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<article xmlns:xlink="http://www.w3.org/1999/xlink">
  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>ImageCLEF Liver CT Image Annotation Task 2014</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Neda B.Marvasti</string-name>
          <email>neda.barzegarmarvasti@boun.edu.tr</email>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Nadin Kkciyan</string-name>
        </contrib>
        <contrib contrib-type="author">
          <string-name>t Trkay</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Abdlkadir Yazc Pnar Yolum</string-name>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Suzan skdarl</string-name>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Burak Acar</string-name>
          <email>acarbu@boun.edu.tr</email>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>Istanbul University, Faculty of Medicine</institution>
          ,
          <addr-line>Istanbul</addr-line>
          ,
          <country country="TR">Turkey</country>
        </aff>
        <aff id="aff1">
          <label>1</label>
          <institution>azii University, Computer Engineering Department</institution>
          ,
          <addr-line>Istanbul</addr-line>
          ,
          <country country="TR">Turkey</country>
        </aff>
      </contrib-group>
      <fpage>329</fpage>
      <lpage>340</lpage>
      <abstract>
        <p>The rst Liver CT annotation challenge was organized during the 2014 Image-CLEF workshop held in Sheeld, UK. This challenge entailed the annotation of Liver CT scans to generate structured reports. This paper describes the motivations for this task, the training and test datasets, the evaluation methods, and discusses the approaches of the participating groups. abstract environment.</p>
      </abstract>
      <kwd-group>
        <kwd>ImageCLEF</kwd>
        <kwd>Liver CT annotation task</kwd>
        <kwd>Automatic annotation</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>-</title>
      <p>2,</p>
    </sec>
    <sec id="sec-2">
      <title>INTRODUCTION</title>
      <p>ImageCLEF [1] was part of the Cross Language Evaluation Forum (CLEF) 2014
consisting of four main tasks: Robot Vision, Image Annotation, Liver CT
Annotation, and Domain Adaptation. It was the rst time that the automatic
annotation of Liver CT images was provided as a challenge.</p>
      <p>The purpose of the Liver CT annotation task was to automatically
generate structured reports with the use of computer generated features of liver CT
volumes. Structured reports are highly valuable in medical contexts due to the
processing opportunities they provide, such as reporting, image retrieval, and
computer-aided diagnosis systems. However, structured reports are cumbersome
and time consuming to create. Furthermore, their creation requires domain
expertise who is time constrained. Consequently, such structured medical reports
are often not found or are incomplete in practice. This challenge was designed
to aid the generation of structured reports.</p>
      <p>
        The datasets provided for this challenge consisted of 50 training and 10 test
datasets. Participants were asked to answer a xed set of multiple-choice
questions about livers. The questions were automatically generated from an
opensource ontology of liver for radiology (onlira) [2]. The answers to the questions
describe the properties of the liver, the hepatic vasculature of the liver, and
a specic lesion within the liver. During this task, the user is presented with
the following training data: (
        <xref ref-type="bibr" rid="ref1">1</xref>
        ) data from a CT scan, (
        <xref ref-type="bibr" rid="ref2">2</xref>
        ) a liver mask, (
        <xref ref-type="bibr" rid="ref3">3</xref>
        ) a
volume-of-interest that highlights the selected lesion, and (
        <xref ref-type="bibr" rid="ref4">4</xref>
        ) a rich set of
imaging observations. The imaging observations are ONLIRA based annotations that
were manually entered by radiologists. Participants were permitted to extract
their own image features from the CT data and use them. The results were
evaluated in terms of the completeness and accuracy of the generated report.
      </p>
      <p>The rest of the paper is organized as follows, Section 2 gives a detailed
description of the task and introduces the participants. Section 3 presents the main
results of the task and the results of the participants, and Section 4 concludes
the paper.
2</p>
    </sec>
    <sec id="sec-3">
      <title>The Liver CT Annotation Challenge</title>
      <p>This section describes the task and introduces the participants.
