ML19343C199

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Contact Doses from Dogs That Have Been Treated with Sn-117m Radiosynoviorthesis
ML19343C199
Person / Time
Issue date: 12/09/2019
From: Irene Wu
NRC/NMSS/DMSST/MSEB
To:
wu i/
Shared Package
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References
Download: ML19343C199 (6)


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Contact Doses from Dogs That Have Been Treated with Sn-117m Radiosynoviorthesis A Report to Serene, LLC 19 February 2018 Richard E. Wendt III, PhD, LMP, DABSNM, DABMP rwendt@mdanderson.org Professor, Department of Imaging Physics 2018.02.19 18:14:57 The University of Texas MD Anderson Cancer Center -06'00' Radiation synoviorthesis is a promising treatment for canine osteoarthritis. Its effective use requires an estimation of the contact dose to those who touch the treated dog in order to determine for how long such contact should be avoided following treatment.

This report reviews the results of a Monte Carlo simulation of an idealized synovial joint in which the synovial tissue bears Sn-117m. It makes recommendations for the safe touching of treated dogs.

Monte Carlo Simulations The GATE Monte Carlo simulation software (1,2) Version 8.0 was used for this study. The definition of the Sn-117m source material was derived from the emission data in ICRP 107(3). Unlike many simulations that have been reported in the literature, which ignore emissions with energies less than 15 or 20 keV or with abundances of less than 1%, every emission that is tabulated in ICRP 107 has been included in this simulation. Two billion events were simulated. This corresponds to 61.856 million disintegrations.

In order to validate the simulations, a point source of Sn-117m in air was simulated at the center of an annular cylinder of water with an inner radius of 1 meter and an outer radius of 1.1 meters. The dose rate constant that was determined from this simulation is 1.54x10-17 Gy-m2/Bq-s. This was at a depth of 1 cm into the cylinder of water. This value falls within the range of those that have been published in the literature, which lie between 1.20x10-17 Gy-m2/Bq-s(4) and 1.89x10-17 Gy-m2/Bq-s(5). There is a nice discussion of why the literature often contains such a wide range of values for the dose rate constant of a particular radionuclide in an AAPM report on PET shielding(6). From this example, we conclude that the simulations are producing reasonable results.

The dose rate in tissue that is in contact with the treated joint was estimated. A stylized model of a synovial joint was constructed and is shown in Figure 1 below. It consists of a ball and a socket (bright and dark yellow, respectively) with radii of 1.5 cm on the ends of cylindrical bones (gray), each covered with a 1 mm thick layer of cartilage (red and magenta). The otherwise empty space within the joint was filled with water (blue outline) to represent the synovial fluid. A superficial layer of tissue (gray outline) surrounds the entire limb. The activity was uniformly distributed in the synovial tissue, which was modeled as an infinitesimally thin-walled cylinder at the outer surface of the synovial fluid colored blue in Figure 1. A block of tissue that is 5 cm thick, 10 cm wide and 30 cm high was placed against the joint as shown in Figures 2 and 3.

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Figure 1: Stylized model of a synovial joint.

Figure 2: Stylized joint with a block of tissue, Figure 3: A top-down view of the joint and outlined in light magenta, pressed against the tissue block in Figure 2.

joint.

The dose was registered in the tissue in a dose actor that had a spatial resolution of 1 mm x 1 mm in the plane of the tissue block that is parallel to the limb (the horizontal direction in Figure 3) and a spatial resolution of 10 m in the direction perpendicular to the limb (the vertical direction in Figure 3).

The dose in the central plane of the first 5 mm of the tissue block that is perpendicular to the limb is shown in Figure 4.

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Figure 4: The 5 mm of the tissue block that is Figure 5: 10 cm2 closest to the joint. Dose is depicted in shades of ROI at 70 m into gray with brighter indicating a higher dose. The the tissue (left) and horizontal axis of this figure is the vertical axis of 1 cm2 ROI at 3 mm Figure 3. The joint is touching the left hand end of into the tissue this figure. The two gray, vertical lines show the (right).

planes at 70 m and 3 mm from the joint. The horizontal direction is expanded 100x compared to the vertical direction.

The average dose at a depth of 70 m in the 10 cm2 circular region of interest shown in Figure 5 was 3.33x10-14 Gy/Bq-s, while the average dose at a depth of 3 mm in the 1 cm2 circular region of interest that is shown in Figure 5 was 3.44x10-14 Gy/Bq-s.

The highest anticipated administered activity to an elbow of 3 mCi would produce 3.996x1011 disintegrations (Bq-s) in the first hour, and thus over the course of that hour the dose at a depth of 70 m would be 13.3 mGy while that at a depth of 3 mm would be 13.7 mGy. Although it seems to be counterintuitive at first glance that the dose farther away is higher, the dose at a depth of 3 mm is determined over a much smaller area that excludes many scattered, lower energy events.

Every two weeks after treatment, the dose from such contact would be halved, given the 14 day physical half-life of Sn-117m.

The duration of time after treatment during which people should avoid more than momentarily touching the dog's elbow may be calculated by solving the following expression for tavoid. This equation sets the dose limit equal to the dose that is accumulated to infinity, taking into account the fraction of time that the contact takes place, E, decayed by the duration of avoidance.

D 0 T 1/ 2 E ln(2)t / T 1/2 e avoid

=D limit (1) ln(2)

T 1/ 2 D ln (2) t avoid = ln [ limit ] (2) ln (2) D 0 T 1 /2 E 3

where D 0 is the initial dose rate, T 1 /2 is the effective half-life, E is sometimes called the occupancy factor, Dlimit is the dose limit and t avoid is the duration of avoiding contact so that the initial dose rate can decay to the point that the subsequently accumulated dose to infinity would remain below the dose limit.

