Molecular Drug Imaging: 89Zr-Bevacizumab PET in Children with Diffuse Intrinsic Pontine Glioma

被引:62
作者
Jansen, Marc H. [1 ]
van Zanten, Sophie E. M. Veldhuijzen [1 ]
van Vuurden, Dannis G. [1 ]
Huisman, Marc C. [2 ]
Vugts, Danielle J. [2 ]
Hoekstra, Otto S. [2 ]
van Dongen, Guus A. [2 ]
Kaspers, Gert-Jan L. [1 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Pediat, Pediat Oncol Hematol, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Radiol & Nucl Med, De Boelelaan 1118, NL-1081 HV Amsterdam, Netherlands
关键词
brain stem neoplasm; PET; Zr-89-bevacizumab; pharmacokinetics; POSITRON-EMISSION-TOMOGRAPHY; BRAIN-TUMOR CONSORTIUM; MONOCLONAL-ANTIBODIES; CLINICAL-TRIALS; LUNG-CANCER; STEM GLIOMA; VEGF-A; BEVACIZUMAB; IRINOTECAN; EXPRESSION;
D O I
10.2967/jnumed.116.180216
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
Predictive tools for guiding therapy in children with brain tumors are urgently needed. In this first molecular drug imaging study in children, we investigated whether bevacizumab can reach tumors in children with diffuse intrinsic pontine glioma (DIPG) by measuring the tumor uptake of Zr-89-labeled bevacizumab by PET. In addition, we evaluated the safety of the procedure in children and determined the optimal time for imaging. Methods: Patients received Zr-89-bevacizumab (0.1 mg/kg; 0.9 MBq/kg) at least 2 wk after completing radiotherapy. Whole-body PET/CT scans were obtained 1, 72, and 144 h after injection. All patients underwent contrast (gadolinium)-enhanced MRI. The biodistribution of Zr-89-bevacizumab was quantified as SUVs. Results: Seven DIPG patients (4 boys; 6-17 y old) were scanned without anesthesia. No adverse events occurred. Five of 7 primary tumors showed focal Zr-89-bevacizumab uptake (SUVs at 144 h after injection were 1.0-6.7), whereas no significant uptake was seen in the healthy brain. In 1 patient, multiple metastases all showed positive PET results. We observed inter- and intratumoral heterogeneity of uptake, and Zr-89-bevacizumab uptake was present predominantly (in 4/5 patients) within MRI contrast -enhanced areas, although Zr-89-bevacizumab uptake in these areas was variable. Tumor targeting results were quantitatively similar at 72 and 144 h after injection, but tumor-to-blood-pool SUV ratios increased with time after injection (P = 0.045). The mean effective dose per patient was 0.9 mSv/MBq (SD, 0.3 mSv/MBq). Conclusion: Zr-89-bevacizumab PET studies are feasible in children with DIPG. The data suggest considerable heterogeneity in drug delivery among patients and within DIPG tumors and a positive, but not 1:1, correlation between MRI contrast enhancement and Zr-89-bevacizumab uptake. The optimal time for scanning is 144 h after injection. Tumor Zr-89-bevacizumab accumulation assessed by PET scanning may help in the selection of patients with the greatest chance of benefit from bevacizumab treatment.
引用
收藏
页码:711 / 716
页数:6
相关论文
共 26 条
  • [1] Aguilera Dolly G, 2013, J Pediatr Hematol Oncol, V35, pe42, DOI 10.1097/MPH.0b013e318279aed8
  • [2] Bevacizumab-Induced Normalization of Blood Vessels in Tumors Hampers Antibody Uptake
    Arjaans, Marlous
    Munnink, Thijs H. Oude
    Oosting, Sjoukje F.
    van Scheltinga, Anton G. T. Terwisscha
    Gietema, Jourik A.
    Garbacik, Erik T.
    Timmer-Bosscha, Hetty
    Lub-de Hooge, Marjolijn N.
    Schroder, Carolina P.
    de Vries, Elisabeth G. E.
    [J]. CANCER RESEARCH, 2013, 73 (11) : 3347 - 3355
  • [3] Pilot study of 89Zr-bevacizumab positron emission tomography in patients with advanced non-small cell lung cancer
    Bahce, Idris
    Huisman, Marc C.
