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E33

GENITOURINARY IMAGING |
RadioGraphics Update:
PI-RADS Version 2.1—A Pictorial Update

Andrei S. Purysko, MD
Editor’s Note.—Articles in the RadioGraphics Update section provide current knowl-
Andrew B. Rosenkrantz, MD edge to supplement or update information found in full-length articles previously
Ismail Baris Turkbey, MD published in RadioGraphics. Authors of the previously published article provide a
Katarzyna J. Macura, MD, PhD brief synopsis that emphasizes important new information such as technological
advances, revised imaging protocols, new clinical guidelines involving imaging, or

RADIOGRAPHICS UPDATE
updated classification schemes. Articles in this section are published solely online
Abbreviations: ADC = apparent diffusion co- and are linked to the original article.
efficient, BPH = benign prostatic hyperplasia,
DCE = dynamic contrast material–enhanced,
DWI = diffusion-weighted imaging, PI-RADS =
Prostate Imaging Reporting and Data System

RadioGraphics 2020; 40:E33–E37 Introduction


https://doi.org/10.1148/rg.2020190207
In 2019, the Prostate Imaging Reporting and Data System (PI-
RADS) steering committee published a document clarifying and up-
Content Codes:
dating the assessment categories and technical parameters described
From the Section of Abdominal Imaging and in PI-RADS version 2 (1,2). The update was considered necessary to
Nuclear Radiology Department, Cleveland
Clinic, Imaging Institute, 9500 Euclid Ave, JB3, address limitations and inconsistencies of the system that had been
Cleveland, OH 44195 (A.S.P.); Department of observed since its release in 2015. Because the overall framework of
Radiology, NYU Langone Medical Center, New
York, NY (A.B.R.); Molecular Imaging Pro-
the system was maintained, the updated version was termed PI-
gram, National Cancer Institute, Bethesda, Md RADS version 2.1 rather than version 3 (3). This article describes
(I.B.T.); and Department of Radiology and Ra- the changes in PI-RADS since our earlier review.
diological Sciences, Johns Hopkins University,
Baltimore, Md (K.J.M.). Received November
14, 2019; revision requested December 10 and Updates in Technical Parameters
received January 7, 2020; accepted January 24.
All authors have provided disclosures (see end of
article). Address correspondence to A.S.P. (e- T2-weighted Imaging
mail: puryska@ccf.org).
The update states that T2-weighted imaging should always be
©
RSNA, 2020 performed in the axial plane and in at least one orthogonal plane,
sagittal or coronal, to facilitate morphologic assessment of lesions.
Assessing lesions on axial images is challenging because of volume
averaging (eg, encapsulation of transition zone nodules). Axial im-
ages—acquired as straight axial images or as oblique axial images
perpendicular to the long axis of the prostate—are used to measure
the transverse diameter of the prostate. Sagittal images can be used
to measure the maximum anteroposterior and longitudinal diam-
eters. Those three diameters are multiplied by 0.52 to obtain the
prostate volume.
E34 November-December 2020 radiographics.rsna.org

Table 1: Updated Transition Zone Assessment

T2-weighted PI-RADS Assessment


Imaging DWI Category (likelihood
Appearance at T2-weighted Imaging* Score Score† of csPCa)
Normal-appearing transition zone (rare) or a 1 NA 1 (highly unlikely)
round completely encapsulated nodule (typical
nodule)
Mostly encapsulated nodule or homogeneous cir- 2 <4 2 (unlikely)
cumscribed nodule without encapsulation (atypi- ≥4 3 (equivocal)
cal nodule) or homogeneous mildly hypointense
area between nodules
Heterogeneous signal intensity with obscured 3 <5 3 (equivocal)
margins; includes other lesions that do not 5 4 (likely)
qualify as 2, 4, or 5
Lenticular or noncircumscribed, homogeneous, 4 NA 4 (likely)
moderately hypointense lesion that is <1.5 cm
in greatest dimension
Same as 4 but ≥1.5 cm in greatest dimension or 5 NA 5 (highly likely)
definite extraprostatic extension or invasive
behavior
Note.—csPCa = clinically significant prostate cancer, NA = not applicable.
*Dominant parameter.
†Ancillary parameter.

