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<article xmlns:xlink="http://www.w3.org/1999/xlink">
  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Ontology-Enhanced Representations of Non-image Data in The Cancer Imaging Archive</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Jonathan P. Bona</string-name>
          <email>jpbona@uams.edu</email>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Tracy S. Nolan</string-name>
          <email>tnolan@uams.edu</email>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Mathias Brochhausen</string-name>
          <email>mbrochhausen@uams.edu</email>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>Department of Biomedical Informatics University of Arkansas for Medical Sciences Little Rock</institution>
          ,
          <addr-line>Arkansas</addr-line>
          ,
          <country country="US">United States</country>
        </aff>
      </contrib-group>
      <pub-date>
        <year>2018</year>
      </pub-date>
      <fpage>7</fpage>
      <lpage>10</lpage>
      <abstract>
        <p>-The Cancer Imaging Archive (TCIA) hosts over 11 million de-identified medical images related to cancer for research reuse. These are organized around DICOM-format radiological collections that are grouped by disease type, modality, or research focus. Many collections also include diverse non-image datasets in a variety of formats without a common approach to representing the entities that the data are about. This paper describes work to make these diverse non-image data more accessible and usable by transforming them into integrated semantic representations using Open Biomedical Ontologies, highlights obstacles encountered in the data, and presents detailed representations data found in select collections.</p>
      </abstract>
      <kwd-group>
        <kwd>cancer</kwd>
        <kwd>imaging</kwd>
        <kwd>ontology development</kwd>
        <kwd>semantics</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>I. INTRODUCTION</title>
      <p>
        Since 2011 the Cancer Imaging Archive [
        <xref ref-type="bibr" rid="ref1">1</xref>
        ] has been NCI’s
primary resource for acquiring, curating, managing and
distributing images and related data to support Cancer Research.
TCIA hosts over 11 million de-identified medical images of
cancer for research reuse, organized around DICOM-format
radiological collections related by disease type, modality, or
research focus. The PRISM (Platform for Imaging in Precision
Medicine) initiative seeks to sustain and expand TCIA’s
capabilities to meet the rapidly evolving requirements of cancer
Precision Medicine research. Through discussions with
investigators in the imaging and cancer research communities,
and through review of TCIA helpdesk tickets, we have identified
a number of near-term goals and challenges. These include
enhanced support for reproducible research and data publication
capabilities; expanded support for additional data types,
including pathology data, and radiomics and pathomics feature
sets; uniform management of non-image data; semantic query
mechanisms and enhanced data exploration; and automatic
curation of current and new data types.
      </p>
      <p>Many TCIA collections include non-image data in a variety
of formats, often as downloadable spreadsheet files without a
common representation scheme. These include patient
demographics, diagnoses, treatments, outcomes, TNM staging,
gene assays and other test results, etc. Some collections provide
data dictionaries or other documentation that aid the human
reader in interpreting these data. However, these are not
machine-interpretable, and hence are difficult to query.
Complicating this is the use of different representations schemes
in different collections to encode the same or similar
information.</p>
      <p>This paper describes work to make these diverse non-image
data more accessible and usable. Our immediate aims are to: 1)
make these data sets queryable; 2) make them
computerinterpretable, and hence available for automated reasoning and
more amenable to exploration and analysis; and 3) establish
links between related data across collections and across data
types.</p>
      <p>To support these aims we are converting these data into
common, semantically-enhanced representations using Open
Biomedical Ontologies Foundry [2] resources, and integrating
the results in a single repository with this shared representation,
to facilitate queries such as “Which patients in lung cancer
collection have been diagnosed with metastatic colon cancer,
and how was that diagnosis obtained?”, or “Which patients
across multiple head and neck cancer collections have tumors
specifically in their oropharynx, and have been diagnosed with
human papillomavirus, and how were those diagnoses
obtained?”</p>
      <p>By using ontologies and semantic web technology we are
making these data more readily available for query, automated
reasoning, exploration, and analysis. TCIA users in general are
not familiar enough with biomedical ontologies and semantic
web technology to write SPARQL queries to access data. This
semantic repository with transformed non-image data will serve
as the back-end data store for user-friendly tools that support
search and exploration of the data.</p>
    </sec>
    <sec id="sec-2">
      <title>II. NON-IMAGE DATA IN TCIA COLLECTIONS</title>
      <sec id="sec-2-1">
        <title>A. Overview</title>
        <p>The Cancer Imaging Archive currently has 74
publiclyavailable collections. We reviewed and compared the
deidentified non-image data provided with these collections as a
first step toward crafting a semantic representation useable to
represent the bulk of non-image data in TCIA collections.</p>
        <p>A large group of 18 of the public collections is provided by
The Cancer Genome Atlas [3]. These collections, whose names
all start with “TCGA”, structure their data using a common,
standardized representation scheme that is published as an RDF
file in Turtle format [4]. TCGA linked data has also been
exposed as a SPARQL endpoint [5]. Our work to integrate
nonimage data from all TCIA collections into a single repository
will be made much easier in the case of TCGA collections
because of their use of a standard scheme and semantic web
technology. Throughout this paper we discuss and describe only
non-TCGA public collections, because those are the collections
that best illustrate the diversity of available data and data
representations, and the need for improved representations.</p>
        <p>Of the 56 non-TCGA public collections, 17 include
downloadable non-image data (often labeled “clinical data”).
