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Random forests to predict rectal toxicity following prostate cancer radiation therapy

  • Juan D. Ospinac, g(Author)
    ,
  • Jian Zhub, c, f, i(Author)
    ,
  • Ciprian Chiraa(Author)
    ,
  • Alberto Bossid(Author)
    ,
  • Jean B. Delobela(Author)
    ,
  • Véronique Beckendorfe(Author)
  • aCentre Georges-François Leclerc
    ,
  • bSoutheast University, Nanjing
    ,
  • cINSERM, U 1099
    ,
  • dDépartement de Radiothérapie, Institut Gustave-Roussy
    ,
  • eCentre Alexis Vautrin
    ,
  • fCentre de Recherche en Information Biomédical Sino-Français
Research Output: Contribution to journal Article Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

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Scopus
Citations
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Citations
55
SciVal
FWCI
5.24
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Author count
12
SciVal
Paper percentile
97
SciVal
Top percentile
5

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Abstract

Purpose To propose a random forest normal tissue complication probability (RF-NTCP) model to predict late rectal toxicity following prostate cancer radiation therapy, and to compare its performance to that of classic NTCP models. Methods and Materials Clinical data and dose-volume histograms (DVH) were collected from 261 patients who received 3-dimensional conformal radiation therapy for prostate cancer with at least 5 years of follow-up. The series was split 1000 times into training and validation cohorts. A RF was trained to predict the risk of 5-year overall rectal toxicity and bleeding. Parameters of the Lyman-Kutcher-Burman (LKB) model were identified and a logistic regression model was fit. The performance of all the models was assessed by computing the area under the receiving operating characteristic curve (AUC). Results The 5-year grade ≥2 overall rectal toxicity and grade ≥1 and grade ≥2 rectal bleeding rates were 16%, 25%, and 10%, respectively. Predictive capabilities were obtained using the RF-NTCP model for all 3 toxicity endpoints, including both the training and validation cohorts. The age and use of anticoagulants were found to be predictors of rectal bleeding. The AUC for RF-NTCP ranged from 0.66 to 0.76, depending on the toxicity endpoint. The AUC values for the LKB-NTCP were statistically significantly inferior, ranging from 0.62 to 0.69. Conclusions The RF-NTCP model may be a useful new tool in predicting late rectal toxicity, including variables other than DVH, and thus appears as a strong competitor to classic NTCP models.

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 1024-1031 (8 pages)

Journal (Volume, Issue Number)

International Journal of Radiation Oncology Biology Physics (Volume 89, Issue 5)

Publication milestones

  • Published
    - 01/08/2014

Publication status

Published
- 01/08/2014

ISSN

0360-3016

External Publication IDs

  • Scopus: 84904123856
  • PubMed: 25035205

Funding Details

This work was funded by the Université Européenne de Bretagne , France, the Institut National de la Santé et la Recherche Médicale , the Departamento Administrativo de Ciencia, Tecnología e Innovación COLCIENCIAS , Colombia, National Natural Science Foundation of China grant 81301298 , and the Institut de Recherche en Santé Publique , France, under the Plan Cancer 2009-2013 Call C13005N5. A part of this work was presented orally at the 31st Annual Meeting of the European Society for Radiotherapy and Oncology, Barcelona, Spain, Month 2012, and in poster form at the 54th Annual Meeting of the American Society for Radiation Oncology, Boston, MA, October 28-31, 2012.
FundersFunding numbers
Inserm
-
UEB
-
Institut de Recherche en Santé Publique
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Departamento Administrativo de Ciencia, Tecnología e Innovación (COLCIENCIAS)
-
NSFC
81301298
NSFC
-