Phase I Study of 2- or 3-Week Dosing of Telisotuzumab Vedotin, an Antibody-Drug Conjugate Targeting c-Met, Monotherapy in Patients with Advanced Non-Small Cell Lung Carcinoma.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
01 11 2021
Historique:
received: 26 02 2021
revised: 11 06 2021
accepted: 16 08 2021
pubmed: 25 8 2021
medline: 1 4 2022
entrez: 24 8 2021
Statut: ppublish

Résumé

Telisotuzumab vedotin (Teliso-V) is an anti-c-Met-directed antibody-drug conjugate. Here, we present safety and efficacy data from a phase I/Ib study of Teliso-V monotherapy evaluated in once every 2 weeks/once every 3 weeks schedules in patients with non-small cell lung cancer (NSCLC). During dose escalation, patients received Teliso-V monotherapy intravenously once every 3 weeks (0.15-3.3 mg/kg) or once every 2 weeks (1.6-2.2 mg/kg). The dose-expansion phase enrolled patients with NSCLC and c-Met Fifty-two patients with NSCLC were enrolled and received ≥1.6 mg/kg Teliso-V once every 2 weeks ( Teliso-V monotherapy was tolerated and showed antitumor activity in c-Met+ NSCLC. On the basis of overall safety, pharmacokinetics, and efficacy outcomes, 1.9 mg/kg Teliso-V once every 2 weeks and 2.7 mg/kg once every 3 weeks schedules were selected for further clinical development.

Identifiants

pubmed: 34426443
pii: 1078-0432.CCR-21-0765
doi: 10.1158/1078-0432.CCR-21-0765
pmc: PMC9401525
doi:

Substances chimiques

Antibodies, Monoclonal 0
Immunoconjugates 0
telisotuzumab vedotin 976X9VXC3Z
MET protein, human EC 2.7.10.1
Proto-Oncogene Proteins c-met EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT02099058']

Types de publication

Clinical Trial, Phase I Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5781-5792

Informations de copyright

©2021 The Authors; Published by the American Association for Cancer Research.

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Auteurs

D Ross Camidge (DR)

University of Colorado Cancer Center, Aurora, Colorado. ross.camidge@cuanschutz.edu.

Daniel Morgensztern (D)

Washington University School of Medicine, St. Louis, Missouri.

Rebecca S Heist (RS)

Massachusetts General Hospital Cancer Center, Boston, Massachusetts.

Minal Barve (M)

Mary Crowley Cancer Research Center, Dallas, Texas.

Everett Vokes (E)

University of Chicago Medicine, Chicago, Illinois.

Jonathan W Goldman (JW)

David Geffen School of Medicine at UCLA, Los Angeles, California.

David S Hong (DS)

The University of Texas MD Anderson Cancer Center, Houston, Texas.

Todd M Bauer (TM)

Sarah Cannon Research Institute, Nashville, Tennessee.
Tennessee Oncology, Nashville, Tennessee.

John H Strickler (JH)

Duke University Medical Center, Durham, North Carolina.

Eric Angevin (E)

Gustave Roussy, Villejuif, France.

Monica Motwani (M)

AbbVie, Inc., North Chicago, Illinois.

Apurvasena Parikh (A)

Clinical Pharmacology and Pharmacometrics, AbbVie Inc., Redwood City, California.

Zhaowen Sun (Z)

AbbVie, Inc., North Chicago, Illinois.

Bruce Allen Bach (BA)

AbbVie, Inc., North Chicago, Illinois.

Jun Wu (J)

AbbVie, Inc., North Chicago, Illinois.

Philip B Komarnitsky (PB)

AbbVie, Inc., North Chicago, Illinois.

Karen Kelly (K)

University of California Davis Comprehensive Cancer Center, Sacramento, California.

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Classifications MeSH