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Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation

Presurgical studies allow study of the relationship between mutations and response of estrogen receptor positive (ER+) breast cancer to aromatase inhibitors (AIs) but have been limited to small biopsies. Here in Phase I of this study, we perform exome sequencing on baseline, surgical core-cuts and blood from 60 patients (40 AI treated, 20 Controls). In poor responders (based on Ki67 change) we find significantly more somatic mutations than good responders. Subclones exclusive to baseline or surgical cores   occur in approximately 30% of tumours. In Phase II we combine targeted sequencing on another 28 treated patients with Phase I. We find six genes frequently mutated: PIK3CA, TP53, CDH1, MLL3, ABCA13 and FLG with 71% concordance between paired cores. TP53 mutations are associated with poor response. We conclude that multiple biopsies are essential for confident mutational profiling of ER+ breast cancer and TP53 mutations are associated with resistance to oestrogen deprivation therapy.

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DATA ACCESS AGREEMENT - The Institute of Cancer Research - Endocrinology Team

DATA ACCESS AGREEMENT These terms and conditions govern access to the managed access datasets (details of which are set out in Appendix I) to which the User Institution has requested access. The User Institution agrees to be bound by these terms and conditions. Definitions Authorised Personnel: The individuals at the User Institution to whom “The Institute of Cancer Research” grants access to the Data. This includes the User, the individuals listed in Appendix II and any other individuals for whom the User Institution subsequently requests access to the Data. Details of the initial Authorised Personnel are set out in Appendix II. Data: The managed access datasets to which the User Institution has requested access. Data Producers: “The Institute of Cancer Research”and the collaborators listed in Appendix I responsible for the development, organisation, and oversight of these Data. External Collaborator: A collaborator of the User, working for an institution other than the User Institution. Project: The project for which the User Institution has requested access to these Data. A description of the Project is set out in Appendix II. Publications: Includes, without limitation, articles published in print journals, electronic journals, reviews, books, posters and other written and verbal presentations of research. Research Participant: An individual whose data form part of these Data. Research Purposes: Shall mean research that is seeking to advance the understanding of genetics and genomics, including the treatment of disorders, and work on statistical methods that may be applied to such research. User: The principal investigator for the Project. User Institution(s): The Institution that has requested access to the Data. XXXXX: Your Institution details here 1. The User Institution agrees to only use these Data for the purpose of the Project (described in Appendix II) and only for Research Purposes. The User Institution further agrees that it will only use these Data for Research Purposes which are within the limitations (if any) set out in Appendix I. 2. The User Institution agrees to preserve, at all times, the confidentiality of these Data. In particular, it undertakes not to use, or attempt to use these Data to compromise or otherwise infringe the confidentiality of information on Research Participants. Without prejudice to the generality of the foregoing, the User Institution agrees to use at least the measures set out in Appendix I to protect these Data. 3. The User Institution agrees to protect the confidentiality of Research Participants in any research papers or publications that they prepare by taking all reasonable care to limit the possibility of identification. 4. The User Institution agrees not to link or combine these Data to other information or archived data available in a way that could re-identify the Research Participants, even if access to that data has been formally granted to the User Institution or is freely available without restriction. 5. The User Institution agrees only to transfer or disclose these Data, in whole or part, or any material derived from these Data, to the Authorised Personnel. Should the User Institution wish to share these Data with an External Collaborator, the External Collaborator must complete a separate application for access to these Data. 6. The User Institution agrees that the Data Producers, and all other parties involved in the creation, funding or protection of these Data: a) make no warranty or representation, express or implied as to the accuracy, quality or comprehensiveness of these Data; b) exclude to the fullest extent permitted by law all liability for actions, claims, proceedings, demands, losses (including but not limited to loss of profit), costs, awards damages and payments made by the Recipient that may arise (whether directly or indirectly) in any way whatsoever from the Recipient’s use of these Data or from the unavailability of, or break in access to, these Data for whatever reason and; c) bear no responsibility for the further analysis or interpretation of these Data. 7. The User Institution agrees to follow the Fort Lauderdale Guidelines (http://www.wellcome.ac.uk/stellent/groups/corporatesite/@policy_communications/documents/web_document/wtd003207.pdf ) and the Toronto Statement (http://www.nature.com/nature/journal/v461/n7261/full/461168a.html). This includes but is not limited to recognising the contribution of the Data Producers and including a proper acknowledgement in all reports or publications resulting from the use of these Data. 8. The User Institution agrees to follow the Publication Policy in Appendix III. This