Skip to main content

Advertisement

Log in

A machine learning risk model based on preoperative computed tomography scan to predict postoperative outcomes after pancreatoduodenectomy

  • Original Article
  • Published:
Updates in Surgery Aims and scope Submit manuscript

Abstract

Clinically relevant postoperative pancreatic fistula (CR-POPF) is a life-threatening complication following pancreaticoduodenectomy (PD). Individualized preoperative risk assessment could improve clinical management and prevent or mitigate adverse outcomes. The aim of this study is to develop a machine learning risk model to predict occurrence of CR-POPF after PD from preoperative computed tomography (CT) scans. A total of 100 preoperative high-quality CT scans of consecutive patients who underwent pancreaticoduodenectomy in our institution between 2011 and 2019 were analyzed. Radiomic and morphological features extracted from CT scans related to pancreatic anatomy and patient characteristics were included as variables. These data were then assessed by a machine learning classifier to assess the risk of developing CR-POPF. Among the 100 patients evaluated, 20 had CR-POPF. The predictive model based on logistic regression demonstrated specificity of 0.824 (0.133) and sensitivity of 0.571 (0.337), with an AUC of 0.807 (0.155), PPV of 0.468 (0.310) and NPV of 0.890 (0.084). The performance of the model minimally decreased utilizing a random forest approach, with specificity of 0.914 (0.106), sensitivity of 0.424 (0.346), AUC of 0.749 (0.209), PPV of 0.502 (0.414) and NPV of 0.869 (0.076). Interestingly, using the same data, the model was also able to predict postoperative overall complications and a postoperative length of stay over the median with AUCs of 0.690 (0.209) and 0.709 (0.160), respectively. These findings suggest that preoperative CT scans evaluated by machine learning may provide a novel set of information to help clinicians choose a tailored therapeutic pathway in patients candidated to pancreatoduodenectomy.

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

The datasets generated during the current study are available from the corresponding author on reasonable request.

Code availability (software application or custom code)

Software code could be available from the corresponding author on reasonable request under written agreement.

References

  1. Pratt WB, Maithel SK, Vanounou T, Huang ZS, Callery MP, Vollmer CM (2007) Clinical and economic validation of the international study group of pancreatic fistula (ISGPF) classification scheme. Ann Surg. https://doi.org/10.1097/01.sla.0000251708.70219.d2

    Article  PubMed  PubMed Central  Google Scholar 

  2. Vollmer CM, Sanchez N, Gondek S et al (2012) A root-cause analysis of mortality following major pancreatectomy. J Gastrointest Surg. https://doi.org/10.1007/s11605-011-1753-x

    Article  PubMed  Google Scholar 

  3. Ahmad SA, Edwards MJ, Sutton JM et al (2012) Factors influencing readmission after pancreaticoduodenectomy: a multi-institutional study of 1302 patients. Ann Surg. https://doi.org/10.1097/SLA.0b013e318265ef0b

    Article  PubMed  Google Scholar 

  4. Williamsson C, Ansari D, Andersson R, Tingstedt B (2017) Postoperative pancreatic fistula-impact on outcome, hospital cost and effects of centralization. HPB. https://doi.org/10.1016/j.hpb.2017.01.004

    Article  PubMed  Google Scholar 

  5. Fuks D, Piessen G, Huet E et al (2009) Life-threatening postoperative pancreatic fistula (grade C) after pancreaticoduodenectomy: incidence, prognosis, and risk factors. Am J Surg 197(6):702–709. https://doi.org/10.1016/j.amjsurg.2008.03.004

    Article  PubMed  Google Scholar 

  6. Callery MP, Pratt WB, Kent TS, Chaikof EL, Vollmer CM (2013) A prospectively validated clinical risk score accurately predicts pancreatic fistula after pancreatoduodenectomy. J Am Coll Surg 216(1):1–14. https://doi.org/10.1016/j.jamcollsurg.2012.09.002

    Article  PubMed  Google Scholar 

  7. Mungroop TH, Van Rijssen LB, Van Klaveren D et al (2019) Alternative fistula risk score for pancreatoduodenectomy (a-FRS): design and international external validation. Ann Surg 269(5):937–943. https://doi.org/10.1097/SLA.0000000000002620

    Article  PubMed  Google Scholar 

  8. Chen JY, Feng J, Wang XQ, Cai SW, Dong JH, Chen YL (2015) Risk scoring system and predictor for clinically relevant pancreatic fistula after pancreaticoduodenectomy. World J Gastroenterol 21(19):5926–5933. https://doi.org/10.3748/wjg.v21.i19.5926

