Pharmacodynamic evaluation of irinotecan therapy by FDG and FLT PET/CT imaging in a colorectal cancer xenograft model.

Purpose: Longitudinal changes of 3'-[(18) F]fluoro-3'-deoxythymidine (FLT) and 2-deoxy-2-[(18) F]fluoro-D-glucose (FDG) in response to irinotecan therapy in an animal model of colorectal cancer were compared.Procedures: SCID/CB-17 mice with HCT116 tumors were treated with 50 mg/kg irinotecan by intr...

Descripción completa

Detalles Bibliográficos
Publicado en:Molecular Imaging & Biology Vol. 14; no. 5; pp. 617 - 625
Autores principales: Mudd SR, Holich KD, Voorbach MJ, Cole TB, Reuter DR, Tapang P, Bukofzer G, Chakravartty A, Donawho CK, Palma JP, Fox GB, Day M, Luo Y, Mudd, Sarah R, Holich, Kimberley D, Voorbach, Martin J, Cole, Todd B, Reuter, David R, Tapang, Paul, Bukofzer, Gail
Formato: research Journal Article
Publicado: Springer Nature Oct2012
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=104383297&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 104383297
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        15361632
        KJU
      jtl: Molecular Imaging & Biology
      issn: 15361632
      maglogo: N
    pubinfo:
      dt: Oct2012
      vid: 14
      iid: 5
      pid: 237
      pub: Springer Nature
      place: New York, New York
    artinfo:
      ui:
        104383297
        NLM22167582
        2011754226
        10.1007/s11307-011-0529-8
        NLM22167582
        104383297
      ppf: 617
      ppct: 8
      formats:
        fmt:
          @attributes:
            type: P
      tig:
        atl: Pharmacodynamic evaluation of irinotecan therapy by FDG and FLT PET/CT imaging in a colorectal cancer xenograft model.
      aug:
        au:
          Mudd SR
          Holich KD
          Voorbach MJ
          Cole TB
          Reuter DR
          Tapang P
          Bukofzer G
          Chakravartty A
          Donawho CK
          Palma JP
          Fox GB
          Day M
          Luo Y
          Mudd, Sarah R
          Holich, Kimberley D
          Voorbach, Martin J
          Cole, Todd B
          Reuter, David R
          Tapang, Paul
          Bukofzer, Gail
        affil: Translational Imaging and Biochemical Biomarkers, Advanced Technology, Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, IL, USA
      sug:
        subj:
          Camptothecin Analogs and Derivatives
          Colorectal Neoplasms Drug Therapy
          Colorectal Neoplasms Radiography
          Deoxyribonucleosides Diagnostic Use
          Fludeoxyglucose F 18 Diagnostic Use
          Animal Studies
          Body Weights and Measures
          Camptothecin Pharmacodynamics
          Camptothecin Therapeutic Use
          Cells
          Colorectal Neoplasms Pathology
          Deoxyribonucleosides Pharmacokinetics
          Female
          Fludeoxyglucose F 18 Pharmacokinetics
          Human
          Immunohistochemistry
          Mice
          Female
      ab: Purpose: Longitudinal changes of 3'-[(18) F]fluoro-3'-deoxythymidine (FLT) and 2-deoxy-2-[(18) F]fluoro-D-glucose (FDG) in response to irinotecan therapy in an animal model of colorectal cancer were compared.Procedures: SCID/CB-17 mice with HCT116 tumors were treated with 50 mg/kg irinotecan by intraperitoneal injection weekly for 3 weeks. FLT and FDG-positron emission tomography (PET) were performed at baseline, the day after each treatment, and 5 days after the first treatment. Proliferation and apoptosis were evaluated by immunohistochemistry (IHC) after day 15 of imaging.Results: Irinotecan treatment resulted in a suppression of tumor growth. Tumor FLT uptake was decreased the day after each treatment but to a lesser extent 5 days after the first treatment. FDG uptake increased the day after each treatment with a continuous increase throughout the experiment. IHC analysis of phospho-H3 and Ki67 confirmed FLT-PET results, indicating a decrease in proliferation the day after the final irinotecan treatment. Increased apoptosis monitored by caspase-3 was observed after day 15 with irinotecan treatment.Conclusions: FLT-PET may be a better method than FDG-PET for assessing treatment response to irinotecan. Changes in imaging occur before changes in tumor volume.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N