Evidence map›Paper›PMID 31005287›Full record

Trial reportGynecologic oncology2019

An international, phase III randomized trial in patients with mucinous epithelial ovarian cancer (mEOC/GOG 0241) with long-term follow-up: and experience of conducting a clinical trial in a rare gynecological tumor.

Martin Gore, Allan Hackshaw, William E Brady, Richard T Penson, Richard Zaino, W Glenn McCluggage, Raji Ganesan, Nafisa Wilkinson, Timothy Perren, Ana Montes and 12 more

Open access · hybridAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Gynecologic oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 4 pooled it
11.6field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 4 syntheses or guidelines pooled it, 102 citations in OpenAlex.

  1. Pooled it
  2. Angiogenesis inhibitors for the treatment of epithelial ovarian cancer.The Cochrane database of systematic reviews · 2023
    Pooled it
  3. Pooled it
  4. Survival outcome and perioperative complication related to neoadjuvant chemotherapy with carboplatin and paclitaxel for advanced ovarian cancer: A systematic review and meta-analysis.European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology · 2020
    Pooled it
  5. Trial
  6. Article
  7. Ovarian cancer.Nature reviews. Disease primers · 2026
    Review
  8. Article
  9. Article
  10. Mucinous ovarian neoplasm - outcomes of a rare tumor.Gynecologic oncology reports · 2025
    Article
  11. Article
  12. Cellular origins of mucinous ovarian carcinoma.The Journal of pathology · 2025
    Review
  13. Article
  14. The Role ofInternational journal of women's health · 2025
    Article
  15. Review
  16. Review
  17. Investigating age and ethnicity as novel high-risk phenotypes in mucinous ovarian cancer: retrospective study in a multi-ethnic population.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2024
    Observational
  18. Review
  19. Article
  20. Review
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

22 authors at 18 institutions in 2 countries.

Martin GoreRoyal Marsden NHS Foundation Trust, London, UK.
Allan HackshawCancer Research UK & UCL Cancer Trials Centre, London, UK. Electronic address: a.hackshaw@ucl.ac.uk.
William E BradyRoswell Park Comprehensive Cancer Centre, Buffalo, USA.
Richard T PensonMassachusetts General Hospital, Boston, USA.
Richard ZainoPenn State Health Milton S. Hershey Medical Centre, PA, USA.
W Glenn McCluggageDept of Pathology, Belfast Health & Social Care Trust, Belfast, UK.
Raji GanesanBirmingham Women's Hospital, Birmingham, UK.
Nafisa WilkinsonUniversity College London Hospitals NHS Foundation Trust, London, UK.
Timothy PerrenLeeds Teaching Hospitals NHS Trust, Leeds, UK.
Ana MontesGuy's and St Thomas' NHS Foundation Trust, London, UK.
Jeffrey SummersMaidstone and Tunbridge Wells NHS Foundation Trust, Kent, UK.
Rosemary LordClatterbridge Cancer Centre NHS Foundation Trust, Liverpool, UK.
Graham DarkNewcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Gordon RustinMount Vernon Cancer Centre, Middlesex, UK.
Melanie MackeanEdinburgh Cancer Centre, Edinburgh, UK.
Nicholas ReedBeatson Oncology Centre, Glasgow, UK.
Sean KehoeInstitute of Cancer and Genomics, University of Birmingham, Birmingham, UK.
Michael FrumovitzThe University of Texas MD Anderson Cancer Centre, Houston, TX, USA.
Helen ChristensenCancer Research UK & UCL Cancer Trials Centre, London, UK.
Amanda FeeneyCancer Research UK & UCL Cancer Trials Centre, London, UK.
Jonathan LedermannCancer Research UK & UCL Cancer Trials Centre, London, UK.
David M GershensonThe University of Texas MD Anderson Cancer Centre, Houston, TX, USA.
Cancer Research UK · GBThe University of Texas MD Anderson Cancer Center · USBeatson West of Scotland Cancer Centre · GBBelfast Health and Social Care Trust · GBBirmingham Women's Hospital · GBClatterbridge Cancer Centre NHS Foundation Trust · GBEdinburgh Cancer Research · GBGenomics (United Kingdom) · GBGuy's and St Thomas' NHS Foundation Trust · GBLeeds Teaching Hospitals NHS Trust · GBMaidstone and Tunbridge Wells NHS Trust · GBMassachusetts General Hospital · USMount Vernon Cancer Centre · GBNewcastle upon Tyne Hospitals NHS Foundation Trust · GBPenn State Milton S. Hershey Medical Center · USRoswell Park Comprehensive Cancer Center · USRoyal Marsden NHS Foundation Trust · GBUniversity College London Hospitals NHS Foundation Trust · GB

