evaluate and compare the doses differences between line source and point source calculation methods...

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the HDR T&R plans for the remaining fractions are adapted to be less restrictive for critical structure sparing. The process is repeated if for any of the T&R plans the dose for the OARs exceeds the maximum allowable dose. Finally, the calculated dose values from the EBRT and the 5 HDR T&R plans are introduced in the BED-EQD2 table and the doses to the critical structures are compared with the corresponding tolerance values. A MIM final composite is also performed to estimate the DVH distribution for the critical structures. If less than 5 T&R implants are performed, the treatment may continue with an SBRT boost. We extrapolated the methodology described above for such EBRT-HDR- SBRT cases. We follow the approach as detailed above to generate realistic HDR T&R plans. After the HDR approach is discontinued, we export to MIM the EBRT plan(s) and all delivered HDR T&R plans. A BED composite plan is done and a DVH analysis is performed to estimate the cumulative D2cc for the critical structures. The maximum allowable doses for the critical structures are then determined and used as constraints for the SBRT plan. Results: We applied the methodology described above for a few cases. One representative case is described below. The patient was treated with 28 fractions of EBRT to 50.4 Gy, using an AP-PA approach. The D2cc for bladder, rectum, and sigmoid in the EBRT plan were 59.4, 59.3, and 59.3 Gy, respectively. By using these values in the BED-EQD2 table, the bladder/rectum/sigmoid tolerances for the HDR T&R approach become 4.1, 2.5, and 2.5 Gy/fraction, respectively. To do a more realistic estimation of those HDR tolerances we contoured in the EBRT plan new partial bladder, rectum, and sigmoid structures, including only the areas around the future HDR treatment region. The D2cc for these new structures were reduced to 55 Gy for the EBRT, resulting in larger HDR tolerances (4.6, 3.2, and 3.2 Gy/fraction for bladder, rectum, and sigmoid, respectively). The final cumulative bladder/rectum/sigmoid D2cc BED for the EBRTand 5 HDR T&R, obtained from our table (worst case scenario) were 132, 117, and 117 when using the partial structures. If we considered the original bladder/ rectum/sigmoid structures these values were 142, 127, and 127, with the rectum and sigmoid doses slightly higher than the stated tolerances. The final MIM composite DVH showed a BED of 120, 107, and 107 for bladder, rectum, and sigmoid, respectively. Conclusions: The approach was successfully used for a few EBRT-HDR and EBRT-HDR-SBRT special cases. PO33 Evaluate and Compare the Doses Differences between Line Source and Point Source Calculation Methods for Episcleral Plaque Brachytherapy Vi Nhan Nguyen, MS, Michael K. Cheung, MD, David Vonk, MD, Baldassarre Stea, MD, PhD, Christopher J. Watchman, PhD, Russell J. Hamilton, PhD, Adam C. Turner, PhD. Radiation Oncology, The University of Arizona, Tucson, AZ. Purpose: Episcleral plaque brachytherapy is a proven modality for treatment of medium-sized ocular melanoma tumors. Radiation dose calculation for this technique was previously performed using the Task Group 43 point-source system. However, the newer Task Group 129 is now recommending using the line-source system. The purpose of this study is to evaluate the dose differences between the two calculation methods on preservation of vision. Materials and Methods: Two programs were created using Matlab for line source and point source approximation methods. The comparison was solely based on the doses differences between the two methods ignoring all other factors such as heterogeneous correction, backscatter and shielding effects from the bowl backing, the Silastics insert and the collimator clips. The doses were calculated for 106 patients treated with I-125 Amersham model 6711 and Best Medical model 2301 seeds. Differences between both methods were compared and correlated with preservation of visual acuity. Results: The average percent doses differences were calculated for 57 patients treated with Amersham model 6711 showing 0.39% ( 0.77%) at apex, 0.31% ( 0.76%) at 5mm point, 1.05% ( 0.63%) at sclera, 