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Volume 70, Issue 5, Pages 907-914 (November 2009)


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EUS-FNA predicts 5-year survival in pancreatic endocrine tumors

Fátima A.F. Figueiredo, MD, PhDCorresponding Author Information, Marc Giovannini, MD, PhD, Genevieve Monges, MD, PhD, Erwan Bories, MD, Christian Pesenti, MD, Fabrice Caillol, MD, Jean Robert Delpero, MD, PhD

Received 17 November 2008; accepted 6 May 2009. published online 30 July 2009.

Background

Pancreatic endocrine tumors (PETs) differ in clinical behavior and prognosis. Determination of malignant potential through specimens obtained by EUS-FNA can help in the management of these patients.

Objective

To determine the value of EUS-FNA for diagnosing PETs and for classifying their underlying malignant potential based on the World Health Organization (WHO) classification.

Design

Single-center, retrospective, cohort study.

Setting

Tertiary referral hospital.

Patients

This study involved 86 consecutive patients (44 men, mean age 58 ± 14 years) who had been diagnosed with PETs and submitted to EUS-FNA from January 1999 to August 2008.

Intervention

EUS-FNA of a pancreatic mass and/or a metastasis site. Immunohistochemistry on microbiopsies or on monolayer cytology was routinely used. The lesions were classified as recommended by the WHO.

Main Outcome Measurements

EUS-FNA sensitivity and 5-year survival rate.

Results

Overall, in 90% (77 of 86) of patients in this study, PET was diagnosed with EUS-FNA. The sensitivity did not vary with tumor size, type, location, or the presence of hormonal secretion. Of 86 patients, 30 (35%) were submitted to surgical resection. The kappa correlation index between the WHO classification obtained by EUS-FNA and by surgery was 0.38 (P = .003). Major discrepancies were found in the group of patients diagnosed with endocrine tumor of uncertain behavior by EUS-FNA, because 72% turned out to have well-differentiated endocrine carcinoma. Sixteen patients (27%) died during a mean follow-up period of 34 ± 27 months. The 5-year survival rates were 100% for endocrine tumors, 68% for well-differentiated endocrine carcinomas, and 30% for poorly differentiated endocrine carcinomas (P = .008, log-rank test).

Limitations

Retrospective design, selection bias, and small sample size.

Conclusions

This largest single-center experience to date demonstrated the accuracy of EUS-FNA in diagnosing and determining the malignant behavior of PETs. EUS-FNA findings predict 5-year survival in patients with PETs.

Marseille, France

Current affiliations: Unité d'Exploration Médico-Chirurgicale Oncologique, Institut Paoli-Calmettes, France (F.A.F.F., M.G., E.B., C.P., F.C.), Gastroenterology Department, University of the State of Rio de Janeiro and Federal University of Rio de Janeiro, Brazil (F.A.F.F.), Biopathology Unit, Institut Paoli-Calmettes, France (G.M.), Surgical Unit, Institut Paoli-Calmettes, France (J.R.D.)

Corresponding Author InformationReprint requests: Fátima Aparecida Ferreira Figueiredo, MD, PhD, Gastroenterology Department - University of the State of Rio de Janeiro, Rua Humaitá 282 Bl II Ap 1703 Humaitá, Rio de Janeiro, Brazil 22261001.

 DISCLOSURE: All authors disclosed no financial relationships relevant to this publication.

 If you would like to chat with an author of this article, you may contact him at faff@gbl.com.br.

PII: S0016-5107(09)01922-1

doi:10.1016/j.gie.2009.05.020


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