Evidence map›Paper›PMID 41994013›Full record

ArticleESMO gastrointestinal oncology2026

Treatment attrition between lines of therapy and its impact on outcomes for well-differentiated neuroendocrine tumors in British Columbia.

R Fedrigo, T do Amaral Miranda, R D'Alpino Peioxoto, S Gill, F Benard, D Wilson, P Martineau, I Alberts, J P Solar Vasconcelos, J M Loree

Abstract read
In one paragraph

Article in ESMO gastrointestinal oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

R FedrigoDivision of Medical Oncology, BC Cancer, Vancouver, Canada.
T do Amaral MirandaDivision of Medical Oncology, BC Cancer, Vancouver, Canada.
R D'Alpino PeioxotoDivision of Medical Oncology, BC Cancer, Vancouver, Canada.
S GillDivision of Medical Oncology, BC Cancer, Vancouver, Canada.
F BenardDepartment of Molecular Imaging and Therapy, BC Cancer, Vancouver, Canada.
D WilsonDepartment of Molecular Imaging and Therapy, BC Cancer, Vancouver, Canada.
P MartineauDepartment of Molecular Imaging and Therapy, BC Cancer, Vancouver, Canada.
I AlbertsDepartment of Molecular Imaging and Therapy, BC Cancer, Vancouver, Canada.
J P Solar VasconcelosDivision of Medical Oncology, BC Cancer, Vancouver, Canada.
J M LoreeDivision of Medical Oncology, BC Cancer, Vancouver, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neuroendocrine neoplasms are uncommon malignancies with variable prognosis. With a growing number of available therapies and recent data supporting earlier initiation of radioligand therapy, we aimed to characterize attrition between lines of therapy to inform treatment sequencing and establish baseline assumptions for future health technology assessments. Patients and methods: In this retrospective chart review, patients with metastatic gastroenteropancreatic neuroendocrine tumors (NETs) who received one or more systemic therapies from January 2010 to December 2023 were reviewed. The primary endpoint was attrition between treatment lines. Logistic regression model was used to identify predictors of attrition. Results: Among 234 patients, 65 (28%) had pancreatic NETs (pNETs) and 169 (72%) had extra-pancreatic gastrointestinal NETs (ep-GI-NETs); median age at diagnosis was 65 years. Maximum number of treatment lines was six for pNETs and four for ep-GI-NETs. First-to-second-line attrition rates were 22% [95% confidence interval (CI) 13% to 36%] and 34% (95% CI 25% to 44%) for pNETs and ep-GI-NETs, respectively. Somatostatin analogs were the preferred first line in 194 patients (83%). Peptide receptor radionuclide therapy was administered to 13 pNETs (20%) and 42 ep-GI-NETs (25%). Median first-line progression-free survival (PFS) was 8.8 months and 26.1 months for pNETs and ep-GI-NETs, respectively. Patients treated in the latter cohort (2021-2023) had a lower risk of attrition compared with those in the earlier cohort (2010-2020) (odds ratio 0.38, 95% CI 0.14-0.94, Conclusions: Despite longer first-line PFS, patients with ep-GI-NETs faced higher attrition rates. These findings emphasize the need to prioritize the most effective therapies early during treatment sequencing to ensure patients are exposed to the most active agents.

Indexed as

attritionlines of therapyneuroendocrine tumors

Identifiers

PMID41994013
PMCPMC13080866

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.