0.21% ( 0.53) at eye center, 0.104%( 0.32%) at contralateral retina, -0.87% ( 1.17) at macula , -0.03%( 0.38%) at lens and -1.08%( 0.8%) at optic disk. For the 49 patients treated with Best Medical model 2301, the average percent doses differences were 0.49% ( 0.73%) at apex, 0.44% ( 0.74%) at 5mm point, 1.31% ( 0.63%) at sclera, 0.33% ( 0.49) at eye center, 0.33%( 0.30%) at contralateral retina, -2.8% ( 1.97) at macula, 2.03%( 0.34%) at lens, and 2.04%( 1.03%) at optic disk. Although, the maximum dose difference was found to be 7% at the macula, there were no significant differences between the doses calculated by point or source methods. Patients with retained visual acuity tended to received lower doses to the macula (p50.001), and optic disk (p ! 0.001), regardless of dose calculation method. Conclusions: The doses calculated by point and line source methods showed similar results for both tumor and normal structures. Furthermore, doses differences calculated by the two methods were not associated with any clinically significant benefit or detriment in visual preservation. Future research on doses calculation should take in account the heterogeneous correction, backscatter and shielding effects from the bowl backing, the Silastics inserts and the collimator lips. PO34 Study of Dosimetric and Spatial Variations Due To Applicator Positioning During Inter-fraction High-dose-rate Brachytherapy in the Treatment of Carcinoma of Cervix - A 3D Dosimetric Analysis Manish K. Goyal, MS 1,2 , Jerry L. Barker, MD 1 , D.V. Rai, PhD 2 , Than S. Kehwar, PhD, DSc 3 , Bret H. Heintz, PhD 1 , Kathleen L. Shide, MD 1 . 1 Texas Oncology, Fort Worth, TX; 2 Biomedical Engineering, Shobhit University, Meerut, UP, India; 3 Penn State Hershey Cancer Institute, Penn State Hershey Medical Center, Hershey, PA. Purpose: This study was designed to study dosimetric and spatial variations in interfraction applicator positioning in high-dose-rate (HDR) brachytherapy. Materials and Methods: This study includes 10 retrospective cervical cancer patients(Ca Cx). Each patient received 5 fractions of high-dose- rate (HDR) intracavitary brachytherapy. In all 50 plans, dose was originally prescribed to point A (ICRU-38), called Pt A. Post treatment, tumor volumes (HR-CTV) were drawn on CT images of each plan by the treating physician. Plan of the first implant is considered as a reference, and all subsequent CT image data sets were rigidly registered on first implant’s CT data set with respect to the cervix or flange location. Another Point A, called Pt A ABS was defined on first plan and all subsequent plans, with reference to the ABS 2011 recommendations. Pt. A and Pt. A ABS of the first plan was carried over to subsequent plans keeping its original location. On subsequent plans, Pt. A and Pt. A ABS had its original location but dose distribution is from different subsequent plans (plan 2-5). Registration properties were recorded for all 50 plans that includes X, Y, Z DICOM offset, Rotational, Translational values and A D90 doses were also recorded. Results: The mean angle of rotation on X, Y and Z axes are 0.49 1.60 deg, -0.67 2.31 deg and -0.10 1.82 deg, respectively. While mean translational motion on X, Y and Z axes are -0.35 3.22 cm, 0.53 2.57 cm and 1.64 9.26 cm, respectively. Mean normalized D90, mean HR_CTV and mean %IDL are 1.18 0.20, 23.25 8.3 cc and 87.36 20.26 cc, respectively. The mean of point A doses of each patient is compared with that of other patients using the method of the analysis of variance (ANOVA). The mean of all 5 plans of each patient do not have statistically significant difference (p50.225). The difference between mean doses of point A ABS (p50.011), mean doses point A registered (p50.005) and mean doses of point A ABS registered (p50.0032), were statistically different. The comparison between the doses of the point As, defined using ICRU-38, ABS 2011 and computed by registering on plan of first implant, are statistically different (p ! 0.05). The mean HR_CTV of each patient were fitted with normalized D90 (ND90) and %IDL data using the method of least square fit. The ND90 has negative correlation with HR_CTV with correlation coefficient of 0.7253, while 100% IDL S101 Abstracts / Brachytherapy 13 (2014) S15eS126