This is in addition to, and separate from, the image metadata
present in many collections. We have manually reviewed each
of the files provided with these collections. This section provides
a summary and discussion that illustrate the richness and
diversity of the data available, and the diversity of representation
schemes currently used. This diversity poses significant
challenges to integration of the non-image data, but also poses
an unique opportunity to vastly improve the usability of this data
with semantic web technology and biomedical ontologies.</p>
        <p>The current submission process for TCIA non-image data
does not specify the use of any common data model or schema,
or require adherence to any specified semantics. This leads to
some of the submitted data being ambiguous, or difficult to
interpret. The semantically-rich representations that we are
designing for this data, as presented in this paper, will become
part of new submission tools TCIA that automate this curation
as much as possible.</p>
        <p>The non-image data contained in these 17 collections can be
placed into 7 major categories: diagnosis, histology, genetic
testing, demographics, treatment, morbidity, and neurological
testing. The latter is a category only found in one of the
collections that currently provide non-imaging data. Most of
those categories are already broken down into subcategories.
E.g. “treatment” is broken down into “primary: chemo”,
“primary: surgery”, and “primary: radiation”, and “adjuvant”.
Table I below indicates for each of these 17 collections the
presence or absence of data in each category and subcategory.
The types of non-imaging data that exist for a collection is
marked green in the table. Types of non-imaging data that do not
exist in a collection are represented by blank cells. If a collection
provides data for at least one subtype of data, the major category
is marked as existing. In very few cases a major category is
represented as existing, when none of their subtypes are part of
the collection’s non-imaging data, but some data that of that
category exists. The diagonally striped cells signify data that was
not described or identified sufficiently and they are represented
based on an assumption of the authors. One example for this is
“laterality”. In the “BREAST_DIAGNOSIS” collection we find
both laterality applied to the diagnosis (on which side the tumor
is located) and laterality for MRI, which specified for which side
an MRI was taken. Other collections did provide laterality
information, but didn’t specify whether that was tumor
localization information or imaging localization information.
We did assume that this data represented the localization of the
tumor, since that was most consistent with the context.</p>
        <p>The following sections describe three of these collections
that we have examined in more detail, highlighting specific
hurdles presented by the representation schemes used. We then
present ontology-based representations we have designed for
use in our transformation of these data into a semantic
repository.</p>
      </sec>
      <sec id="sec-2-2">
        <title>B. LIDC-IDRI Collection</title>
        <p>
          The Lung Image Database Consortium image collection
(LIDC-IDRI)1 [
          <xref ref-type="bibr" rid="ref2">6, 7</xref>
          ] contains non-image data for patients, many
of whose lung cancers are the result of metastasis of other cancer
types from locations other than their lungs. The data is provided
as a spreadsheet labeled as “patient diagnoses”. The sheet has
columns for a de-identified patient ID linking it to other data
about this person (including images), a patient-level diagnosis,
diagnosis method, a primary tumor site for metastatic disease,
and similar diagnosis information about lung nodules. We use
this sheet as a running example throughout this section, focusing
on the patient level diagnosis, including diagnosis method, and
the primary metastatic tumor site.
