Using patient data similarities to predict radiation pneumonitis via a self-organizing map

被引:18
作者
Chen, Shifeng [1 ]
Zhou, Sumin [1 ]
Yin, Fang-Fang [1 ]
Marks, Lawrence B. [1 ]
Das, Shiva K. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC 27710 USA
关键词
D O I
10.1088/0031-9155/53/1/014
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
This work investigates the use of the self-organizing map (SOM) technique for predicting lung radiation pneumonitis (RP) risk. SOM is an effective method for projecting and visualizing high-dimensional data in a low-dimensional space (map). By projecting patients with similar data (dose and non-dose factors) onto the same region of the map, commonalities in their outcomes can be visualized and categorized. Once built, the SOM may be used to predict pneumonitis risk by identifying the region of the map that is most similar to a patient's characteristics. Two SOM models were developed from a database of 219 lung cancer patients treated with radiation therapy (34 clinically diagnosed with Grade 2+ pneumonitis). The models were: SOMall built from all dose and non-dose factors and, for comparison, SOMdose built from dose factors alone. Both models were tested using ten-fold cross validation and Receiver Operating Characteristics (ROC) analysis. Models SOMall and SOMdose yielded ten-fold cross-validated ROC areas of 0.73 (sensitivity/specificity = 71%/68%) and 0.67 (sensitivity/specificity = 63%/66%), respectively. The significant difference between the cross-validated ROC areas of these two models (p < 0.05) implies that non-dose features add important information toward predicting RP risk. Among the input features selected by model SOMall, the two with highest impact for increasing RP risk were: (a) higher mean lung dose and (b) chemotherapy prior to radiation therapy. The SOM model developed here may not be extrapolated to treatment techniques outside that used in our database, such as several-field lung intensity modulated radiation therapy or gated radiation therapy.
引用
收藏
页码:203 / 216
页数:14
相关论文
共 44 条
[1]
[Anonymous], RAD RES S
[2]
The impact of heterogeneity correction on dosimetric parameters that predict for radiation pneumonitis [J].
Chang, Daniel T. ;
Olivier, Kenneth R. ;
Morris, Christopher G. ;
Liu, Chihray ;
Dempsey, James F. ;
Benda, Rashmi K. ;
Palta, Jatinder R. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 65 (01) :125-131
[3]
Breast cancer diagnosis using self-organizing map for sonography [J].
Chen, DR ;
Chang, RF ;
Huang, YL .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2000, 26 (03) :405-411
[4]
Predicting lung radiotherapy-induced pneumonitis using a model combining parametric lyman probit with nonparametric decision trees [J].
Das, Shiva K. ;
Zhou, Sumin ;
Zhang, Junan ;
Yin, Fang-Fang ;
Dewhirst, Mark W. ;
Marks, Lawrence B. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 68 (04) :1212-1221
[5]
Predicting radiotherapy-induced cardiac perfusion defects [J].
Das, SK ;
Baydush, AH ;
Zhou, SM ;
Miften, M ;
Yu, XL ;
Craciunescu, O ;
Oldham, M ;
Light, K ;
Wong, T ;
Blazing, M ;
Borges-Neto, S ;
Dewhirst, MW ;
Marks, LB .
MEDICAL PHYSICS, 2005, 32 (01) :19-27
[6]
RADIATION-INDUCED LUNG DAMAGE AFTER THORACIC IRRADIATION FOR HODGKINS-DISEASE - THE ROLE OF FRACTIONATION [J].
DUBRAY, B ;
HENRYAMAR, M ;
MEERWALDT, JH ;
NOORDIJK, EM ;
DIXON, DO ;
COSSET, JM ;
THAMES, HD .
RADIOTHERAPY AND ONCOLOGY, 1995, 36 (03) :211-217
[7]
Clinical dose-volume histogram analysis for pneumonitis after 3D treatment for non-small cell lung cancer (NSCLC) [J].
Graham, MV ;
Purdy, JA ;
Emami, B ;
Harms, W ;
Bosch, W ;
Lockett, MA ;
Perez, CA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1999, 45 (02) :323-329
[8]
SOUTHWEST-ONCOLOGY-GROUP STANDARD RESPONSE CRITERIA, END-POINT DEFINITIONS AND TOXICITY CRITERIA [J].
GREEN, S ;
WEISS, GR .
INVESTIGATIONAL NEW DRUGS, 1992, 10 (04) :239-253
[9]
Guyon I, 2003, J MACH LEARN RES, P1157, DOI [10.1016/j.aca.2011.07.027, DOI 10.1016/J.ACA.2011.07.027]
[10]
Hastie T., 2002, ELEMENTS STAT LEARNI