TY - JOUR
T1 - Impact of inflammatory marker levels one month after the first-line targeted therapy initiation on progression-free survival prediction in patients with metastatic clear cell renal cell carcinoma
AU - Ito, Keiichi
AU - Masunaga, Ayako
AU - Tanaka, Nobuyuki
AU - Mizuno, Ryuichi
AU - Shirotake, Suguru
AU - Yasumizu, Yota
AU - Ito, Yujiro
AU - Miyazaki, Yasumasa
AU - Hagiwara, Masayuki
AU - Kanao, Kent
AU - Mikami, Shuji
AU - Momma, Tetsuo
AU - Masuda, Takeshi
AU - Nakagawa, Ken
AU - Oyama, Masafumi
AU - Asano, Tomohiko
AU - Oya, Mototsugu
N1 - Funding Information:
The authors would like to thank all members of the Keio Collaboration Study of Renal Cell Carcinoma. The following institutions participated in this study: Keio University School of Medicine, Tokyo, Japan; National Defense Medical College, Tokorozawa, Saitama, Japan; International Medical Center-Comprehensive Cancer Center, Saitama Medical University, Hidaka, Saitama, Japan; Saiseikai Central Hospital, Tokyo, Japan; Saitama City Hospital, Saitama, Japan; National Hospital Organization Saitama Hospital, Wako, Saitama, Japan; and Ichikawa General Hospital, Tokyo Dental College, Ichikawa, Chiba, Japan. This study was performed as a research program of the Project for Development of Innovative Research on Cancer Therapeutics (P-Direct), Ministry of Education, Culture, Sports, Science and Technology of Japan.
Publisher Copyright:
© The Author(s) 2018. Published by Oxford University Press. All rights reserved.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Objectives: Progression-free survival of first-line targeted therapy greatly influences the survival of patients with metastatic renal cell carcinoma. We evaluated whether post-treatment inflammatory markers and lactate dehydrogenase levels had impacts on progression-free survival prediction in addition to those of conventional predictors. Methods: Two hundred and fifteen patients whose tumors were clear cell type and in whom first-line targeted therapies could be continued for >1 month were evaluated. Pretreatment clinical factors, pathological factors and laboratory data 1 month after targeted therapy initiation—including inflammatory markers (neutrophil count, neutrophil-to-lymphocyte ratio and C-reactive protein) and lactate dehydrogenase—were reviewed. To identify progression-free survival predictors, multivariate analyses were done. Results: The 1-year progression-free survival rate was 47%. Female gender, Karnofsky performance status <80%, time from diagnosis to systemic treatment <12 months, pretreatment C-reactive protein >3.0 mg/dl and post-treatment neutrophil-to-lymphocyte ratio >3.0 were independent predictors for progression-free survival. In contrast, neither C-reactive protein increase nor neutrophil-to-lymphocyte ratio increase after targeted therapy initiation were independent predictors. Pretreatment lactate dehydrogenase, post-treatment lactate dehydrogenase and lactate dehydrogenase decline were not independent predictors. When all patients were stratified by these independent factors into three groups (0 risk vs. 1 or 2 risks vs. 3 or more risks), there were significant differences in progression-free survival rates between the groups (P < 0.0001). Furthermore, there were also significant differences in overall survival rates between the groups (P < 0.0001). Conclusions: Integration of post-treatment neutrophil-to-lymphocyte ratio value with pretreatment factors may lead to the establishment of effective predictive model for disease progression in patients with metastatic clear cell renal cell carcinoma who received first-line targeted therapies.
AB - Objectives: Progression-free survival of first-line targeted therapy greatly influences the survival of patients with metastatic renal cell carcinoma. We evaluated whether post-treatment inflammatory markers and lactate dehydrogenase levels had impacts on progression-free survival prediction in addition to those of conventional predictors. Methods: Two hundred and fifteen patients whose tumors were clear cell type and in whom first-line targeted therapies could be continued for >1 month were evaluated. Pretreatment clinical factors, pathological factors and laboratory data 1 month after targeted therapy initiation—including inflammatory markers (neutrophil count, neutrophil-to-lymphocyte ratio and C-reactive protein) and lactate dehydrogenase—were reviewed. To identify progression-free survival predictors, multivariate analyses were done. Results: The 1-year progression-free survival rate was 47%. Female gender, Karnofsky performance status <80%, time from diagnosis to systemic treatment <12 months, pretreatment C-reactive protein >3.0 mg/dl and post-treatment neutrophil-to-lymphocyte ratio >3.0 were independent predictors for progression-free survival. In contrast, neither C-reactive protein increase nor neutrophil-to-lymphocyte ratio increase after targeted therapy initiation were independent predictors. Pretreatment lactate dehydrogenase, post-treatment lactate dehydrogenase and lactate dehydrogenase decline were not independent predictors. When all patients were stratified by these independent factors into three groups (0 risk vs. 1 or 2 risks vs. 3 or more risks), there were significant differences in progression-free survival rates between the groups (P < 0.0001). Furthermore, there were also significant differences in overall survival rates between the groups (P < 0.0001). Conclusions: Integration of post-treatment neutrophil-to-lymphocyte ratio value with pretreatment factors may lead to the establishment of effective predictive model for disease progression in patients with metastatic clear cell renal cell carcinoma who received first-line targeted therapies.
KW - C-reactive protein
KW - Metastatic clear cell renal cell carcinoma
KW - Neutrophil-to-lymphocyte ratio
KW - Progression-free survival
KW - Targeted therapy
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U2 - 10.1093/jjco/hyy154
DO - 10.1093/jjco/hyy154
M3 - Article
C2 - 30407543
AN - SCOPUS:85059494847
SN - 0368-2811
VL - 49
SP - 69
EP - 76
JO - Japanese Journal of Clinical Oncology
JF - Japanese Journal of Clinical Oncology
IS - 1
ER -