includes respecting the moratorium period for the Data Producers to publish the first peer-reviewed report describing and analysing these Data. 9. The User Institution agrees not to make intellectual property claims on these Data and not to use intellectual property protection in ways that would prevent or block access to, or use of, any element of these Data, or conclusion drawn directly from these Data. 10. The User Institution can elect to perform further research that would add intellectual and resource capital to these data and decide to obtain intellectual property rights on these downstream discoveries. In this case, the User Institution agrees to implement licensing policies that will not obstruct further research and to follow the U.S. National Institutes of Health Best Practices for the Licensing of Genomic Inventions (2005) (https://www.icgc.org/files/daco/NIH_BestPracticesLicensingGenomicInventions_2005_en.pdf ) in conformity with the Organisation for Economic Co-operation and Development Guidelines for the Licensing of the Genetic Inventions (2006) (http://www.oecd.org/science/biotech/36198812.pdf ). 11. The User Institution agrees to destroy/discard the Data held, once it is no longer used for the Project, unless obliged to retain the data for archival purposes in conformity with audit or legal requirements. 12. The User Institution will notify “The Institute of Cancer Research” within 30 days of any changes or departures of Authorised Personnel. 13. The User Institution will notify “The Institute of Cancer Research” prior to any significant changes to the protocol for the Project. 14. The User Institution will notify “The Institute of Cancer Research” as soon as it becomes aware of a breach of the terms or conditions of this agreement. 15. “The Institute of Cancer Research” may terminate this agreement by written notice to the User Institution. If this agreement terminates for any reason, the User Institution will be required to destroy any Data held, including copies and backup copies. This clause does not prevent the User Institution from retaining these data for archival purpose in conformity with audit or legal requirements. 16. The User Institution accepts that it may be necessary for the Data Producers to alter the terms of this agreement from time to time. In the event that changes are required, the Data Producers or their appointed agent will contact the User Institution to inform it of the changes and the User Institution may elect to accept the changes or terminate the agreement. 17. If requested, the User Institution will allow data security and management documentation to be inspected to verify that it is complying with the terms of this agreement. 18. The User Institution agrees to distribute a copy of these terms to the Authorised Personnel. The User Institution will procure that the Authorised Personnel comply with the terms of this agreement. 19. This agreement (and any dispute, controversy, proceedings or claim of whatever nature arising out of this agreement or its formation) shall be construed, interpreted and governed by the laws of England and Wales and shall be subject to the exclusive jurisdiction of the English courts. Agreed for User Institution Signature: Name: Title: Date: Principal Investigator I confirm that I have read and understood this Agreement. Signature: Name: Title: Date: Agreed for XXXXX Signature: Name: Title: Date: APPENDIX I – DATASET DETAILS APPENDIX II ––PROJECT DETAILS APPENDIX III –– PUBLICATION POLICY APPENDIX I – DATASET DETAILS Dataset reference (EGA Study ID and Dataset Details) EGAS00001001940 – DNA sequencing data of 86 women with oestrogen receptor positive breast cancer. Name of project that created the dataset Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation Names of other data producers/collaborators - Specific limitations on areas of research - Minimum protection measures required File access: Data can be held in unencrypted files on an institutional compute system, with Unix user group read/write access for one or more appropriate groups but not Unix world read/write access behind a secure firewall. Laptops holding these data should have password protected logins and screenlocks (set to lock after 5 min of inactivity). If held on USB keys or other portable hard drives, the data must be encrypted. APPENDIX II – PROJECT DETAILS (to be completed by the Requestor) Details of dataset requested i.e., EGA Study and Dataset Accession Number Brief abstract of the Project in which the Data will be used (500 words max) All Individuals who the User Institution to be named as registered users Name of Registered User Email Job Title Supervisor* All Individuals that should have an account created at the EGA Name of Registered User Email Job Title APPENDIX III – PUBLICATION POLICY XXXXX intend to publish the results of their analysis of this dataset and do not consider its deposition into public databases to be the equivalent of such publications. XXXXX anticipate that the dataset could be useful to other qualified researchers for a variety of purposes. However, some areas of work are subject to a publication moratorium. The publication moratorium covers any publications (including oral communications) that describe the use of the dataset. For research papers, submission for publication should not occur until 6 months after these data were first made available on the relevant hosting database, unless “The Institute of Cancer Research” has provided written consent to earlier submission. In any publications based on these data, please describe how the data can be accessed, including the name of the hosting database (e.g., The European Genome-phenome Archive at the European Bioinformatics Institute) and its accession numbers (e.g., EGAS00000000029), and acknowledge its use in a form agreed by the User Institution with “The Institute of Cancer Research”.

Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS00001001940 Other

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Quality Report
Located in
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EGAF00001276065 bam 749.8 MB Report
EGAF00001276066 bam 873.0 MB Report
EGAF00001276067 bam 511.2 MB Report
EGAF00001276068 bam 662.4 MB Report
EGAF00001276069 bam 732.5 MB Report
EGAF00001276070 bam 571.1 MB Report
EGAF00001276071 bam 618.9 MB Report
EGAF00001276072 bam 524.2 MB Report
EGAF00001276073 bam 727.8 MB Report
EGAF00001276074 bam 715.3 MB Report
EGAF00001276075 bam 783.0 MB Report
EGAF00001276076 bam 629.9 MB Report
EGAF00001276077 bam 681.2 MB Report
EGAF00001276078 bam 652.0 MB Report
EGAF00001276079 bam 549.6 MB Report
EGAF00001276080 bam 669.8 MB Report
EGAF00001276081 bam 1.0 GB Report
EGAF00001276082 bam 707.4 MB Report
EGAF00001276083 bam 645.2 MB Report
EGAF00001276084 bam 720.9 MB Report
EGAF00001276085 bam 646.7 MB Report
EGAF00001276086 bam 693.7 MB Report
EGAF00001276087 bam 638.7 MB Report
EGAF00001276088 bam 728.5 MB Report
EGAF00001276089 bam 621.2 MB Report
EGAF00001276090 bam 670.3 MB Report
EGAF00001276091 bam 550.7 MB Report
EGAF00001276092 bam 392.6 MB Report
EGAF00001276093 bam 750.3 MB Report
EGAF00001276094 bam 620.5 MB Report
EGAF00001276095 bam 615.8 MB Report
EGAF00001276096 bam 756.3 MB Report
EGAF00001276097 bam 832.8 MB Report
EGAF00001276098 bam 595.8 MB Report
EGAF00001276099 bam 633.7 MB Report
EGAF00001276100 bam 423.3 MB Report
EGAF00001276101 bam 550.5 MB Report
EGAF00001276102 bam 603.2 MB Report
EGAF00001276103 bam 687.3 MB Report
EGAF00001276104 bam 693.0 MB Report
EGAF00001276105 bam 743.5 MB Report
EGAF00001276106 bam 657.8 MB Report
EGAF00001276107 bam 716.9 MB Report
EGAF00001276108 bam 794.9 MB Report
EGAF00001276109 bam 613.3 MB Report
EGAF00001276110 bam 779.8 MB Report
EGAF00001276111 bam 544.5 MB Report
EGAF00001276643 bam 7.8 GB Report
EGAF00001276644 bam 7.1 GB Report
EGAF00001276645 bam 3.2 GB Report
EGAF00001276646 bam 7.0 GB Report
EGAF00001276647 bam 5.4 GB Report
EGAF00001276648 bam 5.6 GB Report
EGAF00001276649 bam 5.2 GB Report
EGAF00001276650 bam 3.2 GB Report
EGAF00001276651 bam 6.0 GB Report
EGAF00001276652 bam 6.7 GB Report
EGAF00001276653 bam 6.4 GB Report
EGAF00001276654 bam 6.1 GB Report
EGAF00001276655 bam 6.1 GB Report
EGAF00001276656 bam 5.4 GB Report
EGAF00001276657 bam 5.3 GB Report
EGAF00001276658 bam 8.4 GB Report
EGAF00001276659 bam 6.2 GB Report
EGAF00001276660 bam 3.8 GB Report
EGAF00001276661 bam 5.8 GB Report
EGAF00001276662 bam 5.2 GB Report
EGAF00001276663 bam 6.3 GB Report
EGAF00001276664 bam 8.4 GB Report
EGAF00001276665 bam 6.6 GB Report
EGAF00001276666 bam 786.6 MB Report
EGAF00001276667 bam 542.0 MB Report
EGAF00001276668 bam 675.5 MB Report
EGAF00001276669 bam 717.6 MB Report
EGAF00001276670 bam 776.9 MB Report
EGAF00001276671 bam 858.0 MB Report
EGAF00001276672 bam 745.5 MB Report
EGAF00001276673 bam 650.3 MB Report
EGAF00001276674 bam 318.5 MB Report
EGAF00001276675 bam 542.6 MB Report
EGAF00001276676 bam 594.8 MB Report
EGAF00001276677 bam 649.2 MB Report
EGAF00001276678 bam 635.7 MB Report
EGAF00001276679 bam 623.1 MB Report
EGAF00001276680 bam 743.4 MB Report
EGAF00001276681 bam 689.9 MB Report
EGAF00001276682 bam 610.7 MB Report
EGAF00001276683 bam 706.2 MB Report
EGAF00001276684 bam 742.8 MB Report
EGAF00001276685 bam 569.2 MB Report
EGAF00001276686 bam 699.0 MB Report
EGAF00001276687 bam 768.1 MB Report
EGAF00001276688 bam 542.0 MB Report
443 Files (1.3 TB)