2.1</p>
      <p>Task Denition and Datasets
The Liver CT annotation task is proposed towards the generation of structured
reports describing the semantic features of the liver, its vascularity, and the types
of lesions in the liver. The goal of proposing this task is to develop automated
mechanisms to assist in the dicult and practically infeasible task of annotating
medical records.</p>
      <p>The training dataset includes 50 cases, each consisting of:
a cropped CT image of the liver a 3D matrix with the same size as cropped
CT image,
a liver mask that species the part corresponding to the liver a 3D matrix
indicating the liver areas with a 1 and nonliver areas with a 0,
a bounding box (ROI) corresponding to the region of the selected lesion
within the liver as a vector of 6 numbers corresponding to the coordinates
of two opposite corners,
a set of 60 computer generated ( CoG) features obtained from an interactive
segmentation software a 60 4 array, and
A set of 73 user expressed features ( UsE) manually entered by a radiologist
and stored in a 73 6 array.</p>
      <p>In training dataset 50 .mat les, each consisting of all the above data were given
to the participants. The format of the test dataset is the same except that the
UsE features are missing, which the participants were expected to predict. The
participants were allowed to extract and use their own image features. It is
important to note that the resolution of CT images may vary ( x : 190 308
pixels, y : 213 238 pixels, and z : 41 588 slices). The spacing may also vary
in the range of (x; y : 0:674 1:007 mm, slice : 0:399 2:5 mm).
Computer Generated Features For each case, there is a set of 60 CoG image
descriptors. Table 4 provides the list of all CoG features for a case. Some of them
have only one value and the rest are vectors with dierent dimension. For
example, the size of "HistogramOfAllLesions" is 67, while the size of "LiverVolume"
is 1. The total dimension of all features is 454. The CoG features were extracted
after interactively marking the liver, vessels, and lesions on a CT image. The
CoG features describe the characteristics of the liver, vessels, and lesions.
Lesion descriptors are categorized into ve types: geometric, locational, gray-scale,
boundary, and texture features. The reader is referred to [3] for the details of
CoG features. In both training and test dataset, CoG features are shown in a 60
array where each columns is stands for:</p>
      <p>Column Feature Type
1 group string
1 name string
3 type string
4 value type of the feature
User Expressed Features Imaging observations of a radiologist for the liver
domain are represented with ONLIRA(Ontology of the Liver for Radiologists).
A web based data collection application, called CaReRa-Web 4.</p>
      <p>For each case, there are 73 user expressed ( UsE) features represented in a 73
6 cell array. These features clinically characterize the liver, hepatic vascularity,
and liver’s lesions. In the training dataset, the UsE features are manually entered
by an expert radiologist. Every UsE feature corresponds to a question answered
by a radiologist. Some UsE features may take on more than one value. Such
features are represented with a multi-selection answers.</p>
      <p>In the test phase, the participants were expected to predict the UsE features.
The format of the 73 6 UsE data is:</p>
      <p>Column Annotation Features Type
1 Group string
2 Concept string
3 Properties string
4 Indices bar separated list of integers
5 Values bar separated list of strings
6 "Free text" related to value Text</p>
      <p>The "Group" and "Concept" are the ONLIRA-based concepts. Each concept
may have several properties. Each property may have multiple values whose
indices and meaning are given in "Indices" and "Values" columns, respectively.
Properties deemed irrelevant are marked as NA by the radiologist. UsE features
are grouped as: Liver, Vessel, General and Lesion. Table 5 lists every group and
its corresponding concepts, properties, possible values and their assigned indices.