Diffusion-weighted Imaging Updates in Imaging


The update clarified that diffusion-weighted Interpretation Criteria
imaging (DWI) should be performed with at
least two b values, including one low b value set Transition Zone Assessment
at 0–100 sec/mm2 (although 50–100 sec/mm2 The criteria for T2-weighted imaging scores of 1
is preferred) and one intermediate b value set and 2 for transition zone lesions have been modi-
at 800–1000 sec/mm2. The data acquired with fied (Table 1). Because of the extremely com-
these b values are used to generate the appar- mon occurrence of benign prostatic hyperplasia
ent diffusion coefficient (ADC) map. In some (BPH), nodules with typical BPH features (ie,
systems, these data can also be used to gener- complete T2-weighted hypointense capsule) now
ate images with high b value (≥1400 sec/mm2), receive a score of 1. The update also clarifies that
which are needed for qualitative assessment nodules differing from the predominant imaging
of abnormalities seen at DWI. If high-b-value appearance of the background transition zone
images cannot be generated from the images should be scored. Nodules with an incomplete
obtained with low and intermediate b values, or absent capsule and areas with homogeneous
these images should be acquired separately to low signal intensity between the nodules now
avoid the kurtosis effect that manifests at DWI receive a T2-weighted imaging score of 2 (Fig 1).
with b values greater than 1000 sec/mm2. This In addition, in recognition of the role of DWI in
kurtosis effect can corrupt the calculation of the transition zone, transition zone lesions that
ADC values. receive a score of 2 at T2-weighted imaging are
to be upgraded to an assessment category of 3 if
Dynamic Contrast–enhanced Imaging they have a DWI score greater than or equal to
For dynamic contrast-enhanced (DCE) imag- 4. As in PI-RADS version 2, lesions that re-
ing, preference is given to three-dimensional ceive a T2-weighted imaging score of 3 are only
acquisitions over two-dimensional acquisitions upgraded to an assessment category of 4 if they
because of the better signal-to-noise ratio. In have a DWI score of 5. Representative examples
addition, a temporal resolution of no more than of lesions in the transition zone according to the
15 seconds instead of 10 seconds or less is now revised criteria are shown in Figure 2.
considered acceptable to mitigate the poten-
tial trade-off in image quality (eg, lower spatial DWI Criteria
resolution) associated with very high temporal As in PI-RADS version 2, the same set of DWI
resolutions. criteria applies to peripheral zone and transi-
RG  •  Volume 40  Number 7 Purysko et al  E35

Figure 1.  Diagram illustrates transition zone findings seen on axial high-b-value DWI and ADC images. A = lenticular or noncircum-
scribed, homogeneous, moderately hypointense lesion; B = heterogeneous signal intensity with obscured margins, includes other
lesions that do not qualify as scores 2, 4, or 5; C = mostly encapsulated nodule; D = homogeneous mildly hypointense area between
nodules; E = homogeneous circumscribed nodule without encapsulation; F = completely encapsulated nodule; G = completely en-
capsulated nodule with cystic change. EPE = extraprostatic extension.

tion zone lesions (Table 2). Changes were made Central Zone and Anterior Fibromuscular
in the criteria for DWI scores of 2 and 3. For a Stroma Assessment
score of 2, the previous morphologic descriptor Clarifications have been made regarding assess-
of indistinct was recognized to be unclear and ment of the central zone and anterior fibromus-
has been replaced with linear or wedge-shaped. cular stroma. If no abnormalities are identified in
For a DWI score of 3, the update indicates that these two normal anatomic regions, they do not
the abnormality needs to be discrete and dif- need to be reported separately. For the central
ferent from the background. In addition, the zone, focal early enhancement plus asymmetries
abnormality may have markedly hypointense at T2-weighted imaging, at DWI, or on the ADC
signal on ADC maps or markedly hyperintense map that cannot be explained by BPH may help
signal at DWI , but not both. The term marked, differentiate tumors from benign anatomy. For
which is used in scores 3 to 5, is also defined the anterior fibromuscular stroma, the assess-
in PI-RADS version 2.1 as a more pronounced ment criteria should be those of the zone from
signal intensity change than any other focus in which the lesion appears to arise (eg, if the focal
the same zone (2). abnormality arises from the transition zone, the
transition zone criteria should be used).
DCE MRI Interpretation
The binary (ie, positive or negative) DCE Considerations regarding
criteria have been clarified. DCE is considered Biparametric MRI
positive if it is focal and occurs earlier than or The PI-RADs update acknowledges the growing
contemporaneously with enhancement of adja- interest in using biparametric MRI (T2-weighted
cent normal prostatic tissues and corresponds imaging and DWI without DCE imaging) to
to suspicious findings at T2-weighted imaging reduce examination time and cost and elimi-
or DWI. DCE is considered negative if no early nate the risks associated with gadolinium-based
or contemporaneous enhancement is noted. In contrast agents. However, a number of concerns
addition, diffuse multifocal enhancement not regarding biparametric MRI are raised in the
corresponding to a focal finding at T2-weighted update and further research is encouraged. The
imaging or DWI and focal enhancement that update states that biparametric MRI should be
corresponds to BPH at T2-weighted imaging currently reserved for select clinical indications
(including ectopic BPH in the peripheral zone) and describes a number of situations in which
are also considered negative. multiparametric MRI is still preferred, including
E36 November-December 2020 radiographics.rsna.org

