Roche uPath IVD User manual

Type
User manual

Roche uPath IVD is an advanced digital pathology system designed to assist pathologists in the evaluation and analysis of tissue samples. With its powerful image analysis capabilities, uPath IVD offers a range of features to enhance diagnostic accuracy and streamline the pathology workflow:

  • Whole Slide Imaging: uPath IVD enables the digitalization of entire glass slides, allowing pathologists to view and analyze high-resolution images of tissue sections on a computer screen.

  • Image Annotation: The system provides tools for annotating and marking specific regions of interest within the digital slides, facilitating effective communication and collaboration among pathologists.

Roche uPath IVD is an advanced digital pathology system designed to assist pathologists in the evaluation and analysis of tissue samples. With its powerful image analysis capabilities, uPath IVD offers a range of features to enhance diagnostic accuracy and streamline the pathology workflow:

  • Whole Slide Imaging: uPath IVD enables the digitalization of entire glass slides, allowing pathologists to view and analyze high-resolution images of tissue sections on a computer screen.

  • Image Annotation: The system provides tools for annotating and marking specific regions of interest within the digital slides, facilitating effective communication and collaboration among pathologists.

uPath PD-L1 (SP263) image analysis for
Non-Small Cell Lung Cancer
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
Data Security 7
Workflow for using the uPath PD-L1 image analysis for NSCLC Algorithm 8
Pathologist Workflow 9
PD-L1 Image Analysis 12
PD-L1 Evaluation 15
PD-L1 Algorithm Stain Evaluation 15
Staining Characteristics 15
Performance Characteristics 26
Method Comparison 26
Pathologist Reproducibility Studies 27
Scanner Reproducibility Studies 28
Troubleshooting 29
References 33
Introduction
The Roche uPath enterprise software (uPath enterprise software)
with the uPath PD-L1 (SP263) image analysis for Non-Small Cell
Lung Cancer (NSCLC) algorithm (uPath PD-L1 (SP263) image
analysis for NSCLC algorithm) is a software system designed to
assist in the quantitative assessment of protein expression in
immunohistochemically (IHC) 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 PD-L1 (SP263) image analysis for NSCLC
algorithm is an adjunctive computer-assisted methodology to aid
in the acquisition and measurement of images from microscope
glass slides of tissue specimens IHC-stained for the presence
of PD-L1 protein. To assure the validity of image analysis scores,
it is the responsibility of the pathologist to verify agreement by
employing appropriate controls as specified in the VENTANA
PD-L1 (SP263) Rabbit Monoclonal Primary Antibody method
sheet (available at www.ventana.com).
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 1
2 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
Algorithm Summary and Explanation
For the image analysis applications, the pathologist may use 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 PD-L1 (SP263)
image analysis for NSCLC algorithm. A count of the total number
of target TC is generated and tumor cells (TC) are stratified by
whether they are stained or unstained. The uPath PD-L1 (SP263)
image analysis for NSCLC algorithm divides the stained TC by
the total number of TC (stained and unstained) to generate the
PD-L1 TC Positivity score on a scale of 0-100%. The uPath PD-L1
(SP263) image analysis for NSCLC algorithm can generate a
score for a particular ROI, or an aggregate score for all selected
ROIs on that slide. Though the algorithm detects non-tumor
cells as part of the overall analysis, the overlay and output only
shows the TC used in the calculation of TC Positivity score. The
pathologist can accept the score provided by the uPath PD-L1
(SP263) image analysis for NSCLC algorithm, or may override
the score with a different score. The pathologist must carefully
review to what the algorithm has marked as positive and negative
TC and confirm the algorithm is correct or provide a manual
override. The uPath PD-L1 (SP263) image analysis for NSCLC
algorithm does not make 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. It is designed and indicated as
an aid to the pathologist for the assessment of PD-L1 expression
at the 50%.
Intended Use
Purpose of Algorithm Guide
This uPath PD-L1 (SP263) image analysis for NSCLC Algorithm
Guide (Algorithm Guide) is intended to:
Provide background information on the intended use of the
uPath PD-L1 (SP263) image analysis for NSCLC algorithm, test
principles and limitations.
Define the necessary materials, IT, data security and network
requirements.
Show step-wise directions for running the uPath PD-L1 (SP263)
