Lu-177 DOTATATE dosimetry for neuroendocrine tumor: single center experience

被引:4
作者
Said, M. A. [1 ]
Masud, M. A. [1 ]
Zaini, M. Z. [1 ]
Salleh, R. A. [1 ]
Lee, B. N. [1 ]
Zainon, R. [2 ]
机构
[1] Inst Kanser Negara, Nucl Med Dept, Presint 7, Putrajaya 62250, Malaysia
[2] Univ Sains Malaysia, Adv Med & Dent Inst, Kepala Batas 13200, Pulau Pinang, Malaysia
来源
10TH INTERNATIONAL SEMINAR ON MEDICAL PHYSICS & 1ST AMDI INTERNATIONAL ONCOLOGY SYMPOSIUM | 2017年 / 851卷
关键词
BONE-MARROW; THERAPY; KIDNEY;
D O I
10.1088/1742-6596/851/1/012017
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Lu-177 labelled with DOTATE is widely acceptable to treat Neuroendocrine Tumor (NET) disease and it better improvement of quality of patients' life since few years ago. However, the radionuclide toxicity becomes the main limitation of the (NET) treatment. Therefore, we performed a pilot study aimed to estimate radiation absorbed doses to dose-limiting organs to develop a systemic therapy with Lu-177 in NET patients. In this study, five set of planar whole body images was acquired every 0.5 hour, 4 hours, 24 hours, 48 hours and 72 hours after Lu-177 administrations. The planar image acquisition was done using Philip Brightview X with Medium Energy General Purpose Collimator (MEGP) collimator. All patients' images in Conjugate View (CV) format were transferred into PMOD 3.7 Software for Region of Interest (ROI) analysis. The ROI were drawn at selected organs such as kidneys, liver, spleen and bladder. This study found that the mean absorbed dose for kidneys 0.62 +/- 0.26 Gy/GBq, liver 0.63 +/- 0.28 Gy/GBq, spleen 0.83 +/- 0.73 Gy/GBq and bladder 0.14 +/- 0.07 Gy/GBq. The radionuclide kinetic for the whole body 99.7 +/- 0.1 percent at 0.5 hours, 79.5 +/- 10.7 percent at 4 hours, 56.6 +/- 10.3 percent at 24 hours, 43.2 +/- 7.9 percent at 48 hours and 37.1 +/- 9.0 percent at 72 hours. This study verifies that this planar quantitative method able to determine organ at risk and the result line with other published data.
引用
收藏
页数:5
相关论文
共 14 条
[1]   Clinical radionuclide therapy dosimetry: the quest for the "Holy Gray" [J].
Brans, B. ;
Bodei, L. ;
Giammarile, F. ;
Linden, O. ;
Luster, M. ;
Oyen, W. J. G. ;
Tennvall, J. .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2007, 34 (05) :772-786
[2]   The Influence of Early Measurements Onto the Estimated Kidney Dose in [177Lu][DOTA0,Tyr3]Octreotate Peptide Receptor Radiotherapy of Neuroendocrine Tumors [J].
Delker, Andreas ;
Ilhan, Harun ;
Zach, Christian ;
Brosch, Julia ;
Gildehaus, Franz Josef ;
Lehner, Sebastian ;
Bartenstein, Peter ;
Boning, Guido .
MOLECULAR IMAGING AND BIOLOGY, 2015, 17 (05) :726-734
[3]   Kidney Dosimetry in 177Lu and 90Y Peptide Receptor Radionuclide Therapy: Influence of Image Timing, Time-Activity Integration Method, and Risk Factors [J].
Guerriero, F. ;
Ferrari, M. E. ;
Botta, F. ;
Fioroni, F. ;
Grassi, E. ;
Versari, A. ;
Sarnelli, A. ;
Pacilio, M. ;
Amato, E. ;
Strigari, L. ;
Bodei, L. ;
Paganelli, G. ;
Iori, M. ;
Pedroli, G. ;
Cremonesi, M. .
BIOMED RESEARCH INTERNATIONAL, 2013, 2013
[4]  
Heikkonen J, 2013, EUR J NUCL MED MOL I, V40, pS265
[5]   Lutetium-labelled peptides for therapy of neuroendocrine tumours [J].
Kam, B. L. R. ;
Teunissen, J. J. M. ;
Krenning, E. P. ;
de Herder, W. W. ;
Khan, S. ;
van Vliet, E. I. ;
Kwekkeboom, D. J. .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2012, 39 :103-112
[6]  
Lammers G.K., 2014, Adv. Mol. Imaging, V4, P27
[7]  
McKay E, 2013, INTERN MED J, V43, P8
[8]   Method dependence, observer variability and kidney volumes in radiation dosimetry of 177Lu-DOTATATE therapy in patients with neuroendocrine tumours [J].
Sandström M. ;
Ilan E. ;
Karlberg A. ;
Johansson S. ;
Freedman N. ;
Garske-Román U. .
EJNMMI Physics, 2 (1) :1-13
[9]   Individualized Dosimetry of Kidney and Bone Marrow in Patients Undergoing 177Lu-DOTA-Octreotate Treatment [J].
Sandstrom, Mattias ;
Garske-Roman, Ulrike ;
Granberg, Dan ;
Johansson, Silvia ;
Widstrom, Charles ;
Eriksson, Barbro ;
Sundin, Anders ;
Lundqvist, Hans ;
Lubberink, Mark .
JOURNAL OF NUCLEAR MEDICINE, 2013, 54 (01) :33-41
[10]  
Schuchardt C, 2014, EUR J NUCL MED MOL I, V41, pS224