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NRG Oncology Network Group Operations Center - GY9 BIQSFP Reports/BudgetsU10CA180868 · NCI · NRG ONCOLOGY FOUNDATION, INC. · PI NORMAN WOLMARK · 2014 to 2026
$206.8M
Statistics CoreU10CA180822 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI James J. Dignam, GREG YOTHERS · 2014 to 2026
$146.4M
GYNECOLOGIC ONCOLOGY GROUP HEADQUARTERSU10CA027469 · NCI · GYNECOLOGIC ONCOLOGY GROUP · PI DISAIA, PHILIP J. · 1985 to 2013
$132.6M
GYNECOLOGIC ONCOLOGY GROUP STATISTICAL OFFICEU10CA037517 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI BLESSING, JOHN A · 1985 to 2013
$67.4M
Cancer Research UK C1569/A9620Department of HealthNCI NIH HHS P30 CA016672NCI NIH HHS U10 CA027469NCI NIH HHS U10 CA037517NCI NIH HHS U10 CA180822NCI NIH HHS U10 CA180868
6 · The paper itself

Abstract

objectivesWe evaluated four different treatment regimens for advanced-stage mucinous epithelial ovarian cancer.

methodsWe conducted a multicenter randomized factorial trial (UK and US). Patients were diagnosed with primary mEOC: FIGO stage II-IV or recurrence after stage I disease. Treatment arms were paclitaxel-carboplatin, oxaliplatin-capecitabine, paclitaxel-carboplatin-bevacizumab, or oxaliplatin-capecitabine-bevacizumab. Chemotherapy was given 3-weekly for 6 cycles, and bevacizumab (3-weekly) was continued as maintenance (for 12 cycles). Endpoints included overall-survival (OS), progression-free survival (PFS), toxicity and quality of life (QoL).

resultsThe trial stopped after 50 patients were recruited due to slow accrual. Median follow-up was 59 months. OS hazard ratios (HR) for the two main comparisons were: 0.78 (p = 0.48) for Oxal-Cape vs. Pac-Carbo (each with/without bevacizumab), and 1.04 (p = 0.92) for bevacizumab vs. no bevacizumab. Corresponding PFS HRs were: 0.84 and 0.80. Retrospective central pathology review revealed only 45% (18/40) cases with available material had confirmed primary mEOC. Among these, OS HR for Oxal-Cape vs. Pac-Carbo was 0.36 (p = 0.14); PFS HR = 0.62 (p = 0.40). Grade 3-4 toxicity was seen in 61% Pac-Carbo, 61% Oxal-Cape, 54% Pac-Carbo-Bev, and 85% Oxal-Cape-Bev. QoL was similar between the four arms.

conclusionmEOC/GOG0241 represents an example of a randomized rare tumor trial. Logistical challenges led to early termination, including difficulties in local histopathological diagnosis and accessing drugs outside their labelled indication. There was misalignment between central funders who support clinical trials in rare cancers and the deprioritisation of such work by those managing and funding research at a local level. Rare cancer trials should include centralised pathology review before treatment. Clinical trial registry number: ISRCTN83438782.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBevacizumabCapecitabineCarboplatinCarcinoma, Ovarian EpithelialFemaleFollow-Up StudiesHumansInternationalityMiddle AgedNeoplasm Recurrence, LocalNeoplasms, Cystic, Mucinous, and SerousOvarian NeoplasmsBevacizumabCapecitabineCarboplatinOxaliplatinPaclitaxelChemotherapyFactorial designMucinous ovarian cancerRare tumor trial

Identifiers

PMID31005287
PMCPMC6559214
OpenAlexW2936836467

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.