Proposal of early CT morphological criteria for response of liver metastases to systemic treatments in gastroenteropancreatic neuroendocrine tumors: Alternatives to RECIST Journal Article


Authors: de Mestier, L.; Resche-Rigon, M.; Dromain, C.; Lamarca, A.; La Salvia, A.; de Baker, L.; Fehrenbach, U.; Pusceddu, S.; Colao, A.; Borbath, I.; de Haas, R.; Rinzivillo, M.; Zerbi, A.; Funicelli, L.; de Herder, W. W.; Selberherr, A.; Wagner, A. D.; Manoharan, P.; De Cima, A.; Lybaert, W.; Jann, H.; Prinzi, N.; Faggiano, A.; Annet, L.; Walenkamp, A.; Panzuto, F.; Pedicini, V.; Pitoni, M. G.; Siebenhuener, A.; Mayerhoefer, M. E.; Ruszniewski, P.; Vullierme, M. P.
Article Title: Proposal of early CT morphological criteria for response of liver metastases to systemic treatments in gastroenteropancreatic neuroendocrine tumors: Alternatives to RECIST
Abstract: RECIST 1.1 criteria are commonly used with computed tomography (CT) to evaluate the efficacy of systemic treatments in patients with neuroendocrine tumors (NETs) and liver metastases (LMs), but their relevance is questioned in this setting. We aimed to explore alternative criteria using different numbers of measured LMs and thresholds of size and density variation. We retrospectively studied patients with advanced pancreatic or small intestine NETs with LMs, treated with systemic treatment in the first-and/or second-line, without early progression, in 14 European expert centers. We compared time to treatment failure (TTF) between responders and non-responders according to various criteria defined by 0%, 10%, 20% or 30% decrease in the sum of LM size, and/or by 10%, 15% or 20% decrease in LM density, measured on two, three or five LMs, on baseline (≤1 month before treatment initiation) and first revaluation (≤6 months) contrast-enhanced CT scans. Multivariable Cox proportional hazard models were performed to adjust the association between response criteria and TTF on prognostic factors. We included 129 systemic treatments (long-acting somatostatin analogs 41.9%, chemotherapy 26.4%, targeted therapies 31.8%), administered as first-line (53.5%) or second-line therapies (46.5%) in 91 patients. A decrease ≥10% in the size of three LMs was the response criterion that best predicted prolonged TTF, with significance at multivariable analysis (HR 1.90; 95% CI: 1.06–3.40; p =.03). Conversely, response defined by RECIST 1.1 did not predict prolonged TTF (p =.91), and neither did criteria based on changes in LM density. A ≥10% decrease in size of three LMs could be a more clinically relevant criterion than the current 30% threshold utilized by RECIST 1.1 for the evaluation of treatment efficacy in patients with advanced NETs. Its implementation in clinical trials is mandatory for prospective validation. Criteria based on changes in LM density were not predictive of treatment efficacy. Clinical Trial Registration: Registered at CNIL-CERB, Assistance publique hopitaux de Paris as “E-NETNET-L-E-CT” July 2018. No number was assigned. Approved by the Medical Ethics Review Board of University Medical Center Groningen. © 2023 The Authors. Journal of Neuroendocrinology published by John Wiley & Sons Ltd on behalf of British Society for Neuroendocrinology.
Keywords: adult; cancer chemotherapy; controlled study; treatment failure; retrospective studies; major clinical study; advanced cancer; systemic therapy; liver neoplasms; cancer patient; computer assisted tomography; tomography, x-ray computed; diagnostic imaging; retrospective study; neuroendocrine tumor; liver metastasis; contrast enhancement; multicenter study; liver tumor; clinical evaluation; drug therapy; university hospital; medical ethics; somatostatin derivative; computed tomography; france; neuroendocrine tumors; pancreas islet cell tumor; molecularly targeted therapy; second-line treatment; response evaluation; cancer prognosis; response evaluation criteria in solid tumors; time to treatment; humans; human; male; female; article; x-ray computed tomography; systemic treatments; gastro-enteropancreatic neuroendocrine tumor; small intestinal neuroendocrine tumor
Journal Title: Journal of Neuroendocrinology
Volume: 35
Issue: 6
ISSN: 0953-8194
Publisher: Wiley Blackwell  
Date Published: 2023-06-01
Start Page: e13311
Language: English
DOI: 10.1111/jne.13311
PUBMED: 37345276
PROVIDER: scopus
DOI/URL:
Notes: Article -- MSK Cancer Center Support Grant (P30 CA008748) acknowledged in PDF -- Source: Scopus
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