Skip to main content
Log in

Is radiomics a useful addition to magnetic resonance imaging in the preoperative classification of PitNETs?

  • Original Article
  • Published:
Acta Neurochirurgica Aims and scope Submit manuscript

Abstract

Background

The WHO 2021 introduced the term pituitary neuroendocrine tumours (PitNETs) for pituitary adenomas and incorporated transcription factors for subtyping, prompting the need for fresh diagnostic methods. Current biomarkers struggle to distinguish between high- and low-risk non-functioning PitNETs. We explored if radiomics can enhance preoperative decision-making.

Methods

Pre-treatment magnetic resonance (MR) images of patients who underwent surgery between 2015 and 2019 with available WHO 2021 classification were used. The tumours were manually segmented on the T1w, T1-contrast enhanced, and T2w images using 3D Slicer. One hundred Pyradiomic features were extracted from each MR sequence. Models were built to classify (1) somatotroph and gonadotroph PitNETs and (2) high- and low-risk subtypes of non-functioning PitNETs. Feature were selected independently from the MR sequences and multi-sequence (combining data from more than one MR sequence) using Boruta and Pearson correlation. Support vector machine (SVM), logistic regression (LR), random forest (RF), and multi-layer perceptron (MLP) were the classifiers used. Data imbalance was addressed using the Synthetic Minority Oversampling TEchnique (SMOTE). Performance of the models were evaluated using area under the receiver operating curve (AUC), accuracy, sensitivity, and specificity.

Results

A total of 222 PitNET patients (train, n = 149; test, n = 73) were enrolled in this retrospective study. Multi-sequence-based LR model discriminated best between somatotroph and gonadotroph PitNETs, with a test AUC of 0.84, accuracy of 0.74, specificity of 0.81, and sensitivity of 0.70. Multi-sequence-based MLP model perfomed best for the high- and low-risk non-functioning PitNETs, achieving a test AUC of 0.76, accuracy of 0.67, specificity of 0.72, and sensitivity of 0.66.

Conclusions

Utilizing pre-treatment MRI and radiomics holds promise for distinguishing high-risk from low-risk non-functioning PitNETs based on the latest WHO classification. This could assist neurosurgeons in making critical decisions regarding surgery or alternative management strategies for PitNETs after further clinical validation.

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

Similar content being viewed by others

Data availability

Available on reasonable request.

Code availability

Codes will be made available on GitHub shortly.

Abbreviations

WHO:

World Health Organization

MR:

Magnetic resonance

PitNETs:

Pituitary neuroendocrine tumours

SVM:

Support vector machine

LR:

Logistic regression

RF:

Random forest

MLP:

Multi-layer perceptron

SMOTE:

Synthetic Minority Oversampling TEchnique

NCA:

Null cell adenoma

GA:

Gonadotroph adenomas

SCA:

Silent corticotroph adenoma

SPA:

Silent PIT-1 positive adenomas

T1w:

T1-weighted MRI

T2w:

T2-weighted MRI

T1-CE:

T1-gadolinium contrast enhanced MRI

GLCM:

Gray-level co-occurrence matrix

GLRLM:

Gray level run length matrix

GLSZM:

Gray level size zone matrix

GLDM:

Gray level dependence matrix

ROC:

Receiver operating characteristic

AUC:

Area under the receiver operating characteristic (ROC) curve

DWI:

Diffusion-weighted imaging

ADC:

Apparent diffusion coefficient

ASL:

Arterial spin labelling

PIT1:

Pituitary-specific positive transcription factor 1

TPIT:

T-box transcription factor

SF1:

Steroidogenic factor

ER:

Estrogen receptor

SA:

Somatotroph adenoma

GATA3:

GATA binding protein 3

References

  1. Ahmadi J, North CM, Segall HD, Zee CS, Weiss MH (1986) Cavernous sinus invasion by pituitary adenomas. AJR Am J Roentgenol 146(2):257–262

    Article  CAS  PubMed  Google Scholar 

  2. Almeida JP, Stephens CC, Eschbacher JM et al (2019) Clinical, pathologic, and imaging characteristics of pituitary null cell adenomas as defined according to the 2017 World Health Organization criteria: a case series from two pituitary centers. Pituitary 22(5):514–519

    Article  CAS  PubMed  Google Scholar 

  3. Asa SL, Mete O, Perry A, Osamura RY (2022) Overview of the 2022 WHO Classification of Pituitary Tumors. Endocr Pathol 33(1):6–26