    Verwer, Eline E.
    Ooijevaar, Rogier
    Boutkourt, Firdaouss
    Vugts, Danielle J.
    van Dongen, Guus A. M. S.
    Boellaard, Ronald
    Smit, Egbert F.
    [J]. EJNMMI RESEARCH, 2014, 4 : 1 - 7
  • [4] Performance of immuno-positron emission tomography with zirconium-89-labeled chimeric monoclonal antibody U36 in the detection of lymph node metastases in head and neck cancer patients
    Börjesson, PKE
    Jauw, YWS
    Boellaard, R
    de Bree, R
    Comans, EFI
    Roos, JC
    Castelijns, JA
    Vosjan, MJWD
    Kummer, JA
    Leemans, CR
    Lammertsma, AA
    van Dongen, GAMS
    [J]. CLINICAL CANCER RESEARCH, 2006, 12 (07) : 2133 - 2140
  • [5] Inert coupling of IRDye800CW and zirconium-89 to monoclonal antibodies for single- or dual-mode fluorescence and PET imaging
    Cohen, Ruth
    Vugts, Danielle J.
    Stigter-van Walsum, Marijke
    Visser, Gerard W. M.
    van Dongen, Guus A. M. S.
    [J]. NATURE PROTOCOLS, 2013, 8 (05) : 1010 - 1018
  • [6] Inert coupling of IRDye800CW to monoclonal antibodies for clinical optical imaging of tumor targets
    Cohen, Ruth
    Stammes, Marieke A.
    de Roos, Inge H. C.
    Stigter-van Walsum, Marijke
    Visser, Gerard W. M.
    van Dongen, Guus A. M. S.
    [J]. EJNMMI RESEARCH, 2011, 1 : 1 - 13
  • [7] Bevacizumab (BVZ)-Associated Toxicities in Children With Recurrent Central Nervous System Tumors Treated With BVZ and Irinotecan (CPT-11) A Pediatric Brain Tumor Consortium Study (PBTC-022)
    Fangusaro, Jason
    Gururangan, Sridharan
    Poussaint, Tina Young
    McLendon, Roger E.
    Onar-Thomas, Arzu
    Warren, Katherine E.
    Wu, Shengjie
    Packer, Roger J.
    Banerjee, Anu
    Gilbertson, Richard J.
    Jakacki, Regina
    Gajjar, Amar
    Goldman, Stewart
    Pollack, Ian F.
    Friedman, Henry S.
    Boyett, James M.
    Kun, Larry E.
    Fouladi, Maryam
    [J]. CANCER, 2013, 119 (23) : 4180 - 4187
  • [8] Lack of Efficacy of Bevacizumab Plus Irinotecan in Children With Recurrent Malignant Glioma and Diffuse Brainstem Glioma: A Pediatric Brain Tumor Consortium Study
    Gururangan, Sridharan
    Chi, Susan N.
    Poussaint, Tina Young
    Onar-Thomas, Arzu
    Gilbertson, Richard J.
    Vajapeyam, Sridhar
    Friedman, Henry S.
    Packer, Roger J.
    Rood, Brian N.
    Boyett, James M.
    Kun, Larry E.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (18) : 3069 - 3075
  • [9] Diffuse brainstem glioma in children: critical review of clinical trials
    Hargrove, D
    Bartels, U
    Bouffet, E
    [J]. LANCET ONCOLOGY, 2006, 7 (03) : 241 - 248
  • [10] A pilot study of bevacizumab-based therapy in patients with newly diagnosed high-grade gliomas and diffuse intrinsic pontine gliomas
    Hummel, Trent R.
    Salloum, Ralph
    Drissi, Rachid
    Kumar, Shiva
    Sobo, Matthew
    Goldman, Stewart
    Pai, Ahna
    Leach, James
    Lane, Adam
    Pruitt, David
    Sutton, Mary
    Chow, Lionel M.
    Grimme, Laurie
    Doughman, Renee
    Backus, Lori
    Miles, Lili
    Stevenson, Charles
    Fouladi, Maryam
    DeWire, Mariko
    [J]. JOURNAL OF NEURO-ONCOLOGY, 2016, 127 (01) : 53 - 61