        </p>
        <p>An immediate obstacle to querying these data is the use of a
terse coding system to indicate values. This system is presented
as a key within column headers in the sheet itself (shown in Fig
2), making it available to a human reader, though not necessarily
easy to interpret. This key is not computer-interpretable, making
the data difficult to query even if it were extracted from the
spreadsheet and used to populate a database table in this form.</p>
        <p>For example, in this representation scheme, a 3 in the patient
level diagnosis column indicates malignant metastatic disease,
while a 3 in the diagnosis method column indicates that the
relevant diagnosis was determined by surgical resection. Similar
information is provided in separate columns for each identified
lung nodule. To make matters worse, files with the same type of
information in other collections use different encoding schemes,
further complicating integrated querying and use of the data.</p>
        <p>Even fields in this file with more explicit entries can be
unclear or ambiguous. For instance, the tumor site column in this
file consists of short, free text (non-standardized) descriptions,
as illustrated in the excerpt in Table III, which shows three
1 http://dx.doi.org/10.7937/K9/TCIA.2015.LO9QL9SX</p>
        <p>Fig. 1. TABLE III.
consecutive entries (ID8 - ID10) that indicate metastatic colon
cancer by using three different values in the tumor site column:
“colon cancer,” “colon,” and “metastatic colon cancer.” In this
case, all three contain the word “colon”, so a string-based text
search for that term would locate these records. However, query
and integration of these data will obviously benefit from
translation to a computer-interpretable, shared representation
that is explicit about which entities are involved.</p>
        <p>Some of these tumor site entries do explicitly denote
anatomical locations, containing only short words like ‘colon’
and ‘bladder.’ Others are descriptions that mention cancer types
mixed with information that indicates locations (‘non small cell
lung left lower lobe’, ‘uterine cancer’, ‘granular cell tumor of
the trachea’). Some only name a disease type (‘lymphoma’,
‘adenocarcinoma’), or use an abbreviation that may allow a
person with domain knowledge to infer the location, such as
‘HCC’ -- hepatocellular carcinoma, which occurs in the liver, or
‘NSCLC’ -- non-small cell lung cancer. As discussed more in
the Methods section below, we found necessary to manually
curate an intermediate spreadsheet with location-denoting terms
before this data could be converted to an OWL representation.</p>
      </sec>
      <sec id="sec-2-3">
        <title>C. Two Head and Neck Cancer Collections</title>
        <p>
          The Head-Neck-PET-CT collection2 [8] contains non-image
data, including diagnostic and treatment information for patients
with head and neck cancer. The HNSCC (Head and Neck
Squamous Cell Carcinoma)[
          <xref ref-type="bibr" rid="ref5">9, 10</xref>
          ] collection3 contains much of
the same information. These collections overlap significantly in
their contents, though with some notational differences. This
section compares a subset of the non-image data provided with
these two collections, focusing on a few key data types in these
2 http://doi.org/10.7937/K9/TCIA.2017.8oje5q00
3 http://doi.org/10.7937/K9/TCIA.2017.umz8dv6s
collections for which we have implemented ontology-based
representations, as discussed more in the Methods section.
        </p>
        <p>Both of these head and neck cancer collections contain
additional types of data not discussed here, many of which we
also will transform into semantic representations for our
integrated repository as this project progresses. As shown in
Tables IV and V below, both collections include the biological
sex of the patient, among other demographic data, as well as
tumor staging information, HPV status, and an indication of the
primary tumor location.</p>
      </sec>
    </sec>
    <sec id="sec-3">
      <title>III. METHODS</title>
      <p>We designed and built representations for these data using
OBO Foundry ontologies, including the Human Disease
Ontology [11] and The Uber Anatomy Ontology, Uberon [12].
Instances for individual entries are linked to ontology classes to
explicitly represent locations, disease types, and diagnosis
methods. These representations are used to transform data from
spreadsheets from these three collection into OWL/RDF files
that are loaded into a triple store database for reasoning and
query. This section presents the details of these representations,
and of the translation process.</p>
      <sec id="sec-3-1">
        <title>A. Ontology-based Representation</title>
        <p>Fig. 1 shows how we represent a patient’s positive HPV
diagnosis in the head and neck collections. In this figure the
labeled ovals stand for ontology classes. The smaller circles
stand for anonymous instances, which are linked to their classes
through rdf:type assertions. The rectangle stands for a labeled
instance. HPV status is provided in these sheets without specific
information about how it was determined, so we can assert only
that an ‘OGMS: diagnostic process’ with some ‘OBI: assay’ has
occurred (this includes physical examinations or other methods
that are not strictly lab tests), and that the output was an ‘OGMS:
diagnosis’ about an instance of ‘DO: papillomavirus infectious
disease’ that inheres in the patient. Not shown in Fig. 1 is
information about the patient’s cancer, though a link exists, both
in reality and in our representation of this data, via the patient.
