Skip to main content
Erschienen in: Cancer Immunology, Immunotherapy 9/2019

03.09.2019 | Clinical Trial Report

A phase II study of the L19IL2 immunocytokine in combination with dacarbazine in advanced metastatic melanoma patients

verfasst von: Benjamin Weide, Thomas Eigentler, Chiara Catania, Paolo Antonio Ascierto, Stefano Cascinu, Jürgen C. Becker, Axel Hauschild, Antonella Romanini, Riccardo Danielli, Reinhard Dummer, Uwe Trefzer, Giuliano Elia, Dario Neri, Claus Garbe

Erschienen in: Cancer Immunology, Immunotherapy | Ausgabe 9/2019

Einloggen, um Zugang zu erhalten

Abstract

Engineered cytokine products represent promising agents for the treatment of immunogenic tumors, such as malignant melanoma, in addition to immune checkpoint inhibitors. Here we describe the results of a controlled, randomized phase II clinical trial, aimed at assessing the therapeutic potential of L19IL2, a fully human fusion protein consisting of the L19 antibody specific to the alternatively spliced extra-domain B of fibronectin, fused to human interleukin-2 in advanced metastatic melanoma. In one arm, patients received dacarbazine (DTIC; 1000 mg/m2 of body surface on day 1 of 21-day cycles) as single agent, while in two other arms L19IL2 (22.5 million international units of IL2 equivalents) was added, based on two different schedules of administration. In total, 69 patients with stage IV melanoma were enrolled (24 in the dacarbazine arm, 23 and 22 in the other combination arms, respectively) and 67 received treatment. Analyses of efficacy results show a statistically significant benefit in terms of overall response rate and median progression-free survival for patients receiving L19IL2 in combination with DTIC, compared to DTIC as single agent. In light of these results, further clinical investigations with L19IL2 (alone or in combination with other agents) are warranted.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
13.
Zurück zum Zitat Penichet ML, Dela Cruz JS, Shin SU, Morrison SL (2001) A recombinant IgG3-(IL-2) fusion protein for the treatment of human HER2/neu expressing tumors. Hum Antibodies 10(1):43–49CrossRefPubMed Penichet ML, Dela Cruz JS, Shin SU, Morrison SL (2001) A recombinant IgG3-(IL-2) fusion protein for the treatment of human HER2/neu expressing tumors. Hum Antibodies 10(1):43–49CrossRefPubMed
37.
Zurück zum Zitat Schwartzentruber DJ (2001) Guidelines for the safe administration of high-dose interleukin-2. J Immunother 24(4):287–293CrossRefPubMed Schwartzentruber DJ (2001) Guidelines for the safe administration of high-dose interleukin-2. J Immunother 24(4):287–293CrossRefPubMed
45.
Zurück zum Zitat Murphy K, Weaver C (2017) Janeway's immunobiology, 9th edn. Garland Science, Taylor & Francis Group, LLC, New York, p 823 Murphy K, Weaver C (2017) Janeway's immunobiology, 9th edn. Garland Science, Taylor & Francis Group, LLC, New York, p 823
51.
Zurück zum Zitat Castellani P, Viale G, Dorcaratto A, Nicolo G, Kaczmarek J, Querze G, Zardi L (1994) The fibronectin isoform containing the ED-B oncofetal domain: a marker of angiogenesis. Int J Cancer 59(5):612–618CrossRefPubMed Castellani P, Viale G, Dorcaratto A, Nicolo G, Kaczmarek J, Querze G, Zardi L (1994) The fibronectin isoform containing the ED-B oncofetal domain: a marker of angiogenesis. Int J Cancer 59(5):612–618CrossRefPubMed
Metadaten
Titel
A phase II study of the L19IL2 immunocytokine in combination with dacarbazine in advanced metastatic melanoma patients
verfasst von
Benjamin Weide
Thomas Eigentler
Chiara Catania
Paolo Antonio Ascierto
Stefano Cascinu
Jürgen C. Becker
Axel Hauschild
Antonella Romanini
Riccardo Danielli
Reinhard Dummer
Uwe Trefzer
Giuliano Elia
Dario Neri
Claus Garbe
Publikationsdatum
03.09.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Cancer Immunology, Immunotherapy / Ausgabe 9/2019
Print ISSN: 0340-7004
Elektronische ISSN: 1432-0851
DOI
https://doi.org/10.1007/s00262-019-02383-z

Weitere Artikel der Ausgabe 9/2019

Cancer Immunology, Immunotherapy 9/2019 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.