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Mechanism of driver mutation positive lung cancer

Research Project

Project/Area Number 15K21525
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Tumor diagnostics
Tumor therapeutics
Research InstitutionKindai University

Principal Investigator

TAKEDA Masayuki  近畿大学, 医学部, 講師 (20510928)

Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2017: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2016: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords薬効評価と予測 / 分子標的治療
Outline of Final Research Achievements

Tumor specimens from 110 patients with lung cancer recruited between July 2013 and March 2015 were analyzed. The most common genetic alterations were TP53 mutations in 42 patients, followed by EGFR mutations in 25, STK11 mutations in 12, and KRAS mutations in 10. Potentially actionable mutations were identified in 44 patients including 50% of those with adenocarcinoma and 14% of those with squamous cell carcinoma. The OS of patients with advanced or recurrent cancer who had an actionable mutation and received targeted therapy (median OS not achieved) was significantly longer than that of those with no mutation (18.1 months, P = 0.041) or of those with a mutation not so treated (6.1 months, P = 0.0027).Multiplex genomic testing was performed on formalin-fixed, paraffin-embedded tumor specimens with a success rate of -95%. Such testing can assist physicians in matching patients with approved or experimental targeted treatments.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report
  • Research Products

    (6 results)

All 2017 2016 2015

All Journal Article (5 results) (of which Peer Reviewed: 5 results,  Open Access: 5 results,  Acknowledgement Compliant: 4 results) Presentation (1 results)

  • [Journal Article] Toxicity profile of epidermal growth factor receptor tyrosine kinase inhibitors in patients with epidermal growth factor receptor gene mutation-positive lung cancer.2017

    • Author(s)
      Takeda M, Nakagawa K.
    • Journal Title

      Mol Clin Oncol

      Volume: 6 Issue: 1 Pages: 3-6

    • DOI

      10.3892/mco.2016.1099

    • Related Report
      2017 Annual Research Report 2016 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Successful human epidermal growth receptor 2-targeted therapy beyond disease progression for extramammary Paget's disease.2016

    • Author(s)
      Watanabe S, Takeda M, Takahama T, Iwasa T, Tsurutani J, Tanizaki J, Shimizu T, Sakai K, Wada Y, Isogai N, Nishio K, Nakagawa K.
    • Journal Title

      Invest New Drugs.

      Volume: Feb 9

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Genome sequencing for nonsmall-cell lung cancer identifies a basis for nintedanib sensitivity.2016

    • Author(s)
      Takeda M, Sakai K, Okamoto K, Hayashi H, Tanaka K, Shimizu T, Nishio K, Nakagawa K.
    • Journal Title

      Ann Oncol

      Volume: 27(4) Issue: 4 Pages: 748-750

    • DOI

      10.1093/annonc/mdw021

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Role of EGFR Monoclonal Antibodies in the Management of Non-small Cell Lung Cancer.2015

    • Author(s)
      Takeda M, Nakagawa K.
    • Journal Title

      Curr Cancer Drug Targets

      Volume: 15(9) Pages: 792-802

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Journal Article] Clinical application of amplicon-based next-generation sequencing to therapeutic decision making in lung cancer.2015

    • Author(s)
      Takeda M, Sakai K, Terashima M, Kaneda H, Hayashi H, Tanaka K, Okamoto K, Takahama T, Yoshida T, Iwasa T, Shimizu T, Nonagase Y, Kudo K, Tomida S, Mitsudomi T, Saigo K, Ito A, Nakagawa K, Nishio K.
    • Journal Title

      Ann Oncol

      Volume: 26(12) Issue: 12 Pages: 2477-2482

    • DOI

      10.1093/annonc/mdv475

    • Related Report
      2015 Research-status Report
    • Peer Reviewed / Open Access / Acknowledgement Compliant
  • [Presentation] 希少がんの新治療法確立に向けての課題2016

    • Author(s)
      武田真幸
    • Organizer
      第54回日本癌治療学会学術集会
    • Place of Presentation
      パシフィコ横浜(横浜)
    • Year and Date
      2016-10-20
    • Related Report
      2016 Research-status Report

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Published: 2015-04-16   Modified: 2020-01-20  

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