Roche uPath IVD User manual

Type
User manual

Roche uPath IVD is a cutting-edge digital pathology solution that empowers pathologists with advanced image analysis and management capabilities. With its user-friendly interface, you can seamlessly acquire, manage, view, analyze, share, and report on digital pathology images. This innovative platform enables you to improve efficiency, accuracy, and collaboration in your pathology workflow.

Roche uPath IVD is a cutting-edge digital pathology solution that empowers pathologists with advanced image analysis and management capabilities. With its user-friendly interface, you can seamlessly acquire, manage, view, analyze, share, and report on digital pathology images. This innovative platform enables you to improve efficiency, accuracy, and collaboration in your pathology workflow.

uPath HER2 (4B5) image analysis for
Breast Algorithm Guide
Table of Contents
Introduction 1
Algorithm Summary and Explanation 2
Intended Use 3
Intended Use of Product 3
Purpose of Algorithm Guide 3
Clinical Significance 4
Test Principles 5
Limitations 6
Network Characteristics 7
Data Security 8
Workflow for Using the uPath HER2 (4B5) Algorithm 9
Pathologist Workflow 11
Staining Characteristics 18
VENTANA anti-HER2/neu (4B5) Antibody Evaluation 18
uPath HER2 (4B5) Algorithm Stain Evaluation 18
Performance Characteristics 30
Method Comparison 30
Pathologist Reproducibility Studies 31
Scanner Reproducibility Studies 32
Troubleshooting 33
References 37
Introduction
The Roche uPath enterprise software (uPath enterprise
software) with the uPath HER2 (4B5) image analysis for Breast
algorithm (uPath HER2 (4B5) algorithm) is a software system
designed to assist in the semi-quantitative assessment of human
epidermal growth factor receptor 2 (HER2) protein expression
in immunohistochemically stained histologic sections from
formalin-fixed, paraffin-embedded (FFPE) normal and neoplastic
tissues.
The uPath enterprise software is an end-to-end digital pathology
software solution that allows pathology laboratories to acquire,
manage, view, analyze, share, and report on digital images of
pathology specimens. Using the uPath enterprise software, the
pathologist can view digital images at various magnifications,
add annotations, make tissue section measurements, perform
image analysis, and generate reports.
Note: The uPath HER2 (4B5) image analysis for Breast algorithm
is an adjunctive computer-assisted methodology to aid in the
acquisition and measurement of images from microscope
glass slides of breast tissue specimens that have undergone
immunohistochemical staining to determine the presence of
HER2 protein. To assure the validity of image analysis scores,
it is the responsibility of the pathologist to verify agreement
and employ appropriate controls as specified in the VENTANA
anti-HER2/ne u (4B5) antibody method sheet (available at dialog.
roche.com).
1 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Algorithm Summary and Explanation
For image analysis applications, the pathologist uses the uPath
enterprise software to select and outline one or several regions
of interest (ROIs), and each ROI may be viewed at various
magnifications and then analyzed by the uPath HER2 (4B5)
algorithm. A count of the total number of target tumor cells
is generated, and tumor cells are stratified by whether they
are stained or unstained. Stained cells are stratified by stain
intensity and completeness of membrane staining. The uPath
HER2 (4B5) algorithm combines percent stained (stained,
unstained), stain intensity (weak, medium, strong) and stain
completeness (unstained, partial, complete) to generate a HER2
score on a scale of 0 to 3+. The uPath HER2 (4B5) algorithm can
generate a score for a particular ROI, or an aggregate score for
all selected ROIs on that slide. The pathologist may accept the
score provided by the uPath HER2 (4B5) algorithm, or override
the score with a different score. The uPath HER2 (4B5) algorithm
makes no independent interpretations of the data and therefore
should only be used by a qualified pathologist in conjunction
with histological examination, relevant clinical information, and
proper controls. The uPath HER2 (4B5) algorithm is designed and
indicated as an aid to the pathologist for the assessment of HER2
protein expression in breast tissue specimens stained with the
VENTANA anti-HER2/neu (4B5) antibody.