    Article  CAS  PubMed  Google Scholar 

  4. Asa SL, Mete O, Riddle ND, Perry A (2023) Multilineage pituitary neuroendocrine tumors (PitNETs) Expressing PIT1 and SF1. Endocr Pathol 34(3):273–278

    Article  CAS  PubMed  Google Scholar 

  5. Asha MJ, Takami H, Velasquez C, Oswari S, Almeida JP, Zadeh G, Gentili F (2019) Long-term outcomes of transsphenoidal surgery for management of growth hormone-secreting adenomas: single-center results. J Neurosurg 11:1–11. https://doi.org/10.3171/2019.6.JNS191187

    Article  Google Scholar 

  6. Cazabat L, Dupuy M, Boulin A, Bernier M, Baussart B, Foubert L, Raffin-Sanson M-L, Caron P, Bertherat J, Gaillard S (2014) Silent, but not unseen: multimicrocystic aspect on T2-weighted MRI in silent corticotroph adenomas. Clin Endocrinol (Oxf) 81(4):566–572

    Article  CAS  PubMed  Google Scholar 

  7. Cordeiro D, Xu Z, Mehta GU et al (2018) Hypopituitarism after gamma knife radiosurgery for pituitary adenomas: a multicenter, international study. J Neurosurg 131(4):1188–1196

    Article  Google Scholar 

  8. Fan Y, Jiang S, Hua M, Feng S, Feng M, Wang R (2019) Machine learning-based radiomics predicts radiotherapeutic response in patients with acromegaly. Front Endocrinol 10:588

    Article  Google Scholar 

  9. Goyal-Honavar A, Sarkar S, Asha HS, Kapoor N, Thomas R, Balakrishnan R, Chacko G, Chacko AG (2021) Impact of experience on outcomes after endoscopic transsphenoidal surgery for acromegaly. World Neurosurgery 151:e1007–e1015

    Article  PubMed  Google Scholar 

  10. Goyal-Honavar A, Sarkar S, Hesarghatta A, Kapoor N, Balakrishnan R, Vanjare H, Chacko G, Chacko A (2021) A clinicoradiological analysis of silent corticotroph adenomas after the introduction of pituitary-specific transcription factors. Acta Neurochir. https://doi.org/10.1007/s00701-021-04911-2

    Article  PubMed  Google Scholar 

  11. Haddad AF, Young JS, Oh T et al (2020) Clinical characteristics and outcomes of null-cell versus silent gonadotroph adenomas in a series of 1166 pituitary adenomas from a single institution. Neurosurg Focus 48(6):E13

    Article  PubMed  Google Scholar 

  12. Jahangiri A, Wagner JR, Pekmezci M, Hiniker A, Chang EF, Kunwar S, Blevins L, Aghi MK (2013) A comprehensive long-term retrospective analysis of silent corticotrophic adenomas vs hormone-negative adenomas. Neurosurgery 73(1):8–18

    Article  PubMed  Google Scholar 

  13. J Jia L Meng G Song S Sun C Li J Tian Y Zhang 2020 Prediction of response to stereotactic radiotherapy for nonfunctioning pituitary adenoma using radiomic feature https://doi.org/10.21203/rs.2.21209/v1

  14. Kiseljak-Vassiliades K, Carlson NE, Borges MT, Kleinschmidt-DeMasters BK, Lillehei KO, Kerr JM, Wierman ME (2015) Growth hormone tumor histological subtypes predict response to surgical and medical therapy. Endocrine 49(1):231–241

    Article  CAS  PubMed  Google Scholar 

  15. Langlois F, Lim DST, Yedinak CG, Cetas I, McCartney S, Cetas J, Dogan A, Fleseriu M (2018) Predictors of silent corticotroph adenoma recurrence; a large retrospective single center study and systematic literature review. Pituitary 21(1):32–40

    Article  CAS  PubMed  Google Scholar 

  16. Louis DN, Perry A, Wesseling P et al (2021) The 2021 WHO Classification of Tumors of the Central Nervous System: a summary. Neuro Oncol 23(8):1231–1251

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. MacFarlane J, Gillett D, Koulouri O, Bashari W, Casey R, Gurnell M (2022) Radiomics as a tool for risk stratification of non-functioning pituitary adenomas following primary surgery. Endocr Abstr. https://doi.org/10.1530/endoabs.86.OC3.5

    Article  Google Scholar 

  18. Machado LF, Elias PCL, Moreira AC, Dos Santos AC, Murta Junior LO (2020) MRI radiomics for the prediction of recurrence in patients with clinically non-functioning pituitary macroadenomas. Comput Biol Med 124:103966

