Rui Wang1 and Xiaoying Wang1
1Peking University First Hospital, Beijing, People's Republic of China
Synopsis
We first investigated the
systemic outcome of a crowd underwent PSA-based screening and pre-biopsy
mp-MRI, and demonstrated the predictive role of pre-biopsy mp-MRI for PCa by using an
advanced machine learning-based approach. Here we answer one important question
at the beginning of the paper: (1) mp-MRI coupled with PSA screening program
can be used to detect PCa. By the constructed nomogram, the outcome of most patients could be accurately
predicted in the first 1-yr follow-up period if they received a pre-biopsy
mp-MRI examination, even without invasive TRUS biopsy.
Background
PSA-based screening has come
in for a lot of criticisms due to noticeable false positive results for
prediction of prostate cancer (PCa). Purpose
To
investigate whether a machine learning analysis of multi-parametric (mp) MRI
can help to improve the predictive performance in PCa. Design, setting, and participants
Based on a support vector
machine classification analysis, we modeled clinical data (age, PSA, DRE, TRUS,
PSAD, prostate volume) and mp-MRI findings on 985 men between Jan 2002 and Dec
2009 to predict the probability of PCa. The model was validated on 493 patients
treated at a same institution during the same period. Median follow-up in the
training and validation cohorts was 40 and 38 mo, respectively.Measurements
5-yr rate of PCa were
measured.Results and limitations
At 5-yr follow-up period,
34.3% of patients had systemic progression of PCa. By adding mp-MRI findings, the
machine learning-based model increased area under curve (Az) from 0.715 to
0.938 (p < 0.001), sensitivity from 27.4% to 83.5% (p < 0.001), positive
predictive value (PPV) from 57.7% to 77.4% (p = 0.004), and negative predictive
value (NPV) from 71.3% to 91.5% (p < 0.001). Scaled by PSA level, the model
had high PPV (93.6%) in patients with PSA > 20 ng/ml, while with
intermediate to low PPVs in group of PSA 10-20 ng/ml (64%), PSA 4-10 ng/ml (55.8%)
and PSA 0-4 ng/ml (29%). Among all predictors, MR PI-RADS score had the highest
Cox hazard ratio (2.112; p < 0.001) associated with time to progression of
PCa, followed by PSA (1.435; p < 0.001), age (1.012; p = 0.043).
Discussion
To our knowledge, this is the
first prospective study to investigate the predictive role of pre-biopsy mp-MRI
for PCa with a long-term follow-up in 1478 consecutive patients. We report
that, at 5-yr follow-up period, 34.3% of patients had systemic progression of PCa,
and 29.6% was detected within initial 1-yr follow-up, while only 2.5% was
detected within the following 4-yr period. In addition, we noted that the machine
learning-based model using the input variables of clinical variables and mp-MRI
findings (SVM-MRI) shows high sensitivity (83.5%) and specificity (87.8%) to
predict PCa statistically more accurate (86.4%) than PSA-based screening
program. And importantly, the high negative predictive values of 91.5% made the
mp-MRI extraordinarily useful for initial evaluation before an invasive biopsy. Conclusion
We first investigated the
systemic outcome of a crowd underwent PSA-based screening and pre-biopsy
mp-MRI, and demonstrated the predictive role of pre-biopsy mp-MRI for PCa by using an
advanced machine learning-based approach. Here we answer one important question
at the beginning of the paper: (1) mp-MRI coupled with PSA screening program
can be used to detect PCa. By the constructed nomogram, the outcome of most patients could be accurately
predicted in the first 1-yr follow-up period if they received a pre-biopsy
mp-MRI examination, even without invasive TRUS biopsy.Acknowledgements
No acknowledgement found.References
No reference found.