2 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Intended Use of Product
The uPath HER2 (4B5) image analysis for Breast algorithm
is intended for use as an aid to the pathologist in the semi-
quantitative detection of HER2 protein in formalin-fixed,
paraffin-embedded neoplastic breast tissue. When used with
the VENTANA anti-HER2/neu (4B5) Rabbit Monoclonal Primary
Antibody, (VENTANA anti-HER2/neu (4B5) antibody) it is
indicated for use as an aid in the assessment of breast cancer
patients for whom Herceptin® (trastuzumab), KADCYLA® (ado-
trastuzumab emtansine) or PERJETA® (pertuzumab) treatments
are being considered.
Note: The uPath HER2 (4B5) image analysis for Breast algorithm
is an adjunctive computer-assisted methodology to aid in the
acquisition and measurement of images from microscope
glass slides of breast tissue specimens that have undergone
immunohistochemical staining to determine the presence of
HER2 protein. To assure the validity of image analysis scores, it
is the responsibility of the pathologist to verify agreement and
employ appropriate controls as specified in the VENTANA anti-
HER2/neu (4B5) antibody method sheet.
This algorithm is intended for in vitro diagnostic (IVD) use.
Intended Use
Purpose of Algorithm Guide
This uPath HER2 (4B5) algorithm guide (algorithm guide) is
intended to:
Provide background information on the intended use of the
uPath HER2 (4B5) algorithm, test principles, and limitations.
Define the necessary materials, IT, data security, and network
requirements.
Show step-wise directions for running the uPath HER2 (4B5)
algorithm.
Provide photographic images that illustrate how the uPath HER2
(4B5) algorithm should be used.
Provide a tool to facilitate the use of the uPath HER2 (4B5)
algorithm on FFPE breast sections stained with the VENTANA
anti-HER2/ne u (4B5) antibody.
Provide example images of challenging cases to provide
guidance on how to use the uPath HER2 (4B5) algorithm in their
evaluation.
Show performance characteristics of the uPath HER2 (4B5)
algorithm.
3 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Clinical Significance
Breast cancer is the most common carcinoma occurring in
women, and the second leading cause of cancer related death.
1,2
In North America, a woman’s chance of contracting breast
cancer is one in eight.
1
Early detection and appropriate treatment
therapies can significantly affect overall survival.
3,4
Small tissue
samples may be easily used in routine immunohistochemistry
(IHC), making this technique, in combination with antibodies
that detect antigens important for carcinoma interpretation, an
effective tool for the pathologist in their diagnosis and prognosis
of disease. One important marker in breast cancer today is
the oncoprotein HER2.
5,6 ,7,8
The therapeutic drugs Herceptin
(trastuzumab), KADCYLA (ado-trastuzumab emtansine), and
PERJETA (pertuzumab), have been shown to benefit some breast
carcinoma patients by arresting, and in some cases reversing
the growth of their cancer.
5,6,7,8,9
The drugs are humanized
monoclonal antibodies that bind to HER2 protein on cancer
cells.
5,8,9,10
In vitro diagnostics for the evaluation of HER2 status in breast
cancer patients are important to aid the clinician in determination
of HER2-targeted therapy.
5,6 ,7,8
The VENTANA anti-HER2/neu
(4B5) antibody is intended for use in the IHC-based detection of
HER2 protein expression in breast cancer. The uPath HER2 (4B5)
algorithm functions as an accessory to the VENTANA anti-HER2/
neu (4B5) antibody to aid in the assessment of breast cancer
patients for whom Herceptin (trastuzumab), KADCYLA (ado-
trastuzumab emtansine), or PERJETA (pertuzumab) treatment is
being considered.
