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dc.contributor.advisorJennifer LaFemina, MD
dc.contributor.authorHendrix, Ryan J.
dc.date2022-08-11T08:08:38.000
dc.date.accessioned2022-08-23T16:02:01Z
dc.date.available2022-08-23T16:02:01Z
dc.date.issued2019-05-06
dc.date.submitted2019-05-28
dc.identifier.doi10.13028/9qvz-4h07
dc.identifier.urihttp://hdl.handle.net/20.500.14038/31248
dc.description.abstractBackground: Pancreatic ductal adenocarcinoma (PDAC) is the third leading cause of US cancer related deaths. This study assessed the oncologic benefit of a neoadjuvant chemotherapy (NAC) treatment strategy for patients with clinical Stage I/II PDAC. Methods: Patients with biopsy confirmed PDAC and clinical Stage I/II disease were treated with a protocol of NAC. The primary study endpoint was median overall survival (OS). Kaplan-Meier survival curves were compared using the log-rank test. Results: 56 patients met inclusion criteria. Of these, 21 patients (38%) had Stage I disease and 35 (62%) had Stage II disease. The median OS for the entire study population was 18.7 months. A total of 22 (39%) patients were managed with NAC+S; 34 (61%) received NAC alone. Median OS and 2-year survival rates were greater in those completing NAC+S compared to NAC alone (median OS 28.8 months vs. 17.3 months: p=0.05; 2-year OS: 55% vs 21%: p=0.01) . Interestingly, patients managed with NAC who were not candidates for surgical resection after restaging demonstrated a survival advantage (17.3 months) compared to what was previously reported in historical controls. Conclusion: NAC+S provided a significant 11.5 month improvement in median OS compared to treatment with NAC alone. Modern NAC may contribute a significant oncologic benefit in the overall treatment strategy for patients with Stage I/II PDAC, even if surgery is not ultimately pursued.
dc.language.isoen_US
dc.rightsCopyright is held by the author, with all rights reserved.
dc.subjectpancreatic ductal adenocarcinoma (PDAC)
dc.subjectneoadjuvant chemotherapy
dc.subjectstage I/II disease
dc.subjectsurvival
dc.subjectNeoplasms
dc.subjectOncology
dc.subjectSurgery
dc.titleImproved Survival after Administration of Neoadjuvant Chemotherapy in Patients with Clinical Stage I/II Pancreatic Ductal Adenocarcinoma
dc.typeMaster's Thesis
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2038&context=gsbs_diss&unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_diss/1029
dc.legacy.embargo2021-06-02T00:00:00-07:00
dc.identifier.contextkey14599411
refterms.dateFOA2022-08-30T04:16:28Z
html.description.abstract<p>Background: Pancreatic ductal adenocarcinoma (PDAC) is the third leading cause of US cancer related deaths. This study assessed the oncologic benefit of a neoadjuvant chemotherapy (NAC) treatment strategy for patients with clinical Stage I/II PDAC.</p> <p>Methods: Patients with biopsy confirmed PDAC and clinical Stage I/II disease were treated with a protocol of NAC. The primary study endpoint was median overall survival (OS). Kaplan-Meier survival curves were compared using the log-rank test.</p> <p>Results: 56 patients met inclusion criteria. Of these, 21 patients (38%) had Stage I disease and 35 (62%) had Stage II disease. The median OS for the entire study population was 18.7 months. A total of 22 (39%) patients were managed with NAC+S; 34 (61%) received NAC alone. Median OS and 2-year survival rates were greater in those completing NAC+S compared to NAC alone (median OS 28.8 months vs. 17.3 months: p=0.05; 2-year OS: 55% vs 21%: p=0.01) . Interestingly, patients managed with NAC who were not candidates for surgical resection after restaging demonstrated a survival advantage (17.3 months) compared to what was previously reported in historical controls.</p> <p>Conclusion: NAC+S provided a significant 11.5 month improvement in median OS compared to treatment with NAC alone. Modern NAC may contribute a significant oncologic benefit in the overall treatment strategy for patients with Stage I/II PDAC, even if surgery is not ultimately pursued.</p>
dc.identifier.submissionpathgsbs_diss/1029
dc.contributor.departmentGeneral Surgery
dc.description.thesisprogramMaster of Science in Clinical Investigation
dc.identifier.orcid0000-0002-2176-4283


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