image analysis for NSCLC algorithm.
Provide photographic images that illustrate how the uPath
PD-L1 (SP263) image analysis for NSCLC algorithm should be
used.
Provide pathologists with a tool to facilitate the use of the uPath
PD-L1 (SP263) image analysis for NSCLC algorithm on FFPE
NSCLC sections stained with the VENTANA PD-L1 (SP263)
Assay.
Provide example images of challenging cases to provide
guidance on how to use the uPath PD-L1 (SP263) image
analysis for NSCLC algorithm in their evaluation.
Show performance characteristics of the uPath PD-L1 (SP263)
image analysis for NSCLC algorithm.
Intended Use of product
The uPath PD-L1 (SP263) Image Analysis for NSCLC algorithm is
intended for use as an aid to the pathologist in the detection and
semi-quantitative measurement of PD-L1 protein in formalin-
fixed, paraffin-embedded NSCLC tissue. When used with the
VENTANA PD-L1 (SP263) Assay, it is indicated for use as an aid
in identifying patients with NSCLC for treatment with therapies
with the ≥ 50% PD-L1 TC positivity cutoff in accordance with the
approved therapeutic product labeling.
Note: The uPath PD-L1 (SP263) Image Analysis for NSCLC is
an adjunctive computer-assisted methodology to aid in the
acquisition and measurement of images from microscope glass
slides of tissue specimens IHC-stained for the presence of
PD-L1 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 PD-L1
(SP263) Assay method sheet (P/N 741-4905).
This algorithm is intended for in vitro diagnostic (IVD) use.
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 3
Clinical Significance
Lung cancer has been the most common cancer in the world for
several decades and remains the leading cause of cancer deaths
worldwide. It is estimated to account for 12.9% of all new cancer
cases and is responsible for nearly 1.76 million deaths annually
worldwide, or approximately one in five cancer-related deaths.
NSCLC, is the most common type of lung cancer accounting
for approximately 85% of all lung cancer cases. The majority of
patients with NSCLC present with inoperable, locally advanced
disease (Stage IIIB) or metastatic disease (Stage IV), neither of
which currently has any curative treatment options. The 5-year
relative survival rate for NSCLC diagnosed in advanced stages is
4.7%.
The programmed death-ligand 1 (PD-L1) is a transmembrane
protein expressed on activated T cells that downregulates the
immune response by binding to its two inhibitory receptors
programmed death-1 (PD-1) and B7-1 (CD80). Binding of PD-
L1 with PD-1 inhibits T cell proliferation, cytokine production,
and cytolytic activity, leading to the functional inactivation or
exhaustion of T cells. PD-L1 also binds with CD80 on antigen
presenting cells and activated T cells mediating downregulation
of immune responses, including inhibition of T-cell activation
and cytokine production. PD-L1 expression is observed in
immune cells and TC.  Aberrant expression of PD-L1 on TC
has been reported to impede anti-tumor immunity, resulting in
immune evasion.  The emergence of immunotherapies that
interrupt the PD-L1 / PD-1 pathway have been shown to improve
survival rates for patients diagnosed with NSCLC. However,
prognosis with treatment is dependent on the level of PD-L1
expression and therefore requires quantification of PD-L1 with
immunohistochemical staining.
Immunohistochemistry can be used to detect specific antigens
present in tissue samples, making it an effective tool for
pathologists in their diagnosis and prognosis of carcinomas. The
VENTANA PD-L1 (SP 263) Assay is a rabbit monoclonal antibody
intended for laboratory use for the semi-quantitative detection
of PD-L1 protein in sections of FFPE normal and neoplastic
tissue. An advantage of histological tissue preparations is that
intact tissue allows morphology to aid in the interpretation of
the PD-L1 positivity of the patient sample. All histological tests
should be interpreted by a specialist in NSCLC morphology,
and/or pathology. The results should be complemented by
morphological studies, proper controls and used in conjunction
with other clinical and laboratory data.
4 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
Test Principles
The uPath enterprise software with the uPath PD-L1 (SP263)
image analysis for NSCLC algorithm employs image analysis
techniques to obtain a TC Positivity score.
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
uses pre-defined parameters to score images of tissue stained
with the VENTANA PD-L1 (SP263) Assay.
Steps involved in image analysis:
Identification of white space and automatic exclusion from
analysis.
Detection of cells across the entire image.
Classification of cells as TC or other cell types.
Identification of stained versus unstained TC.
