<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Sivapalan L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The utility of circulating tumour DNA (ctDNA) for longitudinal tumour monitoring in pancreatic ductal adenocarcinoma (PDAC) has not been explored beyond mutations in the KRAS proto-oncogene. Here, we aimed to characterise and track patient-specific somatic ctDNA variants, to assess longitudinal changes in disease burden and explore the landscape of actionable alterations.&lt;h4>Methods&lt;/h4>We followed 3 patients with resectable disease and 4 patients with unresectable disease, including 4 patients with ≥ 3 serial follow-up samples, of whom 2 were rare long survivors (> 5 years). We performed whole exome sequencing of tumour gDNA and plasma ctDNA (n = 20) collected over a ~ 2-year period from diagnosis through treatment to death or final follow-up. Plasma from 3 chronic panc</pubmed_abstract><journal>BMC cancer</journal><pagination>369</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8991893</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer.</pubmed_title><pmcid>PMC8991893</pmcid><pubmed_authors>Chelala C</pubmed_authors><pubmed_authors>Sivapalan L</pubmed_authors><pubmed_authors>Thorn GJ</pubmed_authors><pubmed_authors>Ross-Adams H</pubmed_authors><pubmed_authors>Kocher HM</pubmed_authors><pubmed_authors>Gadaleta E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Longitudinal profiling of circulating tumour DNA for tracking tumour dynamics in pancreatic cancer.</name><description>&lt;h4>Background&lt;/h4>The utility of circulating tumour DNA (ctDNA) for longitudinal tumour monitoring in pancreatic ductal adenocarcinoma (PDAC) has not been explored beyond mutations in the KRAS proto-oncogene. Here, we aimed to characterise and track patient-specific somatic ctDNA variants, to assess longitudinal changes in disease burden and explore the landscape of actionable alterations.&lt;h4>Methods&lt;/h4>We followed 3 patients with resectable disease and 4 patients with unresectable disease, including 4 patients with ≥ 3 serial follow-up samples, of whom 2 were rare long survivors (> 5 years). We performed whole exome sequencing of tumour gDNA and plasma ctDNA (n = 20) collected over a ~ 2-year period from diagnosis through treatment to death or final follow-up. Plasma from 3 chronic panc</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-26T15:16:45.228Z</modification><creation>2025-04-06T14:50:32.593Z</creation></dates><accession>S-EPMC8991893</accession><cross_references><pubmed>35392854</pubmed><doi>10.1186/s12885-022-09387-6</doi></cross_references></HashMap>