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Materials and Methods:

Investigated sample consisted of 51 patients, af-

fected by Graves’ diseases (47%) and nodular goiter (53%). In the pre-

treatment phase, a 131I sodium-iodide track activity was administered to

identify Umax and T1/2eff (SIE-AIMN-AIFM) and kt, kT and kB (EANM). The

uptake data at about 2, 6 (only for Graves’ disease), 24, 96 hours were fitted

through a bi-exponential curve. Therapeutic activity was calculated also

considering two and one late measurements as described by EANM. The

statistical analysis was performed by SPSS.20 software.

Results:

Therapeutic activities due to SIE-AIMN-AIFM and EANM proce-

dures resulted always significantly different (p

<

0.005), regardless of

pathology and number of pre-treatment measurements. For three or more

uptake assessments, EANM values were always greater than SIE-AIMN-

AIFM ones (Delta A%mean

=

5.6

±

2.7%). Moreover, EANM_3pts activities

resulted to be significantly different (p

<

0.005) from EANM_2pts and

EANM_1pts ones (Delta A%mean

=

2.1

±

4.7% and Delta A%mean

= −

9.8

±

15.8%

respectively).

Conclusion:

The implementation of the EANM method increases the ac-

tivity necessary to achieve a specified clinical dose compared to the SIE-

AIMN-AIFM one. The different values of activity determined through the

three methods of EANM guidelines emphasize the importance of a com-

plete personalized treatment.

http://dx.doi.org/10.1016/j.ejmp.2016.01.345

C.340

CHARACTERIZATION OF AN INTRAOPERATIVE GAMMA SYSTEM

M. Camarda

*

, P. D’Avenia, E. Di Nicola, L. Montani, G. Rossi, S. Fattori.

Servizio

di Fisica Medica ASUR Marche AV3, Macerata, Italy

Introduction:

A home made protocol was set up to characterize a CZT

gamma probe equipped with a new tool for spectral analysis. In addition

to the tests recommended by the Italian Quality Control protocol, spec-

tral analysis at various source activities and lateral scans of 2 point sources

at various separation distances were performed.

Materials and Methods:

Conventional measurements were carried out as

suggested by the Italian protocol.

The count rate linearity test was performed with a 99mTc point source:

count rates (cps) in the 99mTc window, cps in the open energy window

and spectra were acquired at different times.

Lateral profiles of 2 point sources were performed at 1 cm PMMA depth

and at different source distances ranging from 17 mm to 40 mm to eval-

uate at which separation distance they can be detected separately.

Superficial scans of 1 and 2 sources at 1 cm PMMA depth have been ac-

quired, with 3 mm shift step.

Results:

The count rate linearity test shows that the probe is linear within

10% until 25 kcps. Spectral analysis shows that average energy resolution

is 14.6% FWHM (13.5–15.6%) as long as the deviation from linearity is

<

2%

and the ratio between cps in the 99mTc window and open window is

62%

±

3%.

According to the profiles obtained with a single source at 1 cm PMMA depth,

the spatial resolution of the collimated probe is 15 mm FWHM. Profiles ob-

tained with 2 sources show a Peak-to-Valley ratio

<

2 for separation

distance

<

25 mm.

Isoresponse curves were drawn from superficial scans and were of use in

aligning the probe with the point sources.

Conclusions:

Through the home made protocol it is possible to survey the

spectral capability of the probe. As daily quality control, it is recom-

mended to calculate the ratio between cps in the 99mTc energy window

and cps in the open window.

Performing lateral profiles of 2 point sources with different separation dis-

tances it is possible to define the minimal distance at which two lymph

nodes can be detected separately.

http://dx.doi.org/10.1016/j.ejmp.2016.01.346

C.341

RADIATION PROTECTION IMPACT OF RADIOIODINE THERAPY FOR

HYPERTHYROIDISM AFTER A PATIENT SPECIFIC DOSIMETRIC STUDY

C. Canzi

*

, V. Longari, M. Castellani, R. Lambertini, F. Zito, F. Voltini,

R. Benti.

Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milano,

Italy

In hyperthyroid pts treatment with 131I should rapidly obtain a

nonhyperthyroid status. There is a discussion about the method to deter-

mine the therapeutic activity: estimation (fixed activity) vs calculation (based

on radioiodine uptake measurements), however the optimization princi-

ple states that a pt should be given the minimum activity for the clinical

goal. In our Nucl Med Dept all hyperthyroid pts are submitted to a patient

specific pretreatment study to calculate the minimum activity to achieve

euthyroidism, for nodular autonomies, and hypothyroidism, for Graves

disease.

