Jun Teishima1, Kohei Kobatake2, Shunsuke Shinmei2, Shogo Inoue2, Tetsutaro Hayashi2, Shinya Ohara3, Koji Mita3, Yasuhisa Hasegawa4, Satoshi Maruyama5, Mitsuru Kajiwara6, Masanobu Shigeta7, Hideki Mochizuki8, Hiroyuki Moriyama9, Seiji Fujiwara10, Akio Matsubara2. 1. Department of Urology, Graduate School of Biomedical and Health Science, Hiroshima University, Hiroshima, Japan. Electronic address: teishima@hiroshima-u.ac.jp. 2. Department of Urology, Graduate School of Biomedical and Health Science, Hiroshima University, Hiroshima, Japan. 3. Department of Urology, Hiroshima City Asa Citizens Hospital, Hiroshima, Japan. 4. Department of Urology, Fukuyama Medical Center, Fukuyama, Japan. 5. Department of Urology, Hiroshima General Hospital, Hatsukaichi, Japan. 6. Department of Urology, Hiroshima Prefectural Hospital, Hiroshima, Japan. 7. Department of Urology, Kure Medical Center, Kure, Japan. 8. Department of Urology, Miyoshi Central Hospital, Miyoshi, Japan. 9. Department of Urology, Onomichi General Hospital, Onomichi, Japan. 10. Department of Urology, Higashihiroshima Medical Center, Higashihiroshima, Japan.
Abstract
INTRODUCTION AND OBJECTIVES: The aim of this study was to investigate the effect of kinetics of C-reactive protein (CRP) in the prediction of overall survival (OS) in patients with metastatic renal cell carcinoma (mRCC) treated with a tyrosine kinase inhibitor. MATERIALS AND METHODS: The CRP in 118 cases of molecular-targeted therapy for mRCC was measured before starting the prescription of the first-line targeted agents and at the first time a CT scan was conducted during treatments. All cases were classified into higher-CRP groups and lower ones according to their data at the time of starting treatments. A higher-CRP group was further classified into 2 subgroups based on the kinetics after first-line targeted therapy: "decreased-CRP subgroup" and "nondecreased CRP subgroup." RESULTS: The median of the observation period was 23.4 months. The OS in cases with CRP higher than 0.5mg/dl was significantly worse than those in other cases (P<0.0001). Multivariate analysis revealed that the pretreated CRP (hazard ratio = 2.093; 95% CI: 1.176-3.858; P = 0.0179) was an independent predictive factor of OS. In the higher-CRP group, the OS for the decreased-CRP subgroup (1 year, 85.0%) was significantly better than those for the nondecreased CRP subgroup (1 year, 37.2%, P<0.0001). Multivariate analyses in the higher-CRP group revealed that the decrease in the CRP was an independent predictive factor for OS (hazard ratio = 0.176; 95% CI: 0.064-0.488; P = 0.0008). CONCLUSION: A decrease in CRP as well as pretreatment CRP can be a predictive factor for OS in patients with mRCC treated with a tyrosine kinase inhibitor. Cases with mRCC could be stratified into 3 groups with different prognoses using the pretreated CRP and its changes.
INTRODUCTION AND OBJECTIVES: The aim of this study was to investigate the effect of kinetics of C-reactive protein (CRP) in the prediction of overall survival (OS) in patients with metastatic renal cell carcinoma (mRCC) treated with a tyrosine kinase inhibitor. MATERIALS AND METHODS: The CRP in 118 cases of molecular-targeted therapy for mRCC was measured before starting the prescription of the first-line targeted agents and at the first time a CT scan was conducted during treatments. All cases were classified into higher-CRP groups and lower ones according to their data at the time of starting treatments. A higher-CRP group was further classified into 2 subgroups based on the kinetics after first-line targeted therapy: "decreased-CRP subgroup" and "nondecreased CRP subgroup." RESULTS: The median of the observation period was 23.4 months. The OS in cases with CRP higher than 0.5mg/dl was significantly worse than those in other cases (P<0.0001). Multivariate analysis revealed that the pretreated CRP (hazard ratio = 2.093; 95% CI: 1.176-3.858; P = 0.0179) was an independent predictive factor of OS. In the higher-CRP group, the OS for the decreased-CRP subgroup (1 year, 85.0%) was significantly better than those for the nondecreased CRP subgroup (1 year, 37.2%, P<0.0001). Multivariate analyses in the higher-CRP group revealed that the decrease in the CRP was an independent predictive factor for OS (hazard ratio = 0.176; 95% CI: 0.064-0.488; P = 0.0008). CONCLUSION: A decrease in CRP as well as pretreatment CRP can be a predictive factor for OS in patients with mRCC treated with a tyrosine kinase inhibitor. Cases with mRCC could be stratified into 3 groups with different prognoses using the pretreated CRP and its changes.