Seroma Volume Changes

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Presented by Wesley Zoller, B.S.R.T.(T) Medical Dosimetry Student June 19th, 2013 AAMD Annual Meeting San Antonio, TX

Transcript of Seroma Volume Changes

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Presented by Wesley Zoller, B.S.R.T.(T) Medical Dosimetry Student June 19th, 2013 AAMD Annual Meeting San Antonio, TX

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A Little Background on Me

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I’m a Country Fella from Churchtown, Ohio

• Small little farming community by the Ohio River

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My Family!

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B.S.RT(T) from the Ohio State University (2012)

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Cleveland Browns Fan…..

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Honorary Spurs Fan for these few weeks…

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Student in the Cleveland Clinic CMD Program

• Graduating July 19th, 2013!!!!

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When I have time, I like to do a little golfing…

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Presented by Wesley Zoller, B.S.R.T.(T) Medical Dosimetry Student June 19th, 2013 AAMD Annual Meeting San Antonio, TX

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Aims of the Study

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Objectives

• Quantify the changes in seroma volume over the course of RT for early stage breast cancer patients eligible for RTOG 1005.

• Evaluate the dosimetric impact of these changes on sequential boost planning in accordance with Arm I of RTOG 1005.

• Assess the need for adaptive planning and pre-boost CT acquisition for sequentially boosted breast cancer patients based on evaluation with RTOG 1005 criteria.

• Dosimetrically compare two hypofractioned boost methods, concurrent electron versus concomitant tangential IMRT photon, with the planning/evaluation criteria outlined in Arm II of RTOG 1005.

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Background of RTOG 1005

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Reference 1 on Final Slide

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Reference 1 on Final Slide

• For Early Stage Breast Cancer Patients (Stage I-II)

• Post-Lumpectomy Breast Conservation Course

• Shorten Treatment Time

• Objectives of Study

• Primary: determine if accelerated hypofractionated WBI with concomitant tumor bed boosting is non-inferior in local control to Standard of Care sequential boost and fractionation scheme

• Secondary: determine if ARM II is non-inferior to the Standard of Care in terms of cosmesis, treatment symptoms (3 weeks and at 3 years), cardiac toxicity for left sided cases, and treatment costs

• If non-inferior, determine if ARM II hypofractionated scheme is superior to Standard of Care fractionated in same criteria

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Previous Literature

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• 2009 study, aimed to evaluate the change in seroma volume over WBRT prior to boost planning.

• 24 patients with evident seroma on initial CT, received 42.4Gy/16fx with 9.6Gy/4fx boost or 50.4Gy/28fx WBRT with 10Gy/5fx boost

• Second CT acquired at 3-5 weeks, dependent upon fractionation schedule

• Mean CT1 seroma was 65.7 cc and CT2 was 35.6 cc. Mean reduction of 39.6% with an SD of 23.8%, p<0.001, 2 of 24 patients showed increase in size with an increase or 9.7% and 10.7%

• Changes during WBRT found to be significant and group concluded boost planning accuracy can be affected by these changes.

Reference 6 on Final Slide

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Reference 7 on Final Slide

• 2009 study, aimed to determine if lumpectomy cavity decreases in volume during whole breast radiotherapy and contributing factors.

• 43 patients, 44 breast lesions prospectively enrolled. Lumpectomy and CT sim within 60 days of surgery. WBRT 45-50.4 Gy.

• CT2 acquired b/w 21-23 treatments, seroma contoured on new CT and compared.

• Mean volume was 38.2 cc on CT1, 21.7 cc on CT2. Mean decrease of 32% and 11.2 delta cc. Decreased on 38 of 44 patients (86%), p<0.001

• Concluded that tracking change and acquiring a pre-boost CT can lead to decreased doses of radiation to remaining breast and critical structures, and should be considered in patients with larger cavities.

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Methods

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Summary of Methods

• 11 early stage breast cancer patients eligible for RTOG 1005

• Clinically evident seroma at time of initial simulation (CT1)

• Received second CT (CT2) prior to planning of sequential boost

• Seroma volume/Lumpectomy GTV delineated on both datasets

• PHASE I: Characteristics of both CT1 and CT2 seroma volumes recorded

• Fusion of CT2 dataset and contour onto CT1 dataset

• In accordance with RTOG 1005 Arm I, patients retrospectively re-planned giving 50Gy/25fx to whole breast and boosting sequentially with 12Gy/6fx given via electron boost to the cavity (Standard of Care Arm)

• Boost plans individually optimized for each volume (CT1 vs. CT2)

• Plans compared based on dose to Heart, Ipsilateral Lung, Breast PTV Eval (Normal Breast), and coverage of Lumpectomy PTV Eval using specified Arm I evaluation criteria

