Sub-classification of patients with intermediate-risk metastatic renal cell carcinoma treated with targeted therapy.

International Metastatic Renal Cell Carcinoma Database Consortium model Renal cell carcinoma intermediate risk metastatic renal cell carcinoma molecular target therapy

Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
01 Aug 2019
Historique:
received: 11 02 2019
revised: 05 04 2019
accepted: 16 04 2019
pubmed: 8 5 2019
medline: 9 1 2020
entrez: 8 5 2019
Statut: ppublish

Résumé

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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 31063191
pii: 5486425
doi: 10.1093/jjco/hyz067
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

780-785

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Go Kaneko (G)

Department of Uro-Oncology, Saitama Medical University International Medical Center.

Suguru Shirotake (S)

Department of Uro-Oncology, Saitama Medical University International Medical Center.

Koshiro Nishimoto (K)

Department of Uro-Oncology, Saitama Medical University International Medical Center.

Yasumasa Miyazaki (Y)

Department of Urology, Keio University School of Medicine.

Keiichi Ito (K)

Department of Urology, National Defense Medical College.

Yujiro Ito (Y)

Department of Urology, Saiseikai Central Hospital.

Masayuki Hagiwara (M)

Department of Urology, Ichikawa General Hospital, Tokyo Dental College.

Kent Kanao (K)

Department of Urology, Aichi Medical University School of Medicine.

Ken Nakagawa (K)

Department of Urology, Ichikawa General Hospital, Tokyo Dental College.

Tetsuo Momma (T)

Department of Urology, National Hospital Organization Saitama Hospital.

Tomohiko Asano (T)

Department of Urology, National Defense Medical College.

Nobuyuki Tanaka (N)

Department of Urology, Keio University School of Medicine.
Department of Urology, Saitama City Hospital.

Ryuichi Mizuno (R)

Department of Urology, Keio University School of Medicine.

Mototsugu Oya (M)

Department of Urology, Keio University School of Medicine.

Masafumi Oyama (M)

Department of Uro-Oncology, Saitama Medical University International Medical Center.

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