Chemoradiotherapy in Cancer Treatment: Rationale and Clinical Applications

被引:74
作者
Rallis, Kathrine S. [1 ,2 ]
Yau, Thomas Ho Lai [2 ]
Sideris, Michail [3 ]
机构
[1] Queen Mary Univ London, Barts Canc Inst, London, England
[2] Queen Mary Univ London, Barts & London Sch Med & Dent, London, England
[3] Queen Mary Univ London, Womens Hlth Res Unit, London, England
关键词
Chemoradiotherapy; chemotherapy; radiotherapy; cancer treatment; anal cancer; cervical cancer; non-small cell lung cancer; bladder cancer; immunotherapy; combination treatment; review; CELL LUNG-CANCER; DOSE-RATE BRACHYTHERAPY; RADIATION-THERAPY; RANDOMIZED-TRIAL; ANAL CANCER; PHASE-III; CONCURRENT CHEMORADIATION; CERVICAL-CANCER; RADIOTHERAPY; CHEMOTHERAPY;
D O I
10.21873/anticanres.14746
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemoradiotherapy (CRT) refers to the combined administration of both chemotherapy and radiotherapy as an anticancer treatment. Over the years, CRT has become an established treatment for a diverse range of locally advanced solid tumours. The rationale for CRT is based on the two concepts of spatial cooperation and in-field cooperation, whereby the end goal is to achieve synergistic antitumour effects from the combination of both treatment modalities. CRT offers notable patient survival benefits and local disease control without significant long-term toxicities. Although the enhancement of cytotoxic effects inevitably increases damage to normal tissues as well as tumour cells, if the damage to normal tissue is lesser than that to tumour cells, CRT is still deemed beneficial. Thus, the search to optimise dose, timings and fractionation of CRT is of particular interest. Considering the recent success achieved with anticancer immunotherapies including immune checkpoint inhibitors, the combination of CRT and immunotherapy has emerged as an exciting field of research with the potential for significant clinical benefit. This report outlines the rationale underlying CRT and discusses its advantages through clinical examples focusing on anal, cervical, non-small-cell lung cancer and bladder cancer.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 57 条
[41]   The effect of dose escalation for large squamous cell carcinomas of the anal canal [J].
Prasad, R. N. ;
Elson, J. ;
Kharofa, J. .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2018, 20 (10) :1314-1320
[42]  
Provencio Mariano, 2011, J Thorac Dis, V3, P197, DOI 10.3978/j.issn.2072-1439.2011.01.02
[43]   Systemic chemotherapy for advanced non-small cell lung cancer: Recent advances and future directions [J].
Ramalingam, Suresh ;
Belani, Chandra .
ONCOLOGIST, 2008, 13 :5-13
[44]   Propensity matched comparative analysis of survival following chemoradiation or radical cystectomy for muscle-invasive bladder cancer [J].
Ritch, Chad R. ;
Balise, Raymond ;
Prakash, Nachiketh Soodana ;
Alonzo, David ;
Almengo, Katherine ;
Alameddine, Mahmoud ;
Venkatramani, Vivek ;
Punnen, Sanoj ;
Parekh, Dipen J. ;
Gonzalgo, Mark L. .
BJU INTERNATIONAL, 2018, 121 (05) :745-751
[45]  
Rowell NP, 2004, COCHRANE DB SYST REV, DOI DOI 10.1002/14651858.CD002140.PUB2
[46]   The effect of intensity-modulated radiotherapy and high dose rate brachytherapy on acute and late radiotherapy-related adverse events following chemoradiotherapy of anal cancer [J].
Saarilahti, Kauko ;
Arponen, Paeivi ;
Vaalavirta, Leila ;
Tenhunen, Mikko .
RADIOTHERAPY AND ONCOLOGY, 2008, 87 (03) :383-390
[47]   The concurrent chemoradiation paradigm - general principles [J].
Seiwert, Tanguy Y. ;
Salama, Joseph K. ;
Vokes, Everett E. .
NATURE CLINICAL PRACTICE ONCOLOGY, 2007, 4 (02) :86-100
[48]  
Singh P., J CLIN ONCOL, V38, DOI [10.1200/JCO.2020.38.6_suppl.TPS586, DOI 10.1200/JCO.2020.38.6_SUPPL.TPS586]
[49]  
STEEL GG, 1979, INT J RADIAT ONCOL, V5, P85
[50]  
Teply Benjamin A, 2014, J Solid Tumors, V4, P25