- Open Access
Organizing knowledge to enable personalization of medicine in cancer
© Good et al.; licensee BioMed Central Ltd. 2014
- Published: 27 August 2014
Interpretation of the clinical significance of genomic alterations remains the most severe bottleneck preventing the realization of personalized medicine in cancer. We propose a knowledge commons to facilitate collaborative contributions and open discussion of clinical decision-making based on genomic events in cancer.
- Personalized Medicine
- Cancer Genome
- Epidermal Growth Factor Receptor Gene
The landscape of the genomics of tumor progression and heterogeneity has seen incredible advancements in recent years with the maturation of The Cancer Genome Atlas (TCGA) , International Cancer Genome Consortium (ICGC)  and other large-scale tumor sequencing efforts. Software and workflow systems for predicting and annotating genomic changes have proliferated and continue to improve . Caregivers in the healthcare system will soon be faced with a large number of genomic alterations that are potentially relevant to understanding cancer progression and improving clinical decision making for each individual patient. However, there are few resources to help with the prioritization and interpretation of these alterations in a clinical context. Genomic events and the genes or pathways that they affect must be placed in the context of drug-gene or drug-variant interactions and associations with diagnostic or prognostic endpoints. The evidence for these associations must also be captured and characterized to allow risk-benefit analysis for any proposed clinical action. The bulk of this information remains trapped in the masses of published data, clinical trial records, and domain-specific databases. Sifting through this mountain of information is now the most critical bottleneck to making personalized medicine a reality in cancer. In this Opinion article, we propose the creation of a comprehensive, current, and community-based knowledge base to connect cancer genome events with the necessary evidence to evaluate their biological and clinical significance. Such a framework will allow the harnessing of collaborative contributions and open discussion needed to empower the most informed genomics-based clinical decision-making in a rapidly changing landscape.
Cancer genomics promises to revolutionize medicine by identifying tumor-specific alterations that can guide clinical decision-making. To list just two groundbreaking examples, activating mutations in the epidermal growth factor receptor gene EGFR were linked to gefitinib response , and amplification or overexpression of the related gene ERBB2 was shown to predict response to anti-ERBB2 therapies such as lapatinib . Tests for these markers that guide therapy decisions are now part of the standard of care in non-small-cell lung cancer and breast cancer. Since these and other early single-gene findings, large-scale sequencing studies have systematically mapped the landscape of the most common alterations for most common tumor types ,. Increasingly, these alterations are being linked to diagnostic, prognostic, and drug-response outcomes. As the number of these associations increases and sequencing costs decrease, targeted panels are being replaced by genome- and transcriptome-wide approaches. Several proof-of-principle studies have recently demonstrated the potential for use of such data to identify clinically actionable findings -. In a prototypical study, Jones et al. sequenced an oral adenocarcinoma by whole-genome and whole-transcriptome sequencing, identified upregulation of the mitogen activating protein kinase pathways through overexpression of receptor tyrosine kinase (RET) RNA and deletion of the Phosphatase and tensin homolog (PTEN) gene. They proposed a therapeutic intervention by RET inhibition with sunitinib, a therapy that might not otherwise be considered for this disease type. Most recently, Van Allen et al. described an exome sequencing approach that, when applied prospectively, identified clinically relevant alterations in 15 of 16 cancer patients analyzed.
Because computational predictions are inadequate, this challenge of biological and clinical interpretation of genomic events is primarily a challenge in knowledge management. There is a finite collection of knowledge about these events in the biomedical literature, and every cancer genome analyst desires access to the entirety of that knowledge in a concise and consumable form. When analysts reach the interpretation step in Figure 1, each potential tumor-driving event is typically evaluated manually against a disparate set of data sources. For example, candidate fusions might be evaluated against the Mitelman database of chromosomal alterations , Cancer Gene Census , the Gene Ontology , and drug-gene databases such as DGIdb . Similarly, a subset of clinical associations for cancer have been catalogued in databases such as My Cancer Genome (MCG) , and variants associated with genetic diseases are recorded in resources such as ClinVar  and HGMD . Although resources such as these are valuable, the fragmentation of this knowledge in uncoordinated and overlapping efforts is highly inefficient. And given that these efforts do not share a common set of standards and many are proprietary, the products of each group cannot be integrated easily.
