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Editorial
Dear ACGT newsletter readers.
Happy New Year!
Best wishes for a very nice and fruitful year 2010
The New Year is always a time for reflecting - a convenient
benchmark for measuring what has been learned so far. In this
edition, we are presenting an update on the status of the
activities and the tools that have been developed by the ACGT
consortium. In this respect, we are glad to announce the ACGT
competition that will take place during 2010. The competition,
described in this winter 09 newsletter, will be opened to all
interested organizations and individuals to allow the use of the
tools developed by the ACGT consortium. We are looking forward to
collaborating with you on this major event.
We wish you will have a pleasant reading through the
articles and wish to encourage you to contact us for further
collaboration and interaction with the ACGT project.
Samuel Keuchkerian
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Clinical Trials
Antigen scenario of the SIOP clinical trial (Norbert Graf
- USAAR)
Wilms tumour is the most common malignant renal tumour in
children. In the SIOP 2001/ GPOH trial clinical data, molecular
data and pre- and post-chemotherapy DICOM imaging studies are
collected, coming from patients out of more than 50 hospitals in
Germany. Since 2009 anonymized data of the SIOP/GPOH trial are
used in the ACGT scenarios. From a limited set of these patients,
microarray data and data of autoantibodies against tumour specific
antigens of Wilms tumour are provided. The main question is to
answer whether molecular biology helps to define new risk groups
in Wilms tumour and can be used to stratify treatment of these
patients in the future. As ACGT promotes the integration of
heterogeneous data and provides necessary analytic tools, it
facilitates further molecular analysis and allows clinicians to
efficiently analyze data that are presently communicated by mail,
fax or maintained in flat text files at various remote clinical
sites.
One of the scenarios that are analyzed in ACGT is the
Antigen scenario, to analyze if autoantibodies against tumour
specific antigens do correlate with histology and outcome. Up to
now in 133 patients we did receive serum for the Antigen scenario.
Altogether 355 sera are collected from 265 patients out of 36
local hospitals. Out of this cohort 72 sera were from healthy
children and 60 from patients suffering from other cancers than
nephroblastoma. These sera are used as a control groups. Most of
the sera are collected at the time of diagnosis. A preliminary
analysis of the Antigen Scenario regarding the characterization of
found autoantigens against nephroblastoma was reported at the
Nephroblastoma meeting in Chamonix, France in March 2008 and at
the SIOP conference in Berlin in October 2008. In contrast to
adult patients one can find more autoantigens in sera of children.
This is shown in figure 1. The same autoantigen can be found in a
higher frequency in children and children with cancer than in
adult cancer patients. 61 clones could be found that discriminates
between nephroblastoma and neuroblastoma. 39 of these clones can
be selected as best discrimators. Figure 2 shows for a single
antigen the discrimination between sera of patients with
nephroblastoma and neuroblastoma.
[...]
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Products and Services
Literature Based Discovery (Andreas Persidis - Biovista)
Literature-based discovery (or "LBD" for short) is a
relatively new approach to knowledge discovery. It makes the
assumption that by connecting seemingly disparate chunks of
knowledge from within a relatively large corpus of scientific
articles or other textual resources, it is possible to create new
knowledge that does not exist in the original corpus. LBD is
similar to data-mining, the difference being that while the latter
deals with large bodies of numeric data, the former uses running
text as it primary source.
LBD has many applications, including the identification of
biomarkers, predicting Adverse Events (AE) and finding new uses
for existing drugs or compounds. Within ACGT, partner Biovista has
developed versions of its proprietary LBD platform that are
compatible with the basic ACGT infrastructure and can either be
integrated in any workflow created by the ACGT Workflow Editor or
incorporated in any other user application.
The figure 1 above sows the basic architecture of the
system. Information extraction algorithms read scientific articles
that are downloaded from Medline on a regular basis ensuring the
system is always up to date. Extracted information consists of
about 25 classes of biologically relevant concepts, such as genes
and pathways. Once extracted, these concepts are cross-correlated
amongst themselves and these relationships stored in a
custom-design database that ensures very high response rates. This
database is then queried either by the LBD application or the LBD
functions that are accessible via the ACGT infrastructure.
LBD accuracy
As with any predictive system, one of the main concerns is
its predictive accuracy; in other words how confident we can be in
the output of such a system.
To address this question a study was carried out and will
be reported in reference 1. The study looked at Biovista’s LBD
platform for predicting AEs before clinical trials, using
abstracts from PubMed as the primary raw data source. Using a
description of the mode of action (MoA) of a drug as the starting
point, we compared it to the MoA underlying all AEs, for
similarities. The dataset was 66 unique drugs, of which 61 were
oncology, 7 were neurology, and three were both, where the AEs
were reported at the American Society of Clinical Oncology (ASCO)
annual meeting in 2007 and the American Academy of Neurology (AAN)
annual meeting in 2008, respectively. The primary focus was
oncology, where our sample covered 87% of the MoAs of all
FDA-approved cancer drugs. Using data from 1997 to 2007 divided
into five time points, and a total of 881 measurements, a mean of
79±22% of AE prediction was achieved. A similar AE prediction rate
of 79±28% was achieved in the small neurology sample, in an
additional 97 measurements (978 in total). We also found that when
using data that pre-date any publication on a drug by five years,
literature-based analytics predicted 72% of its AEs. The figure 2
shows how the predictive accuracy of the platform varies as a
function of time (ie available data).
