| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | taieb, julien |
| dc.contributor.author | Seufferlein, Thomas |
| dc.contributor.author | Reni, Michele |
| dc.contributor.author | Palmer, Daniel H. |
| dc.contributor.author | Cubillo, Antonio |
| dc.contributor.author | Bridgewater, John |
| dc.contributor.author | Macarulla, Teresa |
| dc.date.accessioned | 2023-09-27T08:52:07Z |
| dc.date.available | 2023-09-27T08:52:07Z |
| dc.date.issued | 2023-09-18 |
| dc.identifier.citation | Taieb J, Seufferlein T, Reni M, Palmer DH, Bridgewater JA, Cubillo A, et al. Treatment sequences and prognostic/predictive factors in metastatic pancreatic ductal adenocarcinoma: univariate and multivariate analyses of a real-world study in Europe. BMC Cancer. 2023 Sep 18;23:877. |
| dc.identifier.issn | 1471-2407 |
| dc.identifier.uri | https://hdl.handle.net/11351/10358 |
| dc.description | Metastatic; Pancreatic cancer; Prognostic factors |
| dc.description.abstract | Background
Real-world data on treatment patterns/outcomes for metastatic pancreatic cancer (mPAC) are limited. This study aims to assess real-world treatment patterns, survival outcomes, and prognostic/predictive factors in patients with mPAC.
Methods
Retrospective, observational, chart-review involving medical oncologists and gastroenterologists from five European countries. Physicians reported information on disease and patient characteristics, diagnosis, and treatment for patients diagnosed with mPAC from January-October 2016. Outcomes included median progression-free survival (mPFS), median overall survival (mOS), and the impact of baseline performance status on survival. Univariate/multivariate regression analyses were undertaken to identify prognostic/predictive factors.
Results
Three hundred four physicians and 3432 patients were included. First-line therapies included modified (m)FOLFIRINOX (28.4%), gemcitabine + nab-paclitaxel (28.0%), and gemcitabine monotherapy (23.0%). Frequent second-line therapies were gemcitabine monotherapy (25.0%), fluorouracil (5-FU) + oxaliplatin (21.8%), and gemcitabine + nab-paclitaxel (16.7%). Most frequent first- to second-line treatment sequences were gemcitabine + nab-paclitaxel followed by fluoropyrimidine combinations. Longest unadjusted estimated mOS was observed with (m)FOLFIRINOX followed by gemcitabine-based combinations (19.1 months). Multivariate analysis identified significant prognostic/predictive factors for OS and PFS including performance status and carbohydrate antigen 19–9 (CA 19–9) levels.
Conclusions
Treatment and treatment sequences were generally in accordance with guidelines at the time of the study. Identification of prognostic/predictive factors for survival may help inform the individualised management of mPAC patients in the future. |
| dc.language.iso | eng |
| dc.publisher | BMC |
| dc.relation.ispartofseries | BMC Cancer;23 |
| dc.rights | Attribution 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
| dc.source | Scientia |
| dc.subject | Pàncrees - Càncer - Tractament |
| dc.subject | Pàncrees - Càncer - Prognosi |
| dc.subject | Adenocarcinoma |
| dc.subject | Metàstasi |
| dc.subject.mesh | Pancreatic Neoplasms |
| dc.subject.mesh | Carcinoma, Pancreatic Ductal |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Prognosis |
| dc.title | Treatment sequences and prognostic/predictive factors in metastatic pancreatic ductal adenocarcinoma: univariate and multivariate analyses of a real-world study in Europe |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1186/s12885-023-11377-1 |
| dc.subject.decs | neoplasias pancreáticas |
| dc.subject.decs | carcinoma ductal pancreático |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | pronóstico |
| dc.relation.publishversion | https://doi.org/10.1186/s12885-023-11377-1 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Taieb J] Department of Gastroenterology and Digestive Oncology, Université de Paris, Georges Pompidou European Hospital, SIRIC CARPEM, Paris, France. Université Paris-Cité, Hôpital Européen Georges Pompidou, Hepatogastroenterology and GI Oncology, Paris, France. [Seufferlein T] Department of Internal Medicine I, University Hospital Ulm, Ulm, Germany. [Reni M] University Vita E Salute, IRCCS, San Rafaele Scientifc Institute, Milan, Italy. [Palmer DH] University of Liverpool, Liverpool, UK. [Bridgewater JA] UCL Cancer Institute, London, UK. [Cubillo A] HM CIOCC University Hospital, Madrid, Spain. [Macarulla T] Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. IOB Quiron, Barcelona, Spain |
| dc.identifier.pmid | 37723453 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |