Literature DB >> 11054522

A quantitative treatment planning study evaluating the potential of dose escalation in conformal radiotherapy of the oesophagus.

J L Bedford1, L Viviers, Z Guzel, P J Childs, S Webb, D M Tait.   

Abstract

BACKGROUND AND
PURPOSE: This study aims to evaluate the reduction in radiation dose to normal thoracic structures through the use of conformal radiotherapy techniques in the treatment of oesophageal cancer, and to quantify the resultant potential for dose escalation.
MATERIALS AND METHODS: Three different CT-derived treatment plans were created and compared for each of ten patients. A two-phase treatment with conventional straight-edged fields and standard blocks (CV2), a two-phase conformal plan (CF2), and a three-phase conformal plan where the third phase was delivered to the gross tumour only (CF3), were considered for each patient. Escalated dose levels were determined for techniques CF2 and CF3, which by virtue of the conformal field shaping, did not increase the mean lung dose. The resulting increase in tumour control probability (TCP) was estimated.
RESULTS: A two-phase conformal technique (CF2) reduced the volume of lung irradiated to 18 Gy from 19.7+/-11.8 (1 SD) to 17.1+/-12.3% (P=0.004), and reduced the normal tissue complication probability (NTCP) from 2.4+/-4.0 to 0.7+/-1.6% (P=0.02) for a standard prescribed dose of 55 Gy. Consequently, technique CF2 permitted a target dose of 59.1+/-3.2 Gy without increasing the mean lung dose. Technique CF3 facilitated a prescribed dose of 60.7+/-4.3 Gy to the target, the additional 5 Gy increasing the TCP from 53. 1+/-5.5 to 68.9+/-4.1%. When the spinal cord tolerance was raised from 45 to 48 Gy, technique CF3 allowed 63.6+/-4.l Gy to be delivered to the target, thereby increasing the TCP to 78.1+/-3.2%.
CONCLUSIONS: Conformal radiotherapy techniques offer the potential for a 5-10 Gy escalation in dose delivered to the oesophagus, without increasing the mean lung dose. This is expected to increase local tumour control by 15-25%.

Entities:  

Mesh:

Year:  2000        PMID: 11054522     DOI: 10.1016/s0167-8140(00)00258-9

Source DB:  PubMed          Journal:  Radiother Oncol        ISSN: 0167-8140            Impact factor:   6.280


  11 in total

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Journal:  Jpn J Radiol       Date:  2011-12-14       Impact factor: 2.374

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3.  Volumetric modulated arc therapy planning for distal oesophageal malignancies.

Authors:  M A Hawkins; J L Bedford; A P Warrington; D M Tait
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6.  A Meta-Analysis of Concurrent Chemoradiotherapy for Advanced Esophageal Cancer.

Authors:  Li-Li Zhu; Ling Yuan; Hui Wang; Lin Ye; Gui-Ying Yao; Cui Liu; Niu-Niu Sun; Xiao-Jing Li; Shi-Cong Zhai; Ling-Juan Niu; Jun-Bo Zhang; Hong-Long Ji; Xiu-Min Li
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7.  Comparison of Acuros (AXB) and Anisotropic Analytical Algorithm (AAA) for dose calculation in treatment of oesophageal cancer: effects on modelling tumour control probability.

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8.  Radiobiological evaluation of simultaneously dose-escalated versus non-escalated intensity-modulated radiation therapy for patients with upper thoracic esophageal cancer.

Authors:  Bao-Tian Huang; Li-Li Wu; Long-Jia Guo; Liang-Yu Xu; Rui-Hong Huang; Pei-Xian Lin; Jian-Zhou Chen; De-Rui Li; Chuang-Zhen Chen
Journal:  Onco Targets Ther       Date:  2017-04-19       Impact factor: 4.147

9.  The effect of dose escalation on gastric toxicity when treating lower oesophageal tumours: a radiobiological investigation.

Authors:  Rhys Carrington; John Staffurth; Samantha Warren; Mike Partridge; Chris Hurt; Emiliano Spezi; Sarah Gwynne; Maria A Hawkins; Thomas Crosby
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10.  Radiobiological determination of dose escalation and normal tissue toxicity in definitive chemoradiation therapy for esophageal cancer.

Authors:  Samantha Warren; Mike Partridge; Rhys Carrington; Chris Hurt; Thomas Crosby; Maria A Hawkins
Journal:  Int J Radiat Oncol Biol Phys       Date:  2014-10-01       Impact factor: 7.038

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