Literature DB >> 8598369

Quantitative comparisons of continuous and pulsed low dose rate regimens in a model late-effect system.

D J Brenner1, E J Hall, G Randers-Pehrson, Y Huang, G W Johnson, R W Miller, B Wu, M E Vazquez, C Medvedovsky, B V Worgul.   

Abstract

PURPOSE: There is increasing interest and usage of pulsed low dose rate (PDR) brachytherapy, in which a single source is shuttled through the catheters of an implant, typically for about 10 min each hour. This study was designed to compare the late effects produced in various PDR regimens with those from the corresponding continuous low dose rate (CLDR) regimens. METHODS AND MATERIALS: A model late-responding system was used, namely, cataract induction in the rat lens. This system has the advantage of being highly quantifiable. The rats eyes were exposed to a total dose of 15 Gy either continuously over 24 h, or with three different PDR regimens, all with the same total dose and overall time. We addressed three questions: (a) are late effects increased when a CLDR regimen is replaced with 10-min pulses repeated every hour? (b) Are late effects increased if hourly 10-min pulses are replaced with 10-min pulses repeated every 4 h? (c) Are late effects increased if 10-min pulses are replaced with 100-s pulses?
RESULTS: We found that the four regimens under test, continuous, 10-min pulses each hour, 10-min pulses every 4 h, and 100-s pulses every hour, showed no significant differences in cataractogenic potential, as estimated with the Wilcoxon-Gehan test. Power tests indicated that the experimental design was adequate to detect relatively small differences in cataractogenicity between regimens.
CONCLUSIONS: The equality of late effects from CLDR and PDR in these experiments must imply that sublethal damage repair is quite slow in this model late-responding system, in agreement with trends observed in the clinic for sublethal damage repair of late sequelae. Such trends would suggest that PDR is unlikely to produce significantly worse late effects than the corresponding CLDR regimen, which is in agreement with early clinical data using PDR. Caution, however, is strongly recommended.

Entities:  

Keywords:  Non-programmatic

Mesh:

Year:  1996        PMID: 8598369     DOI: 10.1016/0360-3016(95)02182-5

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  6 in total

1.  [Effects of fractionation and dose rate in PDR brachytherapy of B14 cells].

Authors:  L Keilholz; M H Seegenschmiedt; M Lotter; R Schulz-Wendtland; J von Erffa; S Pflüger; R Sauer
Journal:  Strahlenther Onkol       Date:  1998-02       Impact factor: 3.621

2.  Lauriston S. Taylor Lecture on radiation protection and measurements: what makes particle radiation so effective?

Authors:  Eleanor A Blakely
Journal:  Health Phys       Date:  2012-11       Impact factor: 1.316

3.  Hyperfractionation of HDR brachytherapy - influence on doses and biologically equivalent doses in clinical target volume and healthy tissues.

Authors:  Janusz Skowronek; Grzegorz Zwierzchowski; Tomasz Piotrowski
Journal:  J Contemp Brachytherapy       Date:  2009-07-17

Review 4.  Pulsed dose rate brachytherapy - is it the right way?

Authors:  Janusz Skowronek
Journal:  J Contemp Brachytherapy       Date:  2010-10-13

5.  Biological equivalence between LDR and PDR in cervical cancer: multifactor analysis using the linear-quadratic model.

Authors:  José Guilherme Couto; Isabel Bravo; Rui Pirraco
Journal:  J Contemp Brachytherapy       Date:  2011-09-30

6.  Influence of length of interval between pulses in PDR brachytherapy (PDRBT) on value of Biologically Equivalent Dose (BED) in healthy tissues.

Authors:  Janusz Skowronek; Julian Malicki; Grzegorz Zwierzchowski; Tomasz Piotrowski
Journal:  J Contemp Brachytherapy       Date:  2010-07-06
  6 in total

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