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Chemotherapy for Well-Differentiated Pancreatic Neuroendocrine Tumours with a Ki-67 Index ≥10%: Is There a More Effective Antitumour Regimen? A Retrospective Multicentre Study of the French Group of Endocrine Tumours (GTE)
Author(s) -
Guillaume Roquin,
Eric Baudin,
Catherine LombardBohas,
Guillaume Cadiot,
Sophie Dominguez,
Rosine Guimbaud,
Patricia Niccoli,
Jean-Louis Legoux,
Emmanuel Mitry,
V. Rohmer,
Philippe Ruszniewski,
Thomas Walter,
Michel Ducreux,
Anne Couvelard,
Jean–Yves Scoazec,
Aline RamondRoquin,
FrançoisXavier CaroliBosc,
Olivia Hentic
Publication year - 2017
Publication title -
neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.493
H-Index - 101
eISSN - 1423-0194
pISSN - 0028-3835
DOI - 10.1159/000457955
Subject(s) - medicine , dacarbazine , temozolomide , chemotherapy , regimen , chemotherapy regimen , neuroendocrine tumors , progression free survival , oncology , gastroenterology , surgery
The best chemotherapy regimen for well- differentiated pancreatic neuroendocrine tumours (pNETs) with a Ki-67 index ≥10% is still debated. We evaluated the antitumour efficacy of various first-line chemotherapy regimens (streptozocin based, platinum based, or dacarbazine/temozolomide based) in this situation.

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