patients were identified by retrospective chart review. The median PFS and OS were 12 and 20 months, respectively. We observed a clear impact of baseline CRP levels on outcome: the median PFS was 25 months in the group with baseline CRP <= 5 mg/L and 8 months in the group with baseline CRP >5 mg/L (hazard ratio [HR] 2.48, 95% CI 1.74-3.59). The median OS in each group was 50 vs 12 months, respectively (HR 3.17, 2.20-4.68). In the group with baseline CRP = 5 mg/L, 61% of patients experienced a partial response compared with 32% of patients in the group with baseline CRP >5 mg/L (difference = 29%, 95% CI 15-42). When adding baseline CRP (with a log transformation) to the six variables of the International Metastatic RCC Database Consortium (IMDC) model in a multivariable Cox regression model, baseline CRP was independently associated with poor PFS (HR for each doubling in CRP level: 1.14, 95% CI 1.03-1.26; P = 0.01) and OS (HR: 1.29, 95% CI 1.16-1.43; P < 0.001). Adding baseline CRP to the model increased the c-statistic of PFS at 5 years from 0.63 (0.59-0.68) to 0.69 (0.65-0.73), and the c-statistic of OS at 5 years from 0.65 (0.60-0.69) to 0.70 (0.66-0.74). Patients with elevated baseline CRP levels had a poor prognosis independent of the IMDC risk group, whereas patients with a low baseline CRP in the IMDC favourable risk group had a very good outcome. Conclusion Baseline serum CRP level is a strong independent variable linked with RR, PFS and OS in patients with mRCC treated with sunitinib.
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页码:81 / 89
页数:9
相关论文
共 41 条
[1]
Interleukin-6 and C-reactive protein in metastatic renal cell carcinoma [J].
Altundag, O ;
Altundag, K ;
Gunduz, E .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (05) :1044-1044
[2]
THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[3]
Blay JY, 1997, INT J CANCER, V72, P424, DOI 10.1002/(SICI)1097-0215(19970729)72:3<424::AID-IJC9>3.0.CO
[4]
2-R
[5]
BLAY JY, 1992, CANCER RES, V52, P3317
[6]
C-reactive protein: A biomarker of survival in patients with metastatic renal cell carcinoma treated with subcutaneous interleukin-2 based immunotherapy [J].
Casamassima, A ;
Picciariello, M ;
Quaranta, M ;
Berardino, R ;
Ranieri, C ;
Paradiso, A ;
Lorusso, V ;
Guida, M .
JOURNAL OF UROLOGY, 2005, 173 (01) :52-55
[7]
Bevacizumab plus interferon alfa-2a for treatment of metastatic renal cell carcinoma: a randomised, double-blind phase III trial [J].
Escudier, Bernard ;
Pluzanska, Anna ;
Koralewski, Piotr ;
Ravaud, Alain ;
Bracarda, Sergio ;
Szczylik, Cezary ;
Chevreau, Christine ;
Filipek, Marek ;
Melichar, Bohuslav ;
Bajetta, Emilio ;
Gorbunova, Vera ;
Bay, Jacques-Olivier ;
Bodrogi, Istvan ;
Jagiello-Gruszfeld, Agnieszka ;
Moore, Nicola .
LANCET, 2007, 370 (9605) :2103-2111
[8]
Sorafenib in advanced clear-cell renal-cell carcinoma [J].
Escudier, Bernard ;
Eisen, Tim ;
Stadler, Walter M. ;
Szczylik, Cezary ;
Oudard, Stephane ;
Siebels, Michael ;
Negrier, Sylvie ;
Chevreau, Christine ;
Solska, Ewa ;
Desai, Apurva A. ;
Rolland, Frederic ;
Demkow, Tomasz ;
Hutson, Thomas E. ;
Gore, Martin ;
Freeman, Scott ;
Schwartz, Brian ;
Shan, Minghua ;
Simantov, Ronit ;
Bukowski, Ronald M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (02) :125-134
[9]
C-reactive protein as a prognostic marker for advanced renal cell carcinoma treated with sunitinib [J].
Fujita, Tetsuo ;
Iwamura, Masatsugu ;
Ishii, Daisuke ;
Tabata, Ken-ichi ;
Matsumoto, Kazumasa ;
Yoshida, Kazunari ;
Baba, Shiro .
INTERNATIONAL JOURNAL OF UROLOGY, 2012, 19 (10) :908-913
[10]
Pretreatment serum markers and lymphocyte response to interleukin-2 therapy [J].
Fumagalli, L ;
Lissoni, P ;
Di Felice, G ;
Meregalli, S ;
Valsuani, G ;
Mengo, S ;
Rovelli, F .
BRITISH JOURNAL OF CANCER, 1999, 80 (3-4) :407-411