Skip to main content

Advertisement

Log in

Deep learning approach of diffusion-weighted imaging as an outcome predictor in laryngeal and hypopharyngeal cancer patients with radiotherapy-related curative treatment: a preliminary study

  • Head and Neck
  • Published:
European Radiology Aims and scope Submit manuscript

Abstract

Objectives

This preliminary study aimed to develop a deep learning (DL) model using diffusion-weighted imaging (DWI) and apparent diffusion coefficient (ADC) maps to predict local recurrence and 2-year progression-free survival (PFS) in laryngeal and hypopharyngeal cancer patients treated with various forms of radiotherapy-related curative therapy.

Methods

Seventy patients with laryngeal and hypopharyngeal cancers treated by radiotherapy, chemoradiotherapy, or induction-(chemo)radiotherapy were enrolled and divided into training (N = 49) and test (N = 21) groups based on presentation timeline. All patients underwent MR before and 4 weeks after the start of radiotherapy. The DL models that extracted imaging features on pre- and intra-treatment DWI and ADC maps were trained to predict the local recurrence within a 2-year follow-up. In the test group, each DL model was analyzed for recurrence prediction. Additionally, the Kaplan-Meier and multivariable Cox regression analyses were performed to evaluate the prognostic significance of the DL models and clinical variables.

Results

The highest area under the receiver operating characteristics curve and accuracy for predicting the local recurrence in the DL model were 0.767 and 81.0%, respectively, using intra-treatment DWI (DWIintra). The log-rank test showed that DWIintra was significantly associated with PFS (p = 0.013). DWIintra was an independent prognostic factor for PFS in multivariate analysis (p = 0.023).

Conclusion

DL models using DWIintra may have prognostic value in patients with laryngeal and hypopharyngeal cancers treated by curative radiotherapy. The model-related findings may contribute to determining the therapeutic strategy in the early stage of the treatment.

Key Points

Deep learning models using intra-treatment diffusion-weighted imaging have prognostic value in patients with laryngeal and hypopharyngeal cancers treated by curative radiotherapy.

The findings from these models may contribute to determining the therapeutic strategy at the early stage of the treatment.

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

Similar content being viewed by others

Abbreviations

ADC:

Apparent diffusion coefficient

ADCintra :

Intra-treatment ADC

ADCpre :

Pretreatment ADC

AUC:

Area under the receiver operating characteristics curve

CNN:

Convolutional neural network

DL:

Deep learning

DWI:

Diffusion-weighted imaging

DWIintra :

Intra-treatment DWI

DWIpre :

Pretreatment DWI

MR:

Magnetic resonance

PFS:

Progression-free survival

ROC:

Receiver operating characteristics.

References

  1. Forastiere AA, Zhang Q, Weber RS et al (2013) Long-term results of RTOG 91-11: a comparison of three nonsurgical treatment strategies to preserve the larynx in patients with locally advanced larynx cancer. J Clin Oncol 31:845–852. https://doi.org/10.1200/JCO.2012.43.6097

  2. Ho AS, Kraus DH, Ganly I, Lee NY, Shah JP, Morris LG (2014) Decision making in the management of recurrent head and neck cancer. Head Neck 36:144–151. https://doi.org/10.1002/hed.23227

  3. Forastiere AA, Ismaila N, Lewin JS et al (2018) Use of larynx-preservation strategies in the treatment of laryngeal cancer: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol 36:1143-1169. https://doi.org/10.1200/JCO.2017.75.7385

  4. Cooper JS, Pajak TF, Forastiere AA et al (2004) Postoperative concurrent radiotherapy and chemotherapy for high-risk squamous-cell carcinoma of the head and neck. N Engl J Med 350:1937–1944. https://doi.org/10.1056/NEJMoa032646

  5. Bernier J, Domenge C, Ozsahin M et al (2004) Postoperative irradiation with or without concomitant chemotherapy for locally advanced head and neck cancer. N Engl J Med 350:1945–1952. https://doi.org/10.1056/NEJMoa032641

