Skip to main content

Advertisement

Log in

Prediction of response after chemoradiation for esophageal cancer using a combination of dosimetry and CT radiomics

  • Chest
  • Published:
European Radiology Aims and scope Submit manuscript

Abstract

Purpose

To investigate the treatment response prediction feasibility and accuracy of an integrated model combining computed tomography (CT) radiomic features and dosimetric parameters for patients with esophageal cancer (EC) who underwent concurrent chemoradiation (CRT) using machine learning.

Methods

The radiomic features and dosimetric parameters of 94 EC patients were extracted and modeled using Support Vector Classification (SVM) and Extreme Gradient Boosting algorithm (XGBoost). The 94-sample dataset was randomly divided into a 70-sample training subset and a 24-sample independent test set while keeping the class proportions intact via stratification. A receiver operating characteristic (ROC) curve was used to assess the performance of models using radiomic features alone and using combined radiomic features and dosimetric parameters.

Results

A total of 42 radiomic features and 18 dosimetric parameters plus the patients’ characteristic parameters were extracted for these 94 cases (58 responders and 36 non-responders). XGBoost plus principal component analysis (PCA) achieved an accuracy and area under the curve of 0.708 and 0.541, respectively, for models with radiomic features combined with dosimetric parameters, and 0.689 and 0.479, respectively, for radiomic features alone. Image features of GlobalMean X.333.1, Coarseness, Skewness, and GlobalStd contributed most to the model. The dosimetric parameters of gross tumor volume (GTV) homogeneity index (HI), Cord Dmax, Prescription dose, Heart-Dmean, and Heart-V50 also had a strong contribution to the model.

Conclusions

The model with radiomic features combined with dosimetric parameters is promising and outperforms that with radiomic features alone in predicting the treatment response of patients with EC who underwent CRT.

Key Points

• The model with radiomic features combined with dosimetric parameters is promising in predicting the treatment response of patients with EC who underwent CRT.

• The model with radiomic features combined with dosimetric parameters (prediction accuracy of 0.708 and AUC of 0.689) outperforms that with radiomic features alone (best prediction accuracy of 0.625 and AUC of 0.412).

• The image features of GlobalMean X.333.1, Coarseness, Skewness, and GlobalStd contributed most to the treatment response prediction model. The dosimetric parameters of GTV HI, Cord Dmax, Prescription dose, Heart-Dmean, and Heart-V50 also had a strong contribution to the model.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Abbreviations

3DCRT:

Three-dimensional conformal radiotherapy

AUC:

Area under curve

CRT:

Chemoradiation

CT:

Computed tomography

EC:

Esophageal cancer

FDG-PET:

Fluorodeoxyglucose positron emission tomography

GLCM:

Gray-level co-occurrence matrix

GTV:

Gross tumor volume

HI:

Homogeneity index

ID:

Intensity direct

IMRT:

Intensity-modulated radiotherapy

NID:

Neighbor intensity difference

NR:

Non-responsive

OARs:

Organs at risk

OS:

Overall survival; CR: complete response

PCA:

Principal component analysis

RBF:

Radial basis function

ROC:

Receiver operating characteristic

RS:

Responsive

SCC:

Squamous cell carcinoma

SVM:

Support vector classification

TPS:

Treatment planning system

VMAT:

Volumetric-modulated arc therapy

XGBoost:

Extreme Gradient Boosting algorithm

References

  1. Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J, Jemal A (2015) Global cancer statistics, 2012. CA Cancer J Clin 65:87–108

    Article  Google Scholar 

  2. Wheeler JB, Reed CE (2012) Epidemiology of esophageal cancer. Surg Clin North Am 92:1077–1087

    Article  Google Scholar 

  3. Kumagai K, Rouvelas I, Tsai JA et al (2014) Meta-analysis of postoperative morbidity and perioperative mortality in patients receiving neoadjuvant chemotherapy or chemoradiotherapy for resectable oesophageal and gastro-oesophageal junctional cancers. Br J Surg 101:321–338

    Article  CAS  Google Scholar 

  4. Li M, Zhang X, Zhao F, Luo Y, Kong L, Yu J (2016) Involved-field radiotherapy for esophageal squamous cell carcinoma: theory and practice. Radiat Oncol 11:18