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S101Abstracts / Brachytherapy 13 (2014) S15eS126

the HDR T&R plans for the remaining fractions are adapted to be lessrestrictive for critical structure sparing. The process is repeated if for anyof the T&R plans the dose for the OARs exceeds the maximum allowabledose. Finally, the calculated dose values from the EBRT and the 5 HDRT&R plans are introduced in the BED-EQD2 table and the doses to thecritical structures are compared with the corresponding tolerance values.A MIM final composite is also performed to estimate the DVHdistribution for the critical structures. If less than 5 T&R implants areperformed, the treatment may continue with an SBRT boost. Weextrapolated the methodology described above for such EBRT-HDR-SBRT cases. We follow the approach as detailed above to generaterealistic HDR T&R plans. After the HDR approach is discontinued, weexport to MIM the EBRT plan(s) and all delivered HDR T&R plans. ABED composite plan is done and a DVH analysis is performed to estimatethe cumulative D2cc for the critical structures. The maximum allowabledoses for the critical structures are then determined and used asconstraints for the SBRT plan.Results: We applied the methodology described above for a few cases. Onerepresentative case is described below. The patient was treated with 28fractions of EBRT to 50.4 Gy, using an AP-PA approach. The D2cc forbladder, rectum, and sigmoid in the EBRT plan were 59.4, 59.3, and 59.3Gy, respectively. By using these values in the BED-EQD2 table, thebladder/rectum/sigmoid tolerances for the HDR T&R approach become4.1, 2.5, and 2.5 Gy/fraction, respectively. To do a more realisticestimation of those HDR tolerances we contoured in the EBRT plan newpartial bladder, rectum, and sigmoid structures, including only the areasaround the future HDR treatment region. The D2cc for these newstructures were reduced to 55 Gy for the EBRT, resulting in larger HDRtolerances (4.6, 3.2, and 3.2 Gy/fraction for bladder, rectum, and sigmoid,respectively).The final cumulative bladder/rectum/sigmoidD2cc BED for the EBRTand 5HDRT&R, obtained from our table (worst case scenario) were 132, 117, and117 when using the partial structures. If we considered the original bladder/rectum/sigmoid structures these values were 142, 127, and 127, with therectum and sigmoid doses slightly higher than the stated tolerances. Thefinal MIM composite DVH showed a BED of 120, 107, and 107 forbladder, rectum, and sigmoid, respectively.Conclusions: The approach was successfully used for a few EBRT-HDRand EBRT-HDR-SBRT special cases.

PO33

Evaluate and Compare the Doses Differences between Line Source

and Point Source Calculation Methods for Episcleral Plaque

Brachytherapy

Vi Nhan Nguyen, MS, Michael K. Cheung, MD, David Vonk, MD,

Baldassarre Stea, MD, PhD, Christopher J. Watchman, PhD, Russell J.

Hamilton, PhD, Adam C. Turner, PhD. Radiation Oncology, The

University of Arizona, Tucson, AZ.

Purpose: Episcleral plaque brachytherapy is a proven modality fortreatment of medium-sized ocular melanoma tumors. Radiation dosecalculation for this technique was previously performed using the TaskGroup 43 point-source system. However, the newer Task Group 129 isnow recommending using the line-source system. The purpose of thisstudy is to evaluate the dose differences between the two calculationmethods on preservation of vision.Materials and Methods: Two programs were created usingMatlab for linesource and point source approximationmethods. The comparisonwas solelybased on the doses differences between the two methods ignoring all otherfactors such as heterogeneous correction, backscatter and shielding effectsfrom the bowl backing, the Silastics insert and the collimator clips. Thedoses were calculated for 106 patients treated with I-125 Amershammodel 6711 and Best Medical model 2301 seeds. Differences betweenboth methods were compared and correlated with preservation of visualacuity.Results: The average percent doses differences were calculated for 57patients treated with Amersham model 6711 showing 0.39% (�0.77%) atapex, 0.31% (�0.76%) at 5mm point, 1.05% (�0.63%) at sclera, 0.21%

