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Overall Survival Prediction and Usefulness of Second-Line Chemotherapy in Advanced Pancreatic Adenocarcinoma.

Authors :
Vienot, Angélique
Beinse, Guillaume
Louvet, Christophe
de Mestier, Louis
Meurisse, Aurélia
Fein, Francine
Heyd, Bruno
Cleau, Denis
d'Engremont, Christelle
Dupont-Gossart, Anne-Claire
Lakkis, Zaher
Tournigand, Christophe
Bouché, Olivier
Rousseau, Benoît
Neuzillet, Cindy
Bonnetain, Franck
Borg, Christophe
Vernerey, Dewi
Source :
JNCI: Journal of the National Cancer Institute. Oct2017, Vol. 109 Issue 10, pN.PAG-N.PAG. 1p.
Publication Year :
2017

Abstract

<bold>Background: </bold>In advanced pancreatic ductal adenocarcinoma (aPDAC), there is no consensual strategy for second-line chemotherapy (L2). Better discrimination of overall survival (OS) may help clinical decision-making. We aimed to predict OS from the beginning of L2 and to assess the benefit from chemotherapy among the identified risk groups.<bold>Methods: </bold>Analyses were derived from all consecutive aPDAC patients treated at Besancon University Hospital, Besancon, France, between January 2003 and December 2013 (n = 462). The association of 50 parameters with OS was evaluated using univariate and multivariable Cox analyses. Based on the final model, a prognostic nomogram and score were developed and externally validated. Patients in the external validation cohort who received L2 (n = 163) were treated at three French institutions between January 2010 and April 2016. All statistical tests were two-sided.<bold>Results: </bold>In the development cohort, 395 patients (85.5%) were eligible for L2, of which 261 (66.1%) were treated. Age, smoking status, liver metastases, performance status, pain, jaundice, ascites, duration of first-line, and type of L2 regimen were identified as independent prognostic factors for OS in L2. The score determined three groups with median OS of 11.3 months (95% confidence interval [CI] = 9.1 to 12.9 months), 3.6 months (95% CI = 2.6 to 4.7 months), and 1.4 months (95% CI = 1.2 to 1.7 months), for low-, intermediate-, and high-risk groups, respectively ( P < .001). By applying the score in the population eligible for L2 but untreated, the chemotherapy benefit was statistically significant across all groups, but with a magnitude of the effect decreased statistically significantly from low- to high-risk groups ( P = .001 for treatment and risk groups interaction term). The ability of the score to discriminate OS was confirmed in the external validation cohort.<bold>Conclusions: </bold>This prognostic nomogram and score in patients with aPDAC can accurately predict OS before administration of L2 and may help clinicians in their therapeutic decisions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278874
Volume :
109
Issue :
10
Database :
Academic Search Index
Journal :
JNCI: Journal of the National Cancer Institute
Publication Type :
Academic Journal
Accession number :
124928812
Full Text :
https://doi.org/10.1093/jnci/djx037