Sequence of therapy and survival in patients with advanced pancreatic neuroendocrine tumours

Curr Oncol. 2020 Aug;27(4):215-219. doi: 10.3747/co.27.5929. Epub 2020 Aug 1.

Abstract

Background: Pancreatic neuroendocrine tumours (pnets) often present as advanced disease. The optimal sequence of therapy is unknown.

Methods: Sequential patients with advanced pnets referred to BC Cancer between 2000 and 2013 who received 1 or more treatment modalities were reviewed, and treatment patterns, progression-free survival (pfs), and overall survival (os) were characterized. Systemic treatments included chemotherapy, small-molecule therapy, and peptide receptor radionuclide therapy.

Results: In 66 cases of advanced pnets, median patient age was 61.2 years (25%-75% interquartile range: 50.8-66.2 years), and men constituted 47% of the group. First-line therapies were surgery (36%), chemotherapy (33%), and somatostatin analogues (32%). Compared with first-line systemic therapy, surgery in the first line was associated with increased pfs and os (20.6 months vs. 6.3 months and 100.3 months vs. 30.5 months respectively, p < 0.05). In 42 patients (64%) who received more than 1 line of therapy, no difference in os or pfs between second-line therapies was observed.

Conclusions: Our results confirm the primary role of surgery for advanced pnets. New systemic treatments will further increase options.

Keywords: Pancreas; neuroendocrine tumours; treatment sequencing.

MeSH terms

  • Aged
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neuroendocrine Tumors / mortality
  • Neuroendocrine Tumors / therapy*
  • Pancreatic Neoplasms / mortality
  • Pancreatic Neoplasms / therapy*
  • Survival Analysis