Influence of Fraction Size on the Development of Late Radiation Enteropathy: An experimental study in the rat

The use of large fraction sizes in radiotherapy may be associated with an increased risk of complications from late responding normal tissues. However, in the intestine, chronic injury may develop either as primary late effect or secondary to disruption of mucosal integrity as so-called consequentia...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Acta oncologica 1996, Vol.35 (1), p.89-94
Hauptverfasser: Langberg, Carl W., Hauer-Jensen, Martin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 94
container_issue 1
container_start_page 89
container_title Acta oncologica
container_volume 35
creator Langberg, Carl W.
Hauer-Jensen, Martin
description The use of large fraction sizes in radiotherapy may be associated with an increased risk of complications from late responding normal tissues. However, in the intestine, chronic injury may develop either as primary late effect or secondary to disruption of mucosal integrity as so-called consequential injury. Mucosal damage is relatively less sensitive to changes in fraction size than late reacting, slowly proliferating cells. The relationship between fraction size and chronic radiation enteropathy in a given situation may thus depend on which of the two mechanisms that predominates. Most previous studies of the influence of fraction size on radiation injury are confounded by differences in treatment time. The present study was therefore designed to assess subacute and chronic radiation enteropathy after three different fractionation regimens where fraction size was the only experimental variable. A total of 96 male Sprague-Dawley rats were orchiectomized and a functionally intact loop of small intestine was transposed into the left scrotum. These 'scrota 1 hernias' containing intestine were subsequently exposed to 50.4 Gy localized fractionated irradiation over 18 days with either 2.8 Gy every 24 h, 4.2 Gy every 36 h, or 5.6 Gy every 48 h. Control animals were sham irradiated. The animals were observed for development of intestinal complications (intestinal obstruction or enterocutaneous fistula formation) up to 6 months after irradiation. Histologic damage was assessed in groups of animals at 2 weeks (subacute injury) and 26 weeks (chronic injury), using a previously validated radiation injury score (RIS). RIS increased significantly with increasing fraction size at both observation times. However, the increase was more pronounced at 26 weeks than at 2 weeks. Increased chronic injury was characterized by increased incidence and severity of mucosal ulceration, serosal thickening, vascular sclerosis and intestinal wall flbrosis. We conclude that increasing fraction size increases both subacute and, even more markedly, chronic injury in the intestine. With the fractionation regimens used here, the chronic radiation enteropathy develops as a combined consequential and primary late effect, but the primary mechanism predominates.
doi_str_mv 10.3109/02841869609098485
format Article
fullrecord <record><control><sourceid>informahealthcare_cross</sourceid><recordid>TN_cdi_crossref_primary_10_3109_02841869609098485</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_3109_02841869609098485</sourcerecordid><originalsourceid>FETCH-LOGICAL-c486t-2961b1b0cb61465b2aa13b0837ff133c91912f226737de355ba39ceb25cc69e33</originalsourceid><addsrcrecordid>eNp9kE9Lw0AQxRdRaq1-AA_CHrxGd7PJJqsnqa0WCoJ_oLcw2czSlHQTNluxfnoTW3oRPA3M-71h3iPkkrMbwZm6ZWEa8VQqyRRTaZTGR2TIZcyDMJSLYzLs9aADFqfkrG1XjLFQJPGADFLJlYrkkKxn1lQbtBppbejUgfZlbelb-d0tLPVLpI_4iVXdrNH6npmDR_oKRQm_5MR6dHUDfrm9ow-W4leDruxhqGjrN8WWlrs7Dvw5OTFQtXixnyPyMZ28j5-D-cvTbPwwD3SUSh-ESvKc50znkkcyzkMALnKWisQYLoRWXPHQdBkTkRQo4jgHoTTmYay1VCjEiPDdXe3qtnVosqb7Cdw24yzrm8v-NNd5rnaeZpOvsTg49lV1-vVeh1ZDZRxYXbYHTDDOWJJ22P0OK62p3RqWCJVfanCYreqNs13sf574AaG0iI8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Influence of Fraction Size on the Development of Late Radiation Enteropathy: An experimental study in the rat</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Taylor &amp; Francis</source><creator>Langberg, Carl W. ; Hauer-Jensen, Martin</creator><creatorcontrib>Langberg, Carl W. ; Hauer-Jensen, Martin</creatorcontrib><description>The use of large fraction sizes in radiotherapy may be associated with an increased risk of complications from late responding normal tissues. However, in the intestine, chronic injury may develop either as primary late effect or secondary to disruption of mucosal integrity as so-called consequential injury. Mucosal damage is relatively less sensitive to changes in fraction size than late reacting, slowly proliferating cells. The relationship between fraction size and chronic radiation enteropathy in a given situation may thus depend on which of