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Sub-classification of patients with intermediate-risk metastatic renal cell carcinoma treated with targeted therapy.
Kaneko, Go; Shirotake, Suguru; Nishimoto, Koshiro; Miyazaki, Yasumasa; Ito, Keiichi; Ito, Yujiro; Hagiwara, Masayuki; Kanao, Kent; Nakagawa, Ken; Momma, Tetsuo; Asano, Tomohiko; Tanaka, Nobuyuki; Mizuno, Ryuichi; Oya, Mototsugu; Oyama, Masafumi.
Afiliação
  • Kaneko G; Department of Uro-Oncology, Saitama Medical University International Medical Center.
  • Shirotake S; Department of Uro-Oncology, Saitama Medical University International Medical Center.
  • Nishimoto K; Department of Uro-Oncology, Saitama Medical University International Medical Center.
  • Miyazaki Y; Department of Urology, Keio University School of Medicine.
  • Ito K; Department of Urology, National Defense Medical College.
  • Ito Y; Department of Urology, Saiseikai Central Hospital.
  • Hagiwara M; Department of Urology, Ichikawa General Hospital, Tokyo Dental College.
  • Kanao K; Department of Urology, Aichi Medical University School of Medicine.
  • Nakagawa K; Department of Urology, Ichikawa General Hospital, Tokyo Dental College.
  • Momma T; Department of Urology, National Hospital Organization Saitama Hospital.
  • Asano T; Department of Urology, National Defense Medical College.
  • Tanaka N; Department of Urology, Keio University School of Medicine.
  • Mizuno R; Department of Urology, Saitama City Hospital.
  • Oya M; Department of Urology, Keio University School of Medicine.
  • Oyama M; Department of Urology, Keio University School of Medicine.
Jpn J Clin Oncol ; 49(8): 780-785, 2019 Aug 01.
Article em En | MEDLINE | ID: mdl-31063191
ABSTRACT

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Terapia de Alvo Molecular / Neoplasias Renais Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Jpn J Clin Oncol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Terapia de Alvo Molecular / Neoplasias Renais Tipo de estudo: Clinical_trials / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Jpn J Clin Oncol Ano de publicação: 2019 Tipo de documento: Article