Imaging early changes in proliferation at 1 week post chemotherapy:: a pilot study in breast cancer patients with 3′-deoxy-3′-[18F]fluorothymidine positron emission tomography

被引:213
|
作者
Kenny, Laura
Coombes, R. Charles
Vigushin, David M.
Al-Nahhas, Adil
Shousha, Sami
Aboagye, Eric O.
机构
[1] Hammersmith Hosp, Mol Therapy Grp, London W12 0NN, England
[2] Hammersmith Hosp, NHS Trust, London, England
[3] Univ London Imperial Coll Sci Technol & Med, London, England
基金
英国医学研究理事会;
关键词
FLT; PET; breast cancer; response;
D O I
10.1007/s00259-007-0379-4
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose 3'-Deoxy-3'-[F-18]fluorothymidine positron emission tomography ([F-18]FLT-PET) has been developed for imaging cell proliferation and findings correlate strongly with the Ki-67 labelling index in breast cancer. The aims of this pilot study were to define objective criteria for [F-18]FLT response and to examine whether [F-18]FLT-PET can be used to quantify early response of breast cancer to chemotherapy. Methods Seventeen discrete lesions in 13 patients with stage II-IV breast cancer were scanned prior to and at 1 week after treatment with combination 5-fluorouracil, epirubicin and cyclophosphamide (FEC) chemotherapy. The uptake at 90 min (SUV90) and irreversible trapping (K-i) of [1(8)F]FLT were calculated for each tumour. The reproducibility of [F-18]FLT-PET was determined in nine discrete lesions from eight patients who were scanned twice before chemotherapy. Clinical response was assessed at 60 days after commencing FEC. Results All tumours showed [F-18]FLT uptake and this was reproducible in serial measurements (SD of mean % difference = 10.5% and 15.1%, for SUV90 and K-i, respectively; test-retest correlation coefficient >= 0.97). Six patients had a significant clinical response (complete or partial) at day 60; these patients also had a significant reduction in [F-18]FLT uptake at 1 week. Decreases in K (i) and SUV90 at 1 week discriminated between clinical response and stable disease (p = 0.022 for both parameters). In three patients with multiple lesions there was a mixed [F-18]FLT response in primary tumours and metastases. [F-18]FLT response generally preceded tumour size changes. Conclusion [F-18]FLT-PET can detect changes in breast cancer proliferation at 1 week after FEC chemotherapy.
引用
收藏
页码:1339 / 1347
页数:9
相关论文
共 50 条
  • [31] 3'-deoxy-3'-[18F]fluorothymidine positron emission tomography is a sensitive method for imaging the response of BRAF-dependent tumors to MEK inhibition
    Solit, David B.
    Santos, Elmer
    Pratilas, Christine A.
    Lobo, Jose
    Moroz, Maxim
    Cai, Shangde
    Blasberg, Ronald
    Sebolt-Leopold, Judith
    Larson, Steven
    Rosen, Neal
    CANCER RESEARCH, 2007, 67 (23) : 11463 - 11469
  • [32] Reproducibility of quantitative 18F-3′-deoxy-3′-fluorothymidine measurements using positron emission tomography
    Adrianus J. de Langen
    Bianca Klabbers
    Mark Lubberink
    Ronald Boellaard
    Marieke D. Spreeuwenberg
    Ben J. Slotman
    Remco de Bree
    Egbert F. Smit
    Otto S. Hoekstra
    Adriaan A. Lammertsma
    European Journal of Nuclear Medicine and Molecular Imaging, 2009, 36 : 389 - 395
  • [33] Reproducibility of quantitative 18F-3'-deoxy-3'-fluorothymidine measurements using positron emission tomography
    de Langen, Adrianus J.
    Klabbers, Bianca
    Lubberink, Mark
    Boellaard, Ronald
    Spreeuwenberg, Marieke D.
    Slotman, Ben J.
    de Bree, Remco
    Smit, Egbert F.
    Hoekstra, Otto S.
    Lammertsma, Adriaan A.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2009, 36 (03) : 389 - 395
  • [34] 3′-deoxy-3′-[18F]fluorothymidine as a new marker for monitoring tumor response to antiproliferative therapy in vivo with positron emission tomography
    Barthel, H
    Cleij, MC
    Collingridge, DR
    Hutchinson, OC
    Osman, S
    He, QM
    Luthra, SK
    Brady, F
    Price, PM
    Aboagye, EO
    CANCER RESEARCH, 2003, 63 (13) : 3791 - 3798
  • [35] Mismatched intratumoral distribution of [18F] fluorodeoxyglucose and 3′-deoxy-3′-[18F] fluorothymidine in patients with lung cancer
    Wang, Xiangcheng
    He, Yulin
    Zhou, Weina
    Bai, Xia
    Wu, Yiwei
    Wang, Xuemei
    Li, Xiao-Feng
    ONCOLOGY LETTERS, 2017, 14 (05) : 5279 - 5284
  • [36] Clinical value of 3'-deoxy-3'-[18F]fluorothymidine-positron emission tomography for diagnosis, staging and assessing therapy response in lung cancer
    Bandar Alwadani
    Sergio Dall’Angelo
    Ian N. Fleming
    Insights into Imaging, 12
  • [37] Molecular imaging of proliferation in vivo: Positron emission tomography with [18F]fluorothymidine
    Buck, Andreas K.
    Herrmann, Ken
    Shen, Changxian
    Dechow, Tobias
    Schwaiger, Markus
    Wester, Hans-Juergen
    METHODS, 2009, 48 (02) : 205 - 215
  • [38] Clinical value of 3'-deoxy-3'-[18F]fluorothymidine-positron emission tomography for diagnosis, staging and assessing therapy response in lung cancer
    Alwadani, Bandar
    Dall'Angelo, Sergio
    Fleming, Ian N.
    INSIGHTS INTO IMAGING, 2021, 12 (01)
  • [39] 3-deoxy-3-[18F]fluorothymidine-positron emission tomography for noninvasive assessment of proliferation in pulmonary nodules
    Buck, AK
    Schirrmeister, H
    Hetzel, M
    von der Heide, M
    Halter, G
    Glatting, G
    Mattfeldt, T
    Liewald, F
    Reske, SN
    Neumaier, B
    CANCER RESEARCH, 2002, 62 (12) : 3331 - 3334
  • [40] Methodological Considerations in Quantification of 3'-Deoxy-3'-[18F]Fluorothymidine Uptake Measured with Positron Emission Tomography in Patients with Non-Small Cell Lung Cancer
    Virginie Frings
    Adrianus J. de Langen
    Maqsood Yaqub
    Robert C. Schuit
    Astrid A. M. van der Veldt
    Otto S. Hoekstra
    Egbert F. Smit
    Ronald Boellaard
    Molecular Imaging and Biology, 2014, 16 : 136 - 145