The representation of this information of head and neck
collection data is nearly identical to the representation used for
the lung collection, as shown in Fig. 4.</p>
        <p>Fig. 2 shows our representation for a patient’s disease and
diagnosis using data from the LIDC collection as an example.
The patient record shown here is for a person whose colon
cancer has spread to their lungs, as determined by a biopsy. This
patient has two instances of ‘DO: cancer’, one that inheres in
the patient’s ‘UBERON: colon’ and one that inheres in the
‘UBERON: lung’. An ‘OGMS: diagnostic process’ with some
‘OBIB: biopsy’ as part has produced as output an ‘OGMS:
diagnosis’ that is about the patient. The biopsy evaluated an
‘UBERON: portion of tissue’ that was derived from an ‘EFO:
neoplasm’ that was located in the patient’s lung. In this case the
dataset does not contain more specific information about which
type of cancer inheres in each location. Note that an OWL
reasoner could infer more specific types for these instances from
the assertions in Figure 2, and from logical definitions in the
Disease Ontology, concluding e.g. that the instance of cancer
inhering in the patient’s lung is an instance of lung cancer.</p>
      </sec>
      <sec id="sec-3-2">
        <title>B. Data Transformation and Populating Repository</title>
        <p>As discussed above, the lung cancer collection uses some
values that require manual interpretation by a human to identify
which anatomical entities, if any, are specified. To facilitate the
transformation of this collection into OWL, we built a
spreadsheet listing all 110 unique values from the primary tumor
site field, and used this to record and track the extent to which
each value in that field indicates an anatomical location. Of these
110 primary tumor site entries, only 9 are short terms that
precisely denote an anatomical location. 54 others explicitly
mention an identifiable location, often as part of a description
that also names the disease type. In total, including entries where
the location can be inferred from use of a standard abbreviation,
76 out of 110 indicate a clear location for the primary tumor of
the metastatic disease. For each these, we manually located and
recorded the matching Uberon class in the sheet for use in our
ontology-based representation of the data. This secondary sheet
was then used as input to a Python script to retrieve and record
the correct anatomical classes for tumor sites even for those
records where the literal value stored in the source sheet did not
strictly identify a location.</p>
        <p>To transform the two head and neck collections, manual
curation of a secondary sheet was unnecessary because the
tumor site entries in those two sheets contain only one of a few
values: 'Larynx', 'Nasopharynx', 'Hypopharynx', 'Oropharynx’,
'Glottis', 'Sinus', 'Oral cavity’, 'unknown', ‘CUP'. A value of
‘CUP’ indicates cancer of unknown primary, so it carries similar
information as the value ‘unknown’. The other seven values
clearly denote anatomical locations found in Uberon.</p>
        <p>These collection data sheets, including a secondary sheet for
the lung collection, were processed with a Python script using
the RDFLib library to build OWL individuals from the instance
data contained in each sheet, asserting the prescribed relations
among these individuals, and saving the results in an OWL file.
As part of this process, the script reads the spreadsheets,
determines which URIs are needed, and automatically generates
OntoFox [13] requests for each external ontology used. OntoFox
is a web-based term extraction tool that supports ontology reuse.
