HDR brachytherapy combined with interstitial hyperthermia in locally advanced cervical cancer patients initially treated with concomitant radiochemotherapy - a phase III study

被引:22
作者
Zolciak-Siwinska, Agnieszka [1 ]
Piotrkowicz, Norbert [1 ,2 ]
Jonska-Gmyrek, Joanna [3 ]
Nicke-Psikuta, Maria [1 ]
Michalski, Wojciech [4 ]
Kawczynska, Maryla [5 ]
Bijok, Michal [5 ]
Bujko, Krzysztof [3 ]
机构
[1] Maria Sklodowska Curie Mem Canc Ctr & Inst Oncol, Dept Brachytherapy, PL-02781 Warsaw, Poland
[2] Maria Sklodowska Curie Mem Canc Ctr & Inst Oncol, Dept Gynecol, PL-02781 Warsaw, Poland
[3] Maria Sklodowska Curie Mem Canc Ctr & Inst Oncol, Dept Teleradiotherapy, PL-02781 Warsaw, Poland
[4] Maria Sklodowska Curie Mem Canc Ctr & Inst Oncol, Dept Clin Trials & Biostat, PL-02781 Warsaw, Poland
[5] Maria Sklodowska Curie Mem Canc Ctr & Inst Oncol, Dept Med Phys, PL-02781 Warsaw, Poland
关键词
HDR brachytherapy; Interstitial hyperthermia; Cervical cancer; Side effects; RADIATION-THERAPY; RADIOTHERAPY; TRIAL; PARAMETERS; CARCINOMA; IMPACT;
D O I
10.1016/j.radonc.2013.04.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: The aim of this randomised trial was to investigate whether hyperthermia (HT) combined with interstitial brachytherapy (ISBT) has any influence on local control (LC), disease-free survival (DFS), or acute and late side effects in patients with advanced cervical cancer. Materials and methods: After radiochemotherapy, consecutive patients with cervical cancer (FIGO stage were randomly assigned to two treatment groups, either ISBT alone or ISBT combined with interstitial hyperthermia (ISHT). A total of 205 patients were included in the statistical analysis. Once a week, HT, at a temperature above 42.5 degrees C, was administered for 45 min before and during the HDR BT. Results: The median follow-up time was 45 months (range 3-72 months). An effect of hyperthermia was not detected for disease-free survival (DFS) (log-rank test: p = 0.178) or for local control (LC) (p = 0.991). According to Cox's analysis, HT did not significantly influence failure or interactions with potential prognostic factors for LC or DFS. Statistical differences were not observed for the distribution of early and late complications between the HT and non HT groups. Conclusions: ISHT is well-tolerated and does not affect treatment-related early or late complications. Improvements in DFS and LC were not observed following the addition of ISHT to ISBT. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:194 / 199
页数:6
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