Evidence map›Paper›PMID 30679780›Full record

ArticleBritish journal of cancer2019

Phase 1 dose-finding and pharmacokinetic study of eribulin-liposomal formulation in patients with solid tumours.

T R Jeffry Evans, Emma Dean, L Rhoda Molife, Juanita Lopez, Malcolm Ranson, Fatima El-Khouly, Ishtiaq Zubairi, Claudio Savulsky, Larisa Reyderman, Yan Jia and 4 more

Abstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Phase II Study of the Liposomal Formulation of Eribulin (E7389-LF) in Combination with Nivolumab: Results from the Gastric Cancer Cohort.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Smart Nanocarrier-Based Cancer Therapeutics.Cancer treatment and research · 2023
    Article
  9. Article
  10. Dose Escalation Data from the Phase 1 Study of the Liposomal Formulation of Eribulin (E7389-LF) in Japanese Patients with Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  11. Efficacy of Eribulin in Soft Tissue Sarcomas.Frontiers in pharmacology · 2022
    Review
  12. Review
  13. Review
  14. 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

14 authors.

T R Jeffry EvansBeatson West of Scotland Cancer Centre, Glasgow, UK. J.Evans@beatson.gla.ac.uk.
Emma DeanThe Christie NHS Foundation Trust, Manchester, UK.
L Rhoda MolifeThe Royal Marsden Hospital NHS Foundation Trust and The Institute of Cancer Research, London, UK.
Juanita LopezThe Royal Marsden Hospital NHS Foundation Trust and The Institute of Cancer Research, London, UK.
Malcolm RansonThe Christie NHS Foundation Trust, Manchester, UK.
Fatima El-KhoulyUCL Cancer Institute, London, UK.
Ishtiaq ZubairiBeatson West of Scotland Cancer Centre, Glasgow, UK.
Claudio SavulskyEisai Ltd., Hatfield, UK.
Larisa ReydermanEisai Inc., Woodcliff Lake, NJ, USA.
Yan JiaEisai Inc., Woodcliff Lake, NJ, USA.
Lorna SweetingBeatson West of Scotland Cancer Centre, Glasgow, UK.
Alastair GreystokeNorthern Institute for Cancer Research, Newcastle University, Newcastle upon Tyne, UK.
Jorge BarriusoThe Christie NHS Foundation Trust, Manchester, UK.
Rebecca KristeleitUCL Cancer Institute, London, UK.

Funding

Cancer Research UK 20409Chief Scientist Office
6 · The paper itself

Abstract

backgroundThis phase 1 study examined the safety, tolerability, pharmacokinetics and preliminary efficacy of eribulin-liposomal formulation (eribulin-LF) in patients with advanced solid tumours.

methodsEligible patients with ECOG PS 0-1 were treated with eribulin-LF either on day 1 every 21 days (Schedule 1), or on days 1 and 15 every 28 days (Schedule 2). Doses ranged from 1.0 to 3.5 mg/m PRIMARY

objectivesmaximum tolerated dose (MTD) and the recommended dose/schedule of eribulin-LF.

resultsTotally, 58 patients were enroled (median age = 62 years). The MTD was 1.4 mg/m

conclusionsEribulin-LF was well tolerated with a favourable pharmacokinetic profile. Preliminary evidence of clinical activity in solid tumours was observed.

Indexed as

AdultAgedDrug CompoundingFemaleFuransHumansKetonesLiposomesMaleMaximum Tolerated DoseMiddle AgedNeoplasmsPolyether PolyketideseribulinFuransKetonesLiposomesPolyether Polyketides

Identifiers

PMID30679780
PMCPMC6461749

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.