We, as a community, need to create a collective resource for this knowledge. Information linking cancer genomic events to clinical interpretations and recommendations needs to be stored, retrieved, edited, and discussed. Only through such a shared knowledge structure will we realize the opportunities for personalized care raised by genomic technology. This knowledge base must be comprehensive. It must incorporate information now distributed across many different databases, scattered through the scientific literature, clinical trials reports, abstracts from conference proceedings, US Food and Drug Administration (FDA) reports and more. At the same time it must be focused. We need to capture detailed evidence for putative connections between genomic events in cancer and their interpretations. This evidence should be captured in structured forms and synthesized in detailed textual summaries that provide biological and clinical interpretations associated with particular genomic events. It must also be kept current. Our collective understanding of clinically important genomic events grows on a daily basis, and the knowledge base should aim to incorporate these advances as they arise.
How can we create and maintain a comprehensive, well-structured knowledge base that captures the relevant findings from hundreds of thousands of new sources each year, as well as the potentially varying interpretations of these findings by thousands of experts? We propose that the only plausible way to achieve this vision is for the community to become the primary contributors of content. Small professional teams can produce excellent resources but they cannot scale with the exponential growth in biomedical knowledge . Of course, numerous attempts have been made in this direction - the great majority of which have failed to attract the critical mass of user contributors needed to thrive. However, there are successes that can be followed, and in the case of N-of-one cancer genomics we have a unique situation that is particularly well suited to a community model.
Every team tasked with an N-of-one analysis now already goes through the process of aggregating content from multiple databases, manually searching through large textual resources such as PubMed and ClinicalTrials.org, identifying relevant content, and translating that content into structured assertions. Dienstmann et al. describe how their team gradually accumulates the information they use to form clinical interpretations of cancer genomes in what they term their `knowledge database’. In addition, they have taken the exemplary step of sharing that knowledge with the public via the Sage Synapse biology information commons  (in the form of a spreadsheet ). Many groups in both academia and industry are currently creating their own internal version of this knowledge base. Nearly all of this work is redundant. If we can convince the community to externalize even a few of the knowledge bases they are already assembling, as Dienstmann et al. have done, we can as a community begin taking real steps in the direction of a common knowledge platform for cancer genomics. The first step is simply to make the choice that knowledge of this nature should remain free.
A draft proposal for the minimal data needed for curation of evidence of a clinically actionable genomic event: evidence details
Gene implicated (Entrez gene id)
Event (gene-level or variant-level)
Genomic event such as SNV, indel, CNV, chimeric transcript, structural variation, epigenetic alteration, expression change, etc. See Table 2 for more details
chr6:g.152419922 T > A (Y537S)
Specific disease or disease subtype that is associated with this event and its clinical implication (Disease Ontology Identifier)
Estrogen-receptor positive breast cancer (DOID:0060075)
Category of clinical action implicated by event. See Table 3 for more details
Levels of evidence for clinical actionability. See Table 3 for more details
Level B - clinical evidence
A positive or negative value indicating whether the evidence statement supports or refutes a clinical association with the event
Positive - the evidence supports the association
Treatment (FDA status)
For predictive evidence, indicates the therapy for which sensitivity or resistance is indicated
Hormone therapy resistance
Positive or negative association with treatment or diagnostic/prognostic end point
Negative - mutation is associated with resistance to therapy
Text summary (wiki-like)
Human readable interpretation. Free-form text summary of this event’s effect on cancer and potential clinical interpretations. This interpretation is the synthesis of all other information about an event and its relevance to clinical action and should be the living product of active discussion
Studies suggest ligand-binding-domain ESR1 mutants mediate clinical resistance to hormonal therapy and suggest that more potent estrogen receptor antagonists may be of substantial therapeutic benefit
Literature where the event is described/explored (PubMed id)
A draft proposal for the minimal data needed for curation of evidence of a clinically actionable genomic event: types of events
Single nucleotide variant (SNV)
Single nucleotide alterations
BRAF c.1799 T > A (V600E)
Small insertion or deletion (Indel)
Small numbers of nucleotides deleted or inserted
PTEN c.800delA (K267fs*9)
Copy number variation (CNV)
Large-scale (for example, chromosomal) or focal changes in copy-number status such as amplifications and deletions
Structural variation (SV)
Large-scale (for example, chromosomal) rearrangements such as translocations or inversions
FLT3 internal tandem duplication
Aberrant expression of messenger RNA involving distant intra- or inter-chromosomal gene pairs
Alterations at the epigenetic level such as DNA methylation or histone modifications
TERT promoter hypermethylation
Significantly increased or decreased expression of RNA or protein
High SPARC expression
A draft proposal for the minimal data needed for curation of evidence of a clinically actionable genomic event: evidence types and levels
Type of evidence
Genomic alteration is predictive of response to therapy
Breast cancer cell lines with H1047R mutation showed increased sensitivity to CH5132799 compared to cells with wild-type PIK3CA gene
Genomic alteration is diagnostic for disease or subtype
DNAJB1:PRKACA fusions are very strongly associated with the fibrolamellar variant of liver cancer
Genomic alteration is prognostic for disease outcome
