Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Article
  • Clinical Research
  • Published:

Development and validation of a multivariable prognostic model in de novo metastatic castrate sensitive prostate cancer

Abstract

Background

Metastatic castrate sensitive prostate cancer (mCSPC) is a heterogeneous disease state with variable prognosis. Although several life-prolonging systemic agents are available, there is no robust multivariable model to predict prognosis and improve risk stratification in mCSPC. The objective of this study was to build and validate a multivariable prognostic model to predict overall survival (OS) in mCSPC.

Methods

We used data from LATITUDE, a phase III randomized controlled trial in which men with de novo mCSPC were randomly allocated to either ADT plus abiraterone or ADT with placebo. Patients with non-missing data (n = 1,058) were randomly split in a 70:30 ratio to training (n = 743) and testing (n = 315) sets. Elastic net regression was used for variable selection. A multivariable Cox regression model for OS was then fitted using the selected variables. The predictive accuracy of the model was assessed on the testing set using the time-dependent area under curve (tAUC) with bootstrapped confidence intervals [CI] primarily for OS and secondarily for radiographic progression-free survival (rPFS).

Results

The 11 prognostic variables in the final model were performance status, number of skeletal metastases, Gleason score, presence of liver metastasis, worst pain score, albumin, lactate dehydrogenase, prostate-specific antigen, hemoglobin, and treatment regimen. The tAUC for predicting OS at 2- and 3-years was 0.74 (95% CI, 0.67–0.80) and 0.72 (95% CI, 0.65–0.77), respectively. The tAUC for rPFS at 2- and 3-years was 0.72 (95% CI, 0.65–0.77) and 0.77 (95% CI, 0.70–0.82), respectively.

Conclusions

A prognostic model for men with de novo mCSPC was developed and validated in an independent testing set. Our model had high accuracy for predicting OS and rPFS. The model includes commonly used clinical and laboratory parameters and can guide risk stratification of these patients for participation in future trials.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Calibration plots for overall survival in the testing dataset.
Fig. 2: Prognostic model predicting overall survival probability.
Fig. 3: Kaplan–Meier survival curves by the two- and three-risk groups in the testing set.

Similar content being viewed by others

Data availability

This study, carried out under YODA Project # 2021–4565, used data obtained from the Yale University Open Data Access Project, which has an agreement with JANSSEN RESEARCH & DEVELOPMENT, L.L.C. The interpretation and reporting of research using this data are solely the responsibility of the authors and does not necessarily represent the official views of the Yale University Open Data Access Project or JANSSEN RESEARCH & DEVELOPMENT, L.L.C.

References

  1. Roy S, Morgan SC. Who dies from prostate cancer? An analysis of the surveillance, epidemiology and end results database. Clin Oncol. 2019;31:630–6. http://www.ncbi.nlm.nih.gov/pubmed/31130340.

    Article  CAS  Google Scholar 

  2. Reese AC, Wessel SR, Fisher SG, Mydlo JH. Evidence of prostate cancer “reverse stage migration” toward more advanced disease at diagnosis: Data from the Pennsylvania Cancer Registry. Urologic Oncol: Semin Original Investig. 2016;34:335.e21–335.e28.

    Article  Google Scholar 

  3. Cornford P, Bellmunt J, Bolla M, Briers E, de Santis M, Gross T, et al. EAU-ESTRO-SIOG Guidelines on Prostate Cancer. Part II: Treatment of relapsing, metastatic, and castration-resistant prostate cancer. Eur Urol. 2017;71:630–42. https://pubmed.ncbi.nlm.nih.gov/27591931/

    Article  PubMed  Google Scholar 

  4. Fizazi K, Tran N, Fein L, Matsubara N, Rodriguez-Antolin A, Alekseev BY, et al. Abiraterone plus prednisone in metastatic, castration-sensitive prostate cancer. N. Engl J Med. 2017;377:352–60. https://doi.org/10.1056/NEJMoa1704174.

