Cargando…
Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy
Melanoma is responsible for most skin cancer-related deaths and is one of the most common cancers diagnosed in young adults. In melanoma, tumors can become established by activation of the negative regulator of cytotoxic T lymphocytes (CTLs), CTL antigen-4 (CTLA-4). Ipilimumab blocks the interaction...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485758/ https://www.ncbi.nlm.nih.gov/pubmed/26155423 http://dx.doi.org/10.1080/2162402X.2015.1008842 |
_version_ | 1782378814153687040 |
---|---|
author | Mozzillo, Nicola Simeone, Ester Benedetto, Lucia Curvietto, Marcello Giannarelli, Diana Gentilcore, Giusy Camerlingo, Rosa Capone, Mariaelena Madonna, Gabriele Festino, Lucia Caracò, Corrado Di Monta, Gianluca Marone, Ugo Di Marzo, Massimiliano Grimaldi, Antonio M Mori, Stefano Ciliberto, Gennaro Ascierto, Paolo A |
author_facet | Mozzillo, Nicola Simeone, Ester Benedetto, Lucia Curvietto, Marcello Giannarelli, Diana Gentilcore, Giusy Camerlingo, Rosa Capone, Mariaelena Madonna, Gabriele Festino, Lucia Caracò, Corrado Di Monta, Gianluca Marone, Ugo Di Marzo, Massimiliano Grimaldi, Antonio M Mori, Stefano Ciliberto, Gennaro Ascierto, Paolo A |
author_sort | Mozzillo, Nicola |
collection | PubMed |
description | Melanoma is responsible for most skin cancer-related deaths and is one of the most common cancers diagnosed in young adults. In melanoma, tumors can become established by activation of the negative regulator of cytotoxic T lymphocytes (CTLs), CTL antigen-4 (CTLA-4). Ipilimumab blocks the interaction of CTLA-4 with CD80/CD86 and augments T-cell activation and proliferation. In electrochemotherapy (ECT), local application of short high-voltage pulses renders cell membranes transiently permeable to chemotherapeutic drugs. The combination of ipilimumab and ECT may be beneficial for the treatment of metastatic melanoma; however, no prospective data are available to date. Here, we report the retrospective analysis of patients treated with ipilimumab in an expanded access program (EAP) who also received ECT. Fifteen patients with previously treated metastatic melanoma who received ipilimumab 3 mg/kg every three weeks for four cycles and underwent ECT for local disease control and/or palliation of cutaneous lesions with bleomycin 15 mg/m(2) after the first ipilimumab infusion were included in the analysis. Over the study period, a local objective response was observed in 67% of patients (27% complete response [CR] and 40% partial response [PR]). According to immune-related response criteria, a systemic response was observed in nine patients (five PR and four stable disease [SD]), resulting in a disease control rate of 60%. Evaluation of circulating T-regulatory (T-reg) cells demonstrated significant differences between responders and non-responders. Overall, treatment was well-tolerated and without notable toxicity. In conclusion, the combination of ipilimumab and ECT appears to be beneficial to patients with advanced melanoma, warranting further investigation in prospective trials. |
format | Online Article Text |
id | pubmed-4485758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-44857582016-02-03 Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy Mozzillo, Nicola Simeone, Ester Benedetto, Lucia Curvietto, Marcello Giannarelli, Diana Gentilcore, Giusy Camerlingo, Rosa Capone, Mariaelena Madonna, Gabriele Festino, Lucia Caracò, Corrado Di Monta, Gianluca Marone, Ugo Di Marzo, Massimiliano Grimaldi, Antonio M Mori, Stefano Ciliberto, Gennaro Ascierto, Paolo A Oncoimmunology Original Research Melanoma is responsible for most skin cancer-related deaths and is one of the most common cancers diagnosed in young adults. In melanoma, tumors can become established by activation of the negative regulator of cytotoxic T lymphocytes (CTLs), CTL antigen-4 (CTLA-4). Ipilimumab blocks the interaction of CTLA-4 with CD80/CD86 and augments T-cell activation and proliferation. In electrochemotherapy (ECT), local application of short high-voltage pulses renders cell membranes transiently permeable to chemotherapeutic drugs. The combination of ipilimumab and ECT may be beneficial for the treatment of metastatic melanoma; however, no prospective data are available to date. Here, we report the retrospective analysis of patients treated with ipilimumab in an expanded access program (EAP) who also received ECT. Fifteen patients with previously treated metastatic melanoma who received ipilimumab 3 mg/kg every three weeks for four cycles and underwent ECT for local disease control and/or palliation of cutaneous lesions with bleomycin 15 mg/m(2) after the first ipilimumab infusion were included in the analysis. Over the study period, a local objective response was observed in 67% of patients (27% complete response [CR] and 40% partial response [PR]). According to immune-related response criteria, a systemic response was observed in nine patients (five PR and four stable disease [SD]), resulting in a disease control rate of 60%. Evaluation of circulating T-regulatory (T-reg) cells demonstrated significant differences between responders and non-responders. Overall, treatment was well-tolerated and without notable toxicity. In conclusion, the combination of ipilimumab and ECT appears to be beneficial to patients with advanced melanoma, warranting further investigation in prospective trials. Taylor & Francis 2015-05-22 /pmc/articles/PMC4485758/ /pubmed/26155423 http://dx.doi.org/10.1080/2162402X.2015.1008842 Text en © 2015 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Original Research Mozzillo, Nicola Simeone, Ester Benedetto, Lucia Curvietto, Marcello Giannarelli, Diana Gentilcore, Giusy Camerlingo, Rosa Capone, Mariaelena Madonna, Gabriele Festino, Lucia Caracò, Corrado Di Monta, Gianluca Marone, Ugo Di Marzo, Massimiliano Grimaldi, Antonio M Mori, Stefano Ciliberto, Gennaro Ascierto, Paolo A Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy |
title | Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy |
title_full | Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy |
title_fullStr | Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy |
title_full_unstemmed | Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy |
title_short | Assessing a novel immuno-oncology-based combination therapy: Ipilimumab plus electrochemotherapy |
title_sort | assessing a novel immuno-oncology-based combination therapy: ipilimumab plus electrochemotherapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485758/ https://www.ncbi.nlm.nih.gov/pubmed/26155423 http://dx.doi.org/10.1080/2162402X.2015.1008842 |
work_keys_str_mv | AT mozzillonicola assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT simeoneester assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT benedettolucia assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT curviettomarcello assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT giannarellidiana assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT gentilcoregiusy assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT camerlingorosa assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT caponemariaelena assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT madonnagabriele assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT festinolucia assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT caracocorrado assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT dimontagianluca assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT maroneugo assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT dimarzomassimiliano assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT grimaldiantoniom assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT moristefano assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT cilibertogennaro assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy AT asciertopaoloa assessinganovelimmunooncologybasedcombinationtherapyipilimumabpluselectrochemotherapy |