The presence of KRAS mutations in acute myelogenous leukemia is associated with shorter survival time
Level of evidence
A - validated association
Proven/consensus association in human medicine
A meta-analysis of clinical studies showed that harboring a BRAF V600E mutation predicts worse prognosis in patients with colorectal cancer
B - clinical evidence
Clinical trial or other primary patient data supports association
In non-small-cell lung cancer patients with EGFR T790M and other activating mutations, their progression-free survival is shorter than those who do not have T790M mutations
C - preclinical evidence
In vivo or in vitro models support association
Experiments showed that AG1296 is effective in triggering apoptosis in cells with the FLT3 internal tandem repeat
D - inferential association
Glioma cells harboring IDH1 mutation may be more susceptible to chemotherapy or radiotherapy due to their reduced ability to respond to oxidative stress
When considering community-generated knowledge bases that have succeeded, Wikipedia stands at the top of the list by far. Although there are undoubtedly a large number of reasons for its success, one distinguishing characteristic is its almost complete lack of gatekeepers. Anyone can edit a Wikipedia article. One powerful result of this openness is that many different types of people with different experience and inclinations can participate . Some produce new text, some fix typos, some add images, some fix references, some write training material, some focus on single articles they care about, while others make minor improvements to thousands of articles. Systems with gatekeepers (for example, any database that says “please email the curators if you have something you would like to add”) make such a diversity of contributors unlikely.
The first principle that we suggest for the collective cancer genomic knowledge base is complete openness. Anyone should be able to add and edit content. This principle not only removes the inevitable slowdown caused by mandatory, top-down curatorial review of all changes, it also facilitates a diversity of ways that people with different kinds of skills can contribute. As an example, one team of clinical researchers might share a spreadsheet of claims linking genomic events to clinical interpretations. A bioinformatician might improve that contribution by exporting it as a comma-separated values (csv) file and replacing the gene and variant names with standard identifiers. Another person with understanding of the shared knowledge-based system might then be able to import that content. Yet another person might notice that there was an error in a particular interpretation and then make a change to the knowledge base. The key thing to note is that these roles can be decoupled across multiple people and even multiple teams. Rather than placing the entire burden on a single individual, this system facilitates iterative and sequential improvement of any contributed content.
Given a gatekeeper-less model, substantial attention must be paid to tracking the provenance of the claims that make their way into the knowledge base. Again, Wikipedia and its underlying MediaWiki software provide a model example. Every edit in Wikipedia is tracked, linked to a user or an IP address, and can be easily reverted. The edit history of an article and of an editor tell a story that can be used to reliably assign trust to either . This information should be made accessible to applications that build on the knowledge base (for example, to generate reports) such that analysts can make their own decisions about whom to trust and for what reasons. In addition to allowing manual and computational decisions about trustworthiness of content, tracking contributions opens up the possibility of using earned reputation as a way of incentivizing contributions.
A final example from Wikipedia, already reflected in the model proposed in Table 1 and a requirement of a gatekeeper-less system, is the requirement for evidence. One of the tenets of the Wikipedia community is that every putatively factual statement should be supported by one or more external sources . This is one of the key factors in making it the reliable resource that it generally is . Readers can always look up the citations associated with a claim and make up their own mind. Any reader who disagrees with the stated claim can edit the article, provided that they too can offer external evidence. This evidence for claims is, of course, much more important in clinical situations. Once an analyst has used the knowledge base to hone in on a small set of events on which to base their interpretations, the next step is for them to examine the list of references produced (such as a list of PubMed identifiers and clinical trials records) and make their own judgment.
A common criticism of any proposal for a community-driven scientific resource is that scientists will not contribute. Reasons include firstly that there is no direct career incentive to do so, secondly that they are too busy already with work that does have career rewards, and thirdly that by sharing their work openly they could lose valuable competitive advantages. However, this issue of the need for career-based incentives to motivate scientific effort is not universal and, in fact, research has shown that it is largely false. Mazumder et al. found that a lack of time (and not a lack of incentives) is the chief factor limiting researchers from contributing to open resources. This contention is further supported by the success of efforts to streamline the processes involved in contributing to open resources. As an example, Flybase increased their rate of community contributions sevenfold by introducing a proactive model in which database curators directly emailed authors of relevant papers , and a similar effort and result was observed with WormBase . In addition to these community-based extensions to curated databases, there are multiple successful community knowledge platforms in the life sciences. Examples of these include the Encyclopedia of Life , the SEQanswers forum , the Gene Wiki ,, the integration of RFAM with Wikipedia , and the BioStar question and answer system for bioinformatics . Each of these efforts has attracted and sustained large communities of active contributors. These results demonstrate that scientists will contribute to effectively designed community content curation efforts without any need for dramatic sociological shifts in the scientific incentive structure.
