Background
Pancreatic neuroendocrine tumors (PNETs) present in more than 50% of cases with liver
metastases as the only systemic localization. Liver metastases are unresectable in
80% of cases at diagnosis. In the context of a metastatic disease, the benefit of
primary tumor removal in terms of survival is controversial.
Methods
A single-center series of patients with PNETs presenting with synchronous unresectable
hepaticmetastases and treated within a framework of a multidisciplinary team was analyzed
retrospectively to assess the prognostic factors and the potential benefit of primary
tumor resection on long-term survival.
Results
At the time of diagnosis, 12 of 43 patients (28%) underwent primary tumor resection.
After a median follow-up of 5 years (range, 0.6–14 years), 22 disease-related deaths
were observed. The corresponding 5-year survival and median disease-specific duration
of survival were 58% and 77 months, respectively. In the operated and nonoperated
patients the 5-year disease-specific survival was 82% and 50%, respectively (P = .027). At multivariate analysis, patients with primary tumor removed had an improved
survival compared with patients who did not (hazard ratio 0.18; 95% CI 0.05–0.66;
P = .010). Other important factors associated with improved survival at multivariate
analysis were lesser age, lesser Ki-67 index, and 25% less liver tumor burden.
Conclusion
In the present series of patients with PNETs and unresectable liver metastases, resection
of the primary tumor was associated with an improved survival. This observation suggests
that resection of the primary tumor should be part of a global therapeutic strategy
and its indication and timing should be discussed within a multidisciplinary team.
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References
- Population-based study of islet cell carcinoma.Ann Surg Oncol. 2007; 14: 3492-3500
- Hepatic neuroendocrine metastases: does intervention alter outcomes?.J Am Coll Surg. 2000; 190: 432-445
- Nonfunctional pancreatic islet cell tumors.in: Doherty G. Skogseid B. Surgical endocrinology. 1st ed. Lippincott Williams & Wilkins, Philadelphia2001: 361-373
- Prognostic factors and survival in endocrine tumor patients: comparison between gastrointestinal and pancreatic localization.Endocr Relat Cancer. 2005; 12: 1083-1092
- Aggressive surgery for metastatic liver neuroendocrine tumors.Surgery. 2003; 134: 1057-1065
- Concurrent resections of pancreatic islet cell cancers with synchronous hepatic metastases: outcomes of an aggressive approach.Surgery. 2002; 132: 976-983
- Clinical and imaging followup after exhaustive liver resection of endocrine metastases: a 15-year monocentric experience.Endocr Relat Cancer. 2009; 16: 977-990
- Cytoreductive hepatic surgery for neuroendocrine tumors.Surgery. 1990; 108: 1091-1096
- Clinical characteristics, treatment and survival in patients with pancreatic tumors causing hormonal syndromes.World J Surg. 1992; 16: 632-639
- Primary tumour resection in metastatic nonfunctioning pancreatic endocrine carcinomas.Dig Liver Dis. 2009; 41: 49-55
- Role of resection of the primary pancreatic neuroendocrine tumour only in patients with unresectable metastatic liver disease: a systematic review.Neuroendocrinology. 2011; 93: 223-229
- Barcelona Consensus Conferencearticipants. ENETS Consensus Guidelines for the management of patients with digestive neuroendocrine neoplasms: functional pancreatic endocrine tumor syndromes.Neuroendocrinology. 2012; 95: 98-119
- ENETS Consensus Guidelines for the management of patients with digestive neuroendocrine neoplasms of the digestive system: well-differentiated pancreatic non-functioning tumors.Neuroendocrinology. 2012; 95: 120-134
- NANETS treatment guidelines: well-differentiated neuroendocrine tumors of the stomach and pancreas.Pancreas. 2010; 39: 735-752
- Neuroendocrine tumors.J Natl Compr Canc Netw. 2012; 10: 724-764
- Nomenclature and classification of neuroendocrine neoplasm of the digestive system.in: Bosman F.T. Carneiro F. Hruban R.H. WHO classification of tumor of the digestive system. International Agency for Research on Cancer (IRAC), Lyon2010: 13-14
- pancreatic endocrine tumors: improve TNM staging and histopathological grading permit a clinically efficient prognostic stratification of patients.Mod Pathol. 2010; 26: 824-833
- Nonfunctioning islet cell carcinoma of the pancreas: survival results in a contemporary series of 163 patients.Surgery. 2001; 130: 1078-1085
- Surgery in malignant pancreatic neuroendocrine tumors.J Surg Oncol. 2007; 96: 397-403
- Gastroenteropancreatic neuroendocrine tumors.Lancet Oncol. 2008; 9: 61-62
- A rationale for multidisciplinary care in treating neuroendocrine tumours.Curr Opin Endocrinol Diabetes Obes. 2012; 19: 306-313
- Radiolabeled somatostatin analog [177Lu-DOTA0,Tyr3]octreotate in patients with endocrine gastroenteropancreatic tumors.J Clin Oncol. 2005; 23: 2754-2762
Article info
Publication history
Published online: December 26, 2013
Accepted:
December 19,
2013
Identification
Copyright
© 2014 Mosby, Inc. Published by Elsevier Inc. All rights reserved.