The effect of the time interval between radiation and hyperthermia on clinical outcome in 400 locally advanced cervical carcinoma patients

M. Kroesen, H.T. Mulder, J.M.L. van Holthe, A.A. Aangeenbrug, J.W.M. Mens, H.C. van Doorn, M.M. Paulides, E. Oomen-de Hoop, R.M. Vernhout, L.C. Lutgens, G.C. van Rhoon, M. Franckena (Corresponding author)

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Samenvatting

Background: Addition of deep hyperthermia to radiotherapy results in improved local control (LC) and overall survival compared to radiotherapy alone in cervical carcinoma patients. Based on preclinical data, the time interval between radiotherapy, and hyperthermia is expected to influence treatment outcome. Clinical studies addressing the effect of time interval are sparse. The repercussions for clinical applications are substantial, as the time between radiotherapy and hyperthermia should be kept as short as possible. In this study, we therefore investigated the effect of the time interval between radiotherapy and hyperthermia on treatment outcome. Methods: We analyzed all primary cervical carcinoma patients treated between 1996 and 2016 with thermoradiotherapy at our institute. Data on patients, tumors and treatments were collected, including the thermal dose parameters TRISE and CEM43T90. Follow-up data on tumor status and survival as well as late toxicity were collected. Data was analyzed using Cox proportional hazards analysis and Kaplan Meier analysis. Results: 400 patients were included. Kaplan Meier and univariate Cox analysis showed no effect of the time interval (range 30–230 min) on any clinical outcome measure. Besides known prognostic factors, thermal dose parameters TRISE and CEM43T90 had a significant effect on LC. In multivariate analysis, the thermal dose parameter TRISE (HR 0.649; 95% CI 0.501–0.840) and the use of image guided brachytherapy (HR 0.432; 95% CI 0.214–0.972), but not the time interval, were significant predictors of LC and disease specific survival. Conclusions: The time interval between radiotherapy and hyperthermia, up to 4 h, has no effect on clinical outcome. These results are re-ensuring for our current practice of delivering hyperthermia within maximal 4 h after radiotherapy.

Originele taal-2Engels
Artikelnummer134
Aantal pagina's11
TijdschriftFrontiers in Oncology
Volume9
DOI's
StatusGepubliceerd - 8 mrt. 2019

Financiering

Eugenia Morselli, Pontificia Universidad Católica de Chile, Chile Alessia Ligresti, National Research Council of Italy – ICB, Italy This study was performed in accordance with the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health (51) and was approved by the Institutional Animal Care and Use Committee of Grand Forks Human Nutrition Research Center. This work was supported by National Institute of Food and Agriculture, U.S. Department of Agriculture, under award number 2014-67017-21758 and through U.S. Department of Agriculture, Agricultural Research Service, research projects 3062-51000-053-00D and 3062-51000-050-00D.

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