Skip to main content
Log in

The role of whole-lesion apparent diffusion coefficient analysis for predicting outcomes of prostate cancer patients on active surveillance

  • Published:
Abdominal Radiology Aims and scope Submit manuscript

Abstract

Purpose

To explore the role of whole-lesion apparent diffusion coefficient (ADC) analysis for predicting outcomes in prostate cancer patients on active surveillance.

Methods

This study included 72 prostate cancer patients who underwent MRI–ultrasound fusion-targeted biopsy at the initiation of active surveillance, had a visible MRI lesion in the region of tumor on biopsy, and underwent 3T baseline and follow-up MRI examinations separated by at least one year. Thirty of the patients also underwent an additional MRI–ultrasound fusion-targeted biopsy after the follow-up MRI. Whole-lesion ADC metrics and lesion volumes were computed from 3D whole-lesion volumes-of-interest placed on lesions on the baseline and follow-up ADC maps. The percent change in lesion volume on the ADC map between the serial examinations was computed. Statistical analysis included unpaired t tests, ROC analysis, and Fisher’s exact test.

Results

Baseline mean ADC, ADC0–10th-percentile, ADC10–25th-percentile, and ADC25–50th-percentile were all significantly lower in lesions exhibiting ≥50% growth on the ADC map compared with remaining lesions (all P ≤ 0.007), with strongest difference between lesions with and without ≥50% growth observed for ADC0–10th-percentile (585 ± 308 vs. 911 ± 336; P = 0.001). ADC0–10th-percentile achieved highest performance for predicting ≥50% growth (AUC = 0.754). Mean percent change in tumor volume on the ADC map was 62.3% ± 26.9% in patients with GS ≥ 3 + 4 on follow-up biopsy compared with 3.6% ± 64.6% in remaining patients (P = 0.050).

Conclusion

Our preliminary results suggest a role for 3D whole-lesion ADC analysis in prostate cancer active surveillance.

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

References

  1. Mottet N, Bellmunt J, Bolla M, et al. (2016) EAU-ESTRO-SIOG guidelines on prostate cancer. Part 1: screening, diagnosis, and local treatment with curative intent. Eur Urol. doi:10.1016/j.eururo.2016.08.003

    Google Scholar 

  2. National Institute for Health and Care Excellence Website (2014) Prostate cancer: diagnosis and management—clinical guideline 175. www.nice.org.uk/guidance/cg175. Accessed 21 October 2016

  3. National Comprehensive Cancer Network Website (2014) Prostate cancer, version 2.2014. https://www.nccn.org/professionals/physician_gls/f_guidelines.asp. Accessed 21 October 2016

  4. Klotz L, Zhang L, Lam A, et al. (2010) Clinical results of long-term follow-up of a large, active surveillance cohort with localized prostate cancer. J Clin Oncol 28:126–131

    Article  PubMed  Google Scholar 

  5. Obek C, Louis P, Civantos F, Soloway MS (1999) Comparison of digital rectal examination and biopsy results with the radical prostatectomy specimen. J Urol 161:494–498

    Article  CAS  PubMed  Google Scholar 

  6. Murphy G, Haider M, Ghai S, Sreeharsha B (2013) The expanding role of MRI in prostate cancer. AJR Am J Roentgenol 201:1229–1238

    Article  PubMed  Google Scholar 

  7. Kvåle R, Møller B, Wahlqvist R, et al. (2009) Concordance between Gleason scores of needle biopsies and radical prostatectomy specimens: a population-based study. BJU Int 103:1647–1654

    Article  PubMed  Google Scholar 

  8. Hu Y, Ahmed HU, Carter T, et al. (2012) A biopsy simulation study to assess the accuracy of several transrectal ultrasonography (TRUS)-biopsy strategies compared with template prostate mapping biopsies in patients who have undergone radical prostatectomy. BJU Int 110:812–820

    Article  PubMed  Google Scholar 

  9. Hoeks CM, Barentsz JO, Hambrock T, et al. (2011) Prostate cancer: multiparametric MR imaging for detection, localization, and staging. Radiology 261:46–66

    Article  PubMed  Google Scholar 

  10. Bjurlin MA, Meng X, Le Nobin J, et al. (2014) Optimization of prostate biopsy: the role of magnetic resonance imaging targeted biopsy in detection, localization and risk assessment. J Urol 192:648–658

    Article  PubMed  PubMed Central  Google Scholar 

  11. Ouzzane A, Renard-Penna R, Marliere F, et al. (2015) Magnetic resonance imaging targeted biopsy improves selection of patients considered for active surveillance for clinically low risk prostate cancer based on systematic biopsies. J Urol 194:350–356

