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dc.contributor.authorLamarca, Angela
dc.contributor.authorBarriuso, Jorge
dc.contributor.authorKulke, M
dc.contributor.authorBorbath, I
dc.contributor.authorLenz, H
dc.contributor.authorRaoul, J
dc.contributor.authorMeropol, N
dc.contributor.authorLombard-Bohas, C
dc.contributor.authorPosey, J
dc.contributor.authorFaivre, S
dc.contributor.authorRaymond, E
dc.contributor.authorValle, Juan W
dc.date.accessioned2017-12-21T10:36:12Z
dc.date.available2017-12-21T10:36:12Z
dc.date.issued2017-11-21
dc.identifier.citationDetermination of an optimal response cut-off able to predict progression-free survival in patients with well-differentiated advanced pancreatic neuroendocrine tumours treated with sunitinib: an alternative to the current RECIST-defined response. 2017, Br J Canceren
dc.identifier.issn1532-1827
dc.identifier.pmid29161241
dc.identifier.doi10.1038/bjc.2017.402
dc.identifier.urihttp://hdl.handle.net/10541/620738
dc.description.abstractSunitinib prolongs progression-free survival (PFS) in patients with advanced pancreatic neuroendocrine tumours (pNET). Response Evaluation Criteria in Solid Tumors (RECIST)-defined partial responses (PR; classically defined as ⩾30% size decrease from baseline) are infrequent.
dc.language.isoenen
dc.rightsArchived with thanks to British journal of canceren
dc.titleDetermination of an optimal response cut-off able to predict progression-free survival in patients with well-differentiated advanced pancreatic neuroendocrine tumours treated with sunitinib: an alternative to the current RECIST-defined response.en
dc.typeArticleen
dc.contributor.department29161241en
dc.identifier.journalBritish Journal of Canceren
refterms.dateFOA2018-12-17T15:10:56Z
html.description.abstractSunitinib prolongs progression-free survival (PFS) in patients with advanced pancreatic neuroendocrine tumours (pNET). Response Evaluation Criteria in Solid Tumors (RECIST)-defined partial responses (PR; classically defined as ⩾30% size decrease from baseline) are infrequent.


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