A Role for Vitamin D in the Gastro-Entero-Pancreatic Neuroendocrine Neoplasms Outcome: Report on a Series from a Single Institute
Abstract
Background/Aims: Vitamin D deficiency is hypothesized to represent a risk factor in several neoplasms. The aim of this study was to determine whether serum 25-hydroxyvitamin D (25-OHvitD) deficiency represents a risk factor for neuroendocrine neoplasms (NEN) and can be associated to overall survival (OS) and progression-free survival (PFS).
Methods: From 2010 to 2015, 138 patients with gastro-entero-pancreatic NENs (F=61, median age 63 years) were included in the study. Serum 25-OHvitD levels, which were measured at baseline, were defined as deficient if <20 ng/ml. In such cases 25-OHvitD supplementation was administered to the patients. The possible associations between 25-OHvitD levels and disease grading, staging, overall OS and PFS were considered. Furthermore, the possible association between 25-OHvitD supplementation and PFS or OS was evaluated by Cox’s proportional hazards regression.
Results: Median 25-OHvitD levels were 12.9 ng/ml (range 2–32): in detail, 94 patients (68%) had <20 ng/ml, with 46 cases (33%) having <10 ng/ml. An inverse correlation was observed between 25-OHvitD levels and OS (p=0.03, r.s.=-0.18) and PFS (p=0.01, r.s.=-0.22). At Cox’s proportional hazards regression, mortality was not related to 25-OHvitD levels; however, there was an association between 25-OHvitD supplementation and OS (p <0.002).
Conclusions: Vitamin D deficiency is highly prevalent among NEN patients. 25-OHvitD supplementation potentially plays an important role not only in the correction of 25-OHvitD values, but also for its influence on the clinical outcome. However, further studies are needed to confirm this observation.
See also:
- Vitamin D (analogues and/or derivatives) and cancer;
- Oesophageal squamocellular carcinoma: a complete and objective response;
- Pancreatic Adenocarcinoma: clinical records on 17 patients treated with Di Bella's Method;
- Complete objective response to biological therapy of plurifocal breast carcinoma;