4 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Test Principles
Criteria for intensity and pattern of cell membrane staining
for the uPath HER2 (4B5) algorithm’s score:
Staining Pattern Score HER2 Staining
Assessment
No membrane staining is observed 0 Negative
Faint, partial staining of the
membrane in any proportion of the
cancer cells
1+ Negative
Weak to moderate complete staining
of the membrane, >10% of cancer
cells
2+ Equivocal*
Intense, complete staining of the
membrane, >10% of cancer cells
3+ Positive
* Recommend reflex to ISH
The uPath enterprise software with the uPath HER2 (4B5)
algorithm employs image analysis techniques to obtain a HER2
score.
The uPath HER2 (4B5) algorithm uses pre-defined parameters to
score images of tissue stained with the VENTANA anti-HER2/neu
(4B5) antibody.
Steps involved in image analysis:
Detection of cells across the entire image.
Classification of cells as tumor cells or other cell types.
Identification of stained membrane and stratification of
membrane into categories: partial or complete staining and
weak, medium, or strong intensity staining.
Computation of the HER2 score by combining cell classification,
stain intensity, and membrane classification.
How HER2 image analysis algorithm identifies tumor cells
and how the score is calculated:
The uPath HER2 (4B5) algorithm identifies tumor cells using
color, intensity, size and morphological features.
Identified tumor cells are classified as stained using detected
membrane and pre-set thresholds.
To calculate the HER2 score, the uPath HER2 (4B5) algorithm
uses the identified stained cells and stratifies them by stain
intensity and completeness.
5 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
The uPath HER2 (4B5) algorithm is designed to work with the
VENTANA anti-HER2/neu (4B5) antibody. The test results are
only as good as the quality and accuracy of the IHC slide that is
imaged, and the subsequent image that is analyzed.
The pathologist must validate the VENTANA anti-HER2/neu
(4B5) antibody staining run by manual microscopic examination
of the HER2 control slides to verify that the expected results have
been obtained before images of slides are accessioned onto the
uPath enterprise software for analysis.
The manufacturer’s recommendations must be followed for
the VENTANA anti-HER2/neu (4B5) antibody including using
all positive and negative quality control materials for each
staining run. If the control slides are not acceptable with manual
microscopic examination, the tissues need to be re-stained with
acceptable results.
The pathologist must follow the recommendations for VENTANA
anti-HER2/ne u (4B5) antibody interpretation.
The uPath HER2 (4B5) algorithm is designed to be used
by a qualified pathologist in conjunction with histological
examination, relevant clinical information, and proper controls. It
is not designed to be a standalone tool, and requires competent
human intervention throughout the analysis process.
The uPath HER2 (4B5) algorithm may generate incorrect scores
if the captured images have abnormal staining (nuclear staining,
pigmentation, etc.).
The uPath HER2 (4B5) algorithm may reject tumor nuclei that
are elongated regardless of the overall shape of the cell. For this
reason, tumors containing large numbers of cells with elongated
tumor nuclei may need to be evaluated manually.
The uPath HER2 (4B5) algorithm has been trained, developed,
and validated on: invasive lobular, ductal, mucinous, medullary,
papillary, and micropapillary carcinomas as well as a few
metastatic lesions.
The uPath HER2 (4B5) algorithm has not been tested, or its
safety and effectiveness validated, when used with a personal
computer (PC) from home.
The uPath HER2 (4B5) algorithm identifies DAB stained
membranes of any intensity and completeness. It uses a noise
threshold of 0.5% of all tumor cells to score a case as 1+. It
does not follow the method sheet guidelines of using a one cell
threshold for a score of 1+. This may result in some cases with
very few cells that have membrane staining being scored as 0
rather than 1+. This noise threshold was implemented to ensure
true negative cases are being called as 0.
The uPath HER2 (4B5) algorithm is designed to be sensitive to
the color brown (DAB staining) to ensure even faint membrane
staining is detected. For this reason, it can incorrectly score a
tissue sample containing brown artifacts such as pigmentation,
background staining in muscle fibers or any other artifacts that
are stained brown. There are tools within the uPath enterprise
software that will allow the pathologist to exclude such areas.
These are discussed in more detail in the staining characteristics
section.