    Article  CAS  Google Scholar 

  5. Minsky BD, Neuberg D, Kelsen DP et al (1999) Final report of intergroup trial 0122 (ECOG PE-289, RTOG 90-12): phase II trial of neoadjuvant chemotherapy plus concurrent chemotherapy and high-dose radiation for squamous cell carcinoma of the esophagus. Int J Radiat Oncol Biol Phys 43:517–523

    Article  CAS  Google Scholar 

  6. Minsky BD, Pajak TF, Ginsberg RJ et al (2002) INT 0123 (radiation therapy oncology group 94-05) phase III trial of combined-modality therapy for esophageal cancer: high-dose versus standard-dose radiation therapy. J Clin Oncol 20:1167–1174

    Article  CAS  Google Scholar 

  7. Ajani JA (2008) Gastroesophageal cancers: progress and problems. J Natl Compr Canc Netw 6:813–814

    Article  Google Scholar 

  8. Luo Y, Mao Q, Wang X, Yu J, Li M (2017) Radiotherapy for esophageal carcinoma: dose, response and survival. Cancer Manag Res 10:13–21

    Article  Google Scholar 

  9. Li JC, Liu D, Chen MQ et al (2012) Different radiation treatment in esophageal carcinoma: a clinical comparative study. J BUON 17:512–516

    PubMed  Google Scholar 

  10. Chen YJ, Liu A, Han C et al (2007) Helical tomotherapy for radiotherapy in esophageal cancer: a preferred plan with better conformal target coverage and more homogeneous dose distribution. Med Dosim 32:166–171

    Article  Google Scholar 

  11. Tong DK, Law S, Kwong DL, Chan KW, Lam AK, Wong KH (2010) Histological regression of squamous esophageal carcinoma assessed by percentage of residual viable cells after neoadjuvant chemoradiation is an important prognostic factor. Ann Surg Oncol 17:2184–2192

    Article  Google Scholar 

  12. Chao YK, Chan SC, Liu YH et al (2009) Pretreatment T3–4 stage is an adverse prognostic factor in patients with esophageal squamous cell carcinoma who achieve pathological complete response following preoperative chemoradiotherapy. Ann Surg 249:392–396

    Article  Google Scholar 

  13. Hammoud ZT, Kesler KA, Ferguson MK et al (2006) Survival outcomes of resected patients who demonstrate a pathologic complete response after neoadjuvant chemoradiation therapy for locally advanced esophageal cancer. Dis Esophagus 19:69–72

    Article  CAS  Google Scholar 

  14. Muijs CT, Beukema JC, Pruim J et al (2010) A systematic review on the role of FDG-PET/CT in tumour delineation and radiotherapy planning in patients with esophageal cancer. Radiother Oncol 97:165–171

    Article  Google Scholar 

  15. Foley KG, Hills RK, Berthon B et al (2018) Development and validation of a prognostic model incorporating texture analysis derived from standardised segmentation of PET in patients with oesophageal cancer. Eur Radiol 28(1):428–436

    Article  Google Scholar 

  16. Miles KA, Lee TY, Goh V et al (2012) Experimental Cancer Medicine Centre Imaging Network Group. Current status and guidelines for the assessment of tumour vascular support with dynamic contrast-enhanced computed tomography. Eur Radiol 22:1430–1441

    Article  CAS  Google Scholar 

  17. Djuric-Stefanovic A, Micev M, Stojanovic-Rundic S, Pesko P, Dj S (2015) Absolute CT perfusion parameter values after the neoadjuvant chemoradiotherapy of the squamous cell esophageal carcinoma correlate with the histopathologic tumor regression grade. Eur J Radiol 84:2477–2484

    Article  CAS  Google Scholar 

  18. Desborders P, Ruan S, Modzelewski R et al (2017) Predictive value of initial FDG-PET features for treatment response and survival in esophageal cancer patients treated with chemo-radiation therapy using a random forest classifier. PLoS One 12:e0173208