    Article  PubMed  Google Scholar 

  12. Da Rosa MR, Milot L, Sugar L, et al. (2015) A prospective comparison of MRI-US fused targeted biopsy versus systematic ultrasound-guided biopsy for detecting clinically significant prostate cancer in patients on active surveillance. J Magn Reson Imaging 41:220–225

    Article  PubMed  Google Scholar 

  13. Siddiqui MM, Rais-Bahrami S, et al. (2013) Magnetic resonance imaging/ultrasound-fusion biopsy significantly upgrades prostate cancer versus systematic 12-core transrectal ultrasound biopsy. Eur Urol 64:713–719

    Article  PubMed  Google Scholar 

  14. Hu JC, Chang E, Natarajan S, et al. (2014) Targeted prostate biopsy in select men for active surveillance: do the Epstein criteria still apply? J Urol 192:385–390

    Article  PubMed  PubMed Central  Google Scholar 

  15. Stamatakis L, Siddiqui MM, Nix JW, et al. (2013) Accuracy of multiparametric magnetic resonance imaging in confirming eligibility for active surveillance for men with prostate cancer. Cancer 119:3359–6336

    Article  PubMed  Google Scholar 

  16. Yerram NK, Volkin D, Turkbey B, et al. (2012) Low suspicion lesions on multiparametric magnetic resonance imaging predict for the absence of high-risk prostate cancer. BJU Int 110:E783–E788

    Article  PubMed  Google Scholar 

  17. Siddiqui MM, Truong H, Rais-Bahrami S, et al. (2015) Clinical implications of a multiparametric magnetic resonance imaging based nomogram applied to prostate cancer active surveillance. J Urol 193:1943–1949

    Article  PubMed  Google Scholar 

  18. Barzell WE, Melamed MR, Cathcart P, et al. (2012) Identifying candidates for active surveillance: an evaluation of the repeat biopsy strategy for men with favorable risk prostate cancer. J Urol 188:762–767

    Article  PubMed  Google Scholar 

  19. Rais-Bahrami S, Türkbey B, Rastinehad AR, et al. (2014) Natural history of small index lesions suspicious for prostate cancer on multiparametric MRI: recommendations for interval imaging follow-up. Diagn Interv Radiol 20:293–298

    Article  PubMed  PubMed Central  Google Scholar 

  20. Walton Diaz A, Shakir NA, George AK, et al. (2015) Use of serial multiparametric magnetic resonance imaging in the management of patients with prostate cancer on active surveillance. Urol Oncol 33:202.e1–202.e7

    Article  Google Scholar 

  21. Sonn GA, Filson CP, Chang E, et al. (2014) Initial experience with electronic tracking of specific tumor sites in men undergoing active surveillance of prostate cancer. Urol Oncol 32:952–957

    Article  PubMed  PubMed Central  Google Scholar 

  22. Abdi H, Pourmalek F, Zargar H, et al. (2015) Multiparametric magnetic resonance imaging enhances detection of significant tumor in patients on active surveillance for prostate cancer. Urology 85:423–428

    Article  PubMed  Google Scholar 

  23. Tran GN, Leapman MS, Nguyen HG, et al. (2016) Magnetic resonance imaging-ultrasound fusion biopsy during prostate cancer active surveillance. Eur Urol. doi:10.1016/j.eururo.2016.08.023

    Google Scholar 

  24. Frye TP, George AK, Kilchevsky A, et al. (2016) MRI-TRUS guided fusion biopsy to detect progression in patients with existing lesions on active surveillance for low and intermediate risk prostate cancer. J Urol. doi:10.1016/j.juro.2016.08.109

    Google Scholar 

  25. Nassiri N, Margolis DJ, Natarajan S, et al. (2016) Targeted biopsy to detect Gleason score upgrading during active surveillance for men with low- vs. intermediate-risk prostate cancer. J Urol. doi:10.1016/j.juro.2016.09.070

    PubMed  Google Scholar 

  26. Donati OF, Mazaheri Y, Afaq A, et al. (2014) Prostate cancer aggressiveness: assessment with whole-lesion histogram analysis of the apparent diffusion coefficient. Radiology 271:143–152

    Article  PubMed  Google Scholar 

  27. Rosenkrantz AB, Triolo MJ, Melamed J, et al. (2015) Whole-lesion apparent diffusion coefficient metrics as a marker of percentage Gleason 4 component within Gleason 7 prostate cancer at radical prostatectomy. J Magn Reson Imaging 41:708–714

    Article  PubMed  Google Scholar 

  28. Rosenkrantz AB, Meng X, Ream JM, et al. (2016) Likert score 3 prostate lesions: Association between whole-lesion ADC metrics and pathologic findings at MRI/ultrasound fusion targeted biopsy. J Magn Reson Imaging 43:325–332

