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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.
Afiliación
  • Miotke L; Division of Medical Oncology, Huntsman Cancer Institute, 2000 Circle of Hope, Salt Lake City, UT, 84112, USA. laura.miotke@hsc.utah.edu.
  • Nevala-Plagemann C; Department of Internal Medicine, University of Utah School of Medicine, 30 North 1900 East, Salt Lake City, UT, 84132, USA. laura.miotke@hsc.utah.edu.
  • Ying J; Division of Medical Oncology, Huntsman Cancer Institute, 2000 Circle of Hope, Salt Lake City, UT, 84112, USA.
  • Florou V; Department of Population Health Sciences, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
  • Haaland B; Division of Medical Oncology, Huntsman Cancer Institute, 2000 Circle of Hope, Salt Lake City, UT, 84112, USA.
  • Garrido-Laguna I; Department of Population Health Sciences, 295 Chipeta Way, Salt Lake City, UT, 84108, USA.
BMC Cancer ; 22(1): 1054, 2022 Oct 12.
Article en En | MEDLINE | ID: mdl-36224524
ABSTRACT

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).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Adenocarcinoma / Carcinoma Ductal Pancreático Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Adenocarcinoma / Carcinoma Ductal Pancreático Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos