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Journal ArticleDOI

Complication Probability as Assessed from Dose-Volume Histograms

TLDR
A recursive algorithm which uses tolerance dose data has been written and can be applied to arbitrary dose-volume histograms to estimate the complication probability.
Abstract
Optimization of a treatment plan for radiation therapy will produce a plan with the highest probability for tumor control without exceeding an acceptable complication rate. To achieve this goal it is necessary to have a means to estimate probabilities of local control and normal tissue complication. In general, good treatment plans deliver a high uniform dose to the target volume and lower doses to the surrounding normal tissues. The tolerance dose values available for various normal tissues are usually assumed to apply to partial or full volumes of the tissue which have been uniformly irradiated. These values are the best guidelines for estimating complication probabilities in tissues that receive a uniform dose to a fraction of the tissue and no dose to the remainder. Dose-volume histograms are one means of evaluating the uniformity of the irradiation on the tissues. Frequently the normal tissues are not uniformly irradiated as is demonstrated by dose-volume histograms for different treatment plans. A recursive algorithm which uses these tolerance dose data has been written and can be applied to arbitrary dose-volume histograms to estimate the complication probability.

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Citations
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Journal ArticleDOI

Use of normal tissue complication probability models in the clinic.

TL;DR: The Quantitative Analysis of Normal Tissue Effects in the Clinic (QUANTEC) review summarizes the currently available three-dimensional dose/volume/outcome data to update and refine the normal tissue dose/ volume tolerance guidelines provided by the classic Emami et al. paper published in 1991.
Journal ArticleDOI

Fitting of normal tissue tolerance data to an analytic function

TL;DR: A four-parameter empirical model has been applied to a compilation of clinical tolerance data developed by Emami et al. and the four parameters to characterize the tissue response have been determined and graphical representations of the derived probability distributions are presented.
Journal ArticleDOI

ICRP PUBLICATION 118: ICRP Statement on Tissue Reactions and Early and Late Effects of Radiation in Normal Tissues and Organs – Threshold Doses for Tissue Reactions in a Radiation Protection Context

TL;DR: Estimates of ‘practical’ threshold doses for tissue injury defined at the level of 1% incidence are provided and it appears that the rate of dose delivery does not modify the low incidence for reactions manifesting very late after low total doses, particularly for cataracts and circulatory disease.
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Reporting and analyzing dose distributions: A concept of equivalent uniform dose

TL;DR: Extensions of the basic EUD concept to include nonuniform density of clonogens, dose per fraction effects, repopulation of clons, and inhomogeneity of patient population are discussed and compared with the basic formula.
Journal ArticleDOI

Quantitative Analyses of Normal Tissue Effects in the Clinic (QUANTEC): An Introduction to the Scientific Issues

TL;DR: Clinical limitations to the current knowledge base include the need for more data on the effect of patient-related cofactors, interactions between dose distribution and cytotoxic or molecular targeted agents, and theeffect of dose fractions and overall treatment time in relation to nonuniform dose distributions.
References
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Journal ArticleDOI

Dose fractionation, dose rate and iso-effect relationships for normal tissue responses

TL;DR: An analysis is presented of responses of a variety of normal tissues in animals to fractionated irradiations and it is shown that the influence of fractionation can be described on the basis of a simple formula relating the effectiveness for induction of cellular effects to the dose per fraction.
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Models in radiotherapy: volume effects.

TL;DR: Experimental data are presented which are consistent with the general model alone and which demonstrate the limits of applicability of previous models.
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Multi-dimensional treatment planning: I. Delineation of anatomy.

TL;DR: Details of techniques for the assessment and delineation of anatomy, including the display of CT information in three dimensions and the ability to draw on and edit the image displays are presented.
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Optimization of radiation therapy: Integral-response of a model biological system

TL;DR: A simple mathematical model of an idealized biological system is presented and an objective function designed to achieve an extremum for that particular plan which minimizes the probabilities of occurrence of unacceptable complications in healthy tissue and of recurrence or spread of disease is derived.
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