4 The CaReRa-Web is a tool that can accessed at https://vavlab.ee.boun.edu.tr:
5904/CareraWeb2. It is available for academic use from the CaReRaproject (Case
Retrieval in Radiological Databases) website http://www.vavlab.ee.boun.edu.tr
2.2</p>
      <p>Evaluation methodology
The evaluation is performed on the basis of the completeness and accuracy of
the predicted annotations with reference to the manual annotations of the test
dataset. Completeness is dened as the number of predicted features divided
by total number of features, while accuracy is the number of correct predicted
features divided by total number of predicted features.</p>
      <p>For answers that allow multiple values to a question, the correct prediction
of a single feature is considered as a correct annotation.</p>
      <p>Completeness =
number of predicted U sE f eatures</p>
      <p>T otal number of U sE f eatures
Accuracy =
number of correctly predicted U sE f eatures</p>
      <p>N umber of predicted U sE f eatures
T otalScore = pCompleteness</p>
      <p>
        Accuracy
(
        <xref ref-type="bibr" rid="ref1">1</xref>
        )
(
        <xref ref-type="bibr" rid="ref2">2</xref>
        )
(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
2.3
      </p>
      <p>Participation
Among 20 groups, which registered for the task and signed the license agreement
to access the datasets, only 3 of them submitted at least one run. The number
of runs per group was limited to ten. Tables 1 describes these runs.
The groups that submitted their results based their prediction on classiers,
image retrieval, and generalized coupled tensor factorization (GCTF).</p>
      <p>The BMET group, achieved the best results using the image retrieval
techniques with total score of %94:7. Classier-based methods were used by both
BMET and CASMIP groups. Only piLabVAVlab used a GCTF method. Table 2
shows the completeness, accuracy and total score achieved by each run on the
test dataset.</p>
      <p>The BMET group [4] submitted 8 runs, of which 4 of them used a
classierbased approach and the remaining used an image retrieval algorithm. They used
two dierent feature sets: the prepared CoG features from the database and a
bag of visual words (BoVW). In the classier-based approach, they used
twostage classication, where each stage consists of a bank of several support vector
machines (SVM), which is used for each UsE feature. A two-stage classication
is proposed to solve the unbalanced training dataset. For each UsE feature, the
rst stage is composed of the 1-vs-all classiers and the second stage is consisted
of the 1-vs-1 classiers. Second classier is activated only if the result of the rst
step is more than one label. In the second stage they run 1-vs-1 classier for the
set of labels resulting from the rst step and a majority voting scheme is used
to select the nal answer. In their rst and second runs, they used linear kernels
while in their third and fourth runs, they employed radial basis function (RBF)
kernel. They examined these two kernels with both sets of features.</p>
      <p>In the image retrieval based approach, they used the most similar training
images to select the UsE features for the test image. Similarity is calculated by
computing the Euclidean distance between image feature vectors. Finally, they
applied a weighted voting scheme to select the label assigned to each UsE
features using the "n" most similar images to the test image, where n = 10 in this
scenario. Basically, this algorithm votes images more similarity to the test image
with higher values. Results of this approach with two dierent sets of features
are seen in 5th and 6th runs. In 7th and 8h runs, they applied a sequential
feature selection method to use the most discriminating features for each question
during the similarity calculation, in order to use the most suitable one. As
mentioned above, BMET group used two kernels for SVM classication, however,
there is no signicant performance dierence in the results, which the
participants attribute to the unbalanced training dataset. Their classication methods
performed best when they employed their expanded feature set. Their retrieval
method performed best when the given CoG features were employed. This
observation suggests that the nature of feature sets are important for utilizing
dierent methods.</p>
      <p>CASMIP group [5] submitted one run to the task, which achieved the second
best performance. They tried four dierent classiers in the learning phase:
linear discriminant analysis (LDA), logistic regression (LR), K-nearest neighbors
(KNN), and nally SVM to predict UsE features. An exhaustive search of
every combination of image features is done using leave-one-out cross validation
method on training data for every UsE feature and classier. As the result, for
each UsE feature the best classier and its related features are learned. They used
only a certain part of provided CoG features, which was achieved by ignoring
21 high-dimension features, i.e. they ignored features with dimensionally more