[...]
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Grid news
Toth - Distributed Logging for ACGT environment (Juliusz
Pukacki – PSNC)
One of the most important paradigms for designing ACGT
architecture is the idea of loosely coupled services cooperating
with each other to provide desired functionality for the end user.
That architectural model is the consequence of Service Oriented
Architecture (SOA) approach chosen for ACGT. There are many
advantages of using SOA solution: flexibility, lower maintenance
costs, well defined integration schema, but there are also some
drawbacks. One of them is the problem with monitoring and
debugging of users actions in the distributed environment. The
reason for that is quite obvious: single action on the level of
user interface can cause multiple services invocations in the
background. The best example of it, is the Workflow Environment
where the user can design his/her experiment as a set of
operations involving usage of databases or grid nodes. The crucial
issue for the ACGT services developers is the ability to track the
flow of actions initiated by the user throughout the whole system.
To fulfill that requirement, Toth the distributed logging system
designed by PSNC, was deployed in the ACGT environment. The main
idea behind to Toth is to provide simple tools for the services to
store the logs in the remote logs repository, and to provide
simple yet powerful mechanisms for analyzing and filtering stored
entries. The main assumptions taken into account during Toth
design and implementation are:
- Open architecture: it is possible to add new modules
enhancing basic functionality
- Flexibility: simplified procedure of client application
configuration with connection of possible further tuning of
logging system by advanced administrators
- Scalability
- Intuitive interface based on web portal and web services
[...]
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Feature article
The data-sharing platform of the NeoBIG research program
The NeoBIG program is a research program led by Breast
International Group (BIG), and aims to organize and set up next
generation clinical trials in the area of breast cancer R&D. A
durable, multidimensional translational research structure
supporting neo-adjuvant trials is expected to be built in order to
share strategies, expertise, technologies, methodologies and
protocols. In addition this will provide a strong foundation for
future adjuvant trials in breast cancer (and research in other
cancers).
Tools and expertise developed in ACGT could be used to
support NeoBIG, especially concerning the data storage, management
and sharing, and with respect to privacy and security. In order to
determine a possible support of the ACGT infrastructure, users
requirements have been collected, scenario refined and finally the
suitability of the ACGT tools and infrastructure to support the
NeoBIG programme have been considered.
The NeoBIG program will include several (five currently
planned) neo-adjuvant trials that will be carried out together
with various Pharma companies (see figure 1). A first trial is
scheduled for 2010. Each trial involves several steps from the
biopsy to the surgery, leading to various types of data that
should be gathered electronically. To provide a platform that
enables data sharing and collaboration between cancer research
centres, NeoBIG requires a robust, secure IT solution that is
compliant with a wide set of regulations and laws in the context
of security, safety and privacy protection. The platform needs to
be able to store, manage, and share the various types of data that
will be generated by NeoBIG trials.
[...]
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Community views
Valencian Cyberinfrastructure for Oncological Medical
Imaging (Ignacio Blanquer - Universidad Politécnica de
Valencia)
The generalisation of digital imaging has lead to the
availability of a vast amount of knowledge in the form of medical
images and reports, which is of enormous relevance to research and
training. In these studies, data are retrieved and structured for
healthcare delivery, around the identity of the patient. However,
research and training requires organizing studies by content,
setting up relations among images of similar or related
pathologies, or morphological similarities. This cannot be
achieved on current image databases, and moreover, the differences
among centres will make studies incomparable.
In this scenario, the project CVIMO
(http://www.grycap.upv.es/cvimo) "Valencian
Cyberinfrastructure for Oncological Medical Imaging (CVIMO
GVEMP06/004)", funded by the Regional Ministry of Industry,
University and Science of the Valencian Government, a middleware
was developed and tested for sharing images and radiology studies
from five hospitals of the Land of Valencia (Quiron Clínic,
University Hospital Dr. Peset, de la Ribera Hospital, Valencian
Foundation for Oncology and the Research Foundation of la Fe
Hospital) with the collaboration of British Telecom. The project
was leaded by the "Universidad Politécnica de
Valencia" and the scientific coordinator was Vicente
Hernández.
[...]
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Events
ACGT competition
The ACGT Competition has been set up by the ACGT Project
Consortium to encourage the creation of Grid enabled services that
can be used for the support of multi-centric clinical trials and
research. The ACGT Competition is open to all parties (academic
groups, individual researchers, companies etc) that are interested
in developing ACGT-compatible services and will take place between
February and April 2010.
- 15th February, 2010, 5pm CET: Deadline
for registering your entry. To register, please send an email to
acgt-mb at inria.fr using the Subject line: ACGT
Competition Registration.
