{"id":210674,"date":"2017-08-09T04:47:33","date_gmt":"2017-08-09T08:47:33","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/grant-to-compare-large-scale-genomic-sequencing-standard-clinical-tests-for-childhood-cancer-patients-baylor-college-of-medicine-news-press\/"},"modified":"2017-08-09T04:47:33","modified_gmt":"2017-08-09T08:47:33","slug":"grant-to-compare-large-scale-genomic-sequencing-standard-clinical-tests-for-childhood-cancer-patients-baylor-college-of-medicine-news-press","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/human-genetics\/grant-to-compare-large-scale-genomic-sequencing-standard-clinical-tests-for-childhood-cancer-patients-baylor-college-of-medicine-news-press\/","title":{"rendered":"Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients &#8211; Baylor College of Medicine News (press&#8230;"},"content":{"rendered":"<p><p>    Baylor College of Medicine is one of six U.S. institutions to    receive a grant through the National Human Genome Research    Institutes Clinical Sequencing    Evidence-Generating Research Consortium, or CSER2. The    four-year grant, including $2.8 million for fiscal year 2017,    co-funded by the National Cancer Institute, will support    Baylors new KidsCanSeq program that will compare the results    of large-scale genomic testing, such as whole exome sequencing,    to targeted clinical tests in childhood cancer patients at five    sites across the state that serve a highly diverse patient    population, including Texas Childrens Cancer Center.  <\/p>\n<p>    In addition to Texas Childrens Cancer Center, pediatric    patients will be enrolled in KidsCanSeq at the Vannie E. Cook    Childrens Cancer Clinic in McAllen, the Childrens Hospital of    San Antonio, the University of Texas Health Science Center at    San Antonio, and Cook Childrens Health Care System in Fort    Worth.  <\/p>\n<p>    KidsCanSeq follows the Baylor Advancing Sequencing in Childhood    Cancer Care(BASIC3) study at Baylor and Texas Childrens    Cancer Center, which developed the initial protocols for    performing clinical genomic testing of pediatric cancer    patients, reporting results and communicating those results to    families and oncologists. BASIC3 was part of the NHGRI Clinical    Sequencing Exploratory Research program, a precursor to CSER2.  <\/p>\n<p>    Through BASIC3 we explored broad questions, such as whether we    could conduct large-scale genomic testing in a clinical    setting, what kind of results it would generate, and how to    communicate the results to families and physicians. KidsCanSeq    is focused more on generating specific data on what tests are    better or worse than standard tests in pediatric cancer    patients, said the studys principal investigator     Dr. Sharon Plon, professor of pediatrics and of molecular    and human genetics at Baylor and director of the Cancer    Genetics Clinical and Research Programs at Texas Childrens    Hospital.  <\/p>\n<p>    BASIC3 was essentially a pilot study, and now that we have a    better idea of how to implement broad-scale genetic testing in    the clinic, we can focus this study more specifically on    determining which patients would be most likely to benefit from    it or for whom it would be most likely to impact care, said        Dr. Will Parsons, co-principal investigator and associate    professor of pediatrics at Baylor and Texas Childrens Cancer    Center. For example, tumor sequencing of cancer types for    which kids are almost always cured at the time of diagnosis is    not likely to be as useful as for high-risk and relapsed    cancers.  <\/p>\n<p>    KidsCanSeq will strive to answer questions such as how    effective is a germline and tumor panel of approximately 150 to    200 genes at picking up hereditary genetic factors and    tumor-specific actionable information compared with larger    scale tests, like whole exome sequencing, which evaluates    thousands of genes. Specifically, the study will compare the    targeted cancer panel to whole exome sequencing of a blood    sample of all enrolled childhood cancer patients to find    hereditary factors and to whole exome sequencing, transcriptome    sequencing and copy number array of tumor samples for the    subset of patients with high-risk or relapsed tumors to find    mutations that might guide treatment. This comprehensive set of    genomic tests will be performed by a unique collaboration    between multiple diagnostic facilities with the involvement of    Dr. Richard Gibbs, director of the Human Genome Sequencing    Center, Drs. Christine Eng and Shashikant Kulkarni, professors    of molecular and human genetics, all of Baylor, and Dr.    Angshumoy Roy, assistant professor of pathology &    immunology at Baylor and Texas Childrens Hospital.  <\/p>\n<p>    The program, in which about 900 patients are expected to be    enrolled over four years, also will include parent and doctor    surveys to determine what they found most useful from the    testing as well as the development of video and other    educational materials in both English and Spanish.    Understanding differences among families from different ethnic    or racial backgrounds as well as in different healthcare    settings, including large academic medical centers versus    smaller clinical settings, also is a goal of KidsCanSeq.  <\/p>\n<p>        Dr. Amy McGuire, Leon Jaworski Professor of Biomedical    Ethics and director of the Center for Medical Ethics and Health    Policy at Baylor, also is co-principal investigator of the    study. She will investigate the ethics and utility of genomic    testing for pediatric cancer patients.  <\/p>\n<p>    It is important to study the clinical and psychosocial risks    and benefits of any new technology in order to plan for its    responsible use, McGuire said. We also want to make sure the    infrastructure is in place so that oncologists in non-academic    settings can understand, effectively communicate and    appropriately manage the results of germline and tumor whole    exome sequencing.  <\/p>\n<p>    Specific aims of the KidsCanSeq study include:  <\/p>\n<p>     Assess the clinical utility of large-scale genomic testing by    measuring the frequency of diagnostic and\/or actionable    germline (blood) and tumor findings and the effect on treatment    decisions    Compare uptake by first-degree relatives for familial    genetic testing and recommended cancer surveillance by race,    ethnicity and clinical settings.    Describe perceived utility of large scale testing by    surveying and interviewing parents and participating pediatric    oncologists.    Work with pediatric cancer stakeholders, including    advocates, BASIC3 study parents and national organizations, to    create and evaluate the use of culturally sensitive educational    materials, including videos in English and Spanish, improved    integrated genomic test reports and counseling materials, and    compare in-person versus telemedicine exome results    disclosure.    Provide data to guide future application of clinical    genomics through three innovative pilot projects focused on    health economics, decision support for cancer surveillance and    whole genome sequencing.  <\/p>\n<p>    Drs. Plon, Parsons and McGuire all are members of the    NCI-designated Dan L Duncan Comprehensive Cancer Center at    Baylor College of Medicine.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Go here to see the original:<br \/>\n<a target=\"_blank\" href=\"https:\/\/www.bcm.edu\/news\/molecular-and-human-genetics\/compare-genomic-sequencing-clinical-tests\" title=\"Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients - Baylor College of Medicine News (press...\">Grant to compare large-scale genomic sequencing, standard clinical tests for childhood cancer patients - Baylor College of Medicine News (press...<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Baylor College of Medicine is one of six U.S. institutions to receive a grant through the National Human Genome Research Institutes Clinical Sequencing Evidence-Generating Research Consortium, or CSER2 <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/human-genetics\/grant-to-compare-large-scale-genomic-sequencing-standard-clinical-tests-for-childhood-cancer-patients-baylor-college-of-medicine-news-press\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":9,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[27],"tags":[],"class_list":["post-210674","post","type-post","status-publish","format-standard","hentry","category-human-genetics"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/210674"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/9"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=210674"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/210674\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=210674"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=210674"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=210674"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}