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clinical findings including physical exam and endoscopy. Endoscopy and physical exam often reveal areas of visible or palpable
disease which are not clearly demonstrated on volumetric imaging. However, interpreting endoscopy images as it relates to the
volumetric imaging is subject to potential error. Localizing disease usually relies on remembering its relationship to fixed anatomic
landmarks that are visible on both CT and endoscopy which, by its nature, may be imprecise or inaccurate. We present and describe
a method of quantitative endoscopy to improve target delineation in planning for head and neck cancer.
Materials/Methods: We have developed technology that registers endoscopic images to CT images by tracking and registering the
position and orientation of the endoscope relative to the CT image set. Software developed by our group overlays this information
in both data sets in the treatment planning space. The endoscopy image and CT data sets are co-registered. After the regions of
disease are identified on the endoscopy image, the same regions are automatically identified in the CT data set.
Results: The endoscopic prototype as well as the capabilities of the registration software will be presented.
Conclusions: Although further testing and prototyping are needed, we believe quantitative endoscopy will be a valuable radiotherapy planning tool, augmenting the accuracy and precision of target delineation for head and neck cancers.
Author Disclosure: J. Cho, None; R. Weershink, None; A. Kashigar, None; D. Jaffray, None; A. Hope, None.
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Utilizing Biological Cost Functions and Monte Carlo Algorithms in Head and Neck IMRT Planning to
Improve Organ at Risk Sparing in Biologic Target Volume Dose Escalation
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Purpose/Objective(s): Visual impairment from radiation induced optic neuropathy (RION) is an uncommon sequela to radiation
therapy. Incidence is related to dose, dose per fraction and other factors. As part of the QUANTEC effort, we analyzed published
studies for consensus on predictors of RION in the ranges of conventional, hypo-fractionation and SRS radiation therapies.
Materials/Methods: The literature was searched for publications relating radiation toxicity of the optic nerves and chiasm to quantitative dose and dose-volume measurements of those structures for fractionations ranging from conventional to SRS. Results from
these authors were inter-compared to seek consensus on predictors of RION. Agreement of models with findings was examined.
Results: Twenty two studies were identified. Average follow-up was 42 and 50 months for studies with and without incidence of
RION, respectively. The interval between RT and development of visual symptoms was generally # 3 years (mode 11.5 years,
median 2.5 years). Most conventional fractionation (1.82.0 Gy/fx) studies were carried out prior to routine use of CT based treatment planning significantly limiting detailed examination of dose-volume response. It was also not possible to asses the impact of
IMRT dose gradients on tolerance. Incidence of RION was unusual for Dmax doses \ 55 Gy, particularly for fraction sizes less
than 2 Gy. The risk rose (310%) in the region 5559 Gy and became more substantial (. 20%) for doses . 60 Gy when fractionations of 1.82.0 Gy were used. For particles, most authors found that incidence of RION was low for Dmax dose \ 54 CGE.
One exception to this range was for pituitary tumors, where authors used constrained Dmax doses \ 46 Gy for 1.8 Gy/fx. For
single-fraction SRS the studies indicated the incidence of RION was rare for Dmax\8 Gy, rose in the region 812 Gy and became
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Cisplatin 30 Mg/M2/Week Decreases Toxicity without Sacrificing Efficacy in Patients Treated with
Concomitant Chemoradiotherapy for Locally Advanced Squamous Cell Carcinoma of the Head and Neck
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Plaque Radiotherapy for Juxtapapillary Choroidal Melanoma: Visual and Systemic Outcomes
Wills Eye Institute, Philadelphia, PA, 2Moorefields Eye Hospital, London, United Kingdom
Purpose/Objective(s): Management of choroidal melanoma adjacent to optic disc (juxtapapillary) is challenging due to the posterior tumor location, difficulty in localization and complexity of radiation field design. Various methods used to treat these tumors
have included enucleation, proton beam radiotherapy, plaque radiotherapy, stereotactic radiotherapy and transpupillary thermotherapy (TTT). The Collaborative Ocular Melanoma Study (COMS) excluded treatment of lesions within 2 mm of the optic
disc. We report the outcomes of treatment of juxtapapillary melanoma with plaque radiotherapy.
Materials/Methods: This was a retrospective, non-comparative review of 520 consecutive cases of juxtapapillary choroidal melanoma treated with custom designed plaque radiotherapy. The variables taken for analysis included the final visual acuity, radiation
complications, recurrence of tumor, need for enucleation, systemic metastasis and mortality.
Results: The median age at presentation was 51years (range, 15 93 years). The most common presenting symptoms were reduced
visual acuity (51%), photopsia (10%) and visual field defect (13%). Optic disc overhang by tumor was absent in 389 eyes (75%),
1% to 50% overhang in 83 (16%) and 51% to 100% overhang in 48 (9%). The quadrantic location of the main tumor was superior in
146 (28%) eyes, inferior in 114 (22%), nasal in 137 (26%) and temporal in 123 (24%). The median tumor basal diameter was 9.5
mm (range, 1.520 mm) and thickness 3.5 mm (range, 1.0 14.8 mm). The radioactive isotopes used were Iodine 125 in 504 eyes
(97%), cobalt 60 in 8 (2%) and iridium 192 in 8 (2%). The plaque shape was notched in 471 eyes (91%), round in 42 eyes (8%) and
rectangular in 7 (1%). The median radiation dose to the apex of the tumor was 8000 cGy, and to the base was 28,500 cGy. KaplanMeier analysis at 2, 5 and 10 years showed poor visual acuity (# 20/200) in 21%, 55%, and 84%; visual loss of more than 5 acuity
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