<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Janssen QP</submitter><funding>ZonMw</funding><funding>KWF Kankerbestrijding</funding><pagination>300</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7989075</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Neoadjuvant therapy has several potential advantages over upfront surgery in patients with localized pancreatic cancer; more patients receive systemic treatment, fewer patients undergo futile surgery, and R0 resection rates are higher, thereby possibly improving overall survival (OS). Two recent randomized trials have suggested benefit of neoadjuvant chemoradiotherapy over upfront surgery, both including single-agent chemotherapy regimens. Potentially, the multi-agent FOLFIRINOX regimen (5-fluorouracil with leucovorin, irinotecan, and oxaliplatin) may further improve outcomes in the neoadjuvant setting for localized pancreatic cancer, but randomized studies are needed. The PREOPANC-2 trial investigates whether neoadjuvant FOLFIRINOX improves OS compared with neoadjuvant </pubmed_abstract><journal>BMC cancer</journal><pubmed_title>Total neoadjuvant FOLFIRINOX versus neoadjuvant gemcitabine-based chemoradiotherapy and adjuvant gemcitabine for resectable and borderline resectable pancreatic cancer (PREOPANC-2 trial): study protocol for a nationwide multicenter randomized controlled trial.</pubmed_title><pmcid>PMC7989075</pmcid><funding_grant_id>10955</funding_grant_id><funding_grant_id>843004108</funding_grant_id><pubmed_authors>Zonderhuis BM</pubmed_authors><pubmed_authors>Wilmink JW</pubmed_authors><pubmed_authors>Groot Koerkamp B</pubmed_authors><pubmed_authors>Loosveld OJL</pubmed_authors><pubmed_authors>Janssen QP</pubmed_authors><pubmed_authors>Karsten TM</pubmed_authors><pubmed_authors>van Dam JL</pubmed_authors><pubmed_authors>Patijn GA</pubmed_authors><pubmed_authors>de Hingh IHJT</pubmed_authors><pubmed_authors>Bosscha KP</pubmed_authors><pubmed_authors>van Santvoort HC</pubmed_authors><pubmed_authors>Bos H</pubmed_authors><pubmed_authors>Besselink MG</pubmed_authors><pubmed_authors>Coene PPLO</pubmed_authors><pubmed_authors>van Eijck CHJ</pubmed_authors><pubmed_authors>van der Kolk MB</pubmed_authors><pubmed_authors>Liem MSL</pubmed_authors><pubmed_authors>Homs MYV</pubmed_authors><pubmed_authors>Bonsing BA</pubmed_authors><pubmed_authors>de Vos-Geelen J</pubmed_authors><pubmed_authors>Dutch Pancreatic Cancer Group</pubmed_authors><pubmed_authors>van Tienhoven G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Total neoadjuvant FOLFIRINOX versus neoadjuvant gemcitabine-based chemoradiotherapy and adjuvant gemcitabine for resectable and borderline resectable pancreatic cancer (PREOPANC-2 trial): study protocol for a nationwide multicenter randomized controlled trial.</name><description>&lt;h4>Background&lt;/h4>Neoadjuvant therapy has several potential advantages over upfront surgery in patients with localized pancreatic cancer; more patients receive systemic treatment, fewer patients undergo futile surgery, and R0 resection rates are higher, thereby possibly improving overall survival (OS). Two recent randomized trials have suggested benefit of neoadjuvant chemoradiotherapy over upfront surgery, both including single-agent chemotherapy regimens. Potentially, the multi-agent FOLFIRINOX regimen (5-fluorouracil with leucovorin, irinotecan, and oxaliplatin) may further improve outcomes in the neoadjuvant setting for localized pancreatic cancer, but randomized studies are needed. The PREOPANC-2 trial investigates whether neoadjuvant FOLFIRINOX improves OS compared with neoadjuvant </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-05-07T17:46:23.576Z</modification><creation>2025-04-04T22:01:35.928Z</creation></dates><accession>S-EPMC7989075</accession><cross_references><pubmed>33757440</pubmed><doi>10.1186/s12885-021-08031-z</doi></cross_references></HashMap>