Evidence map›Paper›PMID 28291776›Full record

ArticleBritish journal of cancer2017

First-in-human phase 1 of YS110, a monoclonal antibody directed against CD26 in advanced CD26-expressing cancers.

Eric Angevin, Nicolas Isambert, Véronique Trillet-Lenoir, Benoit You, Jérôme Alexandre, Gérard Zalcman, Philippe Vielh, Françoise Farace, Fanny Valleix, Thomas Podoll and 8 more

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

Article in British journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 60 citations in OpenAlex.

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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

18 authors at 10 institutions in 3 countries.

Eric AngevinGustave Roussy, Université Paris-Saclay, Drug Development Department (DITEP), Villejuif, France.
Nicolas IsambertCentre Georges-François Leclerc, Unité de Phases Précoces, Dijon, France.
Véronique Trillet-LenoirInstitut de Cancérologie des Hospices Civils de Lyon, CITOHL, Lyon, France.
Benoit YouInstitut de Cancérologie des Hospices Civils de Lyon, CITOHL, Lyon, France.
Jérôme AlexandreHôpital Cochin, Paris, France.
Gérard ZalcmanCentre Hospitalier Universitaire (CHU) de Caen, Centre de Recherche Clinique/Essais de phases précoces, Caen, France.
Philippe VielhGustave Roussy, Translational Research Laboratory, Villejuif, France.
Françoise FaraceGustave Roussy, Translational Research Laboratory, Villejuif, France.
Fanny ValleixFV Clinical subcontractor for SynteractHCR SAS, Levallois-Perret, France.
Thomas PodollY's therapeutics Inc., Redwood City, CA, USA.
Yu KuramochiKissei Pharmaceutical Co., Ltd, Tokyo, Japan.
Itaru MiyashitaKissei Pharmaceutical Co., Ltd, Tokyo, Japan.
Osamu HosonoDepartment of Rheumatology and Allergy, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Nam H DangDivision of Hematology/Oncology, University of Florida, Gainesville, FL, USA.
Kei OhnumaDepartment of Therapy Development and Innovation for Immune Disorders and Cancers, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Taketo YamadaKeio University School of Medicine, Tokyo, Japan.
Yutaro KanekoY's AC Co., Ltd, Tokyo, Japan.
Chikao MorimotoDepartment of Therapy Development and Innovation for Immune Disorders and Cancers, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Institut Gustave Roussy · FRHospices Civils de Lyon · FRJuntendo University · JPKissei Pharmaceutical (Japan) · JPCentre Georges François Leclerc · FRCentre Hospitalier Universitaire de Caen · FRHôpital Cochin · FRSaitama Medical University · JPUniversity of Florida · USUniversity of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundYS110 is a humanised IgG1 monoclonal antibody with high affinity to the CD26 antigen. YS110 demonstrated preclinical anti-tumour effects without significant side effects.

methodsThis FIH study was designed to determine the maximal tolerated dose (MTD) and recommended phase 2 dose (RP2D) to assess the tolerance, pharmacokinetics (PK) and pharmacodynamics profiles of YS110 and preliminary efficacy. YS110 were initially administered intravenously once every 2 weeks (Q2W) for three doses and then, based on PK data, once every week (Q1W) for five doses in patients with CD26-expressing solid tumours.

resultsThirty-three patients (22 mesothelioma) received a median of 3 (range 1-30) YS110 infusions across six dose levels (0.1-6 mg kg

conclusionsYS110 is well tolerated up to 6 mg kg

Indexed as

AdultAgedAntibodies, MonoclonalDipeptidyl Peptidase 4Dose-Response Relationship, DrugDrug-Related Side Effects and Adverse ReactionsFemaleGene Expression Regulation, NeoplasticHumansImmunoglobulin GMaleMaximum Tolerated DoseMesotheliomaMiddle AgedAntibodies, MonoclonalDipeptidyl Peptidase 4DPP4 protein, humanImmunoglobulin GYS110 monoclonal antibody

Identifiers

PMID28291776
PMCPMC5418443
OpenAlexW2607875207

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.