Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

Phase I/II Study of AXL-Specific Antibody-Drug Conjugate Enapotamab Vedotin in Patients with Advanced Solid Tumors

Title: Phase I/II Study of AXL-Specific Antibody-Drug Conjugate Enapotamab Vedotin in Patients with Advanced Solid Tumors
Authors: Rohrberg KS; Lopez JS; Milhem MM; Blank CU; Reijers I; Thistlethwaite F; Plummer R; Piha-Paul SA; Janne PA; Shum E; Shaw HM; Debruyne PR; Lao C; Baurain J-F; Choe JH; Gort E; Zhao Y; Jerusalem G; Schoffski P; Chen AW; Cohen EA; Mankowski WC; Roshkovan L; Katz SI; Kontos D; Brady LK; Qutaish M; Castro PG; Pencheva N; Bajaj G; Fu Y; Windfeld K; Reiter P; Jure-Kunkel M; Higgs BW; Amiri KI; Ahmadi T; Forssmann U; Ramalingam SS; Vergote I
Source: Cancer Research Communications, 1 November 2025
Publisher Information: American Association for Cancer Research
Publication Year: 2025
Collection: Newcastle University Library ePrints Service
Description: ©2025 The Authors; Published by the American Association for Cancer Research. PURPOSE: AXL, a receptor tyrosine kinase related to oncogenic processes, is aberrantly expressed in various cancers and associated with treatment resistance. Enapotamab vedotin (EnaV), a novel anti-AXL human IgG1 and monomethyl auristatin E antibody-drug conjugate, demonstrated antitumor activity in preclinical models, including non-small cell lung cancer (NSCLC). This phase 1/2 study assessed the safety and preliminary efficacy of EnaV in solid tumors. PATIENTS AND METHODS: This study comprised dose-escalation and dose-expansion phases; both phases investigated EnaV once every 3 weeks (Q3W) and EnaV on days 1, 8, and 15 of a 28-day cycle (3Q4W). Primary objectives determined the maximum tolerated dose (dose escalation) and safety (dose expansion). Pharmacokinetic profile, antitumor activity, and AXL expression were also assessed. RESULTS: During dose escalation, 32 patients received EnaV Q3W; 15 received EnaV 3Q4W. The maximum tolerated dose and recommended phase 2 dose were 2.2 mg/kg in Q3W and 1.0 mg/kg in 3Q4W schedules. In dose expansion, 189 patients received EnaV Q3W; 70 received EnaV 3Q4W. Common adverse events in dose expansion included fatigue, constipation, nausea, decreased appetite, and diarrhea. Overall response rates ranged from 4.5% to 12.5% with Q3W dose schedule and from 9.1% to 11.5% with 3Q4W dose schedule. Disease control rates for NSCLC cohorts were 40.9% to 50.0%. NSCLC subset analysis demonstrated correlation between radiomics signature and disease control. The relationship between clinical activity and AXL expression was not apparent. CONCLUSIONS: EnaV had an acceptable safety profile; however, because the evaluation of antitumor activity did not show clinically meaningful responses, clinical development of EnaV was discontinued. SIGNIFICANCE: EnaV, an anti-AXL human IgG1 and monomethyl auristatin E antibody-drug conjugate, showed single-agent antitumor activity in preclinical models. This phase 1/2 study of ...
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: https://eprints.ncl.ac.uk/309187; https://eprints.ncl.ac.uk/fulltext.aspx?url=309187/87513301-72AF-4D76-8C27-572770161952.pdf&pub_id=309187
Availability: https://eprints.ncl.ac.uk/309187
Rights: https://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.B85107D6
Database: BASE