  6. Leeman JE, Li JG, Pei X et al (2017) Patterns of treatment failure and postrecurrence outcomes among patients with locally advanced head and neck squamous cell carcinoma after chemoradiotherapy using modern radiation techniques. JAMA Oncol 3:1487–1494. https://doi.org/10.1001/jamaoncol.2017.0973

  7. Forastiere AA, Adelstein DJ, Manola J (2013) Induction chemotherapy meta-analysis in head and neck cancer: right answer, wrong question. J Clin Oncol 31:2844–2846. https://doi.org/10.1200/JCO.2013.50.3136

  8. Cohen EE, Karrison TG, Kocherginsky M et al (2014) Phase III randomized trial of induction chemotherapy in patients with N2 or N3 locally advanced head and neck cancer. J Clin Oncol 32:2735–2743. https://doi.org/10.1200/JCO.2013.54.6309

  9. Vollenbrock SE, Voncken FEM, Bartels LW, Beets-Tan RGH, Bartels-Rutten A (2020) Diffusion-weighted MRI with ADC mapping for response prediction and assessment of oesophageal cancer: a systematic review. Radiother Oncol 142:17–26

    Article  Google Scholar 

  10. van Rossum PS, van Lier AL, van Vulpen M et al (2015) Diffusion-weighted magnetic resonance imaging for the prediction of pathologic response to neoadjuvant chemoradiotherapy in esophageal cancer. Radiother Oncol 115:163–170. https://doi.org/10.1016/j.radonc.2015.04.027

  11. Iannicelli E, Di Pietropaolo M, Pilozzi E et al (2016) Value of diffusion-weighted MRI and apparent diffusion coefficient measurements for predicting the response of locally advanced rectal cancer to neoadjuvant chemoradiotherapy. Abdom Radiol (NY) 41:1906–1917. https://doi.org/10.1007/s00261-016-0805-9

  12. Schreuder SM, Lensing R, Stoker J, Bipat S (2015) Monitoring treatment response in patients undergoing chemoradiotherapy for locally advanced uterine cervical cancer by additional diffusion-weighted imaging: a systematic review. J Magn Reson Imaging 42:572–594. https://doi.org/10.1002/jmri.24784

  13. Hatakenaka M, Nakamura K, Yabuuchi H et al (2011) Pretreatment apparent diffusion coefficient of the primary lesion correlates with local failure in head-and-neck cancer treated with chemoradiotherapy or radiotherapy. Int J Radiat Oncol Biol Phys 81:339–345. https://doi.org/10.1016/j.ijrobp.2010.05.051

  14. Hatakenaka M, Shioyama Y, Nakamura K et al (2011) Apparent diffusion coefficient calculated with relatively high b-values correlates with local failure of head and neck squamous cell carcinoma treated with radiotherapy. AJNR Am J Neuroradiol 32:1904–1910. https://doi.org/10.3174/ajnr.A2610

  15. Matoba M, Tuji H, Shimode Y et al (2014) Fractional change in apparent diffusion coefficient as an imaging biomarker for predicting treatment response in head and neck cancer treated with chemoradiotherapy. AJNR Am J Neuroradiol 35:379–385.https://doi.org/10.3174/ajnr.A3706

  16. King AD, Chow KK, Yu KH et al (2013) Head and neck squamous cell carcinoma: diagnostic performance of diffusion-weighted MR imaging for the prediction of treatment response. Radiology 266:531–538. https://doi.org/10.1148/radiol.12120167

  17. King AD, Mo FK, Yu KH et al (2010) Squamous cell carcinoma of the head and neck: diffusion-weighted MR imaging for prediction and monitoring of treatment response. Eur Radiol 20:2213–2220. https://doi.org/10.1007/s00330-010-1769-8

  18. Kim S, Loevner L, Quon H et al (2009) Diffusion-weighted magnetic resonance imaging for predicting and detecting early response to chemoradiation therapy of squamous cell carcinomas of the head and neck. Clin Cancer Res 15:986–994. https://doi.org/10.1158/1078-0432.CCR-08-1287

