Late Gastrointestinal Tolerance After Prostate Radiotherapy: Is the Anal Canal the Culprit? A Narrative Critical Review

被引:1
|
作者
Sargos, Paul [1 ]
Faye, Mame Daro [2 ]
Bacci, Manon [1 ]
Supiot, Stephane [3 ]
Latorzeff, Igor [4 ]
Azria, David [5 ]
Niazi, Tamim M. [2 ]
Vuong, Te [2 ]
Vendrely, Veronique [6 ]
de Crevoisier, Renaud [7 ]
机构
[1] Inst Bergonie, Dept Radiat Oncol, Bordeaux, France
[2] Jewish Gen Hosp, Dept Radiat Oncol, Montreal, PQ, Canada
[3] Inst Cancerol Ouest, Dept Radiat Oncol, St Herblain, France
[4] Clin Pasteur, Dept Radiat Oncol, Toulouse, France
[5] Inst Cancerol Montpellier, Dept Radiat Oncol, Montpellier, France
[6] Bordeaux Univ Hosp, Dept Radiat Oncol, Bordeaux, France
[7] Ctr Eugene Marquis, Dept Radiat Oncol, Rennes, France
来源
FRONTIERS IN ONCOLOGY | 2021年 / 11卷
关键词
prostate cancer; radiotherapy; gastrointestinal toxicities; anal canal; rectum; LATE ANORECTAL DYSFUNCTION; RADIATION-THERAPY; CONFORMAL RADIOTHERAPY; FECAL INCONTINENCE; STOOL FREQUENCY; CANCER PATIENTS; TOXICITY; PATHOPHYSIOLOGY; CARCINOMA; SYMPTOMS;
D O I
10.3389/fonc.2021.666962
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Late gastro-intestinal toxicities (LGIT) secondary to pelvic radiotherapy (RT) are well described in the literature. LGIT are mainly related to rectal or ano-rectal irradiation; however, involvement of the anal canal (AC) in the occurrence of LGIT remains poorly described and understood. Materials and Methods The aim of this work was to explore the potential role of the AC in the development of LGIT after prostate irradiation and identify predictive factors that could be optimized in order to limit these toxicities. This narrative literature review was realized using the Pubmed database. We identified original articles published between June 1997 and July 2019, relating to LGIT after RT for localized prostate cancer and for which AC was identified independently. Articles defining the AC as part of an anorectal or rectal volume only were excluded. Results A history of abdominal surgery or cardio-vascular risk, anticoagulant or tobacco use, and the occurrence of acute GIT during RT increases the risk of LGIT. A dose-effect relationship was identified between dose to the AC and development of LGIT. Identification and contouring of the AC and adjacent anatomical structures (muscles or nerves) are justified to apply specific dose constraints. As a limitation, our review mainly considered on 3DCRT which is no longer the standard of care nowadays; we did not identify any reports in the literature using moderately hypofractionated RT for the prostate and AC specific dosimetry. Conclusion These results suggest that the AC may have an important role in the development of LGIT after pelvic RT for prostate cancer. The individualization of the AC during planning should be recommended in prospective studies.
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页数:11
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