Computation of the TC Positivity score by dividing the number of
stained TC by the total number of TC according to the VENTANA
PD-L1 (SP263) Assay method sheet.
How uPath PD-L1 (SP263) image analysis for NSCLC
algorithm identifies TC and how the score is calculated:
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
identifies TC using color, intensity, size and morphological
features.
Identified TC are classified as stained using detected membrane
and pre-set thresholds that are in line with the VENTANA PD-L1
(SP263) Assay method sheet.
To calculate the percentage of stained TC, the number of
stained TC is divided by the total number of TC according to the
VENTANA PD-L1 (SP263) Assay method sheet.
uPath PD-L1 (SP263) image analysis for NSCLC algorithm
white space determination:
The algorithm will automatically exclude white space. Artifacts
such as dirt, scratches or ink may not be automatically excluded.
The user may review the areas determined by the algorithm to
be white space using a false color overlay; see “PD-L1 Image
Analysis: False Color Overlay”.
The uPath PD-L1 (SP263) image analysis for NSCLC
algorithm’s criteria for generating the TC positivity score
output:
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
will report out a score to one digit in the tenths place, e.g. “4.8%”.
It is not recommended to round the score up or down. For
example, “4.8%” should not be rounded up to 5%.
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 5
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm is
designed to work for VENTANA PD-L1 (SP263) Assay. 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 PD-L1 (SP263)
Assay staining run by manual microscopic examination of the
PD-L1 control slides to verify that the expected results have been
obtained before images of slides are accessioned onto the uPath
enterprise software for analysis.
Use the manufacturer's recommendations for the VENTANA
PD-L1 (SP263) Assay, including all positive and negative quality
control materials for each staining run. If the control slides are
not acceptable with manual microscopic examination, restain the
tissue with acceptable results.
The pathologist must follow the recommendations for VENTANA
PD-L1 (SP263) Assay interpretation.
Refer to the VENTANA PD-L1 (SP263) Assay method sheet (P/N
1014258EN) and interpretation guide (P/N 1015317EN) (available
at www.ventana.com).
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
is designed for use 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 PD-L1 (SP263) image analysis for NSCLC algorithm
may generate incorrect scores if the captured images have
abnormal staining (nuclear, cytoplasm, etc.).
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
will 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 nuclei may need to be evaluated
manually.
Limitations
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
has been trained, developed, and validated on NSCLC tissue
samples.
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
has not been tested, or its safety and effectiveness validated,
when used with a personal computer (PC) from home.
The uPath PD-L1 SP263 image analysis algorithm is indicated for
use as an aid in identifying patients with NSCLC for treatment
with therapies with the 50% PD-L1 TC positivity cutoff in
accordance with the approved therapeutic product labeling.
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm
may misidentify cells due to the presence of weak cytoplasmic
and/or membranous staining, strong immune cell staining
overlapping with tumor cell staining where there is significant
intermixed inflammation, TC with cytoplasmic blush, and non-
target staining. This may result in misidentification of TC as non-
TC, and of non-TC as positive TC.
Although it is required for macrophages to be excluded from
the region of analysis, it is not always possible to exclude all
macrophages. As a result, the score generated by the uPath
PD-L1 (SP263) image analysis for NSCLC algorithm may be
influenced by the macrophages in the ROI being analyzed. This is
critical when a patient score is close to the cutoff of 50%.
Cytoplasmic staining is generally diffuse with some cases
displaying a fine granular quality. Rare cases have shown a
perinuclear dot-like body staining with variable intensity. The
total percentage of tumor membrane signal intensities is visually
estimated and used to generate the PD-L1 expression level.
Tumor cell cytoplasmic staining is disregarded for determining
PD-L1 expression. An isotype matched negative control antibody
is used to evaluate the presence of background in test samples
and establish a staining intensity baseline.
6 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
Data Security
