Oesophageal Chemoradiotherapy in the UK¡ªCurrent Practice and Future Directions

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• 作者：S. Gwynne^&lowast ; ; ^&dagger ; ; S. Falk^&Dagger ; ; S. Gollins^§ ; ; ^&dagger ; ; L. Wills^&dagger ; ; A. Bateman^¶ ; ; S. Cummins^|| ; H. Grabsch^&lowast ; &lowast ; ; M.A. Hawkins^&dagger ; &dagger ; ; R. Maggs^&dagger ; ; S. Mukherjee^&dagger ; &dagger ; ; G. Radhakrishna^&Dagger ; &Dagger ; ; R. Roy^§ ; § ; ; R.A. Sharma^&dagger ; &dagger ; ; E. Spezi^&dagger ; ; T. Crosby^&dagger ; ; ^{tom.crosby@wales.nhs.uk}
• 关键词：Chemoradiotherapy ; oesophageal
• 刊名：Clinical Oncology
• 出版年：2013
• 出版时间：June, 2013
• 年：2013
• 卷：25
• 期：6
• 页码：368-377
• 全文大小：162 K

文摘

The SCOPE 1 trial closed to recruitment in early 2012 and has demonstrably improved the quality of UK radiotherapy. It has also shown that there is an enthusiastic upper gastrointestinal clinical oncology community that can successfully complete trials and deliver high-quality radiotherapy. Following on from SCOPE 1, this paper, authored by a consensus of leading UK upper gastrointestinal radiotherapy specialists, attempts to define current best practice and the questions to be answered by future clinical studies.

The two main roles for chemoradiotherapy (CRT) in the management of potentially curable oesophageal cancer are definitive (dCRT) and neoadjuvant (naCRT). The rates of local failure after dCRT are consistently high, showing the need to evaluate more effective treatments, both in terms of optimal local and systemic therapeutic components. This will be the primary objective of the next planned UK dCRT trial and here we discuss the role of dose escalation and systemic therapeutic options that will form the basis of that trial. The publication of the Dutch ¡®CROSS¡¯ trial of naCRT has shown that this pre-operative approach can both be given safely and offer a significant survival benefit over surgery alone. This has led to the development of the UK NeoSCOPE trial, due to open in 2013. There will be a translational substudy to this trial and currently available data on the role of biomarkers in predicting response to therapy are discussed. Postoperative reporting of the pathology specimen is discussed, with recommendations for the NeoSCOPE trial. Both of these CRT approaches may benefit from recent developments, such as positron emission tomography/computed tomography and four-dimensional computed tomography for target volume delineation, planning techniques such as intensity-modulated radiotherapy and ¡®type b¡¯ algorithms and new treatment verification methods, such as cone-beam computed tomography. These are discussed here and recommendations made for their use.