<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Huffman BM</submitter><funding>Stand Up To Cancer</funding><funding>Breakthrough Cancer</funding><funding>National Cancer Institute</funding><funding>Lustgarten Foundation</funding><funding>NCI NIH HHS</funding><funding>Hale Family Center for Pancreatic Cancer Research</funding><pagination>5047-5056</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10842136</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(24)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Combining gemcitabine with CHK1 inhibition has shown promise in preclinical models of pancreatic ductal adenocarcinoma (PDAC). Here, we report the findings from a phase I expansion cohort study (NCT02632448) investigating low-dose gemcitabine combined with the CHK1 inhibitor LY2880070 in patients with previously treated advanced PDAC.&lt;h4>Patients and methods&lt;/h4>Patients with metastatic PDAC were treated with gemcitabine intravenously at 100 mg/m2 on days 1, 8, and 15, and LY2880070 50 mg orally twice daily on days 2-6, 9-13, and 16-20 of each 21-day cycle. Pretreatment tumor biopsies were obtained from each patient for correlative studies and generation of organoid cultures for drug sensitivity testing and biomarker analyses.&lt;h4>Results&lt;/h4>Eleven patients with PDAC were e</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>A Phase I Expansion Cohort Study Evaluating the Safety and Efficacy of the CHK1 Inhibitor LY2880070 with Low-dose Gemcitabine in Patients with Metastatic Pancreatic Adenocarcinoma.</pubmed_title><pmcid>PMC10842136</pmcid><funding_grant_id>P30 CA006516</funding_grant_id><funding_grant_id>P50CA127003</funding_grant_id><funding_grant_id>P50 CA127003</funding_grant_id><pubmed_authors>Sadatrezaei G</pubmed_authors><pubmed_authors>Dunwell S</pubmed_authors><pubmed_authors>Andrews E</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Getchell Z</pubmed_authors><pubmed_authors>Raghavan S</pubmed_authors><pubmed_authors>Perez KJ</pubmed_authors><pubmed_authors>Shapiro GI</pubmed_authors><pubmed_authors>Singh H</pubmed_authors><pubmed_authors>Huffman BM</pubmed_authors><pubmed_authors>Kapner KS</pubmed_authors><pubmed_authors>Rubinson DA</pubmed_authors><pubmed_authors>Schlechter BL</pubmed_authors><pubmed_authors>Aguirre AJ</pubmed_authors><pubmed_authors>Ng K</pubmed_authors><pubmed_authors>Hannigan AM</pubmed_authors><pubmed_authors>Abrams TA</pubmed_authors><pubmed_authors>Giannakis M</pubmed_authors><pubmed_authors>Fortier C</pubmed_authors><pubmed_authors>Kochupurakkal B</pubmed_authors><pubmed_authors>Patel AK</pubmed_authors><pubmed_authors>D'Andrea AD</pubmed_authors><pubmed_authors>Wolpin BM</pubmed_authors><pubmed_authors>Feng H</pubmed_authors><pubmed_authors>Cleary JM</pubmed_authors><pubmed_authors>Parmar K</pubmed_authors><pubmed_authors>Biller LH</pubmed_authors><pubmed_authors>Martignetti DB</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Phase I Expansion Cohort Study Evaluating the Safety and Efficacy of the CHK1 Inhibitor LY2880070 with Low-dose Gemcitabine in Patients with Metastatic Pancreatic Adenocarcinoma.</name><description>&lt;h4>Purpose&lt;/h4>Combining gemcitabine with CHK1 inhibition has shown promise in preclinical models of pancreatic ductal adenocarcinoma (PDAC). Here, we report the findings from a phase I expansion cohort study (NCT02632448) investigating low-dose gemcitabine combined with the CHK1 inhibitor LY2880070 in patients with previously treated advanced PDAC.&lt;h4>Patients and methods&lt;/h4>Patients with metastatic PDAC were treated with gemcitabine intravenously at 100 mg/m2 on days 1, 8, and 15, and LY2880070 50 mg orally twice daily on days 2-6, 9-13, and 16-20 of each 21-day cycle. Pretreatment tumor biopsies were obtained from each patient for correlative studies and generation of organoid cultures for drug sensitivity testing and biomarker analyses.&lt;h4>Results&lt;/h4>Eleven patients with PDAC were e</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2026-05-29T17:08:32.341Z</modification><creation>2026-04-08T05:27:55.968Z</creation></dates><accession>S-EPMC10842136</accession><cross_references><pubmed>37819936</pubmed><doi>10.1158/1078-0432.CCR-23-2005</doi><doi>10.1158/1078-0432.ccr-23-2005</doi></cross_references></HashMap>