Recommendation for Human Touching of the Treated Elbow The annual doses to the skin and to the lens of the eye for members of the general public are not regulated in the United States. The International Atomic Energy Agency(7) and the International Commission on Radiological Protection(8) recommend that the dose limits for the skin and the lens for members of the general public be one-tenth of the occupational limits(9). Thus, prudent limits would be 50 mSv (5 rem) at a depth of 70 m averaged over 10 cm2 for the skin and 15 mSv (1.5 rem) at a depth of 3 mm averaged over 1 cm2 for the lens of the eye, even though these are infrequent exposures of members of the general public to a treated dog and not the annual exposures that are anticipated in the occupational limits.

In order to remain below this skin dose limit for an hour's contact each day between the exact same 10 cm2 of skin and the dog's treated elbow, such touching should be avoided entirely for 34 days. In order to remain below this lens dose limit for an hour's contact each day of an individual's eye with the dog's elbow, such touching should be avoided for 59 days. These durations assume reduction over time of the administered activity only by physical decay, which is appropriate for Sn-117m radiosynoviorthesis in which there is negligible leakage of the radionuclide from the joint.

It is extremely unlikely that either a person or a dog would tolerate the conditions of this ocular contact scenario, and it is quite improbable that the precisely same patch of the person's skin would be touching the dog's elbow for an entire hour each and every day. Even while sleeping, people change position on the average twice or more often an hour(10). There is evidence to corroborate the common perception that sleeping dogs not hold perfectly still for extended periods of time(11), Figure 8 of (12) and Figure 1 of (13).Thus these recommendations that assume contact for an hour a day are extremely conservative and are probably needlessly so.

If one were to suppose only an hour's contact of the precisely same areas each week, contact with the person's skin could commence immediately after treatment while contact with the person's eye should be avoided for 20 days.

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References

1. Jan S, Santin G, Strut D, Staelens S, Assie K, Autret D, et al. GATE: A simulation toolkit for PET and SPECT. Phys Med Biol. 2004;49:4543-61.
2. Visvikis D, Bardies M, Chiavasa S, Danford C, Kirov A, Lamare F, et al. Use of the GATE Monte Carlo Package for Dosimetry Applications. Nucl Instrum Methods Phys Res Sect Accel Spectrometers Detect Assoc Equip [Internet]. 2006;569(2 Special Issue):335-40. Available from:

http://hal.in2p3.fr/docs/00/04/47/03/PDF/Maigne.pdf

3. Eckerman KF, Endo A. ICRP 107: Nuclear Decay Data for Dosimetric Calculations. Ann ICRP.

2008 Jun;38(3):1-96, e1-25.

4. Smith DS, Stabin MG. Exposure Rate Constants and Lead Shielding Values for Over 1,100 Radionuclides. Health Phys [Internet]. 2012;102(3):271-91. Available from: http://www.doseinfo-radar.com/Exposure_Rate_Constants_and_Lead_Shielding_Values%204.pdf
5. Shleien B, Slaback, Jr. LA, Birky BK. Handbook of Health Physics and Radiological Health. Third Edition. Baltimore, MD: Williams and Wilkins; 1998.
6. Madsen MT, Anderson JA, Halama JR, Kleck J, Simpkin DJ, Votaw JR, et al. AAPM Task Group 108: PET and PET/CT Shielding Requirements. Med Phys [Internet]. 2006 Jan;33(1):4-15.

Available from: http://www.aapm.org/pubs/reports/RPT_108.pdf

7. International Atomic Energy Agency. Release of Patients after Radionuclide Therapy [Internet].

Vienna, Austria: International Atomic Energy Agency; 2009 [cited 2013 May 22]. (Safety Reports Series). Report No.: 63. Available from: http://www-pub.iaea.org/MTCD/Publications/PDF/pub1417_web.pdf

8. Valentin J. ICRP 103: The 2007 recommendations of the International Commission on Radiological Protection. Ann ICRP. 37(2-4):1-332.
9. U. S. Nuclear Regulatory Commission. NRC: 10 CFR 20.1201 Occupational dose limits for adults.

[Internet]. [cited 2015 Aug 10]. Available from: http://www.nrc.gov/reading-rm/doc-collections/cfr/part020/part020-1201.html

10. De Koninck J, Lorrain D, Gagnon P. Sleep positions and position shifts in five age groups: an ontogenetic picture. Sleep [Internet]. 1992 [cited 2015 Sep 27];15(2):143-9. Available from:

http://www.journalsleep.org/ViewAbstract.aspx?pid=24878

11. Patel SI, Miller BW, Kosiorek HE, Parish JM, Lyng PJ, Krahn LE. The Effect of Dogs on Human Sleep in the Home Sleep Environment. Mayo Clin Proc [Internet]. [cited 2018 Feb 19];92(9):1368-
72. Available from: http://dx.doi.org/10.1016/j.mayocp.2017.06.014
12. Hansen BD, Lascelles BDX, Keene BW, Adams AK, Thomson AE. Evaluation of an accelerometer for at-home monitoring of spontaneous activity in dogs. Am J Vet Res [Internet]. 2007 May 1 [cited 2018 Feb 20];68(5):468-75. Available from: https://doi.org/10.2460/ajvr.68.5.468 5
13. Dow C, Michel KE, Love M, Brown DC. Evaluation of optimal sampling interval for activity monitoring in companion dogs. Am J Vet Res [Internet]. 2009 Mar 31 [cited 2018 Feb 19];70(4):444-8. Available from: https://doi.org/10.2460/ajvr.70.4.444 6