    Article  CAS  PubMed  Google Scholar 

  5. James ND, de Bono JS, Spears MR, Clarke NW, Mason MD, Dearnaley DP, et al. Abiraterone for prostate cancer not previously treated with hormone therapy. N. Engl J Med. 2017;377:338–51. https://doi.org/10.1056/NEJMoa1702900.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Parker CC, James ND, Brawley CD, Clarke NW, Hoyle AP, Ali A, et al. Radiotherapy to the primary tumour for newly diagnosed, metastatic prostate cancer (STAMPEDE): a randomised controlled phase 3 trial. Lancet. 2018;392:2353–66.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Davis ID, Martin AJ, Stockler MR, Begbie S, Chi KN, Chowdhury S, et al. Enzalutamide with standard first-line therapy in metastatic prostate cancer. N. Engl J Med. 2019;381:121–31. https://doi.org/10.1056/nejmoa1903835.

    Article  CAS  PubMed  Google Scholar 

  8. Chi KN, Agarwal N, Bjartell A, Chung BH, Pereira de Santana Gomes AJ, Given R, et al. Apalutamide for metastatic, castration-sensitive prostate cancer. N. Engl J Med 2019;381:13–24. https://pubmed.ncbi.nlm.nih.gov/31150574/

    Article  CAS  PubMed  Google Scholar 

  9. Sweeney CJ, Chen Y-H, Carducci M, Liu G, Jarrard DF, Eisenberger M, et al. Chemohormonal therapy in metastatic hormone-sensitive prostate cancer. N. Engl J Med. 2015;373:737–46.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. James ND, Sydes MR, Clarke NW, Mason MD, Dearnaley DP, Spears MR, et al. Addition of docetaxel, zoledronic acid, or both to first-line long-term hormone therapy in prostate cancer (STAMPEDE): Survival results from an adaptive, multiarm, multistage, platform randomised controlled trial. Lancet. 2016;387:1163–77.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Kyriakopoulos CE, Chen YH, Carducci MA, Liu G, Jarrard DF, Hahn NM, et al. Chemohormonal therapy in metastatic hormone-sensitive prostate cancer: long-term survival analysis of the randomized phase III E3805 chaarted trial. J Clin Oncol. 2018;36:1080–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Glass TR, Tangen CM, Crawford ED, Thompson I. Metastatic carcinoma of the prostate: Identifying prognostic groups using recursive partitioning. J Urol. 2003;169:164–9.

    Article  CAS  PubMed  Google Scholar 

  13. Gravis G, Boher JM, Fizazi K, Joly F, Priou F, Marino P, et al. Prognostic factors for survival in noncastrate metastatic prostate cancer: validation of the glass model and development of a novel simplified prognostic model. Eur Urol. 2015;68:196–204.

    Article  PubMed  Google Scholar 

  14. Akamatsu S, Kubota M, Uozumi R, Narita S, Takahashi M, Mitsuzuka K, et al. Development and validation of a novel prognostic model for predicting overall survival in treatment-naïve castration-sensitive metastatic prostate cancer. Eur Urol Oncol. 2019;2:320–8. https://doi.org/10.1016/j.euo.2018.10.011. Available from

    Article  PubMed  Google Scholar 

  15. Wallis CJD, Malone S, Cagiannos I, Morgan SC, Hamilton RJ, Basappa NS, et al. Real-world utilization of androgen deprivation therapy-intensification among older canadian men with de novo metastatic prostate cancer. JNCI Cancer Spectrum. 2021; Available from: https://doi.org/10.1093/jncics/pkab082/6379721

  16. Fizazi K, Tran NP, Fein L, Matsubara N, Rodriguez-Antolin A, Alekseev BY, et al. Abiraterone acetate plus prednisone in patients with newly diagnosed high-risk metastatic castration-sensitive prostate cancer (LATITUDE): final overall survival analysis of a randomised, double-blind, phase 3 trial. Lancet Oncol. 2019;20:686–700.