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 trafc.
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.
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 7
Workflow for using the uPath PD-L1 image analysis for NSCLC Algorithm
Materials needed
uPath enterprise software
uPath PD-L1 (SP263) image analysis for NSCLC algorithm
NSCLC tissue slides stained with the VENTANA PD-L1 (SP263) Assay (using OptiView DAB IHC Detection Kit) on the BenchMark
ULTRA instrument
VENTANA DP 200 slide scanner
Workflow
1. An NSCLC tissue sample on a glass slide is stained with the VENTANA PD-L1 (SP263) Assay 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 PD-L1 (SP263) image analysis for NSCLC 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 completed, the pathologist is notified within the uPath enterprise software that “analysis is complete.” The pathologist is
now able to select specific ROIs to score. A pathologist may select a single ROI of any size or multiple ROIs. If multiple ROIs are selected,
an aggregate score is provided as well as an individual score for each ROI.
Staining
Tissue preparation and staining should follow the recommendations provided in the VENTANA PD-L1 (SP263) Assay method sheet.
All proper controls should be reviewed and slides should be restained if the staining does not meet the guidelines outlined in the
VENTANA PD-L1 (SP263) Assay method sheet.
The uPath PD-L1 (SP263) image analysis for NSCLC algorithm requires use of the VENTANA PD-L1 (SP263) Assay, and any additional
material or supplies listed in the VENTANA PD-L1 (SP263) Assay method sheet, to stain tissues prior to analysis. The VENTANA PD-L1
(SP263) Assay detects PD-L1 protein in FFPE NSCLC tissue stained with the OptiView DAB IHC Detection Kit on a BenchMark ULTRA
instrument. Though the VENTANA PD-L1 (SP263) Assay detects PD-L1 protein in FFPE NSCLC tissue stained on thee BenchMark
ULTRA instruments, the uPath PD-L1 (SP263) image analysis for NSCLC algorithm was validated using the OptiView DAB IHC
Detection Kit stained on the BenchMark ULTRA instrument.
Image Capture
The VENTANA DP 200 slide scanner is required for scanning of the slides. Images are required to be scanned at 20x magnification.
If large sections of the image are out of focus, it s recommended that the slides be rescanned. For further information on scanning,
please refer to the VENTANA DP 200 slide scanner User Manual (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 PD-L1 (SP263) image
analysis for NSCLC algorithm only. For further information on the uPath enterprise software, please refer to the uPath enterprise
software User Guide.
8 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
Pathologist Workflow
Opening a Case
Images of NSCLC tissue stained with the VENTANA PD-L1 (SP263) Assay can be accessed by double-clicking on a case or by
selecting a case and pressing the viewer tab within uPath enterprise software (Figure 1).
A screen with all images associated with a case will appear (Figure 2).
Figure 2
Figure 1
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 9
Once a glass slide stained with the VENTANA PD-L1 (SP263) Assay 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 PD-L1 (SP263) image analysis for NSCLC
algorithm will automatically trigger WSA. Times to complete the WSA precomputing step depend on server specifications, image sizes
and 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 and 4). Once the image is completely analyzed via WSA
in the uPath enterprise software, “analysis successful” will be displayed underneath the slide image within the viewer in the uPath
enterprise software (Figure 5). Images cannot be scored prior to successful WSA completion.
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 6 Figure 7
Figure 8
Figure 5
Figure 4
Figure 3
10 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) 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 algorithm, and the stained and unstained TC 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 Freehand exclusions, 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 do the
following:
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 10Figure 9
Figure 11 Figure 12
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 11
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, select the Image Analysis button
either within the Slide Panel (Figure 13) or next to the ROI (Figure 14).
Once the PD-L1 Analysis is complete, the result will appear 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 tumor cell positivity status across all selected ROI(s), which is the score
that will appear in the report.
PD-L1 Image Analysis
Figure 15
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 will also hide this information.
Figure 17