The uPath HER2 (4B5) algorithm is designed to be sensitive for
2+ cases. For this reason, the uPath HER2 (4B5) algorithm may
incorrectly score certain 1+ cases as 2+. Specifically, 1+ cases
with slightly less than 10% of tumor cells with complete staining
or cases with a high amount of tumor cell cytoplasmic staining
may be incorrectly scored as 2+. The pathologist may need to
override the score in these particular types of cases. Cytoplasmic
staining is discussed in more detail in the staining characteristics
section.
Limitations
6 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
7 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Network Characteristics
A 1Gbps network connection between the uPath enterprise software and the image management system (IMS) is recommended.
Table 1. Roche uPath image analysis server specifications for small labs.
Parameter Details
Processor CPU @ 3.6 GHz
Number of cores 4
RAM 6 x 8GB (48 GB)
Hyper-threading Disabled
Hard disk 240 GB SSD
Operating system Microsoft Windows Server 2016
Virtual Machine (VM) support Yes
VM additional information Performance will be different to the physical servers due to VM overhead.
Antivirus Symantec Endpoint Protection Version 12
Power 110V/220V, 800 Watts (2)
Ports 2 USB, HPE Eth 10/25Gb Adaptor
Uninterruptible power supply Recommended
Table 2. Roche uPath image analysis server specifications for medium to large labs.
Parameter Details
Processor CPU @ 3.6 GHz (2 processors)
Number of cores 8 per processor / 16 in total
RAM 12 x 8GB (96 GB)
Hyper-threading Disabled
Hard disk 240 GB SSD (2x)
Operating system Microsoft Windows Server 2016
Virtual Machine (VM) support Yes
VM additional information Performance will be different to the physical servers due to VM overhead.
Antivirus Symantec Endpoint Protection Version 12
Power 110V/220V, 800 Watts (2)
Ports 2 USB, HPE Eth 10/25Gb Adaptor
Uninterruptible power supply Recommended
Malicious software or unauthorized instrument access can result
in data loss or instrument unavailability.
To avoid infection by malicious software or unauthorized access
and misuse of the instrument, the following recommendations
are essential:
Do not install or run any other software on the instrument.
Make sure that other computers and services on the network
are properly secured and protected against malicious software
and unauthorized access. For example, the laboratory
information system (LIS), archiving share, backup share, or
service.
Customers are responsible for the security of their local area
network, especially in protecting it against malicious software
and attacks. This protection might include measures, such as
a firewall, to separate the device from uncontrolled networks.
This protection might also include measures that ensure that the
connected network is free of malicious code.
Restrict physical access to the instrument and all attached IT
infrastructure (computers, cables, network equipment, and so
on).
Make sure that instrument backup and archive files are
protected from any unauthorized access and disaster. This list
includes the remote storage location, disaster discovery sites,
and the secure transfer of backup files.
If possible, use a firewall to restrict network traffic.
USB flash drives can be used for several kinds of backups and
restores. Wrong handling of a USB flash drive may result in data
loss or malfunction of the instrument.
Use only USB flash drives that are tested and installed by your
local Roche service representative.
At any one time only one USB device can be in use. Before
inserting a USB flash drive, check that no other USB device is
inserted.
Before removing a USB flash drive, choose the Eject button in
Windows.
The default operating system (OS) configuration provided with
the server should not be altered as this has implications on the
hardened OS configurations.
To prevent a virus from infecting the uPath enterprise software,
use the USB flash drive exclusively on the instrument. Do not
store other data on this USB flash drive.
Data Security
8 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Workflow for Using the uPath HER2 (4B5) Algorithm
Materials Provided
uPath HER2 (4B5) algorithm
Materials Required but not Provided
uPath enterprise software
Breast tissue slides stained with the VENTANA anti-HER2/neu (4B5) antibody, using the ultraView Universal DAB Detection Kit,
stained on a BenchMark ULTRA instrument.
