Evidence map›Paper›PMID 29719113›Full record

ArticlePediatric blood & cancer2018

A phase 1 study of eribulin mesylate (E7389), a novel microtubule-targeting chemotherapeutic agent, in children with refractory or recurrent solid tumors: A Children's Oncology Group Phase 1 Consortium study (ADVL1314).

Eric S Schafer, Rachel E Rau, Stacey Berg, Xiaowei Liu, Charles G Minard, David D'Adamo, Rachael Scott, Larisa Reyderman, Gresel Martinez, Sandhya Devarajan and 4 more

Open access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in Pediatric blood & cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Evaluation of Eribulin Combined with Irinotecan for Treatment of Pediatric Cancer Xenografts.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  10. Enriching cancer pharmacology with drugs of marine origin.British journal of pharmacology · 2020
    Review
  11. Review
  12. 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 at 7 institutions in 2 countries.

Eric S SchaferDepartment of Pediatrics/Oncology, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.ORCID 0000-0002-7063-512X
Rachel E RauDepartment of Pediatrics/Oncology, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Stacey BergDepartment of Pediatrics/Oncology, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Xiaowei LiuChildren's Oncology Group, Monrovia, California.
Charles G MinardDepartment of Pediatrics/Oncology, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
David D'AdamoEisai, Inc., Woodcliff Lake, New Jersey.
Rachael ScottEisai, Ltd., Hatfield, United Kingdom.
Larisa ReydermanEisai, Inc., Woodcliff Lake, New Jersey.
Gresel MartinezEisai, Inc., Woodcliff Lake, New Jersey.
Sandhya DevarajanMayo Clinic, Rochester, Minnesota.
Joel M ReidMayo Clinic, Rochester, Minnesota.
Elizabeth FoxDivision of Oncology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Brenda J WeigelDepartment of Pediatrics, University of Minnesota, Minneapolis, Minnesota.
Susan M BlaneyDepartment of Pediatrics/Oncology, Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.
Baylor College of Medicine · USEisai (United States) · USMayo Clinic · USChildren's Hospital of Philadelphia · USChildren's Oncology Group · USEisai (United Kingdom) · GBUniversity of Minnesota · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
PEP-CTN EHR to RAVE supplementUM1CA228823 · NCI · PUBLIC HEALTH INSTITUTE · PI Elizabeth Fox · 2018 to 2026
$39.6M
Pediatric Phase 1/Pilot ConsortiumUM1CA097452 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI WEIGEL, BRENDA J. · 2009 to 2018
$17.7M
NCI NIH HHS UM1 CA097452NCI NIH HHS UM1 CA228823
6 · The paper itself

Abstract

backgroundEribulin mesylate is a novel anticancer agent that inhibits microtubule growth, without effects on shortening, and promotes nonproductive tubulin aggregate formation. We performed a phase 1 trial to determine the dose-limiting toxicities (DLTs), maximum tolerated or recommended phase 2 dose (MTD/RP2D), and pharmacokinetics (PK) of eribulin in children with refractory or recurrent solid (excluding central nervous system) tumors.

methodsEribulin was administered intravenously on days 1 and 8 in 21-day cycles. Three dose levels (1.1, 1.4, and 1.8 mg/m

resultsTwenty-three patients, ages 3-17 (median 14) years were enrolled; 20 were evaluable for toxicity. DLTs occurred in 0/6 and 1/6 subjects at the 1.1 and 1.4 mg/m

conclusionsEribulin was well tolerated in children with refractory or recurrent solid tumors with neutropenia identified as the primary DLT. The RP2D of eribulin is 1.4 mg/m

Indexed as

AdolescentAntineoplastic AgentsChildChild, PreschoolDose-Response Relationship, DrugDrug Resistance, NeoplasmFemaleFuransHumansKetonesMaleMaximum Tolerated DoseMicrotubulesNeoplasm Recurrence, LocalNeoplasmsPolyether PolyketidesAntineoplastic AgentseribulinFuransKetonesPolyether PolyketideschildreneribulinpharmacokineticsPhase 1

Identifiers

PMID29719113
PMCPMC6019176
OpenAlexW2801032537

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.