    Article  CAS  PubMed  Google Scholar 

  17. Ali A, Hoyle A, Haran ÁM, Brawley CD, Cook A, Amos C, et al. Association of bone metastatic burden with survival benefit from prostate radiotherapy in patients with newly diagnosed metastatic prostate cancer: a secondary analysis of a randomized clinical trial. JAMA Oncol. 2021;7:555–63. https://jamanetwork.com/journals/jamaoncology/fullarticle/2776418

    Article  PubMed  PubMed Central  Google Scholar 

  18. Bernard B, Burnett C, Sweeney CJ, Rider JR, Sridhar SS. Impact of age at diagnosis of de novo metastatic prostate cancer on survival. Cancer 2020;126:986–93.

    Article  PubMed  Google Scholar 

  19. Kyriakopoulos CE, Chen YH, Carducci MA, Liu G, Jarrard DF, Hahn NM, et al. Chemohormonal therapy in metastatic hormone-sensitive prostate cancer: long-term survival analysis of the randomized phase III E3805 chaarted trial. J Clin Oncol. 2018;36:1080–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Wallis CJD, Shayegan B, Morgan SC, Hamilton RJ, Cagiannos I, Basappa NS, et al. Prognostic association between common laboratory tests and overall survival in elderly men with de novo metastatic castration sensitive prostate cancer: A population-based study in canada. Cancers. 2021;13.

  21. Friedman J, Hastie T, Tibshirani R, Regularization paths for generalized linear models via coordinate descent. J Stat Softw. 2010];33:1. Available from: /pmc/articles/PMC2929880/.

  22. Uno H, Cai T, Tian L, Wei LJ. Evaluating prediction rules for t-year survivors with censored regression models. J Am Stat Assoc [Internet]. 2007;102:527–37. https://www.tandfonline.com/action/journalInformation?journalCode=uasa20

    Article  CAS  Google Scholar 

  23. Harrell FE, Regression Modeling Strategies. Berlin, Heidelberg: Springer-Verlag; 2006.

  24. Morris TP, Jarvis CI, Cragg W, Phillips PPJ, Choodari-Oskooei B, Sydes MR, Proposals on Kaplan–Meier plots in medical research and a survey of stakeholder views: KMunicate. 9, BMJ Open. BMJ Publishing Group; 2019. p. e030215. Available from: http://bmjopen.bmj.com/

  25. Therneau TM, Grambsch PM, Modeling survival data: extending the Cox model. Springer; 2000. 350 p. Available from: https://cran.r-project.org/web/packages/survival/citation.html

  26. Potapov S, Adler W, Schmid Matthias. survAUC: Estimators of prediction accuracy for time-to-event data. R package version 1.0-5. https://CRAN.R-project.org/package=survAUC. 2012.

  27. Rusthoven C, Carlson J, Waxweiler T, Yeh N, Raben D, Flaig T, et al. The prognostic significance of Gleason scores in metastatic prostate cancer. Urol Oncol. 2014;32:707–13. https://pubmed.ncbi.nlm.nih.gov/24629494/

    Article  PubMed  Google Scholar 

  28. Mori K, Kimura S, Parizi MK, Enikeev DV, Glybochko PV, Seebacher V, et al. Prognostic value of lactate dehydrogenase in metastatic prostate cancer: a systematic review and meta-analysis. Clin Genitourin Cancer. 2019;17:409–18.

    Article  PubMed  Google Scholar 

  29. Mori K, Janisch F, Mostafaei H, Lysenko I, Karakiewicz P, Enikeev D, et al. Prognostic value of hemoglobin in metastatic hormone-sensitive prostate cancer: a systematic review and meta-analysis. Clin Genitourin Cancer. 2020;18:e402–9. https://pubmed.ncbi.nlm.nih.gov/32007439/

    Article  PubMed  Google Scholar 

  30. Wallis CJD, Klaassen Z, Bhindi B, Goldberg H, Chandrasekar T, Farrell AM, et al. Comparison of abiraterone acetate and docetaxel with androgen deprivation therapy in high-risk and metastatic hormone-naïve prostate cancer: a systematic review and network meta-analysis. Eur Urol. 2018;73:834–44. https://pubmed.ncbi.nlm.nih.gov/29037513/

    Article  CAS  PubMed  Google Scholar 

  31. Wang L, Paller CJ, Hong H, de Felice A, Alexander C, Brawley OW Comparative effectiveness of systemic treatments for metastatic castration-sensitive prostate cancer: A parametric survival network meta-analysis of randomized controlled trials. https://doi.org/10.1200/JCO20203815_suppl5532. 2020;38(15_suppl):5532–5532.

