Personnel exposure in labelling and administration of 177Lu-DOTA-D-Phe1-Tyr3-octreotide

ObjectiveThe introduction of peptide receptor radionuclide therapy, mainly performed with 90Y and 177Lu-labelled somatostatin analogues, has widened the therapeutic horizon of nuclear medicine.The handling of 177Lu-labelled pharmaceuticals implies an increase of the personnel exposure and this aspect is evaluated in this paper, in comparison with personal exposure in 90Y manipulation. Materials and methodsPersonal dose measurements were performed during 26 177Lu-DOTATOC preparations by using a series of thin active layer LiF: Mg,Cu,P thermoluminescence dosimeters fixed at the operator’s fingertips to evaluate the skin equivalent dose and by means of direct reading dosimeters positioned at the chest to evaluate the personal effective dose. Individual protection devices, such as shielded aprons and anti-X gloves, were also used. ResultsThe 95th percentile of the skin equivalent dose distribution for 177Lu operations by using 0.20-mm anti-X gloves was 0.080 mSv/GBq for the chemist and 0.011 mSv/GBq for the physician, whereas the 75th percentile was 0.058 mSv/GBq for the chemist and 0.006 mSv/GBq for the physician. The use of the 0.25 mm Pb-equivalent anti-X apron halved the personal equivalent dose measured over the apron by a direct reading dosimeter. Skin doses were compared with 90Y-DOTATOC procedures: no relevant exposure reduction is observed for chemists, whereas doses are considerably lower during administration procedures performed by physicians. ConclusionIn this study, an evaluation of the skin equivalent doses during 177Lu-DOTATOC labelling and administration is presented. These data can be useful to assess the risk for workers in centres that are starting to implement PRRT using 177Lu. The use of appropriate protection devices and procedures allows the observance of International Commission for Radiological Protection dose limits for exposed workers.

[1]  T. Gregersen,et al.  Peptide Receptor Radionuclide Therapy with 90Y-DOTATOC and 177Lu-DOTATOC in Advanced Neuroendocrine Tumors: Results from a Danish Cohort Treated in Switzerland , 2011, Neuroendocrinology.

[2]  E. Glatstein Radiation protection in radionuclide therapies with 90Y-conjugates: risks and safety , 2008 .

[3]  J. Guerre,et al.  RADIONUCLIDE AND RADIATION PROTECTION DATA HANDBOOK 2002 , 2002 .

[4]  T. Niewiadomski 25 Years of TL Dosimetry at the Institute of Nuclear Physics, Kraków , 1996 .

[5]  R. Reilly The Radiochemistry of Monoclonal Antibodies and Peptides , 2010 .

[6]  Ch Blunck,et al.  Radiation protection in inhomogeneous beta-gamma fields and modelling of hand phantoms with MCNPX. , 2009, Radiation protection dosimetry.

[7]  A. Rimpler,et al.  Beta radiation exposure of medical staff and implications for extremity dose monitoring. , 2006, Radiation protection dosimetry.

[8]  M. Moscovitch Personnel Dosimetry Using LiF:Mg,Cu,P , 1999 .

[9]  Michael G Stabin,et al.  PHYSICAL MODELS AND DOSE FACTORS FOR USE IN INTERNAL DOSE ASSESSMENT , 2003, Health physics.

[10]  D. Salvo,et al.  Radiation protection in 90Y-labelled DOTA-D-Phe1-Tyr3-octreotide preparations , 2009, Nuclear medicine communications.

[11]  Jack Valentin,et al.  The 2007 Recommendations of the International Commission on Radiological Protection. ICRP publication 103. , 2007, Annals of the ICRP.

[12]  P. Olko,et al.  Ultra-thin LiF:Mg,Cu,P detectors for beta dosimetry , 1995 .

[13]  G. Gualdrini,et al.  Extremity exposure in nuclear medicine: preliminary results of a European study. , 2011, Radiation protection dosimetry.

[14]  E. Kim Monoclonal Antibody and Peptide-Targeted Radiotherapy of Cancer , 2011, The Journal of Nuclear Medicine.

[15]  I. Shimon,et al.  Peptide receptor radioligand therapy is an effective treatment for the long‐term stabilization of malignant gastrinomas , 2011, Cancer.

[16]  F. Forrer,et al.  Diagnostic versus therapeutic doses of [(177)Lu-DOTA-Tyr(3)]-octreotate: uptake and dosimetry in somatostatin receptor-positive tumors and normal organs. , 2007, Cancer biotherapy & radiopharmaceuticals.