  19. Brenet E, Barbe C, Hoeffel C et al (2020) Predictive value of early post-treatment diffusion-weighted MRI for recurrence or tumor progression of head and neck squamous cell carcinoma treated with chemoradiotherapy. Cancers (Basel) 12:1234. https://doi.org/10.3390/cancers12051234

  20. Vandecaveye V, Dirix P, De Keyzer F et al (2012) Diffusion-weighted magnetic resonance imaging early after chemoradiotherapy to monitor treatment response in head-and-neck squamous cell carcinoma. Int J Radiat Oncol Biol Phys 82:1098–1107. https://doi.org/10.1016/j.ijrobp.2011.02.044

  21. Tomita H, Kuno H, Sekiya K et al (2020) Quantitative assessment of thyroid nodules using dual-energy computed tomography: iodine concentration measurement and multiparametric texture analysis for differentiating between malignant and benign lesions. Int J Endocrinol 2020:5484671. https://doi.org/10.1155/2020/5484671

  22. Tomita H, Yamashiro T, Heianna J et al (2021) Nodal-based radiomics analysis for identifying cervical lymph node metastasis at levels I and II in patients with oral squamous cell carcinoma using contrast-enhanced computed tomography. Eur Radiol. https://doi.org/10.1007/s00330-021-07758-4

  23. Kuno H, Qureshi MM, Chapman MN et al (2017) CT texture analysis potentially predicts local failure in head and neck squamous cell carcinoma treated with chemoradiotherapy. AJNR Am J Neuroradiol 38:2334–2340. https://doi.org/10.3174/ajnr.A5407

  24. Zhang H, Graham CM, Elci O et al (2013) Locally advanced squamous cell carcinoma of the head and neck: CT texture and histogram analysis allow independent prediction of overall survival in patients treated with induction chemotherapy. Radiology 269:801–809. https://doi.org/10.1148/radiol.13130110

  25. Koda E, Yamashiro T, Onoe R et al (2020) CT texture analysis of mediastinal lymphadenopathy: combining with US-based elastographic parameter and discrimination between sarcoidosis and lymph node metastasis from small cell lung cancer. PLoS One 15:e0243181. https://doi.org/10.1371/journal.pone.0243181

  26. Tomita H, Yamashiro T, Iida G, Tsubakimoto M, Mimura H, Murayama S (2021) Unenhanced CT texture analysis with machine learning for differentiating between nasopharyngeal cancer and nasopharyngeal malignant lymphoma. Nagoya J Med Sci 83:135–149. https://doi.org/10.18999/nagjms.83.1.135

  27. Tomori Y, Yamashiro T, Tomita H et al (2020) CT radiomics analysis of lung cancers: differentiation of squamous cell carcinoma from adenocarcinoma, a correlative study with FDG uptake. Eur J Radiol 128:109032

    Article  Google Scholar 

  28. Ariji Y, Sugita Y, Nagao T et al (2019) CT evaluation of extranodal extension of cervical lymph node metastases in patients with oral squamous cell carcinoma using deep learning classification. Oral Radiol. https://doi.org/10.1007/s11282-019-00391-4

  29. Yanagawa M, Niioka H, Hata A et al (2019) Application of deep learning (3-dimensional convolutional neural network) for the prediction of pathological invasiveness in lung adenocarcinoma: a preliminary study. Medicine (Baltimore) 98:e16119. https://doi.org/10.1097/MD.0000000000016119

  30. Zhao X, Xie P, Wang M et al (2020) Deep learning-based fully automated detection and segmentation of lymph nodes on multiparametric-mri for rectal cancer: a multicentre study. EBioMedicine 56:102780

    Article  Google Scholar 

  31. Tomita H, Yamashiro T, Heianna J et al (2021) Deep learning for the preoperative diagnosis of metastatic cervical lymph nodes on contrast-enhanced computed tomography in patients with oral squamous cell carcinoma. Cancers (Basel) 13:600. https://doi.org/10.3390/cancers13040600

  32. Xu Y, Hosny A, Zeleznik R et al (2019) Deep learning predicts lung cancer treatment response from serial medical imaging. Clin Cancer Res 25:3266–3275. https://doi.org/10.1158/1078-0432.CCR-18-2495

