Evidence map›Paper›PMID 36629395›Full record

ArticleEndocrine-related cancer2023

Treatment efficacy in a metastatic small intestinal neuroendocrine tumour grade 2 cohort.

Dimitrios Papantoniou, Malin Grönberg, Espen Thiis-Evensen, Halfdan Sorbye, Kalle Landerholm, Staffan Welin, Eva Tiensuu Janson

Open access · hybridAbstract read
In one paragraph

Article in Endocrine-related cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Long-term experience with octreotide and lanreotide for the treatment of gastroenteropancreatic neuroendocrine tumors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  7. Article
  8. Article
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

7 authors at 4 institutions in 2 countries.

Dimitrios PapantoniouDepartment of Medical Sciences, Endocrine Oncology, Uppsala University, Uppsala, Sweden.ORCID 0000-0001-5472-2322
Malin GrönbergDepartment of Medical Sciences, Endocrine Oncology, Uppsala University, Uppsala, Sweden.
Espen Thiis-EvensenOslo University Hospital, Rikshospitalet, Deptartment of Organ Transplant, Oslo, Norway.
Halfdan SorbyeHaukeland Hospital, Deptartment of Oncology, Bergen, Norway.
Kalle LanderholmDepartment of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Staffan WelinDepartment of Medical Sciences, Endocrine Oncology, Uppsala University, Uppsala, Sweden.
Eva Tiensuu JansonDepartment of Medical Sciences, Endocrine Oncology, Uppsala University, Uppsala, Sweden.
Uppsala University · SEHaukeland University Hospital · NOLinköping University · SEOslo University Hospital · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small intestinal neuroendocrine tumours (Si-NET) are often studied as a uniform group. Proliferation index Ki-67 influences prognosis and determines tumour grade. We hypothesized that Si-NET grade 2 (G2) tumours, which have a higher Ki-67 than G1 tumours, might benefit less from established treatments for metastatic disease. We conducted a retrospective cohort study of 212 patients with metastatic Si-NET G2 treated in two Swedish hospitals during 20 years (2000-2019). Median cancer-specific survival on first-line somatostatin analogues (SSA) was 77 months. Median progression-free survival (PFS) was 12.4 months when SSA was given as monotherapy and 19 months for all patients receiving first-line SSA. PFS after SSA dose escalation was 6 months in patients with radiological progression. Treatment efficacies of SSA and peptide receptor radionuclide treatment (PRRT) were studied separately in patients with Ki-67 of 3-5%, 5-10% and 10-20%. For SSA, PFS was significantly shorter at higher Ki-67 levels (31, 18 and 10 months, respectively), while there was only a minor difference in PFS for PRRT (29, 25 and 25 months). Median PFS for sequential treatment with interferon-alpha (IFNα), everolimus and chemotherapy was 6, 5 and 9 months. IFNα seemed to be effective in tumours with low somatostatin-receptor expression. In conclusion, established treatments appeared effective in Si-NET G2, despite their higher proliferation index compared to G1 tumours. However, efficacy of SSA but not PRRT was reduced at higher Ki-67 levels. SSA dose escalation provided limited disease stabilization.

Indexed as

Neuroendocrine TumorsOctreotideHumansIntestinal NeoplasmsKi-67 AntigenPancreatic NeoplasmsRadioisotopesRetrospective StudiesSomatostatinStomach NeoplasmsTreatment OutcomeKi-67 AntigenOctreotideRadioisotopesSomatostatingrade 2interferonKi-67peptide receptor radionuclide treatmentPRRTSi-NETsmall intestinal neuroendocrine tumourssomatostatin analoguessomatostatin receptor negative

Identifiers

PMID36629395
PMCPMC9986391
OpenAlexW4315620216

What OpenQuestion holds

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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.