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Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study
BACKGROUND: A majority of patients undergoing curative intent surgery for pancreatic ductal adenocarcinoma (PDAC) will unfortunately develop recurrent disease. Treatment outcomes for patients with metastatic disease remain suboptimal. In this study, we evaluated clinical outcomes of patients with re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554966/ https://www.ncbi.nlm.nih.gov/pubmed/36224524 http://dx.doi.org/10.1186/s12885-022-10130-4 |
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author | Miotke, Laura Nevala-Plagemann, Christopher Ying, Jian Florou, Vaia Haaland, Benjamin Garrido-Laguna, Ignacio |
author_facet | Miotke, Laura Nevala-Plagemann, Christopher Ying, Jian Florou, Vaia Haaland, Benjamin Garrido-Laguna, Ignacio |
author_sort | Miotke, Laura |
collection | PubMed |
description | BACKGROUND: A majority of patients undergoing curative intent surgery for pancreatic ductal adenocarcinoma (PDAC) will unfortunately develop recurrent disease. Treatment outcomes for patients with metastatic disease remain suboptimal. In this study, we evaluated clinical outcomes of patients with recurrent PDAC who received systemic therapy and compared outcomes to patients with de novo metastatic PDAC undergoing systemic therapy. METHODS: Patients diagnosed with metastatic PDAC between 2014 and 2019 were included using a real-world database. Patients were characterized as either de novo or recurrent based on the date of metastatic diagnosis and history of surgical resection. Overall survival (OS) was summarized within groups via Kaplan–Meier survival estimates and compared using Cox proportional hazards models. RESULTS: We included 5170 patients with metastatic PDAC, of which 1101 (21.3%) were classified as having recurrent disease. Median OS for the recurrent group was significantly greater at 10.8 m (95% CI 9.9–11.7) than in the de novo group at 7.3 m (95% CI 7.0–7.7, p < 0.001). We did not observe a significant difference in OS based on when patients recurred after surgery: 10.0 m (95% CI 8.7–11) within six months of surgery versus 11.6 m (95% CI 10–12, p = 0.256) greater than six months from surgery. CONCLUSIONS: These data support the inclusion of patients with recurrent PDAC in clinical trials for advanced disease, including those who develop recurrent disease within six months of surgery. Due to observed differences in survival, randomization should be stratified by disease presentation (recurrent vs de novo). |
format | Online Article Text |
id | pubmed-9554966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95549662022-10-13 Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study Miotke, Laura Nevala-Plagemann, Christopher Ying, Jian Florou, Vaia Haaland, Benjamin Garrido-Laguna, Ignacio BMC Cancer Research BACKGROUND: A majority of patients undergoing curative intent surgery for pancreatic ductal adenocarcinoma (PDAC) will unfortunately develop recurrent disease. Treatment outcomes for patients with metastatic disease remain suboptimal. In this study, we evaluated clinical outcomes of patients with recurrent PDAC who received systemic therapy and compared outcomes to patients with de novo metastatic PDAC undergoing systemic therapy. METHODS: Patients diagnosed with metastatic PDAC between 2014 and 2019 were included using a real-world database. Patients were characterized as either de novo or recurrent based on the date of metastatic diagnosis and history of surgical resection. Overall survival (OS) was summarized within groups via Kaplan–Meier survival estimates and compared using Cox proportional hazards models. RESULTS: We included 5170 patients with metastatic PDAC, of which 1101 (21.3%) were classified as having recurrent disease. Median OS for the recurrent group was significantly greater at 10.8 m (95% CI 9.9–11.7) than in the de novo group at 7.3 m (95% CI 7.0–7.7, p < 0.001). We did not observe a significant difference in OS based on when patients recurred after surgery: 10.0 m (95% CI 8.7–11) within six months of surgery versus 11.6 m (95% CI 10–12, p = 0.256) greater than six months from surgery. CONCLUSIONS: These data support the inclusion of patients with recurrent PDAC in clinical trials for advanced disease, including those who develop recurrent disease within six months of surgery. Due to observed differences in survival, randomization should be stratified by disease presentation (recurrent vs de novo). BioMed Central 2022-10-12 /pmc/articles/PMC9554966/ /pubmed/36224524 http://dx.doi.org/10.1186/s12885-022-10130-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Miotke, Laura Nevala-Plagemann, Christopher Ying, Jian Florou, Vaia Haaland, Benjamin Garrido-Laguna, Ignacio Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
title | Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
title_full | Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
title_fullStr | Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
title_full_unstemmed | Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
title_short | Treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
title_sort | treatment outcomes in recurrent versus de novo metastatic pancreatic adenocarcinoma: a real world study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554966/ https://www.ncbi.nlm.nih.gov/pubmed/36224524 http://dx.doi.org/10.1186/s12885-022-10130-4 |
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