Evidence map›Paper›PMID 30056611›Full record

ArticleInvestigational new drugs2019

First-in-human study of the anti-HB-EGF antibody U3-1565 in subjects with advanced solid tumors.

Kathleen N Moore, Johanna C Bendell, Patricia M LoRusso, Anthony J Olszanski, Esther Zwick-Wallasch, Mendel Jansen, Alexander G Vandell, Giorgio Senaldi

Open access · greenAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Investigational new drugs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

8 authors at 7 institutions in 3 countries.

Kathleen N MooreStephenson Cancer Center, University of Oklahoma, 800 NE 10th Street, Suite 5050, Oklahoma City, OK, 73104, USA.
Johanna C BendellThe Sarah Cannon Research Institute/Tennessee Oncology, 250 25th Avenue North, Suite 110, Nashville, TN, 37203, USA.
Patricia M LoRussoDivision of Hematology and Oncology, Wayne State University, 4100 John R/4-HWCRC, Detroit, MI, 48201, USA.
Anthony J OlszanskiFox Chase Cancer Center, 333 Cottman Ave, Philadelphia, PA, 19111, USA.
Esther Zwick-WallaschU3 Pharma GmbH, 82152, Martinsried, Germany.
Mendel JansenDaiichi Sankyo Development Ltd., Gerrards Cross, SL9 0BG, UK.
Alexander G VandellDaiichi Sankyo Inc., 211 Mt Airy Rd, Basking Ridge, NJ, 07290, USA. avandell@dsi.com.
Giorgio SenaldiDaiichi Sankyo Inc., 211 Mt Airy Rd, Basking Ridge, NJ, 07290, USA.
Daiichi Sankyo (United States) · USDaiichi Sankyo (United Kingdom) · GBFox Chase Cancer Center · USMax Planck Institute of Neurobiology · DESarah Cannon · USTennessee Oncology · USWayne State University · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
NCI NIH HHS P30 CA022453
6 · The paper itself

Abstract

U3-1565 is a monoclonal antibody directed against heparin-binding epidermal growth factor-like growth factor (HB-EGF), which mediates angiogenesis via induction of vascular endothelial growth factor (VEGF-A). This first-in-human study characterized the safety, tolerability, efficacy, pharmacokinetics, and pharmacodynamics of U3-1565 in subjects with advanced solid tumors. In Part 1 (dose escalation following a modified 3 + 3 design), Cohorts 1-4, U3-1565 was administered at 2, 8, 16, and 24 mg/kg every 3 weeks for Cycle 1 and every 2 weeks thereafter. In Part 1, Cohort 5, and in Part 2 (dose expansion), U3-1565 was administered at 24 mg/kg every week. Thirty-six subjects were enrolled and treated (15 in Part 1; 21 in Part 2). No subject experienced dose limiting toxicity and maximum tolerated dose was not reached. All drug-related events were Grade 1 or 2 in severity, with fatigue and rash predominating. Following treatment with U3-1565, 1 subject with metastatic colorectal cancer experienced partial response and 6 subjects achieved stable disease. Four subjects completed the study main phase (first 12 cycles) and entered the extension phase. Of the 6/36 subjects with high (> 1500 pg/ml) baseline VEGF-A levels, all showed a decrease in VEGF-A (median - 60% [-22% to -97%]). Of the remaining subjects, only 19/30 showed a decrease (median - 18% [-2% to -82%]). Subjects with high VEGF-A baseline levels remained on treatment longer (3/6 entered study extension phase versus 1/30), and were more likely to show disease control (3/6 versus 4/30). In conclusion, U3-1565 demonstrates both proof of mechanism and clinical activity across different tumor types.

Indexed as

Antibodies, Monoclonal, HumanizedFemaleHeparin-binding EGF-like Growth FactorHumansMaleMaximum Tolerated DoseMiddle AgedNeoplasmsPrognosisTissue DistributionAntibodies, Monoclonal, HumanizedHBEGF protein, humanHeparin-binding EGF-like Growth FactorHB-EGFPharmacokineticsPhase 1U3–1565VEGF-A

Identifiers

PMID30056611
PMCPMC6886232
OpenAlexW2884932646

What OpenQuestion holds

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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.