A community knowledgebase will also tap directly into career advancement incentives for cancer genome analysts. If implemented well, the proposed knowledge management system should allow analysts to add content directly to the centralized resource faster than they can assemble and maintain their own internal repositories. Integration of external databases could be accomplished by a few researchers rather than redundantly by everyone. Analysts could record clinically actionable genomic events through interfaces that specifically facilitate this kind of curation (for example, by supporting autocomplete fields that use shared identifiers and vocabularies). Analysts could in turn integrate this community content into their own genome interpretation pipelines. This system could be seeded with enough content to attract the attention of a cancer genomics community clearly starved for such resources. Ideally, this would be the start of a powerful positive feedback loop in which content was curated into the resource, thereby increasing the value of the resource and attracting more users, who in turn add more high quality content. Embedding community contribution seamlessly into the process of completing personal tasks directly addresses the issue of time constraints and directly incentivizes high quality contributions.
We also suggest that a system that is dedicated to remaining an open free public resource will attract a large amount of interest and contributors, particularly those outside of the traditional research enterprise. For example, as patients increasingly become better informed they have the desire, and in many cases also have the ability, to make contributions towards finding cures. This community may be particularly motivated in an area with as much direct clinical relevance as cancer genomics and thus could provide an extremely `long tail’ of curators for this initiative.
Nascent large-scale initiatives, such as the global alliance for genomics and health  (GA4GH) and ClinGen , have been announced to help address a variety of information management problems related here. In particular, they emphasize the development of standards for structuring clinical genetic information for representation in electronic medical records and for deposition in the NCBI’s curated clinical genetic database ClinVar . The visions behind these proposals represent substantial improvements over the current landscape of public information sources for medical genetics.
As these longer-term initiatives unfold, we expect that the bottom-up, community model proposed here will provide an immediately useful resource and will contribute to achieving the shared vision of effective knowledge management for personalized medicine. As GA4GH and ClinGen work to define standards and protocols in a top-down manner, the community can work from the bottom up to share information through the proposed knowledge base. The two initiatives should reinforce each other. The community knowledge base should accept and work towards implementing standards that will be decided on by the expert working groups of ClinGen and GA4GH while at the same time contributing evidence to their discussions and solving real, pressing problems in the interim.
Many other groups are already putting enormous effort into synthesizing the crucial knowledge needed to make effective clinical recommendations and, as Dienstmann et al. exemplify, they are often willing to share this work with the rest of the community. Unfortunately, no existing system provides an effective way to capture and redistribute the ongoing efforts of these teams in a computationally useful way. We have proposed the creation of an open-access, open-source knowledge base to address the challenges of personalized medicine in cancer. This proposal arises, in part, from a recent initiative with the aim of assembling a more general `Network of Biothings’ (NoB) that spans many related problems in biology and medicine . Here we have specifically focused on constructing a NoB for the N-of-one cancer challenge. This NoB should capture the evidence for clinically actionable genomic events as described in Tables 1, 2 and 3. To succeed, it must also meet certain criteria. First, it must be committed to remain an open resource. Numerous closed solutions are being developed in industry to tackle this problem. We need the open alternative. Second, it must stay current. This is a critical and perhaps the most serious challenge. New relevant data, reports, clinical trials and so on join the landscape every day and must be incorporated into the resource in a timely manner. Finally, it must be computable. The NoB should follow the principles of the Semantic Web  in terms of standard data formats, the application of ontologies and the distribution of data via public web APIs.
The N-of-one cancer genomics challenge stands as the tip of the spear in the march towards personalized medicine. Given the complexity of the disease(s), the gravity of the situation for patients, and the limited time available to make decisions, this challenge will continue to test the boundaries of what is possible. The tools created for this case, such as the community knowledge base proposed here, will stand as powerful examples for the many other clinical applications of genomic technology on the horizon.
Ideas presented here were formulated, in part, from research supported by the National Institute of General Medical Sciences (NIGMS) of the NIH under award numbers R01GM089820 and R01GM083924 (AIS), and also by the Scripps Translational Science Institute grant UL1TR001114 from the National Center for Advancing Translational Sciences (NCATS) of the NIH (AIS and BMG). The authors also acknowledge participants in the Network of BioThings satellite meeting, hackathon, and mailing list for helpful discussions.
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