Abstract

Despite the dramatic advancements in pelvic radiotherapy, urinary toxicity remains a significant side-effect. The assessment of clinico-dosimetric predictors of radiation cystitis (RC) based on clinical data has improved substantially over the last decade; however, a thorough understanding of the physiopathogenetic mechanisms underlying the onset of RC, with its variegated acute and late urinary symptoms, is still largely lacking, and data from pre-clinical research is still limited. The aim of this review is to provide an overview of the main open issues and, ideally, to help investigators in orienting future research. First, anatomy and physiology of bladder, as well as the current knowledge of dose and dose-volume effects in humans, are briefly summarized. Subsequently, pre-clinical radiobiology aspects of RC are discussed. The findings suggest that pre-clinical research on RC in animal models is a lively field of research with growing interest in the development of new radioprotective agents. The availability of new high precision micro-irradiators and the rapid advances in small animal imaging might lead to big improvement into this field. In particular, studies focusing on the definition of dose and fractionation are warranted, especially considering the growing interest in hypo-fractionation and ablative therapies for prostate cancer treatment. Moreover, improvement in radiotherapy plans optimization by selectively reducing radiation dose to more radiosensitive substructures close to the bladder would be of paramount importance. Finally, thanks to new pre-clinical imaging platforms, reliable and reproducible methods to assess the severity of RC in animal models are expected to be developed.

Highlights

  • Despite dramatic advance in pelvic radiotherapy, mainly due to the implementation of image-guided intensity-modulated (IMRT) techniques, acute and late urinary toxicity remains a significant sideeffect, especially in the case of high-dose schedules such as those used for prostate and gynecological cancer treatment [1, 2]

  • Rate at 23.4 Gy to ureter = 14/16 Rate at 25 Gy to trigone = 9/11 Many rats died with 37.4 Gy to ureter; No death associated with 40 Gy to trigone Evidence of biphasic change in the bladder reservoir function: acute and late damage

  • All the authors seemed to agree that acute damage is confined to only a few days after irradiation, irrespective of the dose delivered, while late toxicity could emerge at different time lapses and with intensity depending on radiation dose and fractionation; in addition, cystometry has to be considered as a feasible, easy to interpret and reliable way to assess radiation cystitis (RC) functional impairment

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Summary

Introduction

Despite dramatic advance in pelvic radiotherapy, mainly due to the implementation of image-guided intensity-modulated (IMRT) techniques, acute and late urinary toxicity (radiation cystitis [RC] or actinic cystitis) remains a significant sideeffect, especially in the case of high-dose schedules such as those used for prostate and gynecological cancer treatment [1, 2]. A thorough understanding of the pathophysiology at the base of acute and late radiationinduced urinary symptoms, such as urgency, nocturia, urethral stenosis, incontinence, hematuria, etc., is still largely lacking, as well as robust pre-clinical data based on animal models. Animal models of radiation-induced bladder toxicity might improve the current understanding of physio-pathogenetic mechanisms at the base of radiation induced cystitis and expedite the detection and testing of possible radioprotective agents aimed at reducing such damage. The aim of the current paper is to review this suboptimally explored field of research, with the aim of providing both basic researchers and radiation oncologists an overview of the main open issues and, ideally, to assist them in orienting future research.

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