the two mechanisms that predominates. Most previous studies of the influence of fraction size on radiation injury are confounded by differences in treatment time. The present study was therefore designed to assess subacute and chronic radiation enteropathy after three different fractionation regimens where fraction size was the only experimental variable. A total of 96 male Sprague-Dawley rats were orchiectomized and a functionally intact loop of small intestine was transposed into the left scrotum. These 'scrota 1 hernias' containing intestine were subsequently exposed to 50.4 Gy localized fractionated irradiation over 18 days with either 2.8 Gy every 24 h, 4.2 Gy every 36 h, or 5.6 Gy every 48 h. Control animals were sham irradiated. The animals were observed for development of intestinal complications (intestinal obstruction or enterocutaneous fistula formation) up to 6 months after irradiation. Histologic damage was assessed in groups of animals at 2 weeks (subacute injury) and 26 weeks (chronic injury), using a previously validated radiation injury score (RIS). RIS increased significantly with increasing fraction size at both observation times. However, the increase was more pronounced at 26 weeks than at 2 weeks. Increased chronic injury was characterized by increased incidence and severity of mucosal ulceration, serosal thickening, vascular sclerosis and intestinal wall flbrosis. We conclude that increasing fraction size increases both subacute and, even more markedly, chronic injury in the intestine. With the fractionation regimens used here, the chronic radiation enteropathy develops as a combined consequential and primary late effect, but the primary mechanism predominates.</description><identifier>ISSN: 0284-186X</identifier><identifier>EISSN: 1651-226X</identifier><identifier>DOI: 10.3109/02841869609098485</identifier><identifier>PMID: 8619946</identifier><identifier>CODEN: ACTOEL</identifier><language>eng</language><publisher>Basingstoke: Informa UK Ltd</publisher><subject>Acute Disease ; Animals ; Biological and medical sciences ; Chronic Disease ; Cutaneous Fistula - etiology ; Dose-Response Relationship, Radiation ; Fibrosis ; Gastroenterology. Liver. Pancreas. Abdomen ; Ileal Diseases - etiology ; Ileal Diseases - pathology ; Ileum - blood supply ; Ileum - pathology ; Ileum - radiation effects ; Intestinal Fistula - etiology ; Intestinal Mucosa - blood supply ; Intestinal Mucosa - pathology ; Intestinal Mucosa - radiation effects ; Intestinal Obstruction - etiology ; Male ; Medical sciences ; Orchiectomy ; Other diseases. Semiology ; Radiation Injuries - etiology ; Radiation Injuries - pathology ; Radiotherapy - adverse effects ; Radiotherapy Dosage ; Rats ; Rats, Sprague-Dawley ; Sclerosis ; Scrotum ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Time Factors ; Ulcer - etiology</subject><ispartof>Acta oncologica, 1996, Vol.35 (1), p.89-94</ispartof><rights>1996 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1996</rights><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-2961b1b0cb61465b2aa13b0837ff133c91912f226737de355ba39ceb25cc69e33</citedby><cites>FETCH-LOGICAL-c486t-2961b1b0cb61465b2aa13b0837ff133c91912f226737de355ba39ceb25cc69e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/02841869609098485$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/02841869609098485$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,776,780,4009,27902,27903,27904,61197,61378</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3010078$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8619946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Langberg, Carl W.</creatorcontrib><creatorcontrib>Hauer-Jensen, Martin</creatorcontrib><title>Influence of Fraction Size on the Development of Late Radiation Enteropathy: An experimental study in the rat</title><title>Acta oncologica</title><addtitle>Acta Oncol</addtitle><description>The use of large fraction sizes in radiotherapy may be associated with an increased risk of complications from late responding normal tissues. However, in the intestine, chronic injury may develop either as primary late effect or secondary to disruption of mucosal integrity as so-called consequential injury. Mucosal damage is relatively less sensitive to changes in fraction size than late reacting, slowly proliferating cells. The relationship between fraction size and chronic radiation enteropathy in a given situation may thus depend on which of the two mechanisms that predominates. Most previous studies of the influence of fraction size on radiation injury are confounded by differences in treatment time. The present study was therefore designed to assess subacute and chronic radiation enteropathy after three different fractionation regimens where fraction size was the only experimental variable. A total