Figure 16
Figure 13 Figure 14
12 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
PD-L1 Image Analysis: False 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 circles represent cells determined to be positively stained for PD-L1 and blue circles represent cells
determined to be negative for PD-L1. When grabbing the image (left-clicking with the mouse and moving the image) the overlay will
disappear (Figure 19). When the mouse button released, the overlay reappears (Figure 18).
Figure 18
Figure 19
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 13
Manual Override Slide Score Entry
Scores can be manually overridden by clicking on the Slide Score flip-out icon within the Slide Panel next to the Slide Score (Figure
16). The Slide Score flip-out will appear (Figure 20). Selecting the edit button (Figure 20) on the Slide Score flip-out allows the user to
type in a manual score (Figure 21). The Comments field allows notes regarding the case and/or decision to override the automated
score. For PD-L1, scores of 0-100% may be manually entered. Upon entry of a Manual Override score, select the confirm notification
(Figure 22). A confirmation message will appear, select “Yes”.
The score within the Slide Panel will now reflect the manual override score. The image analysis score provided next to the ROI(s) will no
longer be present (Figure 23). The user will have the option to re-analyze the image by pressing the bar graph button (Figure 13, Figure
14).
Figure 21 Figure 22
Figure 20
Figure 23
14 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
Please see the VENTANA PD-L1 (SP263) Assay method sheet and Interpretation Guide.
PD-L1 Evaluation
NSCLC neoplastic cells labeled with the VENTANA PD-L1 (SP263) Assay are evaluated for percent positivity of the TC with membrane
staining at any intensity. The immunohistochemical staining in NSCLC is membranous and/or cytoplasmic, and may be expressed
homogeneously or heterogeneously throughout the neoplasm. Tumor cell cytoplasmic staining is not factored into the TC positivity
score. Membrane staining can have a discontinuous, circumferential or basolateral pattern. An isotype-matched negative control
antibody is used to evaluate the presence of background in test samples.
PD-L1 Algorithm Stain Evaluation
The pathologist using the uPath PD-L1 (SP263) image analysis for NSCLC algorithm should be familiar with manually scoring the
VENTANA PD-L1 (SP263) Assay. The pathologist should use the freehand tool to circle the whole tumor area. The pathologist should
reference the associated H&E and negative control slide prior to using the uPath PD-L1 (SP263) image analysis for NSCLC algorithm.
When selecting the areas to be analyzed, please take into consideration the limitations described in the Limitations and the Areas to
avoid sections. If the pathologist disagrees with the score provided by the uPath PD-L1 (SP263) image analysis for NSCLC algorithm,
the pathologist should manually override the score.
Non-evaluable cases include, but are not limited to, cases with insufcient viable tumor, unacceptable morphology, and interfering
background. NSCLC cases with sufcient viable TC (as determined by the scoring pathologist) and no interfering background on the
PD-L1 IHC slide are acceptable for evaluation.
Staining Characteristics
uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide 15
Figure 24: Scanned images of IHC stained NSCLC tissue in uPath enterprise software; before analysis (above) and after
analysis (below). The red overlay represents cells determined to be positively stained TC and blue overlay represents cells
determined to be negatively stained TC.
Images of various staining patterns and PD-L1 expression levels are provided in the subsequent figures (24-25). PD-L1 expression in
TC is reported as a percentage (0-100).
16 uPath PD-L1 (SP263) image analysis for Non-Small Cell Lung Cancer (NSCLC) Algorithm Guide
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Roche uPath IVD User manual

Type
User manual

Roche uPath IVD is an advanced digital pathology system designed to assist pathologists in the evaluation and analysis of tissue samples. With its powerful image analysis capabilities, uPath IVD offers a range of features to enhance diagnostic accuracy and streamline the pathology workflow:

  • Whole Slide Imaging: uPath IVD enables the digitalization of entire glass slides, allowing pathologists to view and analyze high-resolution images of tissue sections on a computer screen.

  • Image Annotation: The system provides tools for annotating and marking specific regions of interest within the digital slides, facilitating effective communication and collaboration among pathologists.

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