  33. Qu YH, Zhu HT, Cao K, Li XT, Ye M, Sun YS (2020) Prediction of pathological complete response to neoadjuvant chemotherapy in breast cancer using a deep learning (DL) method. Thorac Cancer 11:651–658. https://doi.org/10.1111/1759-7714.13309

  34. Starke S, Leger S, Zwanenburg A et al (2020) 2D and 3D convolutional neural networks for outcome modelling of locally advanced head and neck squamous cell carcinoma. Sci Rep 10:15625-020-70542-9. https://doi.org/10.1038/s41598-020-70542-9

  35. Ha R, Chang P, Karcich J et al (2018) Predicting post neoadjuvant axillary response using a novel convolutional neural network algorithm. Ann Surg Oncol 25:3037–3043. https://doi.org/10.1245/s10434-018-6613-4

  36. Chollet F (2017) Xception: deep learning with depthwise separable convolutions. Proc IEEE CVPR:1251–1258

  37. Szegedy C, Liu W, Jia Y et al (2015) Going deeper with convolutions. Proc IEEE CVPR:1–9

  38. Bulens P, Couwenberg A, Intven M et al (2020) Predicting the tumor response to chemoradiotherapy for rectal cancer: model development and external validation using MRI radiomics. Radiother Oncol 142:246–252

    Article  CAS  Google Scholar 

  39. Shi L, Zhang Y, Nie K et al (2019) Machine learning for prediction of chemoradiation therapy response in rectal cancer using pre-treatment and mid-radiation multi-parametric MRI. Magn Reson Imaging 61:33–40

    Article  Google Scholar 

  40. Driessen JP, Caldas-Magalhaes J, Janssen LM et al (2014) Diffusion-weighted MR imaging in laryngeal and hypopharyngeal carcinoma: association between apparent diffusion coefficient and histologic findings. Radiology 272:456–463. https://doi.org/10.1148/radiol.14131173

  41. Lombardi M, Cascone T, Guenzi E et al (2017) Predictive value of pre-treatment apparent diffusion coefficient (ADC) in radio-chemiotherapy treated head and neck squamous cell carcinoma. Radiol Med 122:345–352. https://doi.org/10.1007/s11547-017-0733-y

  42. Bhatt N, Gupta N, Soni N, Hooda K, Sapire JM, Kumar Y (2017) Role of diffusion-weighted imaging in head and neck lesions: pictorial review. Neuroradiol J 30:356–369. https://doi.org/10.1177/1971400917708582

  43. Yeung DK, Fong KY, Chan QC, King AD (2010) Chemical shift imaging in the head and neck at 3T: initial results. J Magn Reson Imaging 32:1248–1254. https://doi.org/10.1002/jmri.22365

Download references

Acknowledgements

This retrospective study was supported by a grant from the Japanese Ministry of Education, Culture, Sports, Science and Technology (Grant-in-Aid for Young Scientists KAKEN; No. KAKEN No. 21K15814).

Funding

This retrospective study was supported by a grant from the Japanese Ministry of Education, Culture, Sports, Science and Technology (Grant-in-Aid for Young Scientists KAKEN; No. KAKEN No. 21K15814).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hayato Tomita.

Ethics declarations

Guarantor

The scientific guarantor of this publication is Dr. Tomita.

Conflict of interest

The authors declare no competing interests.

Statistics and biometry

No complex statistical methods were necessary for this paper.

Informed consent

Written informed consent was waived by the Institutional Review Board of St. Marianna University School of Medicine.

Ethical approval

Institutional Review Board approval was obtained at St. Marianna University School of Medicine.

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.

Supplementary information

ESM 1

(DOCX 16 kb)

ESM 2

(PNG 2189 kb)

High Resolution Image

(TIFF 3418 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tomita, H., Kobayashi, T., Takaya, E. et al. Deep learning approach of diffusion-weighted imaging as an outcome predictor in laryngeal and hypopharyngeal cancer patients with radiotherapy-related curative treatment: a preliminary study. Eur Radiol 32, 5353–5361 (2022). https://doi.org/10.1007/s00330-022-08630-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00330-022-08630-9

Keywords

Navigation