#PAGE_PARAMS# #ADS_HEAD_SCRIPTS# #MICRODATA#

A prognostic Bayesian network that makes personalized predictions of poor prognostic outcome post resection of pancreatic ductal adenocarcinoma


Autoři: Alison Bradley aff001;  Robert Van der Meer aff001;  Colin J. McKay aff002
Působiště autorů: Department of Management Science, Strathclyde Business School, University of Strathclyde, Glasgow, Scotland, United Kingdom aff001;  West of Scotland Pancreatic Cancer Unit, Glasgow Royal Infirmary, Glasgow, Scotland, United Kingdom aff002
Vyšlo v časopise: PLoS ONE 14(9)
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pone.0222270

Souhrn

Background

The narrative surrounding the management of potentially resectable pancreatic cancer is complex. Surgical resection is the only potentially curative treatment. However resection rates are low, the risk of operative morbidity and mortality are high, and survival outcomes remain poor. The aim of this study was to create a prognostic Bayesian network that pre-operatively makes personalized predictions of post-resection survival time of 12months or less and also performs post-operative prognostic updating.

Methods

A Bayesian network was created by synthesizing data from PubMed post-resection survival analysis studies through a two-stage weighting process. Input variables included: inflammatory markers, tumour factors, tumour markers, patient factors and, if applicable, response to neoadjuvant treatment for pre-operative predictions. Prognostic updating was performed by inclusion of post-operative input variables including: pathology results and adjuvant therapy.

Results

77 studies (n = 31,214) were used to create the Bayesian network, which was validated against a prospectively maintained tertiary referral centre database (n = 387). For pre-operative predictions an Area Under the Curve (AUC) of 0.7 (P value: 0.001; 95% CI 0.589–0.801) was achieved accepting up to 4 missing data-points in the dataset. For prognostic updating an AUC 0.8 (P value: 0.000; 95% CI:0.710–0.870) was achieved when validated against a dataset with up to 6 missing pre-operative, and 0 missing post-operative data-points. This dropped to AUC: 0.7 (P value: 0.000; 95% CI:0.667–0.818) when the post-operative validation dataset had up to 2 missing data-points.

Conclusion

This Bayesian network is currently unique in the way it utilizes PubMed and patient level data to translate the existing empirical evidence surrounding potentially resectable pancreatic cancer to make personalized prognostic predictions. We believe such a tool is vital in facilitating better shared decision-making in clinical practice and could be further developed to offer a vehicle for delivering personalized precision medicine in the future.

Klíčová slova:

Biology and life sciences – Physical sciences – Research and analysis methods – Neuroscience – Cognitive science – Cognitive psychology – Psychology – Social sciences – Mathematics – Medicine and health sciences – Diagnostic medicine – Statistics – Mathematical and statistical techniques – Statistical methods – Clinical medicine – Oncology – Cancer treatment – Cancers and neoplasms – Cognition – Surgical and invasive medical procedures – Gastrointestinal tumors – Clinical oncology – Decision making – Surgical resection – Pancreatic cancer – Surgical oncology – Prognosis


Zdroje

1. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2015. CA Cancer J Clin. 2015;65:5–29 doi: 10.3322/caac.21254 25559415

2. Ferlay J, Steliarova-Foucher E, Lortet-Tieulent J, Rosso S, Coebergh JW, Comber H, et al. Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012. Eur J Cancer. 2013;49:1374–403. doi: 10.1016/j.ejca.2012.12.027 23485231

3. Cancer Research UK. Pancreatic cancer and treatment statistics.https://www.cancerresearchuk.org/about-cancer/pancreatic-cancer/survival. Accessed 7th January 2019.

4. Neoptolemos JP, Dunn JA, Stocken DD, Almond J, Link K, Beger H, et al. Adjuvant chemoradio- therapy and chemotherapy in resectable pancreatic cancer: a randomized controlled trial. Lancet. 2001;358:1576–85. doi: 10.1016/s0140-6736(01)06651-x 11716884

5. Winter JM, Brennan MF, Tang LH, D’Angelica MI, Dematteo RP, Fong Y, et al. Survival after resection of pancreatic adenocarcinoma: results from a single institution over three decades. Ann Surg Oncol. 2012;19:169. doi: 10.1245/s10434-011-1900-3 21761104

6. Bilimoria KY, Bentrem DJ, Ko CY, Tomlinson JS, Stewart AK, Winchester DP, et al. Multimodality therapy for pancreatic cancer in the U.S.: utilization, outcomes, and the effect of hospital volume. Cancer. 2007;110:1227–34. doi: 10.1002/cncr.22916 17654662