than one. Instead, 9 additional features have been added to individual lesion
features extracted in the lesion ROI describing the gray level features of liver,
lesion, and boundary of lesion properties. The learning step was performed using
all UsE features of the training dataset except cluster size, lobe and segments,
which were obtained directly from image features. Python scikit-Learn Machine
learning toolbox was used for implementing each classier with the default
parameters. As the result, for most of the UsE features they got same performance
using any classier and any combination of image features. Hence they assigned
any classier and all image features for them. For 6 of the UsE features that
describe the density, contrast and location of lesions, one of the LDA or KNN
classiers was chosen along with their selected features.</p>
      <p>piLabVAVlab group [6] considered the dataset as heterogeneous data and
GCTF approach was applied to predict UsE features. They considered both
KLdivergence and Euclidean-distance-based cost functions as well as the coupled
matrix factorization models using GCTF framework. They tried to predict
approximately half of the UsE features. In order to achieve this, UsE features with
only 4 indices whose values vary from 0 to 3 were considered as the rst group
and UsE features with binary indices were considered as the second groups. The
reason for this was that the threshold selection needed to be specied for each
type of question. Thus, they considered questions with similar answer ranges in
a study and ignore question with varied answer ranges. Basically, they provide
three matrices for 50 training and 10 test cases:</p>
      <p>X1: A 60
X2: A 60
Z1: A 60
21 matrix (UsE features of rst group).
13 matrix (UsE features of second group).</p>
      <p>447 matrix (all CoG features).</p>
      <p>They estimated the latent matrices: Z2 and Z3 by using coupled matrix
factorization models according to the following formula:</p>
      <p>X1 = Z1
X2 = Z1</p>
      <p>
        Z2
Z3
(
        <xref ref-type="bibr" rid="ref4">4</xref>
        )
(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
      </p>
      <p>The UsE features of the 10 test cases are predicted with Z2 and Z3. Since
the predicted values are not discrete, a binary thresholding method has been
proposed to extract the labels of UsE features.</p>
      <p>This group submitted one run during the submission period, which had the
accuracy of %45. However, after the submission deadline, they claimed that they
had improved their thresholding method and requested that we evaluate their
new results (see Table 2 run2 and run3).</p>
      <p>Among 73 UsE features, 7 of them were excluded from the evaluation
because of their unbounded labels (numeric continuous values). The BMET group
achieved the highest scores with completeness of %98 (See Table 2. In terms of
accuracy, BMET group has also attained the best performance by using an
image retrieval method. In terms of classier-based methods, BMET and CASMIP
groups both obtained the total score of %93.</p>
      <p>Table 3 compares the results of dierent runs in predicting dierent groups
of UsE features. We divide UsE features into 5 groups: liver, vessels and three
lesion groups with area, lesion and component concepts. Results show that all the
groups have completed the vessel UsE features with high accuracy. The BMET
and CASMIP groups completed liver features in full with accuracy more than
%80. None of the groups can completely annotate the area related concepts of
lesions. Components related concepts of lesion are completed fully and annotated
with accuracy higher than %72 by both BIMET and CASMIP groups. Lesion
related concepts of lesions are annotated completely by only BIMET group with
accuracy more than %72.
This was the rst time the liver CT annotation task was proposed. We provided
liver patient data collected via a hybrid patient information entry system whose
liver characteristics are based on the ONLIRA ontology. The challenge presented
to the participants was to predict UsE features of patient records, given CoG
features. As this was the rst time for this challenge, it was not surprising that
few groups were able to submit their runs for this complex task. out of 20 teams
3 teams submitted at least 1 run. The approaches and results were reviewed and
documented in this paper.</p>
      <p>The main challenge of the task was due to the unbalanced dataset and
participants tried to overcome this issue with dierent methods. Among all methods
image retrieval obtained the best performance. It was observed that feature
selection is important for the best performance of the prediction method.
Acknowledgments This work is in part supported by CaReRa Project (TBTAK
Project No: 110E264) and Bogazici University B.A.P (Project No: 5324)
Group
Vessel
General Patient</p>
      <p>
        Concept Properties Possible values(assigned indices)
Left Hepatic Left Hepatic V. Lu- decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Vein men Diam.
