Pre-treatment number of clonogenic cells and their radiosensitivity are major determinants of local turnour control after fractionated irradiation

被引:129
作者
Yaromina, Ala
Krause, Marie
Thames, Howard
Rosner, Andrea
Krause, Mechthild
Hessel, Franziska
Grenman, Reidar
Zips, Daniel
Baumann, Michael
机构
[1] Tech Univ Dresden, Dept Radiat Oncol, Med Fac Carl Gustav Carus, D-01307 Dresden, Germany
[2] Tech Univ Dresden, OncoRay Ctr Radiat Res Oncol, D-01307 Dresden, Germany
[3] Tech Univ Dresden, Expt Ctr, D-01307 Dresden, Germany
[4] Tech Univ Dresden, Dept Transfus Med, D-01307 Dresden, Germany
[5] Univ Texas, MD Anderson Canc Ctr, Div Quantitat Sci, Houston, TX 77030 USA
[6] Turku Univ, Dept Otorhinolaryngol Head & Neck Surg & Med Bioc, Turku, Finland
关键词
human tumour xenograft; fractionated radiation; local tumour control; clonogenic cells; cancer stem cells; intrinsic radiosensitivity; predictive assays;
D O I
10.1016/j.radonc.2007.04.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: The response of tumours to fractionated radiotherapy is determined by many factors including repopulation, reoxygenation, the number of clonogenic cells, and their intrinsic radiosensitivity. However, after single radiation doses given under conditions of clamp hypoxia, the dose to control a tumour locally is dependent only on the number of clonogenic cells and their cellular radiosensitivity. Therefore, these parameters were investigated using local control after single doses given under hypoxia, to predict the outcome of fractionated irradiation. Materials and methods: Ten hSCC cell lines (FaDu, UT-SCC-15, UT-SCC-14, XF354, UT-SCC-5, UT-SCC-45, SAS, CAL-33, UT-SCC-8, and HSC-4) were transplanted subcutaneously into the right hind-leg of NMRI nude mice. At 7 mm in diameter, tumours were irradiated either with graded single doses under clamp blood flow conditions (n = 873) or with 30 graded fractions within 6 weeks (n = 905) under ambient conditions. Local tumour control was determined 120 days after irradiation. Radiation response was quantified in terms of TCD(50), i.e. the dose required to control 50% of tumours locally. Results: Ten tumour lines investigated showed a pronounced heterogeneity in both TCD(50(30fx/6w)) after fractionated irradiation and TCD(50(SDclamp)) after single dose irradiation. TCD(50(30fx/6w)) varied between 45 Gy for UT-SCC-45 and 127 Gy for SAS; TCD(50(SDclamp)) varied between 42 Gy for UT-SCC-14 and 66 Gy for CAL-33. Two tumours were excluded from further analysis due to immunogenicity or non-defined TCD50. Linear regression analysis revealed a significant positive correlation between TCD(50(SDclamp)) and TCD(50(30fx/6w)) (R(2) = 0.82, p = 0.002). Conclusions: Significant association between TCD(50(SDclamp)) and TCD(50(30fx/6w)) suggests that the pre-treatment number of clonogenic tumour cells and their cellular radiosensitivity have a major impact on local control after fractionated radiotherapy. (C) 2007 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 83 (2007) 304-310.
引用
收藏
页码:304 / 310
页数:7
相关论文
共 38 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   RESPONSE OF HUMAN SQUAMOUS-CELL CARCINOMA XENOGRAFTS OF DIFFERENT SIZES TO IRRADIATION - RELATIONSHIP OF CLONOGENIC CELLS, CELLULAR RADIATION SENSITIVITY INVIVO, AND TUMOR RESCUING UNITS [J].
BAUMANN, M ;
DUBOIS, W ;
SUIT, HD .
RADIATION RESEARCH, 1990, 123 (03) :325-330
[3]  
BAUMANN M, 1992, CONTR ONCOL, V42, P98
[4]   Epidermal growth factor receptor expression in pretreatment biopsies from head and neck squamous cell carcinoma as a predictive factor for a benefit from accelerated radiation therapy in a randomized controlled trial [J].
Bentzen, SM ;
Atasoy, BM ;
Daley, FM ;
Dische, S ;
Richman, PI ;
Saunders, MI ;
Trott, KR ;
Wilson, GD .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (24) :5560-5567
[5]  
Bentzen SM, 1997, INT J RADIAT BIOL, V71, P531, DOI 10.1080/095530097143860
[6]  
Clarke Michael F, 2006, Cancer Res, V66, P9339, DOI 10.1158/0008-5472.CAN-06-3126
[7]   THE RADIORESPONSIVENESS OF HUMAN-TUMORS AND THE INITIAL SLOPE OF THE CELL-SURVIVAL CURVE [J].
DEACON, J ;
PECKHAM, MJ ;
STEEL, GG .
RADIOTHERAPY AND ONCOLOGY, 1984, 2 (04) :317-323
[8]  
Efron B., 1986, STAT SCI, V1, P54, DOI [DOI 10.1214/SS/1177013815, 10.1214/ss/1177013815]
[9]   The influence of epidermal growth factor receptor and tumor differentiation on the response to accelerated radiotherapy of squamous cell carcinomas of the head and neck in the randomized DAHANCA 6 and 7 study [J].
Eriksen, JG ;
Steiniche, T ;
Overgaard, J .
RADIOTHERAPY AND ONCOLOGY, 2005, 74 (02) :93-100
[10]   The prognostic value of epidermal growth factor receptor is related to tumor differentiation and the overall treatment time of radiotherapy in squamous cell carcinomas of the head and neck [J].
Eriksen, JG ;
Steiniche, T ;
Askaa, J ;
Alsner, J ;
Overgaard, J .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 58 (02) :561-566