    Article  PubMed  Google Scholar 

  29. Meng X, Rosenkrantz AB, Mendhiratta N, et al. (2016) Relationship between prebiopsy multiparametric magnetic resonance imaging (MRI), biopsy indication, and MRI-ultrasound fusion-targeted prostate biopsy outcomes. Eur Urol 69:512–517

    Article  PubMed  Google Scholar 

  30. Rosenkrantz AB, Babb JS, Taneja SS, Ream JM (2017) Proposed adjustments to PI-RADS version 2 decision rules: impact on prostate cancer detection. Radiology 283:119–129

    Article  Google Scholar 

  31. Henderson DR, de Souza NM, Thomas K, et al. (2016) Nine-year follow-up for a study of diffusion-weighted magnetic resonance imaging in a prospective prostate cancer active surveillance cohort. Eur Urol 69:1028–1033

    Article  PubMed  Google Scholar 

  32. van As NJ, de Souza NM, Riches SF, et al. (2009) A study of diffusion-weighted magnetic resonance imaging in men with untreated localised prostate cancer on active surveillance. Eur Urol 56:981–987

    Article  PubMed  Google Scholar 

  33. Giles SL, Morgan VA, Riches SF, et al. (2011) Apparent diffusion coefficient as a predictive biomarker of prostate cancer progression: value of fast and slow diffusion components. AJR Am J Roentgenol 196:586–591

    Article  PubMed  Google Scholar 

  34. Rozenberg R, Thornhill RE, Flood TA, et al. (2013) Whole-tumor quantitative apparent diffusion coefficient histogram and texture analysis to predict gleason score upgrading in intermediate-risk 3 + 4 = 7 prostate cancer. AJR Am J Roentgenol 206:775–782

    Article  Google Scholar 

  35. Peng Y, Jiang Y, Antic T, et al. (2014) Validation of quantitative analysis of multiparametric prostate MR images for prostate cancer detection and aggressiveness assessment: a cross-imager study. Radiology 271:461–471

    Article  PubMed  Google Scholar 

  36. Peng Y, Jiang Y, Yang C, et al. (2013) Quantitative analysis of multiparametric prostate MR images: differentiation between prostate cancer and normal tissue and correlation with Gleason score—a computer-aided diagnosis development study. Radiology 267:787–796

    Article  PubMed  Google Scholar 

  37. Rosenkrantz AB, Ream JM, Nolan P, et al. (2015) Prostate cancer: utility of whole-lesion apparent diffusion coefficient metrics for prediction of biochemical recurrence after radical prostatectomy. AJR Am J Roentgenol 205:1208–1214

    Article  PubMed  PubMed Central  Google Scholar 

  38. Felker ER, Wu J, Natarajan S, et al. (2016) Serial Magnetic resonance imaging in active surveillance of prostate cancer: incremental value. J Urol 195:1421–1427

    Article  PubMed  Google Scholar 

  39. Mazaheri Y, Hricak H, Fine SW, et al. (2009) Prostate tumor volume measurement with combined T2-weighted imaging and diffusion-weighted MR: correlation with pathologic tumor volume. Radiology 252:449–457

    Article  PubMed  PubMed Central  Google Scholar 

  40. Scarpato KR, Barocas DA (2016) Use of mpMRI in active surveillance for localized prostate cancer. Urol Oncol 34:320–325

    Article  PubMed  Google Scholar 

  41. Recabal P, Ehdaie B (2015) The role of MRI in active surveillance for men with localized prostate cancer. Curr Opin Urol 25:504–509

    Article  PubMed  Google Scholar 

  42. Barrett T, Haider MA (2017) The emerging role of MRI in prostate cancer active surveillance and ongoing challenges. AJR Am J Roentgenol 208:131–139

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tsutomu Tamada.

Ethics declarations

Funding

This study was funded by Joseph and Diane Steinberg Charitable Trust.

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

Informed consent

The local institutional review board provided a waiver of the requirement for written informed consent.

Disclosures

Rosenkrantz (royalties from Thieme Medical Publishers). Taneja (consultant for Hitachi-Aloka; nonfinancial support from Biobot). Remaining authors (no disclosures).

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tamada, T., Dani, H., Taneja, S.S. et al. The role of whole-lesion apparent diffusion coefficient analysis for predicting outcomes of prostate cancer patients on active surveillance. Abdom Radiol 42, 2340–2345 (2017). https://doi.org/10.1007/s00261-017-1135-2

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00261-017-1135-2

Keywords

Navigation