    Article  Google Scholar 

  19. Tixier F, Rest CC, Hatt M et al (2011) Intratumor heterogeneity characterized by textural features on baseline 18F-FDG PET images predicts response to concomitant radiochemotherapy in esophageal cancer. J Nucl Med 52:369–378

    Article  Google Scholar 

  20. Ganeshan B, Skogen K, Pressney I, Coutroubis D, Miles K (2012) Tumour heterogeneity in esophageal cancer assessed by CT texture analysis: preliminary evidence of an association with tumour metabolism, stage, and survival. Clin Radiol 67:157–164

    Article  CAS  Google Scholar 

  21. Hou Z, Ren W, Li S et al (2017) Radiomic analysis in contrast-enhanced CT: predict treatment response to chemoradiotherapy in esophageal carcinoma. Oncotarget 8:104444–104454

    PubMed  PubMed Central  Google Scholar 

  22. Jin X, Yi J, Zhou Y, Yan H, Han C, Xie C (2013) CRT combined with a sequential VMAT boost in the treatment of upper thoracic esophageal cancer. J Appl Clin Med Phys 14:153–161

    Article  Google Scholar 

  23. Wu Z, Xie C, Hu M et al (2014) Dosimetric benefits of IMRT and VMAT in the treatment of middle thoracic esophageal cancer: is the conformal radiotherapy still an alternative option? J Appl Clin Med Phys 15:93–101

    Article  Google Scholar 

  24. Zhang L, Fried DV, Fave XJ, Hunter LA, Yang J, Court LE (2015) IBEX: an open infrastructure software platform to facilitate collaborative work in radiomics. Med Phys 42:1341–1353

    Article  Google Scholar 

  25. Blaas J, Botha CP, Post FH (2008) Extensions of parallel coordinates for interactive exploration of large multi-timepoint data sets. IEEE Trans Vis Comput Graph 14:1436–1443

    Article  Google Scholar 

  26. Burges CJC (1998) A tutorial on support vector machines for pattern recognition. Data Min Knowl Discov 2:121–167

    Article  Google Scholar 

  27. Chen T, Guestrin C (2016) XGBoost: a scalable tree boosting system. AcmSigkdd international conference on Knowledge Discovery & Data Mining, pp 785–94

  28. Minka TP (2001) Automatic choice of dimensionality for PCA. In: Advances in neural information processing systems, pp 598–604

    Google Scholar 

  29. Ganeshan B, Skogen K, Pressney I, Coutroubis D, Miles K (2012) Tumour heterogeneity in oesophageal cancer assessed by CT texture analysis: preliminary evidence of an association with tumour metabolism, stage, and survival. Clin Radiol 67:157–164

    Article  CAS  Google Scholar 

  30. Yip C, Davnall F, Kozarski R, Landau DB et al (2015) Assessment of changes in tumor heterogeneity following neoadjuvant chemotherapy in primary esophageal cancer. Dis Esophagus 28:172–179

    Article  CAS  Google Scholar 

  31. Lloyd S, Chang BW (2014) Current strategies in chemoradiation for esophageal cancer. J Gastrointest Oncol 5:156–165

    PubMed  PubMed Central  Google Scholar 

  32. O'Sullivan KE, Hurley ET, Hurley JP (2015) Understanding complete pathologic response in oesophageal cancer: implications for management and survival. Gastroenterol Res Pract 2015(2015):518281

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Funding

This study has received funding by National Natural Science Foundation of China (11675122).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Cong Liu or Congying Xie.

Ethics declarations

Guarantor

The scientific guarantor of this publication is Congying Xie.

Conflict of interest

The authors of this manuscript declare no relationships with any companies whose products or services may be related to the subject matter of the article.

Statistics and biometry

One of the authors has significant statistical expertise: Cong Liu.

Informed consent

Written informed consent was waived by the Institutional Review Board.

Ethical approval

Institutional Review Board approval was obtained.

Methodology

• retrospective

• observational

• performed at one institution

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Jin, X., Zheng, X., Chen, D. et al. Prediction of response after chemoradiation for esophageal cancer using a combination of dosimetry and CT radiomics. Eur Radiol 29, 6080–6088 (2019). https://doi.org/10.1007/s00330-019-06193-w

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00330-019-06193-w

Keywords

Navigation