7. Asare EA, Evans DB, Erickson BA, Aburajab M, Tolat P, Tsai S. Neoadjuvant treatment sequencing adds value to the care of patients with operable pancreatic cancer. Journal of Surgical Oncology. 2016;114(3):291–295. doi: 10.1002/jso.24316 27264017

8. Lee J, Ahn S, Paik K, Kim HW, Kang J, Kim J, et al. Clinical impact of neoadjuvant treatment in resectable pancreatic cancer: a systematic review and meta-analysis protocol. BMJ. 2016;6(3):1–9

9. Versteijne E, Vogel JA, Besselink MG, Busch ORC, Wilmink JW, Daams JG, et al. Meta‐analysis comparing upfront surgery with neoadjuvant treatment in patients with resectable or borderline resectable pancreatic cancer. The British Journal of Surgery. 2018;105(8):946–958. doi: 10.1002/bjs.10870 29708592

10. Sharma G, Whang EE, Ruan DT, Ito H. Efficacy of neoadjuvant versus adjuvant versus adjuvant therapy for resectable pancreatic adenocarcinoma: a decision analysis. Ann Surg Oncol. 2015;22(suppl 3):1229–37.

11. Xu CP, Xue XJ, Laing N, Xu DG, Liu FJ, Yu XS, et al. Effect of chemoradiotherapy and neoadjuvant chemoradiotherapy in resectable pancreatic cancer: a systematic review and meta-analysis. J Cancer Res Clin Oncol. 2014;140:549–59. doi: 10.1007/s00432-013-1572-4 24370686

12. Andriulli A, Festa V, Botteri E, Valvano MR, Koch M, Bassi C, et al. Neoadjuvant/preoperative gemcitabine for patients with localized pancreatic cancer: a meta-analysis of prospective studies. Ann Surg Oncol. 2012;19:1644–62. doi: 10.1245/s10434-011-2110-8 22012027

13. Petrelli F, Coinu A, Borgnovo K, Cabiddu M, Ghilardi M, Lonati V, et al. FOLFIRINOX-based neoadjuvant therapy in borderline resectable or unresectable pancreatic cancer: a meta-analytical review of published studies. Pancreas. 2015;44(4):515–21. doi: 10.1097/MPA.0000000000000314 25872127

14. de Gus SW, Evans DB, Bliss LA, Eskander MF, Smith JK, Wolff RA, et al. Neoadjuvant therapy versus upfront surgical strategies in resectable pancreatic cancer: a markov decision analysis. Eur J Surg. 2016; 42(10):1552–60.

15. Van Houten JP, White RR, Jackson GP. A decision model of therapy for potentially resectable pancreatic cancer. The Journal of Surgical Research. 2012;174(2):222–230. doi: 10.1016/j.jss.2011.08.022 22079845

16. Velikova M, Scheltinga JT, Lucas PJF, Spaanderman M. Exploiting causal functional relationships in Bayesian network modeling for personalized healthcare. Int Journal of Approximate Reasoning. 2014: 55:59–73

17. School R, Kaplan D, Denissen J, Asendorpf JB, Neyer FJ, van Aken MAG. A Gentle introduction to Bayesian analysis: applications to development research. Child Development. 2013: 85:3:842–860. doi: 10.1111/cdev.12169 24116396

18. Lewis RS Jr, Vollmer CM Jr. Risk scores and prognostic models in surgery: pancreas resection as a paradigm. Curr Probl Surg. 2012. 49:12:731–95. doi: 10.1067/j.cpsurg.2012.08.002 23131540

19. Verduijn M, Peek N, Rosseel PM, de Jonge E, de Mol BAJM. Prognostic Bayesian networks I: rationale, learning procedure, and clinical use. Journal of Biomedical Informatics. 2007:609–618. doi: 10.1016/j.jbi.2007.07.003 17704008

20. Fenton N, Neil M. Risk assessment and decision analysis with Bayesian networks. 2nd ed. London: CRC Press;2019.

21. Stajduhar I, Dalbelo-Basic B. Learning Bayesian networks from survival data using weighting censored instances. Journal of Biomedical Informatics. 2010: 43:613–622. doi: 10.1016/j.jbi.2010.03.005 20332035

22. Lucas PJF, van der Gaag, Abu-Hanna A. Bayesian networks in biomedicine and health-care. Artificial Intelligence in Medicine. 2004: 201–214. doi: 10.1016/j.artmed.2003.11.001 15081072

23. Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. Open Med. 2009; 3:e123–e130. 21603045

24. Guyatt GH, Oxman AD, Visit G, Kunz R, Brozek J, Alonso-Coello P et al. GRADE guidelines: 4. Rating the qyality of evidence-study limitations (risk of bias). Journal of Clinical Epidemiology. 2011; 64:407–415. doi: 10.1016/j.jclinepi.2010.07.017 21247734

25. Zhu X., Zhou X., Zhang Y., Sun X., Liu H., & Zhang Y. Reporting and methodological quality of survival analysis in articles published in Chinese oncology journals. Medicine. 2017: 96(50), e9204. doi: 10.1097/MD.0000000000009204 29390340

26. Zhao D, Weng C. Combining PubMed knowledge and EHR data to develop a weighted Bayesian network for pancreatic cancer prediction. Journal of Biomedical Informatics. 2011: 44:5:859–868. doi: 10.1016/j.jbi.2011.05.004 21642013

27. Agenarisk. Bayesian network software for risk analysis and decision analysis. https://www.agenarisk.com.

28. Kanda M, Fujii T, Takami H, Suenaga M, Inokawa Y, Yamada S, et al. The combination of the serum carbohydrate antigen 19–9 and carcinoembryonic antigen is a simple and accurate predictor of mortality in pancreatic cancer patients. Surg Today. 2014: 44:1692–1701 doi: 10.1007/s00595-013-0752-9 24114022

29. Hsu CC, Wolfgang CL, Laheru DA, Pawlik TM, Swartz MJ, Winter JM, et al. Early mortality risk score: identification of poor outcomes following upfront surgery for resectable pancreatic cancer. J Gastrointest Surg. 2012; 16:4:753–761 doi: 10.1007/s11605-011-1811-4 22311282

30. Shen Y-N, Bai X-L, Gang J, Zhang Q, Lu JH, Quin RY, et al. A preoperative nomogram predicts prognosis of up front resectable patients with pancreatic with pancreatic head cancer and suspected venous invasion. HPB. 2018: 1–10.

31. Balzano G, Dugnani E, Crippa S, Scavini M, Pasquale V, Aleotti V, et al. A preoperative score to predict early death after pancreatic cancer resection. Digestive and Liver Disease. 2017: 49:1050–1056. doi: 10.1016/j.dld.2017.06.012 28734776

32. Walczak S & Velanovich V. An evaluation of Artificial Neural Networks in predicting pancreatic cancer survival. J Gastrointest Surg. 2017; 21:1606–1612 doi: 10.1007/s11605-017-3518-7 28776157

33. Smith BJ & Mezhir JJ. An interactive Bayesian model for prediction of lymph node ratio and survival in pancreatic cancer patients. J Am Med Inform Assoc. 2014;21:e203–e211 doi: 10.1136/amiajnl-2013-002171 24444460

34. Tonelli MR, Shirts BH. Knowledge for precision medicine mechanistic reasoning and methodological pluralism. JAMA. 2017;318:17:1649–1650. doi: 10.1001/jama.2017.11914 29052713

35. MacConaill LE, Lindeman NI, Rollins BJ. Brave-ish new world—what’s needed to make precision oncology a practical reality. JAMAOncol. 2015:1:7:879–880.

36. Dzau VJ, Ginsburg GS. Realizing the full potential of precision medicine in health and health care. JAMA.2016:316:16:1659–1660. doi: 10.1001/jama.2016.14117 27669484

37. Obermeyer ZMD, Lee TH. Lost in thought—the limits of the human mind and the future of medicine. N Engl J Med. 2017:377:1209–1211. doi: 10.1056/NEJMp1705348 28953443


Článok vyšiel v časopise

PLOS One


2019 Číslo 9
Najčítanejšie tento týždeň
Najčítanejšie v tomto čísle
Kurzy

Zvýšte si kvalifikáciu online z pohodlia domova

Získaná hemofilie - Povědomí o nemoci a její diagnostika
nový kurz

Eozinofilní granulomatóza s polyangiitidou
Autori: doc. MUDr. Martina Doubková, Ph.D.

Všetky kurzy
Prihlásenie
Zabudnuté heslo

Zadajte e-mailovú adresu, s ktorou ste vytvárali účet. Budú Vám na ňu zasielané informácie k nastaveniu nového hesla.

Prihlásenie

Nemáte účet?  Registrujte sa

#ADS_BOTTOM_SCRIPTS#