Literature DB >> 9588929

Pulse frequency in pulsed brachytherapy based on tissue repair kinetics.

P Sminia1, C J Schneider, K Koedooder, G van Tienhoven, L E Blank, D G González.   

Abstract

PURPOSE: Investigation of normal tissue sparing in pulsed brachytherapy (PB) relative to continuous low-dose rate irradiation (CLDR) by adjusting pulse frequency based on tissue repair characteristics.
METHOD: Using the linear quadratic model, the relative effectiveness (RE) of a 20 Gy boost was calculated for tissue with an alpha/beta ratio ranging from 2 to 10 Gy and a half-time of sublethal damage repair between 0.1 and 3 h. The boost dose was considered to be delivered either in a number of pulses varying from 2 to 25, or continuously at a dose rate of 0.50, 0.80, or 1.20 Gy/h.
RESULTS: The RE of 20 Gy was found to be identical for PB in 25 pulses of 0.80 Gy each h and CLDR delivered at 0.80 Gy/h for any alpha/beta value and for a repair half-time > 0.75 h. When normal tissue repair half-times are assumed to be longer than tumor repair half-times, normal tissue sparing can be obtained, within the restriction of a fixed overall treatment time, with higher dose per pulse and longer period time (time elapsed between start of pulse n and start of pulse n + 1). An optimum relative normal tissue sparing larger than 10% was found with 4 pulses of 5 Gy every 8 h. Hence, a therapeutic gain might be obtained when changing from CLDR to PB by adjusting the physical dose in such a way that the biological dose on the tumor is maintained. The normal tissue-sparing phenomenon can be explained by an increase in RE with longer period time for tissue with high alpha/beta ratio and fast or intermediate repair half-time, and the RE for tissue with low alpha/beta ratio and long repair half-time remains almost constant.
CONCLUSION: Within the benchmark of the LQ model, advantage in normal tissue-sparing is expected when matching the pulse frequency to the repair kinetics of the normal tissue exposed. A period time longer than 1 h may lead to a reduction of late normal tissue complications. This theoretical advantage emphasizes the need for better knowledge of human tissue-repair kinetics.

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Year:  1998        PMID: 9588929     DOI: 10.1016/s0360-3016(98)00023-6

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


  5 in total

Review 1.  A review of the clinical experience in pulsed dose rate brachytherapy.

Authors:  Brian V Balgobind; Kees Koedooder; Diego Ordoñez Zúñiga; Raquel Dávila Fajardo; Coen R N Rasch; Bradley R Pieters
Journal:  Br J Radiol       Date:  2015-08-20       Impact factor: 3.039

Review 2.  Pulsed dose rate brachytherapy.

Authors:  A Polo
Journal:  Clin Transl Oncol       Date:  2008-06       Impact factor: 3.405

3.  Pulsed brachytherapy: a modelled consideration of repair parameter uncertainties and their influence on treatment duration extension and daytime-only "block-schemes".

Authors:  T S A Underwood; R G Dale; A M Bidmead; C A Nalder; P R Blake
Journal:  Br J Radiol       Date:  2011-01-25       Impact factor: 3.039

4.  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

5.  IMRT and brachytherapy comparison in gynaecological cancer treatment: thinking over dosimetry and radiobiology.

Authors:  Valentina Pinzi; Valeria Landoni; Federica Cattani; Roberta Lazzari; Barbara Alicja Jereczek-Fossa; Roberto Orecchia
Journal:  Ecancermedicalscience       Date:  2019-12-17
  5 in total

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