2018
DOI: 10.1093/annonc/mdy282.007
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The nationwide cancer genome screening project in Japan, SCRUM Japan GISCREEN: Efficient identification of cancer genome alterations in advanced biliary tract cancer

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Cited by 3 publications
(5 citation statements)
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“…In total, 5743 patients with advanced GI cancers, including colorectal (n = 2791), gastric (n = 1141), esophageal (n = 369), pancreatic (n = 652), biliary tract (n = 416), liver (n = 67), small intestine (n = 93), appendiceal (n = 47), anal canal cancers (n = 13), GI stromal tumors (n = 79), and neuroendocrine tumors (n = 75), were enrolled. The landscape of genomic alterations was comparable to that reported in other profiling studies in Western countries, and revealed a high prevalence of mutations in trunk genes such as TP53 , and a considerable number of alterations were detected at a low prevalence showing a “long‐tail” distribution 10‐14 . RNA sequencing performed using the OCA assay aided the successful identification of rare fusions involving ERBB2 , FGFR2 or 3 , RET , ROS1 , NTRK , and others.…”
Section: Gi‐screensupporting
confidence: 72%
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“…In total, 5743 patients with advanced GI cancers, including colorectal (n = 2791), gastric (n = 1141), esophageal (n = 369), pancreatic (n = 652), biliary tract (n = 416), liver (n = 67), small intestine (n = 93), appendiceal (n = 47), anal canal cancers (n = 13), GI stromal tumors (n = 79), and neuroendocrine tumors (n = 75), were enrolled. The landscape of genomic alterations was comparable to that reported in other profiling studies in Western countries, and revealed a high prevalence of mutations in trunk genes such as TP53 , and a considerable number of alterations were detected at a low prevalence showing a “long‐tail” distribution 10‐14 . RNA sequencing performed using the OCA assay aided the successful identification of rare fusions involving ERBB2 , FGFR2 or 3 , RET , ROS1 , NTRK , and others.…”
Section: Gi‐screensupporting
confidence: 72%
“…The landscape of genomic alterations was comparable to that reported in other profiling studies in Western countries, and revealed a high prevalence of mutations in trunk genes such as TP53 , and a considerable number of alterations were detected at a low prevalence showing a “long‐tail” distribution. 10 , 11 , 12 , 13 , 14 RNA sequencing performed using the OCA assay aided the successful identification of rare fusions involving ERBB2 , FGFR2 or 3 , RET , ROS1 , NTRK , and others.…”
Section: Gi‐screenmentioning
confidence: 99%
“…In addition, a Nationwide Cancer Genome Screening Project in Japan is currently ongoing and is recruiting patients with a variety of gastrointestinal cancers, including advanced BTC, with a view to evaluating the frequency of cancer genome alterations using NGS technology (SCRUM-Japan GI-SCREEN). Most recently reported results confirm enrolment of 167 patients into the BTC cohort with successful sequencing of 65.7% of patients suggesting that a nationwide screening system may be an efficient way to detect rare mutations in advanced BTC and provide data which is more representative of the patient population as a whole [106]. The successful sequencing of the majority of screened patients is reassuring given difficulties in obtaining good quality tissue from biopsies of BTC.…”
Section: Overcoming the Challenges For Precision Medicine In Rare Canmentioning
confidence: 66%
“…First, the frequency of HER2 amplification is normally <10% in GI cancer; except for gastric cancer. 34,58,65,113 To address this issue, broad screening using NGS and several basket trials, such as MyPathway, have recently been applied. 42,67 In Japan, a nationwide cancer genome screening project, GI-SCREEN, has been in place since 2015, with more than 5,000 genome sequencing results from GI cancer tissue samples generated to date.…”
Section: Future Perspectivesmentioning
confidence: 99%
“…Project in Japan, for metastatic BTC (mBTC) samples analysed by NGS, HER2 amplification was detected in three of 92 tumours (3.3%) 65. Another comprehensive genomic profiling study of 260 BTCs demonstrated that HER2 mutation was identified in 4-5%, and was mutually exclusive to RAS, BRAF and NF1 mutations 66.…”
mentioning
confidence: 99%