    Article  PubMed  PubMed Central  Google Scholar 

  9. Kim JY, Park JS, Kim JK, Yoon DS (2013) A model for predicting pancreatic leakage after pancreaticoduodenectomy based on the international study group of pancreatic surgery classification. Korean J Hepato Biliary Pancreatic Surg 17(4):166. https://doi.org/10.14701/kjhbps.2013.17.4.166

    Article  Google Scholar 

  10. Roberts KJ, Hodson J, Mehrzad H et al (2014) A preoperative predictive score of pancreatic fistula following pancreatoduodenectomy. HPB 16(7):620–628. https://doi.org/10.1111/hpb.12186

    Article  PubMed  Google Scholar 

  11. Yamamoto Y, Sakamoto Y, Nara S, Esaki M, Shimada K, Kosuge T (2011) A preoperative predictive scoring system for postoperative pancreatic fistula after pancreaticoduodenectomy. World J Surg 35(12):2747–2755. https://doi.org/10.1007/s00268-011-1253-x

    Article  PubMed  Google Scholar 

  12. Pratt WB, Callery MP, Vollmer CM (2008) Risk prediction for development of pancreatic fistula using the ISGPF classification scheme. World J Surg 32(3):419–428. https://doi.org/10.1007/s00268-007-9388-5

    Article  PubMed  Google Scholar 

  13. Sandini M, Bernasconi DP, Fior D et al (2016) A high visceral adipose tissue-to-skeletal muscle ratio as a determinant of major complications after pancreatoduodenectomy for cancer. Nutrition 32(11–12):1231–1237. https://doi.org/10.1016/j.nut.2016.04.002

    Article  PubMed  Google Scholar 

  14. Pecorelli N, Carrara G, De Cobelli F et al (2016) Effect of sarcopenia and visceral obesity on mortality and pancreatic fistula following pancreatic cancer surgery. Br J Surg. https://doi.org/10.1002/bjs.10063

    Article  PubMed  Google Scholar 

  15. Wellner UF, Kayser G, Lapshyn H et al (2010) A simple scoring system based on clinical factors related to pancreatic texture predicts postoperative pancreatic fistula preoperatively. HPB 12(10):696–702. https://doi.org/10.1111/j.1477-2574.2010.00239.x

    Article  PubMed  PubMed Central  Google Scholar 

  16. Sandini M, Bernasconi DP, Ippolito D et al (2015) Preoperative computed tomography to predict and stratify the risk of severe pancreatic fistula after pancreatoduodenectomy. Med (US) 94(31):1–7. https://doi.org/10.1097/MD.0000000000001152

    Article  Google Scholar 

  17. Lambin P, Leijenaar RTH, Deist TM et al (2017) Radiomics: the bridge between medical imaging and personalized medicine. Nat Rev Clin Oncol 14(12):749–762. https://doi.org/10.1038/nrclinonc.2017.141

    Article  PubMed  Google Scholar 

  18. Tempero MA, Malafa MP, Chiorean EG et al (2019) Pancreatic adenocarcinoma, version 1.2019 featured updates to the NCCN guidelines. JNCCN J Natl Compr Cancer Netw. 17(3):203–210. https://doi.org/10.6004/jnccn.2019.0014

    Article  Google Scholar 

  19. Dindo D, Demartines N, Clavien P (2004) Classification of Surgical Complications. Ann Surg 240(2):205–213. https://doi.org/10.1097/01.sla.0000133083.54934.ae

    Article  PubMed  PubMed Central  Google Scholar 

  20. Bassi C, Marchegiani G, Dervenis C et al (2017) The 2016 update of the International Study Group (ISGPS) definition and grading of postoperative pancreatic fistula: 11 Years After. Surg (US) 161(3):584–591. https://doi.org/10.1016/j.surg.2016.11.014

    Article  Google Scholar 

  21. Pecorelli N, Carrara G, De Cobelli F et al (2016) Effect of sarcopenia and visceral obesity on mortality and pancreatic fistula following pancreatic cancer surgery. Br J Surg 103(4):434–442. https://doi.org/10.1002/bjs.10063

    Article  CAS  PubMed  Google Scholar 

  22. Haralick RM, Dinstein I, Shanmugam K (1973) Textural features for image classification. IEEE Trans Syst Man Cybern SMC-3(6):610–621. https://doi.org/10.1109/TSMC.1973.4309314

    Article  Google Scholar 

  23. Xu DH, Kurani AS, Furst JD, Raicu DS (2004) Run-length encoding for volumetric texture. Image Process Proc Fourth IASTED Int Conf Vis Imaging 27:534–539

