Evidence map›Paper›PMID 31089155›Full record

Trial reportScientific reports2019

A phase II study of ENMD-2076 in advanced soft tissue sarcoma (STS).

Zachary Veitch, Alona Zer, Herbert Loong, Samer Salah, Maryam Masood, Abha Gupta, Penelope A Bradbury, David Hogg, Andrew Wong, Rita Kandel and 2 more

Open access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  3. Review
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  5. The two sides of chromosomal instability: drivers and brakes in cancer.Signal transduction and targeted therapy · 2024
    Review
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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

12 authors at 4 institutions in 1 country.

Zachary VeitchPrincess Margaret Cancer Centre, Toronto, Canada.
Alona ZerPrincess Margaret Cancer Centre, Toronto, Canada.
Herbert LoongPrincess Margaret Cancer Centre, Toronto, Canada.
Samer SalahPrincess Margaret Cancer Centre, Toronto, Canada.
Maryam MasoodPrincess Margaret Cancer Centre, Toronto, Canada.
Abha GuptaPrincess Margaret Cancer Centre, Toronto, Canada.
Penelope A BradburyPrincess Margaret Cancer Centre, Toronto, Canada.
David HoggPrincess Margaret Cancer Centre, Toronto, Canada.
Andrew WongDepartment of Pathology and Lab Medicine, Mount Sinai Hospital, Toronto, Canada.
Rita KandelDepartment of Pathology and Lab Medicine, Mount Sinai Hospital, Toronto, Canada.ORCID http://orcid.org/0000-0003-4047-3913
George S CharamesDepartment of Pathology and Lab Medicine, Mount Sinai Hospital, Toronto, Canada.
Albiruni R Abdul RazakPrincess Margaret Cancer Centre, Toronto, Canada. albiruni.razak@uhn.ca.
University of Toronto · CAMount Sinai Hospital · CAPrincess Margaret Cancer Centre · CAUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ENMD-2076, an aurora-A kinase inhibitor with anti-angiogenic properties, has shown activity in solid and hematologic malignancies. We investigated oral ENMD-2076 in an open-label, single-arm phase II study using 275 mg daily on a 28-day cycle in patients with advanced soft-tissue sarcomas (STS) receiving ≤1 line of prior therapy. Primary endpoint was 6-month progression-free survival (PFS) with ≤15% indicating no interest, and ≥40% indicating further interest in ENMD-2076. Secondary/exploratory endpoints included clinical benefit (CBR ≥6-months) and objective response (ORR) rates, PFS, OS, safety, and whole-exome sequencing (WES) for potentially associated biomarkers. Overall, 23/25 (92%) patients receiving ENMD-2076 were efficacy evaluable with median follow-up of 14 months (range 2.2-39.5). Common subtypes were leiomyosarcoma (n = 10), undifferentiated pleomorphic sarcoma (n = 3), angiosarcoma (n = 3), and alveolar soft-part sarcoma (n = 3). The 6-month PFS was 20.8% (95% CI:3.2-38.4) with a CBR of 17% (95% CI:1.55-33.23) and ORR of 9% (95% CI:3.08-20.46). Median PFS was 2.5 months (95% CI:2.20-4.47) and OS was 14.1 months (95% CI:6.07-20.07). The most common high-grade treatment-related adverse event was hypertension (60%). WES identified PTPRB mutations in 3/4 patients (p = 0.018) benefiting from ENMD-2076. Although this study failed to meet its primary endpoint, occasional responses and prolonged stable disease was noted. ENMD-2076 evaluation in PTPRB mutated tumors and/or angiosarcoma is warranted.

Indexed as

AdultAgedAurora Kinase ABiomarkers, TumorDrug Administration ScheduleExome SequencingFemaleFollow-Up StudiesHumansHypertensionMaleMiddle AgedMutationNeoplasm GradingProgression-Free SurvivalProtein Kinase InhibitorsAURKA protein, humanAurora Kinase ABiomarkers, TumorENMD 2076Protein Kinase InhibitorsPTPRB protein, humanPyrazolesPyrimidinesReceptor-Like Protein Tyrosine Phosphatases, Class 3

Identifiers

PMID31089155
PMCPMC6517396
OpenAlexW2945151271

What OpenQuestion holds

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LicenceCC BY
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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.