    Article  PubMed  Google Scholar 

  19. Mendi BAR, Batur H, Çay N, Çakır BT (2023) Radiomic analysis of preoperative magnetic resonance imaging for the prediction of pituitary adenoma consistency. Acta Radiol 64(8):2470–2478

    Article  PubMed  Google Scholar 

  20. Mete O, Lopes MB (2017) Overview of the 2017 WHO Classification of Pituitary Tumors. Endocr Pathol 28(3):228–243

    Article  CAS  PubMed  Google Scholar 

  21. Micko ASG, Wöhrer A, Wolfsberger S, Knosp E (2015) Invasion of the cavernous sinus space in pituitary adenomas: endoscopic verification and its correlation with an MRI-based classification. JNS 122(4):803–811

    Article  Google Scholar 

  22. Osborn AG, Louis DN, Poussaint TY, Linscott LL, Salzman KL (2022) The 2021 World Health Organization Classification of Tumors of the Central Nervous System: what neuroradiologists need to know. Am J Neuroradiol. https://doi.org/10.3174/ajnr.A7462

    Article  PubMed  PubMed Central  Google Scholar 

  23. Peng A, Dai H, Duan H, Chen Y, Huang J, Zhou L, Chen L (2020) A machine learning model to precisely immunohistochemically classify pituitary adenoma subtypes with radiomics based on preoperative magnetic resonance imaging. Eur J Radiol 125:108892

    Article  PubMed  Google Scholar 

  24. Rui W, Qiao N, Wu Y, Zhang Y, Aili A, Zhang Z, Ye H, Wang Y, Zhao Y, Yao Z (2022) Radiomics analysis allows for precise prediction of silent corticotroph adenoma among non-functioning pituitary adenomas. Eur Radiol 32(3):1570–1578

    Article  PubMed  Google Scholar 

  25. Wang H, Chang J, Zhang W et al (2023) Radiomics model and clinical scale for the preoperative diagnosis of silent corticotroph adenomas. J Endocrinol Invest 46(9):1843–1854

    Article  CAS  PubMed  Google Scholar 

  26. Won SY, Lee N, Park YW, Ahn SS, Ku CR, Kim EH, Lee S-K (2022) Quality reporting of radiomics analysis in pituitary adenomas: promoting clinical translation. Br J Radiol 95(1139):20220401

    Article  PubMed  PubMed Central  Google Scholar 

  27. Zhang Y, Luo Y, Kong X, Wan T, Long Y, Ma J (2022) A preoperative MRI-based radiomics-clinicopathological classifier to predict the recurrence of pituitary macroadenoma within 5 years. Front Neurol 12:780628

    Article  PubMed  PubMed Central  Google Scholar 

  28. Zhang S, Song G, Zang Y, Jia J, Wang C, Li C, Tian J, Dong D, Zhang Y (2018) Non-invasive radiomics approach potentially predicts non-functioning pituitary adenomas subtypes before surgery. Eur Radiol 28(9):3692–3701. https://doi.org/10.1007/s00330-017-5180-6

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors acknowledge the support provided by Mr. Reji towards data anonymization and transfer of images.

Author information

Authors and Affiliations

Authors

Contributions

The authors confirm contribution to the paper as follows: study conception and design: AGC, AJ, GC, DD, BKS, SPP, HMTT; data collection: SA, AGH, JAS. Author; analysis, and interpretation of results: SA, AGH, AGC, AJ, GC, DD, JAS, BKS, SPP, HMTT; draft manuscript preparation: SA, AGH; revised manuscript critically for important intellectual content: AGC, AJ, GC, DD, BKS, SPP, HMTT. All authors reviewed the results and approved the final version of the manuscript.

Corresponding author

Correspondence to Hannah Mary T Thomas.

Ethics declarations

Ethical approval

This study was conducted in accordance with the 1964 Declaration of Helsinki and was approved by the Institutional Review Board with the need for informed consent waived due to the retrospective nature of the study.

Consent to participate

Waiver granted due to retrospective nature of study.

Consent for publication

All authors have consented to publishing this manuscript.

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher's Note

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

Sathya A and Abhijit Goyal-Honavar are equal contributing first authors.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 439 KB)

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sathya A, Goyal-Honavar, A., Chacko, A.G. et al. Is radiomics a useful addition to magnetic resonance imaging in the preoperative classification of PitNETs?. Acta Neurochir 166, 91 (2024). https://doi.org/10.1007/s00701-024-05977-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00701-024-05977-4

Keywords

Navigation