Isotope Technologies Garching GmbHCERN 2010 Radiation Protection Aspects Related to Lutetium-177 Use in Hospitals R. Henkelmann, A. Hey, O. Buck, K. Zhernosekov,

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Isotope Technologies Garching GmbHCERN 2010 Radiation Protection Aspects Related to Lutetium-177 Use in Hospitals R. Henkelmann, A. Hey, O. Buck, K. Zhernosekov, T. Nikula

Isotope Technologies Garching GmbHCERN 2010 PRRT for neuroendrocrine tumors  Peptide Receptor Radionuclide Therapy – PRRT  How is it performed?  Choice of peptide: DOTA-TATE, DOTA-TOC  Choice of radionuclide: 177 Lu, 90 Y  Aspects: kidney protection, tumor and organ dosimetry, monitoring of toxicity  Nuclide Half-life beta energy path length(mm) gamma (keV) 177 Lu 6.7 d 133 keV 2 208, Y 2.7 d 935 keV 12 no

Isotope Technologies Garching GmbHCERN 2010 Lu-177 Hf-177 Lu-176 2,59 σ d 6,7d β γ 208.  Irradiate enriched 176 Lu sample in typical neutron flux of (1-3)·10 14 n./cm 2 /s.  max. specific activity of 177 Lu at EOI: 925 – 1220 GBq/mg ( depending on enrichment of target material ), “carrier-added form” more than 3 stable Lu atoms for every 177 Lu  long-lived radioactive impurities: > 0.01 % of 177m Lu  easy target processing  easy chemistry Direct production: (easy) route 176 Lu(n,  ) 177 Lu

Isotope Technologies Garching GmbHCERN 2010  Irradiate highly enriched 176 Yb sample in high neutron flux (1-20)·10 14 n./cm 2 /s, then separate chemically Lu from Yb.  highest specific activity: up to 4000 GBq/mg, i.e. nearly every Lu atom is 177 Lu  “no-carrier-added” form  highest radionuclidic purity Lu-177 Hf-177 Lu-176 2,59 σ d 6.7d β γ 208. Yb-177Yb ,76 σ <3 1.9 h β Indirect production route 176 Yb(n,  ) 177 Yb (β - ) 177 Lu

Isotope Technologies Garching GmbHCERN 2010 Chemical Separation Yb-Lu

Isotope Technologies Garching GmbHCERN 2010  During direct irradiation of 176 Lu a remarkable amount of 177m Lu (T 1/2 = 160 d) is produced via 176 Lu(n,γ) (σ= 2 barn).  It is known that minute amounts of 152 Eu (T 1/2 = 13.3 a), 154 Eu (T 1/2 = 8.8 a), 178 Hf (T 1/2 =31 a), and 46 Sc (T 1/2 = 84 d) are also present in the final product.  The 177m Lu content in a labelling solution is mainly depending on two factors: irradiation time and time after end of the irradiation (EOI).  Under the above mentioned conditions reported values for the 177m Lu/ 177 Lu ratio from several reactors vary between 0.01% % at EOI. The hospitals are using their 177 Lu up to one week after EOI when the 177m Lu/ 177 Lu ratio has doubled. Impurities in the carrier-added Lutetium-177 solution

Isotope Technologies Garching GmbHCERN 2010 Amount of Lutetium-177m  Lutetium-177 is mainly used for peptide labelling. A typical dose is GBq. When the 177m Lu/ 177 Lu ratio is 0.02%, it means that a dose includes approximately 1.4 – 1.8 MBq 177m Lu.

Isotope Technologies Garching GmbHCERN 2010 Radioactive Material Licence  To handle radioactive materials, which have more activity than the free limit, it is required to have a radioactive material licence. For 177m Lu the free limit is 1 MBq.  If the free limit is exceeded the nuclide has to be included in the licence or it should be licenced as a byproduct.  Hence, hospitals which are using over 5 GBq c.a. 177 Lu should have a radioactive material licence also for 177m Lu  (According to the German Radiation Safety Regulation)

Isotope Technologies Garching GmbHCERN 2010 Laboratory Waste  During the labelling process and treatment the loss of radioactivity is typically 2 to 5% of the activity - that is equal to kBq 177m Lu.  The release limit for 177m Lu is 10 Bq/g waste. All waste should be collected and shipped to a radioactive deposit or left to decay (if the total waste amount is 0,5 kg per treatment it requires at least 5 half-lives (2 years) to reach the limit).  (According to the German Radiation Safety Regulation)

Isotope Technologies Garching GmbHCERN 2010 Waste Water  A patient excretes approximately 80% of the dose (1.45 MBq 177m Lu) through the urine relatively fast.  The highest allowed radioactive concentration in the sewage water canal is 50 kBq/m 3. This means that a patient dose needs to be diluted in 30 m 3 after the cooling time, which is required for 177 Lu decay (2.5 months after treatment the total volume should be 60 m 3 ).  Great variation how regulatory bodies are calculating the total amount of water that is required and how the radioactive concentration is calculated in a sewage water canal.

Isotope Technologies Garching GmbHCERN 2010 Waste Water Gamma-Ray Spectrum

Isotope Technologies Garching GmbHCERN 2010 Waste Water in the Tank  The waste water sample (1 litre) from a nuclear medicine department contained approximately 30 Bq/l of 177m Lu, so the 177m Lu content was under the release limit.  BUT:  The 177m Lu content was much higher than the estimation of the hospital.  The sample contained less than 1‰ of solid material. After filtration 50% of the activity was found on the filter.  How representative was the sample from the waste water tank?  If the 177m Lu content in the solid residual is estimated from the liquid, it might be underestimated by a factor 1000.

Isotope Technologies Garching GmbHCERN 2010 Conclusions  177 Lu includes a remarkable amount of long-lived 177m Lu when produced from the direct route.  A radioactive licence might be needed for 177m Lu.  Laboratory waste should be collected separately and sent to a radioactive deposit.  In the waste water tanks 177m Lu might exceed the limits alone or with other nuclides (sum activity).  Indirectly produced n.c.a. 177 Lu is the only way to guarantee highest specific activity and best radionuclidic purity, i.e. absence of the 177m Lu problem.  n.c.a. 177 Lu requires high-flux reactors and more involved chemical separation.