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Summary of Methods

• PHASE II: Comparison of Concurrent Hypofractionated Boost Methods

• In accordance with RTOG 1005 Arm II, patients retrospectively re-planned giving 40Gy/15fx to whole breast tangents and boosting concurrently with 8 Gy in the same 15 fx

• Boost plans individually optimized for CT1 target volumes

• Concurrent Electron Cavity Boost

• Concomitant IMRT Photon Cavity Boost

• Plans compared based on dose to Heart, Ipsilateral Lung, Breast PTV Eval (Normal Breast), and coverage of Lumpectomy PTV Eval using specified Arm II evaluation criteria

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Contouring for the Study (Using RTOG 1005 Delineation Guidelines)

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Lumpectomy GTV (per RTOG 1005) • Excision cavity volume, architectural distortion, lumpectomy scar,

seroma and/or extend of surgical clips (clips strongly recommended)

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Lumpectomy CTV (per RTOG 1005) • Lumpectomy GTV + 1 cm 3D Expansion, Limiting Borders: Pectoralis

and Serratus Anterior Muscles, Midline, and 5 mm from skin surface

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Lumpectomy PTV (per RTOG 1005) • Lumpectomy CTV + 7 mm uniform 3D Expansion (Excluding Heart)

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Lumpectomy PTV Eval (per RTOG 1005) • Lumpectomy PTV minus area outside of ipsilateral breast, first 5 mm

of skin, and the chest wall/pectoralis muscles/lungs.

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Breast PTV Eval (per RTOG 1005) • Breast CTV (palpable breast volume – CW and 5mm skin) + 7 mm PTV

expansions in same Manner as Lumpectomy PTV Eval (avoid CW, 5mm)

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Critical Normal Structures (per RTOG 1005) • In this study: Ipsilateral Lung, Heart (Split of Pulmonary trunk into

Pulmonary Arteries superiorly to apex inferiorly), and Contralateral Lung.

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Image Fusion

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GTV Delineation (RTOG 1005) and Image Fusion

CT1 GTV Delineation CT2 GTV Delineation

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GTV Delineation (RTOG 1005) and Image Fusion

Box-Based Fusion using chest wall and Ipsilateral Breast

CT-CT Fusion done in PhilipsTM Pinnacle® SyntegraTM

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Evaluation/Results of Seroma Volume Changes CT1 versus CT2 Volume

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Results – Table 1 Seroma Volume Changes

Max Percent Decrease = 77.3%

Min Decrease = 46.1%

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Planning for Phase I: Sequential Electron Boost for CT1 and CT2 (RTOG Arm I)

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Phase I of Study, Sequential Boosting (Arm I)

• 11 patients, retrospectively re-planned for 50 Gy in 25 fractions tangentially to the whole breast.

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• Sequential Electron boosts given 12 Gy in 6 fractions to Lumpectomy GTV using Lumpectomy PTV as Block Margin

• Optimized for both CT1 and CT2 Scans for the 11 patients (Available MEV 6, 9, 12, 15, 18, 21)

Phase I of Study, Sequential Boosting (Arm I)

Boost BEV for CT1 Volume Boost BEV for new CT2 Volume

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Evaluation of Sequential Boost (RTOG Arm I) Phase I: CT1 versus CT2 Seroma Volume

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V58.9 of Lumpectomy PTV Eval >/= 95% (Arm I)

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V47.5 of Breast PTV Eval >/= 95% (Arm I)

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V56 of Breast PTV Eval </= 50% (Arm I)

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V62 of Breast PTV Eval </= 30% (Arm I)

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V20 of Ipsilateral Lung </= 20% (Arm I)

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Mean Heart Dose < 500 cGy (RTOG 1005 Arm I)

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Results for Sequential Boost (RTOG Arm I) Phase I: CT1 versus CT2 Seroma Volume

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Comparison (Phase I)

For Phase I, the lung and heart dose are comparable for both plans.

However, V56 of Breast PTV Eval drops by 6.8% for boost plan optimized to new volume

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Phase I of Study, Sequential Boosting (Arm I) • Comparison of Sequential Electron Boosts

Boost Plan for Lumpectomy PTV Eval CT1 Boost Plan for Lumpectomy PTV Eval CT2

Reduced V56 for Re-CT Optimized Plan

59.8 Gy

56 Gy

47.5 Gy

20 Gy

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Results - Table 2 for Sequential Boost (Phase I)

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Comparison of V58.9 of Lumpectomy PTV Eval

Old Plan still maintains coverage of re-scan Lumpectomy PTV Eval

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Planning for Phase II: Hypofractionated Concurrent Electron versus Concomitant IMRT Photon (RTOG Arm II)

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Phase II of Study, Hypofractionated Course with Concurrent Boosting (Arm II) • 11 patients, retrospectively re-planned for 40 Gy in 15 fractions

tangentially to the whole breast.

