TY - JOUR
T1 - Sub-classification of patients with intermediate-risk metastatic renal cell carcinoma treated with targeted therapy
AU - Kaneko, Go
AU - Shirotake, Suguru
AU - Nishimoto, Koshiro
AU - Miyazaki, Yasumasa
AU - Ito, Keiichi
AU - Ito, Yujiro
AU - Hagiwara, Masayuki
AU - Kanao, Kent
AU - Nakagawa, Ken
AU - Momma, Tetsuo
AU - Asano, Tomohiko
AU - Tanaka, Nobuyuki
AU - Mizuno, Ryuichi
AU - Oya, Mototsugu
AU - Oyama, Masafumi
N1 - Funding Information:
This work was supported in part by a JSPS Grants-in-Aid for Scientific Research (grant no. JP17K18062) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
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; Saitama Medical University International Medical Center, Hidaka, Saitama, Japan; National Defense Medical College, Tokorozawa, 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 work was supported in part by a JSPS Grants-in-Aid for Scientific Research (grant no. JP17K18062) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
Publisher Copyright:
© The Author(s) 2019. Published by Oxford University Press. All rights reserved.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Background: International Metastatic Renal Cell Carcinoma Database Consortium model predicts the outcomes of metastatic renal cell carcinoma stratified into favorable, intermediate, and poor risk groups (FG, IG, and PG, respectively), with approximately 50% of patients being classified as IG. We aimed to generate better risk model based on the sub-classification of IG. Methods: We analyzed records of 213 consecutive patients receiving molecular targeted therapy. Age, gender, histology, type of initial molecular targeted therapy, serum laboratory data, previous nephrectomy and immunotherapy, and metastatic sites were used for IG sub-stratification. Modified and original models were compared using a concordance correlation coefficient analysis. Results: Median follow-up was 17.8 months. Serum albumin, serum C-reactive protein, and bone metastases were independent predictors of overall survival (OS) in IG. IG was sub-classified into low-, middle-, and high-risk IG according to the number of predictors. The following modified model was developed: modified FG (FG & low-risk IG), modified IG (middle-risk IG), and modified PG (PG & high-risk IG). Concordance indices for original and modified models were 0.68 and 0.73, respectively (P < 0.001). OS was significantly longer in modified PG treated with mammalian target of rapamycin inhibitors as second-line therapy than with tyrosine kinase inhibitors, whereas this was not observed in the original model. Conclusions: We successfully developed modified IMDC model using a two-step process: the original IMDC plus an IG sub-stratification, and demonstrated that it predicts outcomes more accurately than original model.
AB - Background: International Metastatic Renal Cell Carcinoma Database Consortium model predicts the outcomes of metastatic renal cell carcinoma stratified into favorable, intermediate, and poor risk groups (FG, IG, and PG, respectively), with approximately 50% of patients being classified as IG. We aimed to generate better risk model based on the sub-classification of IG. Methods: We analyzed records of 213 consecutive patients receiving molecular targeted therapy. Age, gender, histology, type of initial molecular targeted therapy, serum laboratory data, previous nephrectomy and immunotherapy, and metastatic sites were used for IG sub-stratification. Modified and original models were compared using a concordance correlation coefficient analysis. Results: Median follow-up was 17.8 months. Serum albumin, serum C-reactive protein, and bone metastases were independent predictors of overall survival (OS) in IG. IG was sub-classified into low-, middle-, and high-risk IG according to the number of predictors. The following modified model was developed: modified FG (FG & low-risk IG), modified IG (middle-risk IG), and modified PG (PG & high-risk IG). Concordance indices for original and modified models were 0.68 and 0.73, respectively (P < 0.001). OS was significantly longer in modified PG treated with mammalian target of rapamycin inhibitors as second-line therapy than with tyrosine kinase inhibitors, whereas this was not observed in the original model. Conclusions: We successfully developed modified IMDC model using a two-step process: the original IMDC plus an IG sub-stratification, and demonstrated that it predicts outcomes more accurately than original model.
KW - Intermediate risk
KW - International Metastatic Renal Cell Carcinoma Database Consortium model
KW - Metastatic renal cell carcinoma
KW - Molecular target therapy
KW - Renal cell carcinoma
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U2 - 10.1093/jjco/hyz067
DO - 10.1093/jjco/hyz067
M3 - Article
C2 - 31063191
AN - SCOPUS:85074378644
SN - 0368-2811
VL - 49
SP - 780
EP - 785
JO - Japanese journal of clinical oncology
JF - Japanese journal of clinical oncology
IS - 8
ER -