Our script uses OntoFox to retrieve hierarchical information and
select other details only for those classes and relations that are
needed to represent the data. It invokes the ROBOT command
line tool [14] to convert between RDF serializations, e.g. to
convert OntoFox’s default RDF/XML output into turtle format
for ease of use with RDFLib. The resulting OWL files are added
to a triple store, making them available for reasoning and query.</p>
        <p>PREFIX inheres: &lt;http://purl.obolibrary.org/obo/RO_0000052&gt;
PREFIX human: &lt;http://purl.obolibrary.org/obo/NCBITaxon_9606&gt;
PREFIX rdfs: &lt;http://www.w3.org/2000/01/rdf-schema#&gt;
PREFIX identifier: &lt;http://purl.obolibrary.org/obo/IAO_0020000&gt;
PREFIX denotes: &lt;http://purl.obolibrary.org/obo/IAO_0000219&gt;
PREFIX oroph: &lt;http://purl.obolibrary.org/obo/UBERON_0001729&gt;
PREFIX cancer: &lt;http://purl.obolibrary.org/obo/DOID_162&gt;
PREFIX has_part: &lt;http://purl.obolibrary.org/obo/BFO_0000051&gt;
PREFIX hpv: &lt;http://purl.obolibrary.org/obo/DOID_11166&gt;
PREFIX disease: &lt;http://purl.obolibrary.org/obo/DOID_4&gt;
select ?idl {
# the person and identifier
?person rdf:type human: .
?id denotes: ?person .
?id rdf:type identifier: .
?id rdfs:label ?idl .
idl
HNSCC-01-0050
HNSCC-01-0054
HN-HGJ-018
HNSCC-01-0098
HNSCC-01-0116
# the person has hpv
?hpv rdf:type hpv: .
?hpv inheres: ?person .
# the person's oropharynx
?person has_part: ?o .
?o rdf:type oroph: .
# cancer in the oropharynx
?d inheres: ?o .</p>
        <p>?d rdf:type cancer: .
} limit 5</p>
      </sec>
    </sec>
    <sec id="sec-4">
      <title>IV. RESULTS</title>
      <p>The resulting triple store contains assertions linking patient
identifiers to RDF instances representing patients, affected body
parts, diagnoses, relations among those, etc. OBO Foundry
Ontologies provide the types (OWL classes) for these instances
and define the relations (OWL object properties).</p>
      <p>This database can be queried using SPARQL to identify
patient records matching criteria based on these fields that were
previously inaccessible, as well as queries that operate across
collections. For example, the query shown above gets a list of
patient identifiers for patients who have been diagnosed with
HPV, and who have also been diagnosed with a cancerous tumor
in their oropharynx. This query is able to retrieve results from
both the Head-Neck-PET-CT collection and the Head and Neck
Squamous Cell Carcinoma collection because the relevant data
are now represented in the same way in the triple store. This
enhanced data is immediately available for simple reasoning
tasks allowed by the use of ontologies, e.g. using the partonomic
information built into UBERON to support queries at different
levels of anatomical granularity.</p>
    </sec>
    <sec id="sec-5">
      <title>V. DISCUSSION AND FUTURE WORK</title>
      <p>The Cancer Imaging Archive contains a wealth of diverse
non-image data that is currently difficult to work with because
much of it, though publicly available, is locked away in
spreadsheet files that must to be downloaded and interpreted
individually. As part of ongoing development work for TCIA
and for the PRISM platform, we are examining the contents of
these files, cataloging and characterizing the data therein, and
designing realist ontology-based representations that explicitly
the entities that these data are about.</p>
      <p>The examples presented in this paper demonstrate the
usefulness of ontologies and semantic web tools for knowledge
representation to enable querying of otherwise opaque
nonimage data in these TCIA collections. We are expanding this
work beyond the collections presented here to include more data
from the archive. The graph-based nature of RDF stores allows
us to incrementally add and link knowledge from different
collections and files within them as the representation work
proceeds, simplifying the task of integrating these data.</p>
      <p>Because most users prefer not to write SPARQL queries, a
next step is the development of user-friendly interfaces to help
end users search, explore, and interpret these data. We also plan
to provide ontology-driven submission tools that will
automatically generate the same representations, allowing for
seamless integration of new datasets.</p>
    </sec>
    <sec id="sec-6">
      <title>VI. REFERENCES</title>
      <p>This project has been funded in whole or in part with federal funds from the National Cancer Institute, National Institutes of Health
under Contract No. HHSN261200800001E. The content of this publication does not necessarily reflect the views or policies of the
Department of Health and Human Services, nor does mention of trade names, commercial products, or organizations imply
endorsement by the U.S. Government. Under this contract the University of Arkansas is funded by Leidos Biomedical Research
subcontract 16X011. Funding was also provided by U24CA215109.</p>
    </sec>
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