Angiogenic, inflammatory and immunologic markers in predicting response to sunitinib in metastatic renal cell carcinoma. Issue 9 (20th August 2017)
- Record Type:
- Journal Article
- Title:
- Angiogenic, inflammatory and immunologic markers in predicting response to sunitinib in metastatic renal cell carcinoma. Issue 9 (20th August 2017)
- Main Title:
- Angiogenic, inflammatory and immunologic markers in predicting response to sunitinib in metastatic renal cell carcinoma
- Authors:
- Mizuno, Ryuichi
Kimura, Go
Fukasawa, Satoshi
Ueda, Takeshi
Kondo, Tsunenori
Hara, Hidehiko
Shoji, Sunao
Kanao, Kent
Nakazawa, Hayakazu
Tanabe, Kazunari
Horie, Shigeo
Oya, Mototsugu - Other Names:
- Yuasa T. investigator.
Horiguchi A. investigator.
Nakaigawa N. investigator.
Oyama M. investigator.
Nagata H. investigator.
Ishida M. investigator.
Kawata N. investigator.
Hatano T. investigator.
Kishida T. investigator.
Morita J. investigator.
Yamaguchi R. investigator.
Nakagawa T. investigator.
Kume H. investigator. - Abstract:
- Abstract : The objective of this prospective study was to identify baseline angiogenic and inflammatory markers in serum as well as the baseline levels of immune cells in whole blood to predict progression‐free survival in patients with metastatic renal cell carcinoma treated with sunitinib. Blood samples were collected at baseline in all 90 patients to analyze serum angiogenic and inflammatory markers together with peripheral blood immunological marker. The association between each marker and sunitinib efficacy was analyzed. Univariate and multivariate Cox proportional model analyses were used to assess the correlation between those markers with survival. Baseline levels of interleukin‐6, interleukin‐8, high sensitivity C‐reactive protein and myeloid‐derived suppressor cells were significantly higher in patients who progressed when compared with those with clinical benefit. Analysis by the Cox regression model showed that baseline interleukin‐8, high sensitivity C‐reactive protein and percentage of T helper type 1 cells were significantly associated with progression‐free survival in univariate analysis. Furthermore, in multivariate analysis, those three markers were independent indices to predict progression‐free survival. In conclusion, angiogenic (interleukin‐8), inflammatory (interleukin‐6, high sensitivity C‐reactive) and immunologic (myeloid‐derived suppressor cells, percentage of T helper type 1 cells) markers at baseline would predict the response to sunitinibAbstract : The objective of this prospective study was to identify baseline angiogenic and inflammatory markers in serum as well as the baseline levels of immune cells in whole blood to predict progression‐free survival in patients with metastatic renal cell carcinoma treated with sunitinib. Blood samples were collected at baseline in all 90 patients to analyze serum angiogenic and inflammatory markers together with peripheral blood immunological marker. The association between each marker and sunitinib efficacy was analyzed. Univariate and multivariate Cox proportional model analyses were used to assess the correlation between those markers with survival. Baseline levels of interleukin‐6, interleukin‐8, high sensitivity C‐reactive protein and myeloid‐derived suppressor cells were significantly higher in patients who progressed when compared with those with clinical benefit. Analysis by the Cox regression model showed that baseline interleukin‐8, high sensitivity C‐reactive protein and percentage of T helper type 1 cells were significantly associated with progression‐free survival in univariate analysis. Furthermore, in multivariate analysis, those three markers were independent indices to predict progression‐free survival. In conclusion, angiogenic (interleukin‐8), inflammatory (interleukin‐6, high sensitivity C‐reactive) and immunologic (myeloid‐derived suppressor cells, percentage of T helper type 1 cells) markers at baseline would predict the response to sunitinib therapy and/or disease progression in patients with metastatic renal cell carcinoma. Abstract : Angiogenic (interleukin‐8), inflammatory (interleukin‐6, high sensitivity C‐reactive), and immunologic (myeloid‐derived suppressor cells, percentage of T helper type 1 cells) markers at baseline would predict response to sunitinib therapy and/or disease progression in patients with mRCC. … (more)
- Is Part Of:
- Cancer science. Volume 108:Issue 9(2017)
- Journal:
- Cancer science
- Issue:
- Volume 108:Issue 9(2017)
- Issue Display:
- Volume 108, Issue 9 (2017)
- Year:
- 2017
- Volume:
- 108
- Issue:
- 9
- Issue Sort Value:
- 2017-0108-0009-0000
- Page Start:
- 1858
- Page End:
- 1863
- Publication Date:
- 2017-08-20
- Subjects:
- High sensitivity C‐reactive protein -- interleukin 8 -- renal cell carcinoma -- sunitinib -- T helper type 1 lymphocyte
Cancer -- Periodicals
Neoplasms -- Periodicals
Research -- Periodicals
Electronic journals
616.994005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1347-9032;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1349-7006 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cas.13320 ↗
- Languages:
- English
- ISSNs:
- 1347-9032
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.603000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26623.xml