Evidence map›Paper›PMID 37969399›Full record

ArticleTranslational cancer research2023

The clinicopathological characteristics and survival outcomes of primary expansile

Sabina Nistor, Sally El-Tawab, Flora Wong, Andreas Zouridis, Rene Roux, Sanjiv Manek, Kezia Gaitskell, Ahmed Ashour Ahmed, Sean Kehoe, Hooman Soleymani Majd

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Article in Translational cancer research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

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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 at 3 institutions in 3 countries.

Sabina NistorDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Sally El-TawabDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Flora WongDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Andreas ZouridisDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Rene RouxDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Sanjiv ManekDepartment of Cellular Pathology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Kezia GaitskellDepartment of Cellular Pathology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Ahmed Ashour AhmedMRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.
Sean KehoeDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Hooman Soleymani MajdDepartment of Gynaecology Oncology, Churchill Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
University of Oxford · GBChurchill Hospital · GBOxford University Hospitals NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mucinous ovarian carcinomas (MOCs) are rare ovarian tumours accounting for 3% of all epithelial ovarian carcinomas (EOCs). They are either expansile or infiltrative, based on the tumour's histological pattern of invasion. MOCs have a distinct molecular profile, natural history, chemo-sensitivity, and prognosis compared to other EOCs. The aim of this study was to describe patient and tumour characteristics, as well as survival outcomes of expansile and infiltrative primary MOCs. Methods: This was a retrospective cohort study conducted at a tertiary cancer centre. Patients had surgery for primary MOC between Jul 1, 2010 and Oct 28, 2022. All patients discussed at the Oxford multidisciplinary team (MDT) meeting with a diagnosis of MOC were included. We excluded patients with mucinous metastatic carcinoma (MMC), dual histological diagnoses, those who died before treatment was initiated, and patients with incomplete records. Results: A total of 47 patients were identified and 14 were excluded. Out of the remaining 33 MOCs, 23 (70.6%) were expansile and 10 (30.4%) were infiltrative. The median follow-up was 37 months (95% CI: 14.1-69.8). Patients with infiltrative tumours were older than those with expansile tumours (median age 62 Conclusions: Patients with infiltrative tumours were older, more likely to have bilateral tumours and more likely to have an advanced FIGO stage at diagnosis. Adjuvant treatment was more likely to be administered to patients with infiltrative tumours, however, this did not prevent relapse. PFS at 3 years was significantly higher in patients with expansile tumours. PAX8 was more frequently expressed by expansile tumours.

Indexed as

expansileinfiltrativeMucinous ovarian carcinomas (MOCs)

Identifiers

PMID37969399
PMCPMC10643958
OpenAlexW4387952848

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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.