論文

査読有り 国際誌
2017年9月

Effect of ABO blood type on the outcomes of patients with metastatic renal cell carcinoma treated with first-line tyrosine kinase inhibitors

Urologic Oncology: Seminars and Original Investigations
  • Kenji Omae
  • ,
  • Shingo Fukuma
  • ,
  • Tatsuyoshi Ikenoue
  • ,
  • Tsunenori Kondo
  • ,
  • Toshio Takagi
  • ,
  • Hiroki Ishihara
  • ,
  • Kazunari Tanabe
  • ,
  • Shunichi Fukuhara

35
9
開始ページ
540.e7
終了ページ
540.e12
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.urolonc.2017.04.004
出版者・発行元
ELSEVIER SCIENCE INC

Objectives: To assess the effect of blood type on survival outcomes and adverse events (AEs) in patients treated with tyrosine kinase inhibitors (TKIs) for metastatic renal cell carcinoma (mRCC).Materials and methods: Patients who received TKIs as first-line therapy for mRCC between 2008 and 2015 at our hospital were included in the study (n = 136). Patients were divided into 2 groups based on their blood type as 0 and non-O. Survival outcomes and AEs were compared according to blood type. Cox regression models were used for univariate and multivariate survival analyses.Results: Of the 136 patients, 34 (25%) and 102 (75%) had 0 and non-O blood types, respectively. Blood type 0 was associated with an increased number of disease sites. There were no differences between the 2 groups with respect to other baseline characteristics. The progression-free survival in patients with 0 and non-O blood types was 12.1 and 11.6 months, respectively; the overall survival was 34.4 and 24.8 months, respectively. On univariate and multivariate analyses, the ABO blood type was not a significant prognostic factor for progression-free survival or overall survival. Furthermore, the incidences of serious AEs were similar in the 2 blood groups.Conclusions: ABO blood type was not associated with survival outcomes or incidences of serious AEs in mRCC patients treated with TKIs. However, blood type 0 may be associated with an increased number of disease sites. (C) 2017 Published by Elsevier Inc.

リンク情報
DOI
https://doi.org/10.1016/j.urolonc.2017.04.004
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28624136
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000410681000005&DestApp=WOS_CPL
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85020744205&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85020744205&origin=inward
ID情報
  • DOI : 10.1016/j.urolonc.2017.04.004
  • ISSN : 1078-1439
  • eISSN : 1873-2496
  • PubMed ID : 28624136
  • SCOPUS ID : 85020744205
  • Web of Science ID : WOS:000410681000005

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