Literature DB >> 21128242

Reaction of plasma hepatocyte growth factor levels in non-small cell lung cancer patients treated with EGFR-TKIs.

Hidenori Tanaka1, Tatsuo Kimura, Shinzoh Kudoh, Shigeki Mitsuoka, Tetsuya Watanabe, Tomohiro Suzumura, Keisei Tachibana, Masayuki Noguchi, Seiji Yano, Kazuto Hirata.   

Abstract

Hepatocyte growth factor induces resistance to epidermal growth factor receptor tyrosine kinase inhibitors. It has been hypothesized that epidermal growth factor receptor tyrosine kinase inhibitors administration may influence the levels of plasma hepatocyte growth factor. Patients with advanced non-small cell lung cancer and relapsed after chemotherapies were eligible. Plasma hepatocyte growth factor levels were analyzed on pretreatment and post-treatment day 15 and 30. We also investigated the correlation between plasma hepatocyte growth factor levels and sensitivity to epidermal growth factor receptor tyrosine kinase inhibitors, tissue immunoreactivity for hepatocyte growth factor and MET gene status. Thirty-one patients were enrolled. Plasma hepatocyte growth factor levels on post-treatment day 15 (630.1 ± 366.9 pg/ml) were significantly higher (p = 0.029) than the pretreatment plasma hepatocyte growth factor levels (485.9 ± 230.2 pg/ml). Plasma hepatocyte growth factor levels on the post-treatment day 30 (581.5 ± 298.1 pg/ml) tend to be higher than those before treatment (p = 0.057). Pretreatment plasma hepatocyte growth factor levels in patients with progressive disease (724.1 ± 216.4 pg/ml) were significantly higher than those in patients with stable disease (396.5 ± 148.3 pg/ml; p = 0.0008) and partial response (381.7 ± 179.0 pg/ml; p = 0.0039). The optimal pretreatment plasma hepatocyte growth factor cut-off value for diagnosis of responder was 553.5 pg/ml, and its sensitivity and specificity were 90% and 65%, respectively. Pretreatment plasma hepatocyte growth factor levels had no correlation with tissue immunoreactivities for hepatocyte growth factor, MET gene status and active EGFR mutations. Administration of epidermal growth factor receptor tyrosine kinase inhibitors significantly increased plasma hepatocyte growth factor levels. High levels of pretreatment plasma hepatocyte growth factor indicated intrinsic resistance to epidermal growth factor receptor tyrosine kinase inhibitors. Plasma hepatocyte growth factor can serve as a useful biomarker for the early diagnosis of tumor relapse treated with epidermal growth factor receptor tyrosine kinase inhibitors.
Copyright © 2010 UICC.

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Year:  2011        PMID: 21128242     DOI: 10.1002/ijc.25799

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  11 in total

Review 1.  Redundant kinase activation and resistance of EGFR-tyrosine kinase inhibitors.

Authors:  Min Luo; Li-Wu Fu
Journal:  Am J Cancer Res       Date:  2014-11-19       Impact factor: 6.166

2.  IL6 is associated with response to dasatinib and cetuximab: Phase II clinical trial with mechanistic correlatives in cetuximab-resistant head and neck cancer.

Authors:  L P Stabile; A M Egloff; M K Gibson; W E Gooding; J Ohr; P Zhou; N J Rothenberger; L Wang; J L Geiger; J T Flaherty; J R Grandis; J E Bauman
Journal:  Oral Oncol       Date:  2017-04-09       Impact factor: 5.337

Review 3.  MET/HGF pathway activation as a paradigm of resistance to targeted therapies.

Authors:  Brian Ko; Tianfang He; Shirish Gadgeel; Balazs Halmos
Journal:  Ann Transl Med       Date:  2017-01

Review 4.  Hepatocyte Growth Factor/c-Met Signaling in Head and Neck Cancer and Implications for Treatment.

Authors:  Natalie J Rothenberger; Laura P Stabile
Journal:  Cancers (Basel)       Date:  2017-04-24       Impact factor: 6.639

Review 5.  Hepatocyte growth factor/MET in cancer progression and biomarker discovery.

Authors:  Kunio Matsumoto; Masataka Umitsu; Dinuka M De Silva; Arpita Roy; Donald P Bottaro
Journal:  Cancer Sci       Date:  2017-03       Impact factor: 6.716

6.  Triple inhibition of EGFR, Met, and VEGF suppresses regrowth of HGF-triggered, erlotinib-resistant lung cancer harboring an EGFR mutation.

Authors:  Junya Nakade; Shinji Takeuchi; Takayuki Nakagawa; Daisuke Ishikawa; Takako Sano; Shigeki Nanjo; Tadaaki Yamada; Hiromichi Ebi; Lu Zhao; Kazuo Yasumoto; Kunio Matsumoto; Kazuhiko Yonekura; Seiji Yano
Journal:  J Thorac Oncol       Date:  2014-06       Impact factor: 15.609

7.  Four Is Better Than 1-Strength in Numbers!

Authors:  Ann M Bode; Zigang Dong
Journal:  EBioMedicine       Date:  2016-08-31       Impact factor: 8.143

8.  Multiplexed Serum Biomarkers for the Detection of Lung Cancer.

Authors:  Shenglin Ma; Wenzhe Wang; Bing Xia; Shirong Zhang; Haining Yuan; Hong Jiang; Wen Meng; Xiaoliang Zheng; Xiaoju Wang
Journal:  EBioMedicine       Date:  2016-08-14       Impact factor: 8.143

9.  Targeting the tumor-promoting microenvironment in MET-amplified NSCLC cells with a novel inhibitor of pro-HGF activation.

Authors:  Benjamin Y Owusu; Shantasia Thomas; Phanindra Venukadasula; Zhenfu Han; James W Janetka; Robert A Galemmo; Lidija Klampfer
Journal:  Oncotarget       Date:  2017-05-29

10.  Phase I Study of Ficlatuzumab and Cetuximab in Cetuximab-Resistant, Recurrent/Metastatic Head and Neck Cancer.

Authors:  Julie E Bauman; James Ohr; William E Gooding; Robert L Ferris; Umamaheswar Duvvuri; Seungwon Kim; Jonas T Johnson; Adam C Soloff; Gerald Wallweber; John Winslow; Autumn Gaither-Davis; Jennifer R Grandis; Laura P Stabile
Journal:  Cancers (Basel)       Date:  2020-06-11       Impact factor: 6.639

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