Literature DB >> 18378028

Comparison of biologically equivalent dose-volume parameters for the treatment of prostate cancer with concomitant boost IMRT versus IMRT combined with brachytherapy.

Bradley R Pieters1, Jeroen B van de Kamer, Yvonne R J van Herten, Niek van Wieringen, Greet M D'Olieslager, Uulke A van der Heide, Caro C E Koning.   

Abstract

BACKGROUND AND
PURPOSE: The two main modalities to deliver high dose to the prostate and prevent high doses to neighboring organs are intensity modulated radiotherapy (IMRT) or external beam radiotherapy combined with brachytherapy. Because of the different biological effectiveness the physical dose distributions were converted to 3-dimensional linear quadratic dose at 2 Gy per fraction (EQD(2)). From the latter, cumulative EQD(2)-volume histograms were determined for comparison of the modalities.
MATERIAL AND METHODS: An IMRT plan was made on the contoured planning target volume (PTV1) and organs at risk (OAR) of 20 patients (IMRT-only). A dose of 70 Gy was prescribed on the PTV1 with a concomitant boost to a total of 76 Gy on a subvolume (PTV2). Also a 46 Gy IMRT plan was made combined with either a pulsed dose-rate (PDR) or a high dose-rate (HDR) brachytherapy boost. The EQD(2) on the PTV1 of the combined IMRT-PDR and IMRT-HDR plans were made equivalent to the EQD(2) of the 70 Gy IMRT-only plan. The alpha/beta-ratio for prostate was set to 1.5 Gy and 10 Gy. For normal tissues an alpha/beta-ratio of 3.0 Gy was taken. Several EQD(2)-volume histogram parameters were calculated for comparison and analyzed by two-way ANOVA.
RESULTS: The mean EQD(2) to 95% of the prostate volume was slightly higher for the IMRT-only plan than for the brachytherapy modalities (P<0.001), in contrast to the mean EQD(2) to 50% of the prostate volume in which the opposite was the case (P<0.001). Rectum and bladder doses for IMRT-only are significantly higher (P<0.001). The urethra dose for IMRT-HDR was much higher than the other modalities only when the alpha/beta-ratio for prostate was 10 Gy.
CONCLUSION: Because of the high doses within an implant, the dose in 50% of the prostate volume is much higher with the brachytherapy modalities than IMRT-only which may have clinical consequences. With brachytherapy the doses to the OAR are lower or similar to IMRT-only. Dose escalation for prostate tumors is more easily achieved with brachytherapy than with IMRT alone. Therefore, brachytherapy might be the preferred modality to achieve further dose escalation.

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Mesh:

Year:  2008        PMID: 18378028     DOI: 10.1016/j.radonc.2008.02.023

Source DB:  PubMed          Journal:  Radiother Oncol        ISSN: 0167-8140            Impact factor:   6.280


  10 in total

1.  Dosimetric evaluation of high-dose-rate interstitial brachytherapy boost treatments for localized prostate cancer.

Authors:  Georgina Fröhlich; Péter Agoston; József Lövey; András Somogyi; János Fodor; Csaba Polgár; Tibor Major
Journal:  Strahlenther Onkol       Date:  2010-06-24       Impact factor: 3.621

2.  [Long-term outcomes of two different treatment concepts with HDR brachytherapy boost for intermediate-risk prostate cancer].

Authors:  Nina Seibold; György Kovács
Journal:  Strahlenther Onkol       Date:  2016-03       Impact factor: 3.621

3.  A comparison of HDR brachytherapy and IMRT techniques for dose escalation in prostate cancer: a radiobiological modeling study.

Authors:  M Fatyga; J F Williamson; N Dogan; D Todor; J V Siebers; R George; I Barani; M Hagan
Journal:  Med Phys       Date:  2009-09       Impact factor: 4.071

4.  Comparison of tumor control and toxicity outcomes of high-dose intensity-modulated radiotherapy and brachytherapy for patients with favorable risk prostate cancer.

Authors:  Michael J Zelefsky; Yoshiya Yamada; Xin Pei; Margie Hunt; Gilad Cohen; Zhigang Zhang; Marco Zaider
Journal:  Urology       Date:  2010-12-31       Impact factor: 2.649

5.  Biological dose summation of intensity-modulated arc therapy and image-guided high-dose-rate interstitial brachytherapy in intermediate- and high-risk prostate cancer.

Authors:  Georgina Fröhlich; Péter Ágoston; Kliton Jorgo; Csaba Polgár; Tibor Major
Journal:  J Contemp Brachytherapy       Date:  2020-06-30

6.  Choline PET based dose-painting in prostate cancer--modelling of dose effects.

Authors:  Maximilian Niyazi; Peter Bartenstein; Claus Belka; Ute Ganswindt
Journal:  Radiat Oncol       Date:  2010-03-18       Impact factor: 3.481

7.  A comparison of outcomes for patients with intermediate and high risk prostate cancer treated with low dose rate and high dose rate brachytherapy in combination with external beam radiotherapy.

Authors:  Finbar Slevin; Sree Lakshmi Rodda; Peter Bownes; Louise Murray; David Bottomley; Clare Wilkinson; Ese Adiotomre; Bashar Al-Qaisieh; Emma Dugdale; Oliver Hulson; Joshua Mason; Jonathan Smith; Ann M Henry
Journal:  Clin Transl Radiat Oncol       Date:  2019-10-14

Review 8.  X-change symposium: status and future of modern radiation oncology-from technology to biology.

Authors:  Stefanie Corradini; Maximilian Niyazi; Dirk Verellen; Vincenzo Valentini; Seán Walsh; Anca-L Grosu; Kirsten Lauber; Amato Giaccia; Kristian Unger; Jürgen Debus; Bradley R Pieters; Matthias Guckenberger; Suresh Senan; Wilfried Budach; Roland Rad; Julia Mayerle; Claus Belka
Journal:  Radiat Oncol       Date:  2021-02-04       Impact factor: 4.309

9.  Use of deformable image registration techniques to estimate dose to organs at risk following prostate external beam radiation therapy and high-dose-rate brachytherapy.

Authors:  Marie Vozzo; Joel Poder; Johnson Yuen; Joseph Bucci; Annette Haworth
Journal:  J Contemp Brachytherapy       Date:  2021-02-18

Review 10.  High-dose-rate brachytherapy for prostate cancer: Rationale, current applications, and clinical outcome.

Authors:  Iosif Strouthos; Efstratios Karagiannis; Nikolaos Zamboglou; Konstantinos Ferentinos
Journal:  Cancer Rep (Hoboken)       Date:  2021-06-23
  10 in total

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