    CAS  Google Scholar 

  24. Amadasun M, King R (1989) Texural features corresponding to texural properties. IEEE Trans Syst Man Cybern. https://doi.org/10.1109/21.44046

    Article  Google Scholar 

  25. Thibault G, Fertil B, Navarro C et al (2014) Texture indexes and gray level size zone matrix application to cell nuclei classification. Pattern Recognit Inf Process 2009:140–145

    Google Scholar 

  26. Mitsiopoulos N, Baumgartner RN, Heymsfield SB, Lyons W, Gallagher D, Ross R (1998) Cadaver validation of skeletal muscle measurement by magnetic resonance imaging and computerized tomography. J Appl Physiol 85(1):115–122. https://doi.org/10.1152/jappl.1998.85.1.115

    Article  CAS  PubMed  Google Scholar 

  27. Van Griethuysen JJM, Fedorov A, Parmar C et al (2017) Computational radiomics system to decode the radiographic phenotype. Cancer Res. https://doi.org/10.1158/0008-5472.CAN-17-0339

    Article  PubMed  PubMed Central  Google Scholar 

  28. Bergstra J, Bengio Y (2012) Random search for hyper-parameter optimization. J Mach Learn Res 13:281–305

    Google Scholar 

  29. Tibshirani R (1996) Regression shrinkage and selection via the lasso. J R Stat Soc Ser B. https://doi.org/10.1111/j.2517-6161.1996.tb02080.x

    Article  Google Scholar 

  30. Chawla NV, Bowyer KW, Hall LO, Kegelmeyer WP (2002) SMOTE: synthetic minority over-sampling technique. J Artif Intell Res. https://doi.org/10.1613/jair.953

    Article  Google Scholar 

  31. Shen W, Punyanitya M, Wang ZM et al (2004) Total body skeletal muscle and adipose tissue volumes: estimation from a single abdominal cross-sectional image. J Appl Physiol. https://doi.org/10.1152/japplphysiol.00744.2004

    Article  PubMed  Google Scholar 

  32. Mourtzakis M, Prado CMM, Lieffers JR, Reiman T, McCargar LJ, Baracos VE (2008) A practical and precise approach to quantification of body composition in cancer patients using computed tomography images acquired during routine care. Appl Physiol Nutr Metab. https://doi.org/10.1139/H08-075

    Article  PubMed  Google Scholar 

  33. Bihorac A, Ozrazgat-Baslanti T, Ebadi A et al (2019) MySurgeryRisk: development and validation of a machine-learning risk algorithm for major complications and death after surgery. Ann Surg 269(4):652–662. https://doi.org/10.1097/SLA.0000000000002706

    Article  PubMed  Google Scholar 

  34. Merath K, Hyer JM, Mehta R et al (2020) Use of machine learning for prediction of patient risk of postoperative complications after liver, pancreatic, and colorectal surgery. J Gastrointest Surg. https://doi.org/10.1007/s11605-019-04338-2

    Article  PubMed  Google Scholar 

  35. Kambakamba P, Mannil M, Herrera PE et al (2020) The potential of machine learning to predict postoperative pancreatic fistula based on preoperative, non-contrast-enhanced CT: a proof-of-principle study. Surg (US) 167(2):448–454. https://doi.org/10.1016/j.surg.2019.09.019

    Article  Google Scholar 

  36. Han IW, Cho K, Ryu Y et al (2020) Risk prediction platform for pancreatic fistula after pancreatoduodenectomy using artificial intelligence. World J Gastroenterol. https://doi.org/10.3748/WJG.V26.I30.4453

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Funding

No funding.

Author information

Authors and Affiliations

Authors

Contributions

All authors contributed to the study concept and design, data interpretation, drafting, final approval, and accountability for all aspects of the work.

Corresponding author

Correspondence to Victor Savevski.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. This study was approved by the institutional Ethics Committee of Humanitas Clinical and Research Center-IRCCS, Milan.

Consent to participate

For this type of study, formal consent is not required.

Consent for publication

Not applicable.

Research involving human participants and/or animals

The study was approved by the institutional research committee. This article does not contain any studies on animals performed by any of the authors.

Additional information

Publisher's Note

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

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 1137 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Capretti, G., Bonifacio, C., De Palma, C. et al. A machine learning risk model based on preoperative computed tomography scan to predict postoperative outcomes after pancreatoduodenectomy. Updates Surg 74, 235–243 (2022). https://doi.org/10.1007/s13304-021-01174-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13304-021-01174-5

Keywords

Navigation