VENTANA DP 200 slide scanner
Warnings and Precautions
1. For in vitro diagnostic (IVD) use.
2. For professional use only.
3. CAUTION: In the United States, Federal law restricts this device to sale by or on the order of a physician. (Rx Only)
4. To report suspected serious incidents related to this device, contact the local Roche representative and the competent authority of
the Member State or Country in which the user is established.
Workflow
1. The breast tissue on a glass slide is stained with the VENTANA anti-HER2/neu (4B5) antibody using a BenchMark ULTRA instrument.
2. Image acquisition (whole slide scanning) is performed with the VENTANA DP 200 slide scanner at 20x magnification at one z-plane.
3. Once digital images are acquired, these images are transferred from the computer associated with the VENTANA DP 200 slide
scanner to the image management system (IMS) on a centralized server.
4. Following transfer to the server, a case will be created in the uPath enterprise software. Case creation can occur automatically
through communication with the laboratory information system (LIS) using identification information (i.e., tissue type and primary
antibody) contained in the barcode label of the glass slide or entered manually into the uPath enterprise software. Refer to the uPath
enterprise software User Guide (PN 1018943EN).
5. If the uPath HER2 (4B5) algorithm is installed (must be installed on a separate server from the uPath enterprise software and the IMS)
and a 20x image is accessioned with the appropriate stain and tissue type, the uPath enterprise software then automatically triggers
whole slide analysis (WSA).
6. WSA automatically analyzes the entire scanned image.
7. Once WSA is complete, the pathologist is notified within the uPath enterprise software viewer with a blue bar that reads “analysis
successful”.
8. The pathologist may select specific ROIs to score using the ROI and Exclusion tools within the uPath enterprise software.
9. The pathologist reviews the image analysis results and either accepts the score or manually overrides it.
Staining
Tissue preparation and staining should follow the recommendations provided in the VENTANA anti-HER2/neu (4B5) antibody method
sheet.
All proper controls should be reviewed and slides should be re-stained if the staining does not meet the guidelines outlined in the
VENTANA anti-HER2/neu (4B5) antibody method sheet.
9 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
The uPath HER2 (4B5) algorithm requires use of the VENTANA anti-HER2/neu (4B5) antibody, and any additional material or supplies
listed in the VENTANA anti-HER2/neu (4B5) antibody method sheet, to stain tissues prior to analysis.
The VENTANA anti-HER2/neu (4B5) antibody detects HER2 protein in FFPE breast tissue stained with the ult raView Universal DAB
Detection Kit on a BenchMark ULTRA instrument.
Image Capture
A VENTANA DP 200 slide scanner is required for scanning the slides. Images are required to be scanned at 20x magnification. It
is recommended that the tissue be free of folds and ink. If large sections of the image are out of focus, it is recommended that the
slides be rescanned. For further information on scanning, please refer to the VENTANA DP 200 slide scanner IVD User Guide (PN
1017149EN).
General Navigation: uPath enterprise software
The uPath enterprise software is meant to be customizable to individual and site needs including but not limited to report
configuration and user interface. This algorithm guide will focus on the tools necessary for using the uPath HER2 (4B5) algorithm only.
For further information on the uPath enterprise software, please refer to the uPath enterprise software User Guide.
10 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Pathologist Workflow
Opening a Case in uPath Enterprise Software
To access images of breast tissue stained with the VENTANA anti-HER2/neu (4B5) antibody, double-click on a case, or select a case
and press the viewer tab (Figure 1).
A screen with all images associated with a case will appear (Figure 2).
Figure 2
Figure 1
11 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Once a glass slide stained with the VENTANA anti-HER2/neu (4B5) antibody is scanned on a VENTANA DP 200 slide scanner at
20x, the image is imported into the uPath enterprise software and associated with a case. The uPath HER2 (4B5) algorithm will
automatically trigger WSA. Times to complete the WSA precomputing step depends on server specifications, image sizes, and the
number of images in the queue. When displayed, “waiting to start auto-analysis” specifies the images are in queue and yet to be
analyzed and “analyzing” is used when WSA is being performed (Figures 3 & 4).
