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A Genetic Polymorphism in CTLA-4 Is Associated with Overall Survival in Sunitinib-Treated Patients with Clear Cell Metastatic Renal Cell Carcinoma.
Liu, Xiaoyan; Swen, Jesse J; Diekstra, Meta H M; Boven, Epie; Castellano, Daniel; Gelderblom, Hans; Mathijssen, Ron H J; Vermeulen, Sita H; Oosterwijk, Egbert; Junker, Kerstin; Roessler, Max; Alexiusdottir, Kristin; Sverrisdottir, Asgerdur; Radu, Marius T; Ambert, Valentin; Eisen, Tim; Warren, Anne; Rodríguez-Antona, Cristina; García-Donas, Jesus; Böhringer, Stefan; Koudijs, Karel K M; Kiemeney, Lambertus A L M; Rini, Brian I; Guchelaar, Henk-Jan.
Afiliação
  • Liu X; Department of Clinical Pharmacy and Toxicology, Leiden University Medical Center, Leiden, the Netherlands.
  • Swen JJ; Institute of Clinical Pharmacology, Qilu Hospital of Shandong University, Jinan, China.
  • Diekstra MHM; Department of Clinical Pharmacy and Toxicology, Leiden University Medical Center, Leiden, the Netherlands.
  • Boven E; Department of Clinical Pharmacy and Toxicology, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Castellano D; Department of Medical Oncology, VU University Medical Center, Amsterdam, the Netherlands.
  • Gelderblom H; Oncology Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
  • Mathijssen RHJ; Department of Medical Oncology, Leiden University Medical Center, Leiden, the Netherlands.
  • Vermeulen SH; Department of Medical Oncology, Erasmus MC Cancer Institute, Rotterdam, the Netherlands.
  • Oosterwijk E; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Junker K; Department of Urology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Roessler M; Clinic of Urology and Paediatric Urology, Saarland University, Homburg, Germany.
  • Alexiusdottir K; CESAR Central Office, CESAR Central European Society for Anticancer Drug Research-EWIV, Vienna, Austria.
  • Sverrisdottir A; Department of Medicine, Landspitali-University Hospital, Reykjavik, Iceland.
  • Radu MT; Department of Oncology, Landspitali-University Hospital, Reykjavik, Iceland.
  • Ambert V; University of Medicine and Pharmacy Carol Davila, Bucuresti, Romania.
  • Eisen T; University of Medicine and Pharmacy Carol Davila, Bucuresti, Romania.
  • Warren A; Department of Oncology, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • Rodríguez-Antona C; Department of Pathology, Cambridge University Hospitals NHS Foundation Trust, Addenbrooke's Hospital, Cambridge Biomedical Campus, Cambridge, United Kingdom.
  • García-Donas J; Hereditary Endocrine Cancer Group, Spanish National Cancer Research Centre (CNIO) and Biomedical Network on Rare Diseases (CIBERER), Madrid, Spain.
  • Böhringer S; Medical Oncology, HM Hospitales, Centro Integral Oncológico HM Clara Campal, Madrid, Spain.
  • Koudijs KKM; Department of Medical Statistics and Bioinformatics, Leiden University Medical Center, Leiden, the Netherlands.
  • Kiemeney LALM; Department of Clinical Pharmacy and Toxicology, Leiden University Medical Center, Leiden, the Netherlands.
  • Rini BI; Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Guchelaar HJ; Department of Solid Tumor Oncology, Cleveland Clinic Taussig Cancer Institute (CCF), Cleveland, Ohio.
Clin Cancer Res ; 24(10): 2350-2356, 2018 05 15.
Article em En | MEDLINE | ID: mdl-29490989
ABSTRACT

Purpose:

The survival of patients with clear cell metastatic renal cell carcinoma (cc-mRCC) has improved substantially since the introduction of tyrosine kinase inhibitors (TKI). With the fact that TKIs interact with immune responses, we investigated whether polymorphisms of genes involved in immune checkpoints are related to the clinical outcome of cc-mRCC patients treated with sunitinib as first TKI.Experimental

Design:

Twenty-seven single-nucleotide polymorphisms (SNP) in CD274 (PD-L1), PDCD1 (PD-1), and CTLA-4 were tested for a possible association with progression-free survival (PFS) and overall survival (OS) in a discovery cohort of 550 sunitinib-treated cc-mRCC patients. SNPs with a significant association (P < 0.05) were tested in an independent validation cohort of 138 sunitinib-treated cc-mRCC patients. Finally, data of the discovery and validation cohort were pooled for meta-analysis.

Results:

CTLA-4 rs231775 and CD274 rs7866740 showed significant associations with OS in the discovery cohort after correction for age, gender, and Heng prognostic risk group [HR, 0.84; 95% confidence interval (CI), 0.72-0.98; P = 0.028, and HR, 0.73; 95% CI, 0.54-0.99; P = 0.047, respectively]. In the validation cohort, the associations of both SNPs with OS did not meet the significance threshold of P < 0.05. After meta-analysis, CTLA-4 rs231775 showed a significant association with OS (HR, 0.83; 95% CI, 0.72-0.95; P = 0.008). Patients with the GG genotype had longer OS (35.1 months) compared with patients with an AG (30.3 months) or AA genotype (24.3 months). No significant associations with PFS were found.

Conclusions:

The G-allele of rs231775 in the CTLA-4 gene is associated with an improved OS in sunitinib-treated cc-mRCC patients and could potentially be used as a prognostic biomarker. Clin Cancer Res; 24(10); 2350-6. ©2018 AACR.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Polimorfismo de Nucleotídeo Único / Antígeno CTLA-4 Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma de Células Renais / Polimorfismo de Nucleotídeo Único / Antígeno CTLA-4 Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article