- 30th April, 2010, 5pm CET: Deadline for
submitting your entry
- 1st May - 15th May, 2010: Judging
Process by a panel of judges from ACGT Consortium based on 3
criteria: 1) Utility for end users 2) Integration within ACGT
infrastructure 3) Novelty
- 20th May 2010: Announcement of winning
entrie, prizes will include monetary awards and/or selected gift
while all entrants will receive a Certificate of Participation,
signed by the ACGT Competition Committee.
- Award Ceremony: Date to be announced
A WIKI is available for the competition entrants: http://www.biovista.com/ACGTCompetition/Main_Page.
[...]
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Legal & Ethical
Analysis of the Grid infrastructure and its implications
on intellectual property issues (Marcelo Corrales - LUH)
In the realm of a clinical trial scenario a Grid computing
infrastructure has been identified as a key to support and
facilitate the cooperation of scientists and resources through
scalable computation and the management of data systems.
The ACGT platform consists of multiple interconnected IT
resources networks allowing users to execute a variety of
scientific applications requiring a trustworthy, steady and
prevalent access to computational capabilities. This complex
collection of servers and communication protocols poses legal
intellectual property questions: should copyrights or patents
protect the grid? What about software licenses in a Grid
environment?
For a better legal analysis, it is important to know what
the grid is. A Grid infrastructure is generally described with
three different layers. The lowest layer is usually called
"platform", consisting of the hardware resources such as
computers, networks and interface devices which are geographically
distributed, presenting their data in a variety of formats. The
second layer, also called the “middleware“, is defined as the
software layer that lies between the operating system and the
applications on each site of the system. The last layer provides
the user with application services including workflow engines,
data visualization tools, semantic web and web portals.
Intellectual property rights can be applicable to different
aspects of the Grid infrastructure:
[...]
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Life in ACGT
Workshop on European-Japanese Research Collaboration in
Medical ICT’ held at Hokkaido University, Japan (Aran Lunzer and
Yuzuru Tanaka- Hokkaido University)
In September 2009 ACGT partner Hokkaido University hosted a
two-day workshop that brought ACGT’s technical, medical and legal
representatives together with planners from the Japan Science and
Technology Agency (JST), and the leaders of academic and
industrial research teams. As well as disseminating the EU's
clinical-trial infrastructure strategy, as embodied in ACGT, the
workshop provided a forum for discussing increased cooperation
between Japan and the EU on future medical ICT (Information and
Communication Technologies) projects.
It is still rare for a European Commission-funded project
to include a Japanese research partner. Although participation
from outside Europe has been allowed since the Fourth Framework
Programme (FP4), under FP6 there was a Japanese partner in only
ten projects under the Information Society Technologies theme, of
which just seven (including ACGT) are Integrated Projects. One
barrier to participation is that partners in Japan cannot receive
any EC funding; Hokkaido University has funded its work in ACGT
using separately obtained competitive research grants from the
Japanese government.
Hokkaido University, based in Sapporo, is one of Japan’s
seven former “imperial universities”, which also include Kyoto
University and the University of Tokyo. When the proposal for ACGT
was put together in 2005, Professor Yuzuru Tanaka’s Meme Media
Laboratory had been collaborating with the technical leaders,
FORTH, for over ten years, including numerous researcher
exchanges. In 2004, Tanaka had helped set up a new graduate school
whose mix of computer science and bioinformatics expertise gave it
a clear fit with ACGT’s mission.
[...]
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ACGT people
‘Workshop on European-Japanese Research Collaboration in
Medical ICT’ held at Hokkaido University, Japan (Aran Lunzer and
Yuzuru Tanaka- Hokkaido University)
In September 2009 ACGT partner Hokkaido University hosted a
two-day workshop that brought ACGT’s technical, medical and legal
representatives together with planners from the Japan Science and
Technology Agency (JST), and the leaders of academic and
industrial research teams. As well as disseminating the EU's
clinical-trial infrastructure strategy, as embodied in ACGT, the
workshop provided a forum for discussing increased cooperation
between Japan and the EU on future medical ICT (Information and
Communication Technologies) projects.
It is still rare for a European Commission-funded project
to include a Japanese research partner. Although participation
from outside Europe has been allowed since the Fourth Framework
Programme (FP4), under FP6 there was a Japanese partner in only
ten projects under the Information Society Technologies theme, of
which just seven (including ACGT) are Integrated Projects. One
barrier to participation is that partners in Japan cannot receive
any EC funding; Hokkaido University has funded its work in ACGT
using separately obtained competitive research grants from the
Japanese government.
Hokkaido University, based in Sapporo, is one of Japan’s
seven former “imperial universities”, which also include Kyoto
University and the University of Tokyo. When the proposal for ACGT
was put together in 2005, Professor Yuzuru Tanaka’s Meme Media
Laboratory had been collaborating with the technical leaders,
FORTH, for over ten years, including numerous researcher
exchanges. In 2004, Tanaka had helped set up a new graduate school
whose mix of computer science and bioinformatics expertise gave it
a clear fit with ACGT’s mission.
[...]
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