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IMAGING
The
Utility of Magnetic Resonance Imaging and Spectroscopy for Predicting
Insignificant Prostate Cancer: an Initial Analysis
Shukla-Dave A, Hricak H, Kattan MW, Pucar D, Kuroiwa K, Chen HN, Spector
J, Koutcher JA, Zakian KL, Scardino PT
Department of Medical Physics, Memorial Sloan-Kettering Cancer Center,
New York, NY, USA
BJU Int. 2007; 99:786-93
- Objective:
To
design new models that combine clinical variables and biopsy data with
magnetic resonance imaging (MRI) and MR spectroscopic imaging (MRSI)
data, and assess their value in predicting the probability of insignificant
prostate cancer.
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Patients and Methods:
In all, 220 patients (cT stage T1c or T2a, prostate-specific antigen
level < 20 ng/mL, biopsy Gleason score 6) had MRI/MRSI before surgery
and met the inclusion criteria for the study. The probability of insignificant
cancer was recorded retrospectively and separately for MRI and combined
MRI/MRSI on a 0-3 scale (0, definitely insignificant; - 3, definitely
significant). Insignificant cancer was defined from surgical pathology
as organ-confined cancer of </= 0.5 cm (3) with no poorly differentiated
elements. The accuracy of predicting insignificant prostate cancer was
assessed using areas under receiver operating characteristic curves
(AUCs), for previously reported clinical models and for newly generated
MR models combining clinical variables, and biopsy data with MRI data
(MRI model) and MRI/MRSI data (MRI/MRSI model).
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Results: At
pathology, 41% of patients had insignificant cancer; both MRI (AUC 0.803)
and MRI/MRSI (AUC 0.854) models incorporating clinical, biopsy and MR
data performed significantly better than the basic (AUC 0.574) and more
comprehensive medium (AUC 0.726) clinical models. The P values for the
differences between the models were: base vs. medium model, < 0.001;
base vs. MRI model, < 0.001; base vs. MRI/MRSI model, < 0.001;
medium vs. MRI model, < 0.018; medium vs. MRI/MRSI model, < 0.001.
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Conclusions: The
new MRI and MRI/MRSI models performed better than the clinical models
for predicting the probability of insignificant prostate cancer. After
appropriate validation, the new MRI and MRI/MRSI models might help in
counseling patients who are considering choosing deferred therapy.
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Editorial Comment
Insignificant prostate cancer defined as pathologically organ-confined
cancer with a total volume of ≤ 0.5 cm 3 and no poorly differentiated
component (Gleason grade 4 or 5) on histology is not infrequent but
patients with this cancer are very difficult to identify clinically.
The authors presented their pioneering work emphasizing that after appropriate
validation this new magnetic resonance imaging (MRI) and MRI / magnetic
resonance spectroscopic imaging (MRSI) models, might improve the overall
accuracy of clinical models in predicting the likelihood of insignificant
prostate cancer .Information obtained with conventional MRI and with
magnetic resonance spectroscopic imaging were combined with clinical
variables and biopsy results in order to build this new clinical nomogram.
Both MRI models and the MRI/MRSI model were more accurate than the clinical
models for discriminating insignificant prostate cancer from significant
prostate cancer. Since MRSI is more specific than conventional MRI for
identification of prostate cancer, one could expect that the MRI/MRSI
model was the most discriminating (area under the curve 0.854) and performed
significantly better than MRI model alone and other clinical models.
As pointed out by the authors the major limitation of the model is that
they are vulnerable to upgrading of the biopsy Gleason grade after radical
prostatectomy; 26% of the patients of this series had their Gleason
scores upgraded. This was particularly important in 7% of the patients
of this series. The authors emphasizes that their goal was not produce
MRI models ready for clinical use, but rather to test the feasibility
of creating such models. In our institution, we already started a prospective
clinical study in order to validate this MRI/MRSI model.
Dr. Adilson Prando
Chief, Department of Radiology
Vera Cruz Hospital
Campinas, São Paulo, Brazil
E-mail: aprando@mpc.com.br
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