  32. Mori K, Mostafaei H, Motlagh RS, Pradere B, Quhal F, Laukhtina E, et al. Systemic therapies for metastatic hormone-sensitive prostate cancer: network meta-analysis. BJU International. 2021; Available from: https://doi.org/10.1111/bju.15507

  33. Mori K, Janisch F, Parizi MK, Mostafaei H, Lysenko I, Enikeev DV, et al. Prognostic value of alkaline phosphatase in hormone-sensitive prostate cancer: a systematic review and meta-analysis. Int J Clin Oncol. 2019;25:247–57. https://link.springer.com/article/10.1007/s10147-019-01578-9

    Article  PubMed  PubMed Central  Google Scholar 

  34. Metwalli AR, Rosner IL, Cullen J, Chen Y, Brand T, Brassell SA, et al. Elevated alkaline phosphatase velocity strongly predicts overall survival and the risk of bone metastases in castrate resistant prostate cancer. Urol Oncol. 2014;32:761. cited 2021 Available from: /pmc/articles/PMC4129955/

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Brown JE, Sim S. Evolving role of bone biomarkers in castration-resistant prostate cancer. Neoplasia 2010;12:685–96.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Funding

The original LATITUDE study was funded by Janssen Oncology. However, the employees of the funder had no role in study design, data collection, data analysis, data interpretation, and writing of the report. The corresponding author had full access to all data in the study and final responsibility for the decision to submit for publication.

Author information

Authors and Affiliations

Authors

Contributions

Conception and design: SR and SM. Administrative support: SM, CW, SR, DM, JM, and DS. Provision of study material or patients: SM, SM, SR, CW, and FS. Collection and assembly of data: SM, SR, YS, SM, FS, AUK, DM, and SG. Data analysis and interpretation: SR, YS. Manuscript writing: All authors. Final approval of manuscript: All authors. Accountable for all aspects of the work: All authors.

Corresponding authors

Correspondence to Soumyajit Roy or Shawn Malone.

Ethics declarations

Competing interests

Outside of this work, Dr. Malone has received honoraria from Astellas, Bayer, Janssen, and Sanofi; and travel and accommodations support from TerSera and Sanofi. Outside of this work, Dr. Morgan reports personal fees from Astellas, Bayer, Janssen, and TerSera. Dr. Roy reports a research grant from Abbvie-Canadian Association of Radiation Oncology. Dr. Wallis reports other from Janssen Oncology, other from SESEN Bio, outside the submitted work. Honoraria. Dr. Kishan reports personal fees and research support from ViewRay, Inc., and personal fees from Varian Medical Systems, Inc., and Intelligent Automation, Inc., outside the submitted work. Dr. Saad reports grants, personal fees, and non-financial support from Janssen, during the conduct of the study; grants, personal fees, and non-financial support from Astellas, grants, personal fees, and non-financial support from Bayer, outside the submitted work. Dr. Spratt reports personal fees from Blue Earth, personal fees from Janssen, personal fees from AstraZeneca, outside the submitted work. The other coauthors have no competing financial interests.

Additional information

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

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Roy, S., Sun, Y., Wallis, C.J.D. et al. Development and validation of a multivariable prognostic model in de novo metastatic castrate sensitive prostate cancer. Prostate Cancer Prostatic Dis 26, 119–125 (2023). https://doi.org/10.1038/s41391-022-00560-3

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41391-022-00560-3

This article is cited by

Search

Quick links