Clinical development of new drug-radiotherapy combinations

被引:249
作者
Sharma, Ricky A. [1 ,2 ]
Plummer, Ruth [3 ]
Stock, Julie K. [4 ]
Greenhalgh, Tessa A. [5 ]
Ataman, Ozlem [6 ]
Kelly, Stephen [7 ]
Clay, Robert [8 ]
Adams, Richard A. [9 ,10 ]
Baird, Richard D. [11 ]
Billingham, Lucinda [12 ]
Brown, Sarah R. [13 ]
Buckland, Sean
Bulbeck, Helen [14 ]
Chalmers, Anthony J. [15 ]
Clack, Glen [16 ]
Cranston, Aaron N. [17 ]
Damstrup, Lars [18 ]
Ferraldeschi, Roberta [19 ]
Forster, Martin D. [1 ,2 ]
Golec, Julian [20 ]
Hagan, Russell M. [21 ]
Hall, Emma [22 ]
Hanauske, Axel-R. [23 ]
Harrington, Kevin J. [22 ]
Haswell, Tom [14 ]
Hawkins, Maria A. [5 ]
Illidge, Tim [24 ]
Jones, Hazel [4 ]
Kennedy, Andrew S. [25 ]
McDonald, Fiona [22 ]
Melcher, Thorsten [26 ]
O'Connor, James P. B. [24 ]
Pollard, John R. [20 ]
Saunders, Mark P. [24 ]
Sebag-Montefiore, David [13 ]
Smitt, Melanie [27 ]
Staffurth, John [9 ,10 ]
Stratford, Ian J. [24 ]
Wedge, Stephen R. [3 ]
机构
[1] UCL, UCL Canc Inst, 72 Huntley St, London WC1E 6DD, England
[2] UCL, London, England
[3] Newcastle Univ, Newcastle Upon Tyne, Tyne & Wear, England
[4] Canc Res UK, London, England
[5] Univ Oxford, Oxford, England
[6] Eisai, Hatfield Business Pk, Hatfield, Herts, England
[7] Pfizer Ltd, Tadworth, Surrey, England
[8] Kinapse Ltd, London, England
[9] Cardiff Univ, Cardiff, S Glam, Wales
[10] Velindre Canc Ctr, Cardiff, S Glam, Wales
[11] Univ Cambridge, Cambridge, England
[12] Univ Birmingham, Birmingham, W Midlands, England
[13] Univ Leeds, Leeds, W Yorkshire, England
[14] Natl Inst Canc Res, London, England
[15] Univ Glasgow, Glasgow, Lanark, Scotland
[16] AstraZeneca Cheshire UK, Alderley Pk, Cheshire, England
[17] MISSION Therapeut Ltd, Cambridge, England
[18] Merck KGaA, Darmstadt, Germany
[19] Astex Pharmaceut, Cambridge, England
[20] Vertex Pharmaceut Europe Ltd, Abingdon, Oxon, England
[21] BTG Int Ltd, London, England
[22] Royal Marsden NIHR Biomed Res Ctr, Inst Canc Res, London, England
[23] Eli Lilly & Co, Indianapolis, IN 46285 USA
[24] Univ Manchester, Manchester, Lancs, England
[25] Sarah Cannon Res Inst, Nashville, TN USA
[26] J&J Innovat, Menlo Pk, CA USA
[27] Genentech Inc, San Francisco, CA 94080 USA
关键词
SURROGATE END-POINTS; CELL LUNG-CANCER; POSITRON-EMISSION-TOMOGRAPHY; MOLECULARLY TARGETED AGENTS; ADVANCED RECTAL-CANCER; EARLY BREAST-CANCER; PHASE-II TRIAL; RADIATION-THERAPY; PROSTATE-CANCER; NORMAL-TISSUE;
D O I
10.1038/nrclinonc.2016.79
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In countries with the best cancer outcomes, approximately 60% of patients receive radiotherapy as part of their treatment, which is one of the most cost-effective cancer treatments. Notably, around 40% of cancer cures include the use of radiotherapy, either as a single modality or combined with other treatments. Radiotherapy can provide enormous benefit to patients with cancer. In the past decade, significant technical advances, such as image-guided radiotherapy, intensity-modulated radiotherapy, stereotactic radiotherapy, and proton therapy enable higher doses of radiotherapy to be delivered to the tumour with significantly lower doses to normal surrounding tissues. However, apart from the combination of traditional cytotoxic chemotherapy with radiotherapy, little progress has been made in identifying and defining optimal targeted therapy and radiotherapy combinations to improve the efficacy of cancer treatment. The National Cancer Research Institute Clinical and Translational Radiotherapy Research Working Group (CTRad) formed a Joint Working Group with representatives from academia, industry, patient groups and regulatory bodies to address this lack of progress and to publish recommendations for future clinical research. Herein, we highlight the Working Group's consensus recommendations to increase the number of novel drugs being successfully registered in combination with radiotherapy to improve clinical outcomes for patients with cancer.
引用
收藏
页码:627 / 642
页数:16
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