Figure 2. Representative examples of lesions in the transition zone according to the revised PI-RADS version 2.1 criteria. T2WI = T2-
weighted image, TZ = transition zone.
RG  •  Volume 40  Number 7 Purysko et al  E37

Table 2: Updated Peripheral Zone Assessment

DWI PI-RADS Assessment Category


Appearance at DWI* Score DCE† (Likelihood of csPCa)
No abnormality (ie, normal) on ADC map and at high-b- 1 NA PI-RADS 1 (highly unlikely)
value DWI
Linear or wedge-shaped hypointensity on ADC map or lin- 2 NA PI-RADS 2 (unlikely)
ear or wedge-shaped hyperintensity at high-b-value DWI
Focal (discrete and different from the background) hypoin- 3 Negative‡ PI-RADS 3 (equivocal)
tensity on ADC map or focal hyperintensity at high-b-val- Positive§ PI-RADS 4 (likely)
ue DWI, may be markedly hypointense on ADC map or
markedly hyperintense at high-b-value DWI, but not both
Focal markedly hypointense on ADC map and markedly 4 NA PI-RADS 4 (likely)
hyperintense at high-b-value DWI, <1.5 cm in greatest
dimension
Same as 4 but ≥1.5 cm in greatest dimension or definite 5 NA PI-RADS 5 (highly likely)
extraprostatic extension or invasive behavior
Note.—csPCa = clinically significant prostate cancer, NA = not applicable.
*Dominant parameter. DWI criteria used for the peripheral zone also apply for the transition zone.

Ancillary parameter.

Negative DCE: no early or contemporaneous enhancement or diffuse multifocal enhancement not correspond-
ing to a focal finding at T2-weighted imaging or DWI or focal enhancement corresponding to a lesion demon-
strating features of BPH at T2-weighted imaging (including features of extruded BPH in the peripheral zone).
§
Positive DCE: enhancement that is focal and occurs earlier than or contemporaneously with enhancement of
adjacent normal prostatic tissues and corresponds to a suspicious finding at T2-weighted imaging or DWI.

when clinical parameters indicate a high likeli- activities: disclosed no relevant relationships. I.B.T. Ac-
hood of clinically significant prostate cancer and tivities related to the present article: disclosed no relevant
relationships. Activities not related to the present article:
when adequate DWI cannot be performed.
cooperative research and development agreements with
Philips and NVIDIA; royalties from Invivo. Other ac-
Conclusion tivities: disclosed no relevant relationships. K.J.M. Ac-
Adjustments in the technical parameters and tivities related to the present article: disclosed no relevant
refinements in the interpretation criteria intro- relationships. Activities not related to the present article:
grants from Siemens Healthineers and Profound Medi-
duced in PI-RADS version 2.1 address important
cal; royalties from Elsevier. Other activities: disclosed no
limitations of the system’s predecessor. Further relevant relationships.
changes are expected to be made as more data
become available. References
1. Purysko AS, Rosenkrantz AB, Barentsz JO, Weinreb JC,
Disclosures of Conflicts of Interest.—A.S.P. Activi- Macura KJ. PI-RADS Version 2: a pictorial update. Radio-
ties related to the present article: support from Profound Graphics 2016;36(5):1354–1372.
Medical. Activities not related to the present article: grants 2. American College of Radiology. PI-RADS: Prostate Imaging
from the RSNA R&E Foundation; payment from the – Reporting and Data System. Version 2.1. https://www.acr.
American College of Radiology for development of edu- org/-/media/ACR/Files/RADS/Pi-RADS/PIRADS-V2-1.
cational presentations; support from Profound Medical; pdf?la=en. Published 2019. Accessed November 12, 2019.
3. Turkbey B, Rosenkrantz AB, Haider MA, et al. Prostate
research support provided to Invivo. Other activities: dis- Imaging Reporting and Data System Version 2.1: 2019
closed no relevant relationships. A.B.R. Activities related Update of Prostate Imaging Reporting and Data System
to the present article: disclosed no relevant relationships. Version 2. Eur Urol 2019;76(3):340–351.
Activities not related to the present article: institution re-
ceived royalties from Thieme Medical Publishers. Other

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