of 96 male Sprague-Dawley rats were orchiectomized and a functionally intact loop of small intestine was transposed into the left scrotum. These 'scrota 1 hernias' containing intestine were subsequently exposed to 50.4 Gy localized fractionated irradiation over 18 days with either 2.8 Gy every 24 h, 4.2 Gy every 36 h, or 5.6 Gy every 48 h. Control animals were sham irradiated. The animals were observed for development of intestinal complications (intestinal obstruction or enterocutaneous fistula formation) up to 6 months after irradiation. Histologic damage was assessed in groups of animals at 2 weeks (subacute injury) and 26 weeks (chronic injury), using a previously validated radiation injury score (RIS). RIS increased significantly with increasing fraction size at both observation times. However, the increase was more pronounced at 26 weeks than at 2 weeks. Increased chronic injury was characterized by increased incidence and severity of mucosal ulceration, serosal thickening, vascular sclerosis and intestinal wall flbrosis. We conclude that increasing fraction size increases both subacute and, even more markedly, chronic injury in the intestine. With the fractionation regimens used here, the chronic radiation enteropathy develops as a combined consequential and primary late effect, but the primary mechanism predominates.</description><subject>Acute Disease</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chronic Disease</subject><subject>Cutaneous Fistula - etiology</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Fibrosis</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Ileal Diseases - etiology</subject><subject>Ileal Diseases - pathology</subject><subject>Ileum - blood supply</subject><subject>Ileum - pathology</subject><subject>Ileum - radiation effects</subject><subject>Intestinal Fistula - etiology</subject><subject>Intestinal Mucosa - blood supply</subject><subject>Intestinal Mucosa - pathology</subject><subject>Intestinal Mucosa - radiation effects</subject><subject>Intestinal Obstruction - etiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Orchiectomy</subject><subject>Other diseases. Semiology</subject><subject>Radiation Injuries - etiology</subject><subject>Radiation Injuries - pathology</subject><subject>Radiotherapy - adverse effects</subject><subject>Radiotherapy Dosage</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Sclerosis</subject><subject>Scrotum</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Time Factors</subject><subject>Ulcer - etiology</subject><issn>0284-186X</issn><issn>1651-226X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9Lw0AQxRdRaq1-AA_CHrxGd7PJJqsnqa0WCoJ_oLcw2czSlHQTNluxfnoTW3oRPA3M-71h3iPkkrMbwZm6ZWEa8VQqyRRTaZTGR2TIZcyDMJSLYzLs9aADFqfkrG1XjLFQJPGADFLJlYrkkKxn1lQbtBppbejUgfZlbelb-d0tLPVLpI_4iVXdrNH6npmDR_oKRQm_5MR6dHUDfrm9ow-W4leDruxhqGjrN8WWlrs7Dvw5OTFQtXixnyPyMZ28j5-D-cvTbPwwD3SUSh-ESvKc50znkkcyzkMALnKWisQYLoRWXPHQdBkTkRQo4jgHoTTmYay1VCjEiPDdXe3qtnVosqb7Cdw24yzrm8v-NNd5rnaeZpOvsTg49lV1-vVeh1ZDZRxYXbYHTDDOWJJ22P0OK62p3RqWCJVfanCYreqNs13sf574AaG0iI8</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>Langberg, Carl W.</creator><creator>Hauer-Jensen, Martin</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1996</creationdate><title>Influence of Fraction Size on the Development of Late Radiation Enteropathy: An experimental study in the rat</title><author>Langberg, Carl W. ; Hauer-Jensen, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-2961b1b0cb61465b2aa13b0837ff133c91912f226737de355ba39ceb25cc69e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acute Disease</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chronic Disease</topic><topic>Cutaneous Fistula - etiology</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Fibrosis</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Ileal Diseases - etiology</topic><topic>Ileal Diseases - pathology</topic><topic>Ileum - blood supply</topic><topic>Ileum - pathology</topic><topic>Ileum - radiation effects</topic><topic>Intestinal Fistula - etiology</topic><topic>Intestinal Mucosa - blood supply</topic><topic>Intestinal Mucosa - pathology</topic><topic>Intestinal Mucosa - radiation effects</topic><topic>Intestinal Obstruction - etiology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Orchiectomy</topic><topic>Other diseases. Semiology</topic><topic>Radiation Injuries - etiology</topic><topic>Radiation Injuries - pathology</topic><topic>Radiotherapy - adverse effects</topic><topic>Radiotherapy Dosage</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Sclerosis</topic><topic>Scrotum</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Time Factors</topic><topic>Ulcer - etiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Langberg, Carl W.