Once the image is completely analyzed via WSA in the uPath enterprise software, “analysis successful” is displayed underneath the
slide image within the viewer (Figure 5). Images cannot be scored prior to successful WSA completion.
Figure 5
Figure 4
Figure 3
12 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Drawing Whole Tumor ROI(s): Selecting Tumor Area
Use the Freehand tool button within the ROI dropdown menu (Figure 6) to select the tumor area(s) on the IHC slide image to be
analyzed. Figure 7 illustrates an image that has a single ROI drawn. Additional ROIs can be drawn. Each area selected will cause an
ROI to appear in the Slide Panel (Figure 8).
Figure 7
Figure 8
Figure 6
13 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Drawing Whole Tumor ROI(s): Exclusion Area
When drawing the ROIs, the exclusion of certain areas may be required; specific areas to be avoided or omitted as well as examples
will be addressed within the staining characteristics section below. Use the Freehand exclusion tool within the Exclusion dropdown
menu (Figure 9) to exclude specific areas (Figure 10). If large areas of the image are blurry or out of focus, rescan the slide.
Excluded areas will not be analyzed by the uPath HER2 (4B5) algorithm, and the stained and unstained tumor cells within this area
will be excluded from the total analysis area. If the ROI has already been analyzed, and an exclusion is used, the ROI will need to be
reanalyzed and the overlay and score will be updated appropriately.
Drawing a high number of exclusions, especially complicated exclusions using the Freehand tool, can be time consuming and impact
workflow efficiency with only a marginal impact on the final score. If a case requires a high number of exclusions, the pathologist
should
Draw multiple ROIs and exclude portions of tissue they deem unscorable with minimal use of the Exclusion tool.
Limit exclusions and manually override the score with another score.
Drawing Whole Tumor ROI(s): Deletion
If a selected whole tumor ROI is not optimal, it can be deleted. Select the whole tumor ROI by clicking on the center of the ROI on
the image and then clicking the Delete button within the Slide Panel (Figure 11) or within the slide image near the ROI (Figure 12). A
confirmation window will appear. Select Confirm to delete the selected ROI. Select Cancel to retain the ROI.
Figure 9
Figure 11
Figure 12
Figure 10
14 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
Once all whole tumor ROI(s) and/or exclusion areas have been drawn, the image is ready to be analyzed. Select the whole tumor ROI by
clicking on the center of the ROI to be analyzed or clicking on the ROI in the Slide Panel. For each ROI, click the Image Analysis button
either within the Slide Panel (Figure 13) or next to the ROI (Figure 14).
Once the HER2 analysis is complete, the result appears in the Slide Panel in two locations: under Slide Score and next to the ROIs
(Figure 15). The Slide Score is based on a summation of the HER 2 status across all selected ROI(s), which is the score that will appear
in the report.
You can also see more detailed information in the Slide Score flip-out and the ROI Details flip-out, by clicking the flip-out icon (Figure
16). The Slide Score flip-out will appear (Figure 17). Clicking the same flip-out icon again will also hide this information.
Figure 15
Figure 17
Figure 16
Figure 13
Figure 14
15 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
HER2 Image Analysis: Color Overlay
Once the ROI(s) Analysis button has been pressed and the tissue analyzed, a color overlay will be displayed on the ROI. In the image
below (Figure 18), the red overlay represents cell membranes determined to be positively stained for HER2. When grabbing the image
(left-clicking with the mouse and moving the image) the overlay disappears (Figure 19). When the mouse button is no longer pressed,
the overlay reappears (Figure 18).
Figure 18
Figure 19
16 uPath HER2 (4B5) image analysis for Breast Algorithm Guide
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Roche uPath IVD User manual

Type
User manual

Roche uPath IVD is a cutting-edge digital pathology solution that empowers pathologists with advanced image analysis and management capabilities. With its user-friendly interface, you can seamlessly acquire, manage, view, analyze, share, and report on digital pathology images. This innovative platform enables you to improve efficiency, accuracy, and collaboration in your pathology workflow.

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