(�0.53) at eye center, 0.104%(�0.32%) at contralateral retina, -0.87%(�1.17) at macula , -0.03%(�0.38%) at lens and -1.08%(�0.8%) at opticdisk. For the 49 patients treated with Best Medical model 2301, theaverage percent doses differences were 0.49% (�0.73%) at apex, 0.44%(�0.74%) at 5mm point, 1.31% (�0.63%) at sclera, 0.33% (�0.49) at eyecenter, 0.33%(�0.30%) at contralateral retina, -2.8% (�1.97) at macula,2.03%(�0.34%) at lens, and 2.04%(�1.03%) at optic disk. Although, themaximum dose difference was found to be 7% at the macula, there wereno significant differences between the doses calculated by point or sourcemethods. Patients with retained visual acuity tended to received lowerdoses to the macula (p50.001), and optic disk (p!0.001), regardless ofdose calculation method.Conclusions: The doses calculated by point and line source methodsshowed similar results for both tumor and normal structures.Furthermore, doses differences calculated by the two methods werenot associated with any clinically significant benefit or detriment invisual preservation. Future research on doses calculation should takein account the heterogeneous correction, backscatter and shieldingeffects from the bowl backing, the Silastics inserts and the collimatorlips.

PO34

Study of Dosimetric and Spatial Variations Due To Applicator

Positioning During Inter-fraction High-dose-rate Brachytherapy in

the Treatment of Carcinoma of Cervix - A 3D Dosimetric Analysis

Manish K. Goyal, MS1,2, Jerry L. Barker, MD1, D.V. Rai, PhD2, Than S.

Kehwar, PhD, DSc3, Bret H. Heintz, PhD1, Kathleen L. Shide, MD1. 1Texas

Oncology, Fort Worth, TX; 2Biomedical Engineering, Shobhit University,

Meerut, UP, India; 3Penn State Hershey Cancer Institute, Penn State

Hershey Medical Center, Hershey, PA.

Purpose: This study was designed to study dosimetric and spatial variationsin interfraction applicator positioning in high-dose-rate (HDR)brachytherapy.Materials and Methods: This study includes 10 retrospective cervicalcancer patients(Ca Cx). Each patient received 5 fractions of high-dose-rate (HDR) intracavitary brachytherapy. In all 50 plans, dose wasoriginally prescribed to point A (ICRU-38), called Pt A. Posttreatment, tumor volumes (HR-CTV) were drawn on CT images ofeach plan by the treating physician. Plan of the first implant isconsidered as a reference, and all subsequent CT image data sets wererigidly registered on first implant’s CT data set with respect to thecervix or flange location. Another Point A, called Pt A ABS wasdefined on first plan and all subsequent plans, with reference to theABS 2011 recommendations. Pt. A and Pt. A ABS of the first planwas carried over to subsequent plans keeping its original location. Onsubsequent plans, Pt. A and Pt. A ABS had its original location butdose distribution is from different subsequent plans (plan 2-5).Registration properties were recorded for all 50 plans that includes X,Y, Z DICOM offset, Rotational, Translational values and A D90 doseswere also recorded.Results: The mean angle of rotation on X, Yand Z axes are 0.49� 1.60 deg,-0.67 � 2.31 deg and -0.10 � 1.82 deg, respectively. While meantranslational motion on X, Y and Z axes are -0.35 � 3.22 cm, 0.53 � 2.57cm and 1.64 � 9.26 cm, respectively. Mean normalized D90, meanHR_CTV and mean %IDL are 1.18 � 0.20, 23.25 � 8.3 cc and 87.36 �20.26 cc, respectively. The mean of point A doses of each patient iscompared with that of other patients using the method of the analysis ofvariance (ANOVA). The mean of all 5 plans of each patient do not havestatistically significant difference (p50.225). The difference betweenmean doses of point A ABS (p50.011), mean doses point A registered(p50.005) and mean doses of point A ABS registered (p50.0032), werestatistically different. The comparison between the doses of the point As,defined using ICRU-38, ABS 2011 and computed by registering on planof first implant, are statistically different (p!0.05). The mean HR_CTVof each patient were fitted with normalized D90 (ND90) and %IDL datausing the method of least square fit. The ND90 has negative correlationwith HR_CTV with correlation coefficient of 0.7253, while 100% IDL