</creatorcontrib><creatorcontrib>Hauer-Jensen, Martin</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Acta oncologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Langberg, Carl W.</au><au>Hauer-Jensen, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Fraction Size on the Development of Late Radiation Enteropathy: An experimental study in the rat</atitle><jtitle>Acta oncologica</jtitle><addtitle>Acta Oncol</addtitle><date>1996</date><risdate>1996</risdate><volume>35</volume><issue>1</issue><spage>89</spage><epage>94</epage><pages>89-94</pages><issn>0284-186X</issn><eissn>1651-226X</eissn><coden>ACTOEL</coden><abstract>The use of large fraction sizes in radiotherapy may be associated with an increased risk of complications from late responding normal tissues. However, in the intestine, chronic injury may develop either as primary late effect or secondary to disruption of mucosal integrity as so-called consequential injury. Mucosal damage is relatively less sensitive to changes in fraction size than late reacting, slowly proliferating cells. The relationship between fraction size and chronic radiation enteropathy in a given situation may thus depend on which of the two mechanisms that predominates. Most previous studies of the influence of fraction size on radiation injury are confounded by differences in treatment time. The present study was therefore designed to assess subacute and chronic radiation enteropathy after three different fractionation regimens where fraction size was the only experimental variable. A total of 96 male Sprague-Dawley rats were orchiectomized and a functionally intact loop of small intestine was transposed into the left scrotum. These 'scrota 1 hernias' containing intestine were subsequently exposed to 50.4 Gy localized fractionated irradiation over 18 days with either 2.8 Gy every 24 h, 4.2 Gy every 36 h, or 5.6 Gy every 48 h. Control animals were sham irradiated. The animals were observed for development of intestinal complications (intestinal obstruction or enterocutaneous fistula formation) up to 6 months after irradiation. Histologic damage was assessed in groups of animals at 2 weeks (subacute injury) and 26 weeks (chronic injury), using a previously validated radiation injury score (RIS). RIS increased significantly with increasing fraction size at both observation times. However, the increase was more pronounced at 26 weeks than at 2 weeks. Increased chronic injury was characterized by increased incidence and severity of mucosal ulceration, serosal thickening, vascular sclerosis and intestinal wall flbrosis. We conclude that increasing fraction size increases both subacute and, even more markedly, chronic injury in the intestine. With the fractionation regimens used here, the chronic radiation enteropathy develops as a combined consequential and primary late effect, but the primary mechanism predominates.</abstract><cop>Basingstoke</cop><pub>Informa UK Ltd</pub><pmid>8619946</pmid><doi>10.3109/02841869609098485</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0284-186X
ispartof Acta oncologica, 1996, Vol.35 (1), p.89-94
issn 0284-186X
1651-226X
language eng
recordid cdi_crossref_primary_10_3109_02841869609098485
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Taylor & Francis
subjects Acute Disease
Animals
Biological and medical sciences
Chronic Disease
Cutaneous Fistula - etiology
Dose-Response Relationship, Radiation
Fibrosis
Gastroenterology. Liver. Pancreas. Abdomen
Ileal Diseases - etiology
Ileal Diseases - pathology
Ileum - blood supply
Ileum - pathology
Ileum - radiation effects
Intestinal Fistula - etiology
Intestinal Mucosa - blood supply
Intestinal Mucosa - pathology
Intestinal Mucosa - radiation effects
Intestinal Obstruction - etiology
Male
Medical sciences
Orchiectomy
Other diseases. Semiology
Radiation Injuries - etiology
Radiation Injuries - pathology
Radiotherapy - adverse effects
Radiotherapy Dosage
Rats
Rats, Sprague-Dawley
Sclerosis
Scrotum
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Time Factors
Ulcer - etiology
title Influence of Fraction Size on the Development of Late Radiation Enteropathy: An experimental study in the rat
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T05%3A53%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-informahealthcare_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Influence%20of%20Fraction%20Size%20on%20the%20Development%20of%20Late%20Radiation%20Enteropathy:%20An%20experimental%20study%20in%20the%20rat&rft.jtitle=Acta%20oncologica&rft.au=Langberg,%20Carl%20W.&rft.date=1996&rft.volume=35&rft.issue=1&rft.spage=89&rft.epage=94&rft.pages=89-94&rft.issn=0284-186X&rft.eissn=1651-226X&rft.coden=ACTOEL&rft_id=info:doi/10.3109/02841869609098485&rft_dat=%3Cinformahealthcare_cross%3E10_3109_02841869609098485%3C/informahealthcare_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/8619946&rfr_iscdi=true