Evidence map›Paper›PMID 20304628›Full record

Trial reportEuropean journal of cancer (Oxford, England : 1990)2010

Phase II trial of the histone deacetylase inhibitor belinostat in women with platinum resistant epithelial ovarian cancer and micropapillary (LMP) ovarian tumours.

Helen J Mackay, Hal Hirte, Terrence Colgan, Al Covens, Katrina MacAlpine, Pamela Grenci, Lisa Wang, Jaqueline Mason, Pnu-An Pham, Ming-S Tsao and 3 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in European journal of cancer (Oxford, England : 1990), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

66 citing papers in PubMed, 146 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Epigenetic regulation in gynecological cancers: a paradigm shift in immunotherapy strategies.Journal of experimental & clinical cancer research : CR · 2025
    Review
  6. Review
  7. Epigenetic Modulation of Estrogen Receptor Signaling in Ovarian Cancer.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review

6 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 2 countries.

Helen J MackayPrincess Margaret Phase II Consortium, Toronto, Canada. helen.mackay@uhn.on.ca
Hal Hirte
Terrence Colgan
Al Covens
Katrina MacAlpine
Pamela Grenci
Lisa Wang
Jaqueline Mason
Pnu-An Pham
Ming-S Tsao
James Pan
James Zwiebel
Amit M Oza
Princess Margaret Cancer Centre · CANational Cancer Institute · USSunnybrook Health Science Centre · CA

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Christine Hui · 1994 to 2026
$57.9M
NCI NIH HHS N01 CM062203NCI NIH HHS N01-CM-62203
6 · The paper itself

Abstract

aimMicropapillary/borderline (LMP) ovarian tumours are rarely included in clinical trials and are intrinsically resistant to radiation and chemotherapy. Platinum resistant epithelial ovarian cancer (EOC) has a poor prognosis. The histone deacetylase inhibitor belinostat demonstrated antitumour activity in pre-clinical ovarian cancer models.

methodsA phase II study was performed to evaluate the activity of belinostat in two patient populations: women with metastatic or recurrent platinum resistant (progression within 6 months) EOC and LMP ovarian tumours, both groups had received no more than 3 prior lines of chemotherapy. Belinostat 1000 mg/m(2)/d was administered iv days 1-5 of a 21 d cycle. Peripheral blood mononuclear cells (PBMCs) and tumour biopsies, where possible, for correlative studies were obtained prior to and following treatment.

resultsEighteen patients with EOC and 14 patients with LMP tumours were enrolled on study. Belinostat was well tolerated with no grade four toxicity (179 cycles). Grade 3 toxicity consisted of thrombosis (3 patients), hypersensitivity (1) and elevated ALP (1). One patient with LMP tumour had a partial response (unconfirmed) and 10 had stable disease (SD), 3 were non-evaluable. Median progression-free survival (PFS) was 13.4 months (95% confidence interval (CI), 5.6--not reached). Best response in patients with EOC was SD (nine patients) and median PFS was 2.3 months (95% CI, 1.2-5.7 months). An accumulation of acetylated histones H3 and H4 was noted in PBMCs and in tumour tissue.

conclusionsBelinostat is well tolerated in both patient groups and shows some activity in patients with micropapillary (LMP) disease.

Indexed as

AcetylationAdultAgedAged, 80 and overAntineoplastic AgentsCarcinoma, PapillaryDrug Resistance, NeoplasmFemaleHistone Deacetylase InhibitorsHistonesHumansHydroxamic AcidsInfusions, IntravenousMiddle AgedNeoplasm Recurrence, LocalOvarian NeoplasmsAntineoplastic AgentsbelinostatHistone Deacetylase InhibitorsHistonesHydroxamic AcidsSulfonamides

Identifiers

PMID20304628
PMCPMC3244274
OpenAlexW2017583298

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.