Progression of Site-specific Recurrence of Pancreatic Cancer and Implications for Treatment

To analyze postrecurrence progression in the context of recurrence sites and assess implications for postrecurrence treatment. Most patients with resected pancreatic ductal adenocarcinoma (PDAC) recur within 2 years. Different survival outcomes for location-specific patterns of recurrence are report...

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Veröffentlicht in:Annals of surgery 2024-08, Vol.280 (2), p.317-324
Hauptverfasser: Rompen, Ingmar F, Levine, Jonah, Habib, Joseph R, Sereni, Elisabetta, Mughal, Nabiha, Hewitt, Daniel Brock, Sacks, Greg D, Welling, Theodore H, Simeone, Diane M, Kaplan, Brian, Berman, Russell S, Cohen, Steven M, Wolfgang, Christopher L, Javed, Ammar A
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Sprache:eng
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Zusammenfassung:To analyze postrecurrence progression in the context of recurrence sites and assess implications for postrecurrence treatment. Most patients with resected pancreatic ductal adenocarcinoma (PDAC) recur within 2 years. Different survival outcomes for location-specific patterns of recurrence are reported, highlighting their prognostic value. However, a lack of understanding of postrecurrence progression and survival remains. This retrospective analysis included surgically treated patients with PDAC at NYU Langone Health (2010-2021). Sites of recurrence were identified at the time of diagnosis and further follow-up. Kaplan-Meier curves, log-rank test, and Cox regression analyses were applied to assess survival outcomes. Recurrence occurred in 57.3% (196/342) patients with a median time to recurrence of 11.3 months (95% CI: 12.6-16.5). The first site of recurrence was local in 43.9% of patients, liver in 23.5%, peritoneal in 8.7%, lung in 3.6%, whereas 20.4% had multiple sites of recurrence. Progression to secondary sites was observed in 11.7%. Only lung involvement was associated with significantly longer survival after recurrence compared with other sites (16.9 vs 8.49 months, P = 0.003). In local recurrence, 21 (33.3%) patients were alive after 1 year without progression to secondary sites. This was associated with a CA19-9 of
ISSN:0003-4932
1528-1140
1528-1140
DOI:10.1097/SLA.0000000000006142