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World Congress of Brachytherapy 10-12 May, 2012 - Estro-events.org

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S136 <strong>World</strong> <strong>Congress</strong> <strong>of</strong> <strong>Brachytherapy</strong> 20<strong>12</strong><br />

PO338<br />

VAGINAL CUFF BRACHYTHERAPY USING OVOIDS: COMPARISON OF<br />

POINT BASED AND TARGET BASED PRESCRIPTION<br />

S. Sharma 1 , D. Manigandan 1 , A.K. Gandhi 1 , D.N. Sharma 1 , V.<br />

Subramani 1 , P.K. Julka 1 , G.K. Rath 1<br />

1<br />

All India Institute <strong>of</strong> Medical Sciences (AIIMS), Radiation Oncology,<br />

Delhi, India<br />

: To compare the treatment plans with point based<br />

and target dose point based prescription methods for vaginal cuff<br />

brachytherapy with two ovoids.<br />

: Twenty previously treated sessions <strong>of</strong> post<br />

operative carcinoma uterine cervix patients were studied. For all the<br />

patients, application was done by using two Fletcher ovoids under<br />

sedation. After application, CT scan was done at 3mm slice thickness.<br />

The target volume was contoured and it assumed to be around the<br />

applicator, however, in some cases, modification was done according<br />

to the clinical and planning CT findings. Similarly, <strong>org</strong>ans at risk (OAR)<br />

i.e. bladder and rectum were contoured. The ICRU38 bladder and<br />

rectum points were also marked on CT images. Applicators were<br />

reconstructed using 2.5mm source step size and plans were generated<br />

for Nucletron HDRV2 machine using PLATO planning system. In both<br />

the ovoids, first four dwell positions were activated and dose<br />

prescription was done by using two different prescription methods.<br />

One is conventional point dose (PD) based and the second is target<br />

dose point (TDP) based. For conventional PD method, the dose<br />

prescription point was at 5mm above the superior surface <strong>of</strong> mid<br />

dwell position <strong>of</strong> two ovoids. For TDP based method, target dose<br />

points were created 5mm around the target. No optimization was<br />

done after prescription. For comparison purposes, dose was<br />

prescribed at <strong>10</strong>0cGy. For plan evaluation, following dose volume<br />

indices were used: Volume <strong>of</strong> target that receive <strong>10</strong>0% (V<strong>10</strong>0), 95%<br />

(V95), and 90% (V90) <strong>of</strong> prescription dose, coverage index<br />

(CI=V<strong>10</strong>0/Target volume) and overdose volume index (OI=V200/V<strong>10</strong>0). For<br />

bladder and rectum, doses received by 0.1cc (D0.1cc), 1cc (D1cc), 2cc<br />

(D2cc), 5cc (D5cc), and <strong>10</strong>cc (D<strong>10</strong>cc) <strong>of</strong> volumes were noted. The ICRU38<br />

bladder and rectum point doses were also noted to correlate with<br />

volumetric doses.<br />

: The plan comparison is summarized in Table.1. Volumetric<br />

evaluation shows that target coverage was lower in PD based plans<br />

than the TDP based plans. However, the OI index shows that high dose<br />

volume was more in TDP based plans compared to PD plans. In<br />

addition, the OAR doses were higher in TDP based method than the PD<br />

based. In the both TDP and PD methods, the bladder doses received<br />

by 0.1cc, 1cc, 2cc and 5cc volumes were higher compared to ICRU38<br />

bladder point doses and doses to <strong>10</strong>cc bladder volume were in closer<br />

agreement with the ICRU38 bladder points. Similarly, for rectum, the<br />

doses received by 0.1cc, and 1cc volumes were higher compared to<br />

ICRU38 rectum point doses and doses to 2–5cc volume <strong>of</strong> rectum were<br />

in closer agreement with the ICRU38 rectum points.<br />

: In the CT guided PD prescription method, lesser target<br />

coverage and lower OAR doses were observed. In TDP based<br />

prescription, target coverage was higher and resulted in higher OAR<br />

doses. Doses received by <strong>10</strong>cc <strong>of</strong> bladder and 2–5cc <strong>of</strong> rectum were<br />

closer to ICRU38 bladder and rectum points, respectively.<br />

PO339<br />

MRIDUMMY MARKERS OF MRIGUIDED HDR BRACHYTHERAPY FOR<br />

INTERSTITIAL PROSTATE AND INTRACAVITARY GYN CANCERS<br />

J. Schindel 1 , M. Muruganandham 1 , A. Eagle 2 , M. Hewitt 2 , T.<br />

Stockman 2 , C. Pigge 3 , Y. Kim 1<br />

1<br />

University <strong>of</strong> Iowa, Radiation Oncology, Iowa City, USA<br />

2<br />

University <strong>of</strong> Iowa, Electrical Computer Engineering, Iowa City, USA<br />

3<br />

University <strong>of</strong> Iowa, Chemistry, Iowa City, USA<br />

: Compare seven different MRIdummy markers for<br />

interstitial prostate and intracavitary GYN HDR brachytherapy.<br />

: Seven markers were used: Saline, Conray60<br />

(Mallinckrodt medical), CuSO4 (1.5g/L), liquid Vitamin E, fish oil, 1%<br />

Agarose gel (AGEL: 1g Agarose powder/ <strong>10</strong>0 ml distilled water), and a<br />

cobaltchloride complex contrast (C4) (CoCl2: Glycine=4:1). Interstitial<br />

and intracavitary phantoms were designed. The interstitial phantom<br />

consisted <strong>of</strong> eight flexi needles (outer/inner diameter <strong>of</strong><br />

1.98mm/1.45mm) that were filled with each MRImarker and<br />

embedded in 450 mL <strong>of</strong> 3% AGEL. The intracavitary phantom consisted<br />

<strong>of</strong> 4L <strong>of</strong> 3% AGEL, a plastic tandem and ring applicator (Varian), and<br />

MRIdummy catheters (outer/inner diameter <strong>of</strong> 2.66mm/1.87mm).<br />

Clinical 3T MRI protocols (both T1weightedMRI (T1MRI:1mm slice<br />

thickness) and T2weightedMRI scans (T2MRI: 3mm slice thickness))<br />

were used. Signal intensities for each marker were characterized as<br />

percentages compared to the 3% AGEL background using ImageJ<br />

s<strong>of</strong>tware.<br />

: Some interstitial markers, even though small agent volume,<br />

could generate favorable signals (> <strong>10</strong>0%), implying their feasibility for<br />

MRIguided prostate HDR. The markers <strong>of</strong> CuSO4, C4, and Vitamin E on<br />

T1MRI and 1% AGEL, Saline, and fish oil on T2MRI showed higher than<br />

<strong>10</strong>0% signals on both phantoms. The volume effect on signals was<br />

found due to different marker volumes in the different dummy<br />

catheters. The markers <strong>of</strong> CuSO4 and Saline showed highest signals on<br />

T1MRI and T2MRI, respectively. Sourcereconstruction is<br />

recommended on T1MRI, so CuSO4 and C4 markers have great<br />

potentials as a dummy marker for both interstitial and intracavitary<br />

brachytherapy.<br />

: The use <strong>of</strong> interstitial markers for MRIguided prostate<br />

HDR seems feasible. The markers <strong>of</strong> CuSO4 and C4 showed<br />

considerably high signals on T1MRI, as did Saline on T2MRI, for<br />

interstitial needles for prostate HDR and for a tandemandring<br />

applicator for GYN.<br />

<strong>World</strong> <strong>Congress</strong> <strong>of</strong> <strong>Brachytherapy</strong> 20<strong>12</strong> S 137<br />

PO340<br />

DOSIMETRIC IMPACT OF NOT CORRECTING FOR THE DISTAL SHIFT<br />

REPORTED IN VARIAN TANDEM AND RING (T&R) APPLICATORS<br />

O. Craciunescu 1 , J. Sánchez Mazón 2 , L. Lan 3 , J. Maurer 1 , B. Steffey 1 ,<br />

J. Cai 1 , J. Adamson 1 , J. Chino 1<br />

1<br />

Duke University Medical Center, Radiation Oncology, Durham NC,<br />

USA<br />

2<br />

Hospital Universitario Marqués de Valdecilla, Servicio de Radi<strong>of</strong>ísica<br />

y Protección Radiológica, Santander, Spain<br />

3<br />

Duke University Medical Center, Department <strong>of</strong> Biostatistics and<br />

Bioinformatics, Durham NC, USA<br />

: Studies have shown that source stop positions<br />

within Varian’s HDR CT/MR compatible ring applicators can deviate<br />

from the intended positions by several millimeters, and that a<br />

corrective shift has to be applied to limit the effect <strong>of</strong> these inherent<br />

<strong>of</strong>fsets. The purpose <strong>of</strong> this study was to investigate the dosimetric<br />

impact <strong>of</strong> NOT applying this correction.<br />

: Twentyseven HDR T&R clinical plans (cP)<br />

from six different patients treated for cervical cancer in our clinic<br />

were used in this study. Both CT and MR were acquired for each plan.<br />

The dose per fraction was 5.5 Gy. GECESTRO guidelines were<br />

followed for HRCTV and <strong>org</strong>ans at risk (OARs): bladder, rectum,<br />

sigmoid. ICRU 38 points A were also defined. The planning was done in<br />

BrachyVision with a hybrid volume optimization method based on<br />

HRCTV and ABS recommended reference lines. Depending on the<br />

shape <strong>of</strong> the HRCTV, the posterior ring dwell positions were allowed<br />

in the optimization for 5 patients. For 1 patient, a standard ring<br />

loading that mimicks ovoid placement was used. To show the<br />

dosimetric impact <strong>of</strong> NOT applying distal corrections, plans were<br />

generated by shifting the dwells in the ring in the opposite direction<br />

incrementally by 1 5 mm. The plans were calculated using the TG43<br />

formalism and ACUROS, a modelbased analytical solver that<br />

accounts for inhomogeneities. To establish clinical significance, the<br />

mean percent difference between all metrics in each <strong>of</strong> the shifted<br />

plans and the cP were calculated. The Wilcoxon signedrank test was<br />

used to determine if the differences have any statistical significance,<br />

for all cases together, but also separating patients depending on the<br />

ring dwells activated.<br />

: For brevity, only D2cc results for OARs for all 27 plans are<br />

presented. Ring loading strategy did not impact the dosmetric results.<br />

The mean percent differences between the largest shift (5mm) and<br />

the cP for the D2cc bladder, rectum and sigmoid were 1.6, 1.7, 2.5%<br />

for TG43, and 1.2, 1.8 and 1.4 % for ACUROS. The Wilcoxon rank sum<br />

pvalues were > 0.05 for all the OAR metrics, shift amounts, and<br />

method <strong>of</strong> calculation. For A_RT, A_LT and HRCTV D90, the mean<br />

percent differences were 0.8, 0.5 and 0.6 %, and 0.6, 0.8 and 0.9 %<br />

for TG43 and ACUROS, respectively. However, the Wilcoxon signed<br />

rank pvalues for Point A_RT were < 0.05 for both TG43 and ACUROS,<br />

for all shifts. Only when using ACUROS, the pvalues for HRCTV D90<br />

were < 0.05 for all shifts.<br />

: The dosimetric impact <strong>of</strong> NOT applying corrective shifts<br />

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