What is the normal tissues morbidity following Helical Intensity Modulated Radiation Treatment for cervical cancer?. Issue 3 (June 2015)
- Record Type:
- Journal Article
- Title:
- What is the normal tissues morbidity following Helical Intensity Modulated Radiation Treatment for cervical cancer?. Issue 3 (June 2015)
- Main Title:
- What is the normal tissues morbidity following Helical Intensity Modulated Radiation Treatment for cervical cancer?
- Authors:
- Mouttet-Audouard, Raphaelle
Lacornerie, Thomas
Tresch, Emmanuelle
Kramar, Andrew
Le Tinier, Florence
Reynaert, Nick
Leblanc, Eric
Narducci, Fabrice
Lartigau, Eric
Nickers, Philippe - Abstract:
- <abstract xml:lang="en" abstract-type="author" id="ab005"> <title id="st065">Abstract</title> <sec> <title id="st035">Background and purpose</title> <p id="sp0005">To report on normal tissues morbidity following IMRT for cervix cancer.</p> </sec> <sec> <title id="st040">Material and methods</title> <p id="sp0010">The first 61 patients of a prospective series were included. 50 Gy to the PTV 1(pelvis) and 60 Gy to the PTV 2 (centro-pelvic disease and GTV nodes) were delivered concomitantly in 28 fractions, followed by a brachytherapy boost. For the small bowel, 50 Gy was the maximal dose, while V45 and V40 had to be &lt;50 cc and 200 cc, respectively. For the bladder, rectum and sigmoid structures, 60 Gy was the maximal dose, and V45 and V40 had to be &lt;20% and &lt;50%. Acute and late toxicity data were prospectively collected.</p> </sec> <sec> <title id="st045">Results</title> <p id="sp0015">The median follow-up period was 40 months (range: 23–60). 30% and 90% of acute and moderate late side effects were reported respectively. Considering the AUC data of the organs at risk (OAR) DVH, late morbidity and doses were significantly linked (<italic>p</italic> ⩽ 0.03), predominantly between 10 Gy and 40 Gy, considering the small bowel and sigmoid colon. The high dose regions exhibited no significant impact.</p> </sec> <sec> <title id="st050">Conclusion</title> <p id="sp0020">The moderate dose volumes represent the predominant cause of morbidity after IMRT. Prospective trials are<abstract xml:lang="en" abstract-type="author" id="ab005"> <title id="st065">Abstract</title> <sec> <title id="st035">Background and purpose</title> <p id="sp0005">To report on normal tissues morbidity following IMRT for cervix cancer.</p> </sec> <sec> <title id="st040">Material and methods</title> <p id="sp0010">The first 61 patients of a prospective series were included. 50 Gy to the PTV 1(pelvis) and 60 Gy to the PTV 2 (centro-pelvic disease and GTV nodes) were delivered concomitantly in 28 fractions, followed by a brachytherapy boost. For the small bowel, 50 Gy was the maximal dose, while V45 and V40 had to be &lt;50 cc and 200 cc, respectively. For the bladder, rectum and sigmoid structures, 60 Gy was the maximal dose, and V45 and V40 had to be &lt;20% and &lt;50%. Acute and late toxicity data were prospectively collected.</p> </sec> <sec> <title id="st045">Results</title> <p id="sp0015">The median follow-up period was 40 months (range: 23–60). 30% and 90% of acute and moderate late side effects were reported respectively. Considering the AUC data of the organs at risk (OAR) DVH, late morbidity and doses were significantly linked (<italic>p</italic> ⩽ 0.03), predominantly between 10 Gy and 40 Gy, considering the small bowel and sigmoid colon. The high dose regions exhibited no significant impact.</p> </sec> <sec> <title id="st050">Conclusion</title> <p id="sp0020">The moderate dose volumes represent the predominant cause of morbidity after IMRT. Prospective trials are thus required to investigate new ways of dose distribution within the OAR.</p> </sec> </abstract> … (more)
- Is Part Of:
- Radiotherapy and oncology. Volume 115:Issue 3(2015:Jun.)
- Journal:
- Radiotherapy and oncology
- Issue:
- Volume 115:Issue 3(2015:Jun.)
- Issue Display:
- Volume 115, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 115
- Issue:
- 3
- Issue Sort Value:
- 2015-0115-0003-0000
- Page Start:
- 386
- Page End:
- 391
- Publication Date:
- 2015-06
- Subjects:
- Oncology -- Periodicals
Radiotherapy -- Periodicals
Tumors -- Periodicals
Medical Oncology -- Periodicals
Neoplasms -- radiotherapy -- Periodicals
Radiotherapy -- Periodicals
Radiothérapie -- Périodiques
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Electronic journals
616.9940642 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01678140 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01678140 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01678140 ↗
http://www.estro.org/ ↗
http://www.elsevier.com/journals ↗
http://www.journals.elsevier.com/radiotherapy-and-oncology/ ↗ - DOI:
- 10.1016/j.radonc.2015.02.010 ↗
- Languages:
- English
- ISSNs:
- 0167-8140
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7240.790000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3548.xml