      </p>
      <p>
        Left Hepatic V. Lu- obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
men Type
Middle Middle Hepatic V. decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Hepatic Vein Lumen Diam.
      </p>
      <p>
        Middle Hepatic V. obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Lumen Type
Right Hepatic Right Hepatic V. Lu- decreased(0), increased(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), normal(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
Vein men Diam.
      </p>
      <p>
        Right Hepatic V. Lu- obliterated(0), open(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), partially obliterated(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), other(
        <xref ref-type="bibr" rid="ref3">3</xref>
        )
men Type
      </p>
      <p>Diagnosis
Lesion</p>
      <p>Lesion
is Leveling
served?
Leveling Type</p>
      <p>Diagnosis of given image using ICD10 codes (bar
separated) and in the free text MD’s comments are written
(bar separated).</p>
      <p>
        Cluster Size 1(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), 2(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), 3(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), 4(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), 5(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ), multiple(6)
      </p>
      <p>
        For simple cases this value shows number of lesions inside
the ROI, but in case of having more than one lesions of a
certain type, the biggest lesion is annotated as a sample of
that cluster and number of lesions with same properties
is written here
Contrast Uptake NA(-1), dense(0), heterogeneous(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), homogeneous(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
minimal(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), moderate(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
Contrast Pattern NA(-1), central(0), early uptake then wash out(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),
xing contrast in late phase(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), heterogeneous(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ),
homogeneous(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), peripheric(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ), peripheric nodular(6), spokes
wheel(7), undecided(8), other(9)
Lesion Composition SolidCycsticMix(0), Solid(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), SolidWithCystic(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
PureSolid(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), PredominantSolid(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), Cystic(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ),
PureCystic(6), PredominantCystic(7),
CysticWithSolidComponent(8), CysticWithDebris(9), Abcess(10)
Ob- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0)
      </p>
      <p>
        NA(-1), uid uid(0), uid gas(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), uid solid(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), gas
solid(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), other(
        <xref ref-type="bibr" rid="ref4">4</xref>
        )
is Debris observed? True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0),NA(-1)
Debris Location NA(-1), oating inside(0), located on dependent
position(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),other(
        <xref ref-type="bibr" rid="ref2">2</xref>
        )
is Close to Vein NA(-1), HepaticArtery(0), HepaticPortalVein(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),
RightPortalVein(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), LeftPortalVein(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), HepaticVein(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ),
RightHepaticVein(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ), MiddleHepaticVein(6),
LeftHepaticVein(7), VenacavaInferior(8),
PosteriorBranchOfRightPortalVein(9), AnteriorBranchOfRightPortalVein(10),
other(11)
Vasculature Proxim- NA(-1), adjacent(0), adjunct to contact(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), bended(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ),
ity circumscribed(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ), invaded(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), other(
        <xref ref-type="bibr" rid="ref5">5</xref>
        )
Lobe LeftLobe(0), CaudateLobe(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), RightLobe(
        <xref ref-type="bibr" rid="ref2">2</xref>
        )
Segment SegmentI(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ), SegmentII(
        <xref ref-type="bibr" rid="ref2">2</xref>
        ), SegmentIII(
        <xref ref-type="bibr" rid="ref3">3</xref>
        ),
SegmentIV(
        <xref ref-type="bibr" rid="ref4">4</xref>
        ), SegmentV(
        <xref ref-type="bibr" rid="ref5">5</xref>
        ), SegmentVI(6), SegmentVII(7),
      </p>
      <p>
        SegmentVIII(8)
width a number in mm which represents width of the lesion
height a number in mm which represents heigth of the lesion
is Gallbladder Adja- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0)
cent?
is Peripherical Local- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0)
ized?
is Subcapsular Local- True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0)
ized?
is Central Localized True(
        <xref ref-type="bibr" rid="ref1">1</xref>
        ),False(0)
,
      </p>
    </sec>
  </body>
  <back>
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