Aim:

To retrospectively evaluate the radioprotection impact of 131I thera-

pies for hyperthyroidism after patient specific dosimetric studies, with

respect to a standard administration of 600 MBq (max activity allowed by

Italian law).

Materials and Methods:

532 pts were considered (207 Graves, 388 F, median

age

=

65 y [17–89 y]). They all reached a nonhyperthyroid status within 1 y.

Results:

Median 131I therapeutic administered activity

=

398 MBq [66–

629 MBq]. Total administered activity was 228 GBq. If the standard activity

of 600 MBq had been administered to all pts total activity would have been

319 GBq, 40% greater than the really used one. This acts also on the patient

mean effective dose equivalent and on the mean absorbed dose to the

stomach wall (critical organ for 131I iodide-ICRP 53) that were 6 Sv instead

of 9 Sv and 0.20 Gy instead of 0.28 Gy respectively, with a maximum of dose

saving (8 times) for the patient who was given 66 MBq. The reduction of

131I administered activity also acts on the exposure of the nucl med staff

and of population: the mean dose rate at 1 m at the dismission time is

12 μSv/h instead of 20 μSv/h. This approach involves also the environ-

ment, as in the first 24 h 60% of administered activity is excreted.

Conclusion:

The application of a patient specific pretreatment dosimet-

ric study can reduce to 40% the radioprotection impact of 131I treatments

of hyperthyroidism with clinical results guaranteed.

http://dx.doi.org/10.1016/j.ejmp.2016.01.347

C.342

STUDY OF INTER-FRACTION VARIABILITY OF ABSORBED DOSE TO BONE

METASTASES AND FOLLOW-UP FOR A PATIENT WHO UNDERWENT

223RA-DICHLORIDE THERAPY

M. Pacilio

a ,

B. Cassano

*

, b ,

G. Ventroni

c ,

P. Ialongo

d ,

L. Lorenzon

b ,

E. Di Castr

o e ,

F. Recine

f ,

C.N. Sternberg

f ,

L. Mango

c .

a

Department of Medical

Physics, Azienda Ospedaliera San Camillo Forlanini, Roma, Italy;

b

Postgraduate

School of Medical Physics, Sapienza University of Rome, Roma, Italy;

c

Department of Nuclear Medicine, Azienda Ospedaliera San Camillo Forlanini,

Roma, Italy;

d

Department of Radiology, Azienda Ospedaliera San Camillo

Forlanini, Roma, Italy;

e

Department of Radiological, Oncological and Anatomo

Pathological Sciences, Sapienza University of Rome, Roma, Italy;

f

Department

of Medical Oncology, Azienda Ospedaliera San Camillo Forlanini, Roma, Italy

Introduction:

A 70 year old man, affected by bone metastases from

castration-resistant prostate cancer, underwent 223Ra-dichloride therapy

(6 administrations of 50 kBq per kg of body weight). The inter-administration

variability of absorbed dose to lesions was evaluated, and the lesion uptake

was monitored with 99mTc-MDP imaging.

Materials and Methods:

Biokinetic studies were performed for 4 lesions,

after the 1°, 3°, 5° and 6° injections, acquiring antero-posterior planar static

images at 1 h, 1 day, between 2 and 4 days and 7–9 days, using MEGP col-

limator and double-peak acquisition. Lesions were delineated on 99mTc-

MDP WB images acquired before the therapy, and the ROIs superimposed

on the 223Ra images after image coregistration and Wiener filtering. The

activity was quantified with background, attenuation, and scatter correc-

tion, and absorbed doses assessed with the MIRD approach, after delineation

of the lesions on the CT images. Uptake of 8 lesions (i.e., uptake ratio between

lesion and normal bone, TNT) was monitored 4 days before the 3° injec-

tion, 11 days before the 5° injection, and 16, 45 and 93 days after the 6°

injection.

e100

Abstracts/Physica Medica 32 (2016) e97–e115