Tumor regressions observed in patients with metastatic melanoma treated with an antigenic peptide encoded by geneMAGE-3 and presented by HLA-A1

Marie Marchand(Ludwig Cancer Research), Nicolas van Baren(UCLouvain), P. Weynants(UCLouvain), Vincent Brichard(Ludwig Cancer Research), Brigitte Dr�no(Centre Hospitalier Universitaire de Nantes), Marie-H�l�ne Tessier(Centre Hospitalier Universitaire de Nantes), Elaine M. Rankin(The Netherlands Cancer Institute), Giorgio Parmiani(Fondazione IRCCS Istituto Nazionale dei Tumori), Flavio Arienti(Fondazione IRCCS Istituto Nazionale dei Tumori), Yves Humblet(UCLouvain), A Bourlond(UCLouvain), R Vanwijck(Cliniques Universitaires Saint-Luc), Danielle Li�nard(Ludwig Cancer Research), M. Beauduin(Hôpital de Jolimont), Pierre‐Yves Dietrich(Hôpital Beau-Séjour), Vincenzo Russo(The San Raffaele Telethon Institute for Gene Therapy), Joseph Kerger(Université Libre de Bruxelles), Giuseppe Masucci(Sophiahemmet Hospital), Elke J�ger(Krankenhaus Nordwest), Jacques De Grève(Vrije Universiteit Brussel), Jens Atzpodien(Medizinische Hochschule Hannover), Francis Brasseur(Ludwig Cancer Research), Pierre G. Coulie(UCLouvain), Pierre van der Bruggen(Ludwig Cancer Research), Thierry Boon(UCLouvain)
International Journal of Cancer
January 18, 1999
Cited by 786

Abstract

Thirty-nine tumor-bearing patients with metastatic melanoma were treated with 3 subcutaneous injections of the MAGE-3.A1 peptide at monthly intervals. No significant toxicity was observed. Of the 25 patients who received the complete treatment, 7 displayed significant tumor regressions. All but one of these regressions involved cutaneous metastases. Three regressions were complete and 2 of these led to a disease-free state, which persisted for more than 2 years after the beginning of treatment. No evidence for a cytolytic T lymphocyte (CTL) response was found in the blood of the 4 patients who were analyzed, including 2 who displayed complete tumor regression. Our results suggest that injection of the MAGE-3.A1 peptide induced tumor regression in a significant number of the patients, even though no massive CTL response was produced. Int. J. Cancer 80:219–230, 1999. © 1999 Wiley-Liss, Inc.


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