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Phase II of Study, Hypofractionated Course with Concurrent Boosting (Arm II)

• Concurrent Electron Boost (Same blocking as Initial Sequential Phase I) given concurrently 8 Gy over 15 fractions for 11 patients

• 8 Gy Concomitant IMRT Photon Boost “mini-tangents” for same 11 patients

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Evaluation of Concurrent Boost on Hypofractionated Course (RTOG Arm II) Phase II: Electron versus Concomitant IMRT Photon

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V45.6 of Lumpectomy PTV Eval >/= 95% (Arm II)

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V38 of Breast PTV Eval >/= 95% (Arm II)

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V44.8 of Breast PTV Eval </= 50% (Arm II)

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V48 of Breast PTV Eval </= 30% (Arm II)

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V16 of Ipsilateral Lung </= 20% (Arm II)

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Mean Heart Dose < 400 cGy (RTOG 1005 Arm II)

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Results for Concurrent Boost on Hypofractionated Course (RTOG Arm II) Phase II: Electron versus Concomitant IMRT Photon

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For Phase II, the ipsilateral lung and heart dose are comparable for both plans.

However, V44.8 of Breast PTV Eval dropped by 28.1% for Electron Boost vs. IMRT Photon Boosts

Comparison (Phase II)

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45.6 Gy

44.8 Gy

38 Gy

16 Gy

Phase II of Study, Concurrent Hypofractionated Boosting (Arm II)

Much higher V44.8 for Concomitant IMRT Photon Boost Plan

Concurrent 8 Gy Electron Boost Concomitant 8 Gy Photon IMRT Boost

• Comparison of Boost Methods

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Results - Table 3 for Hypofractionated Concurrent Boost (Phase II)

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Discussion

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Discussion

• Average seroma volume decrease of 57.1% +/- 8.96% from CT1 to CT2

• Time elapsed between CT acquisition was 33.6 days +/- 5.1 days

• ARM I SEQUENTIAL: V56 for Breast PTV Eval decreased by an average of 9.2% +/- 3.3% by optimizing the boost plan on a 2nd CT for the current standard of care WB + Boost (50 Gy + 12 Gy Boost)

• Lung and Heart Dose discrepancies were minimal b/w plans

• Coverage of Lumpectomy PTV Eval CT2 volume maintained using CT1-optimized plan

• Under-treating not found to be a concern in this study

• ARM II Hypofractionated: V44.8 for Breast PTV Eval decreased by an average of 16.2% +/- 8.1% on all Electron Boosts when compared to concomitant IMRT photon boost methods

• Lung and Heart Dose discrepancies were minimal b/w plans

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Discussion

• Findings showed significant dose differences to the Breast PTV Eval

• Reduced by re-planning sequential boost using pre-boost CT

• Reduced using electron boost versus IMRT photon

• Significance of findings?

• Beyond WB prescription, breast tissue deemed to be normal tissue

• Reducing amount of normal breast tissue in boost field could potentially decrease some of the acute side effects associated with treatment of the site4,5

• Potential also exists to reduce late effects from breast irradiation, such as the development of fibrosis4,5

• RTOG 1005 does not currently allow planning from a pre-boost CT

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• 2008 trial to investigate predictors of long-term risk of fibrosis

• Between 1989 and 1996, 5318 patients receive 50 Gy/25 fx WBRT

• 2661 not boosted, 2657 boosted w/ 16 Gy/8fx with electrons to tumor bed

• Median Follow-up 10.7 years in both, 1079 pt (20.8%) had developed moderate or severe fibrosis, 482 (9.3%) local recurrences, and 1013 (19.6% ) died

• Development dataset: 26.9% in boost arm had moderate or severe fibrosis versus 12.6% in non-boosted

• Boost reduced the risk of local recurrence by 41%

Reference 4 on Final Slide

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Conclusions

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Take Home Message • Breast volume beyond tangential prescription should be treated as normal

tissue and should be spared as much as possible

• Potential to minimize both acute and late RT effects

• Adaptive Planning, or optimizing using a pre-boost CT showed to significantly decrease excess irradiation to normal breast tissue

• Electron cavity boosting also showed to be significantly superior to photon mini-tangents

• Lung and Heart dose discrepancies minimal between respective comparisons

• Simply acquiring one CT and adaptively optimizing a new boost plan has the potential to significantly decrease excess dose to normal breast tissue

• 4th or so week of treatment, ample time for dosimetry to generate boost plan

• In a world of CBCT and IGRT, the simple acquisition of one additional CT may be considered worthwhile in terms of potential to better patient outcomes

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References and Co-authors of Manuscript

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Thank you all so much for your time and your attention!!!

Have a great afternoon and everyone travel home safely!!!