| Literature DB >> 27294607 |
Markus V Heppt1, Thomas K Eigentler2, Katharina C Kähler3, Rudolf A Herbst4, Daniela Göppner5, Thilo Gambichler6, Jens Ulrich7, Edgar Dippel8, Carmen Loquai9, Beatrice Schell10, Bastian Schilling11,12, Susanne G Schäd13, Erwin S Schultz14, Fanny Matheis1, Julia K Tietze1, Carola Berking15.
Abstract
Growing evidence suggests that concurrent loco-regional and systemic treatment modalities may lead to synergistic anti-tumor effects in advanced melanoma. In this retrospective multicenter study, we evaluate the use of electrochemotherapy (ECT) combined with ipilimumab or PD-1 inhibition. We investigated patients with unresectable or metastatic melanoma who received the combination of ECT and immune checkpoint blockade for distant or cutaneous metastases within 4 weeks. Clinical and laboratory data were collected and analyzed with respect to safety and efficacy. A total of 33 patients from 13 centers were identified with a median follow-up time of 9 months. Twenty-eight patients received ipilimumab, while five patients were treated with a PD-1 inhibitor (pembrolizumab n = 3, nivolumab n = 2). The local overall response rate (ORR) was 66.7 %. The systemic ORR was 19.2 and 40.0 % in the ipilimumab and PD-1 cohort, respectively. The median duration of response was not reached in either group. The median time to disease progression was 2.5 months for the entire population with 2 months for ipilimumab and 5 months for PD-1 blockade. The median overall survival was not reached in patients with ipilimumab and 15 months in the PD-1 group. Severe systemic adverse events were detected in 25.0 % in the ipilimumab group. No treatment-related deaths were observed. This is the first reported evaluation of ECT and simultaneous PD-1 inhibition and the largest published dataset on ECT with concurrent ipilimumab. The local response was lower than reported for ECT only. Ipilimumab combined with ECT was feasible, tolerable and showed a high systemic response rate.Entities:
Keywords: Electrochemotherapy; Immune checkpoint blockade; Ipilimumab; Melanoma; Nivolumab; Pembrolizumab
Mesh:
Year: 2016 PMID: 27294607 DOI: 10.1007/s00262-016-1856-z
Source DB: PubMed Journal: Cancer Immunol Immunother ISSN: 0340-7004 Impact factor: 6.968