Dr. Genti Xhepa (Varese/CH) et al. were awarded this year’s Magna Cum Laude Poster Award for their research on Percutaneous electrochemotherapy for soft tissue tumors: local tumor control, pain palliation, and safety outcomes.
CIRSE Insider: Can you tell us a little bit about your academic background?
Xhepa: My training started at the University of Insubria’s Varese Medical School, followed by a radiology residency with Prof. Gianpaolo Carrafiello, who introduced me to interventional radiology and oncology. After working as an interventional and abdominal radiologist at ASST Rhodense in Garbagnate Milanese for several years, I moved to Switzerland in 2021, continuing at EOC in Lugano and HUG in Geneva. In June 2025, I joined the Institut Gustave Roussy as a research fellow under Prof. Lambros Tselikas and Dr. Frédéric Deschamps, focusing on interventional oncology research, especially electrochemotherapy.
CIRSE Insider: Your research topic was on percutaneous electrochemotherapy for soft tissue tumors. What led you to study this topic?
Xhepa: This topic is one of the reasons I joined Gustave Roussy, a world-leading centre for electrochemotherapy (ECT), largely thanks to Prof. Lluis Mir’s long-standing work on electroporation. The technique is at a pivotal stage: for superficial metastases, evidence has been strong for over a decade through the standard operating procedures for electrochemotherapy and electrogenetherapy (ESOPE) protocol; for deep tissues, it’s still developing. ECT uses low-dose bleomycin and electric pulses to temporarily permeabilize cell membranes, boosting cytotoxicity up to 1000-fold while sparing nearby tissue. My clinical question was simple: which patients benefit, and for how long?
CIRSE Insider: What were the key findings of your study? How do you see these findings impacting care for cancer patients?
Xhepa: Our research examined the GRECT series’ soft-tissue cohort: 44 patients with 48 lesions, most treated after exhausting other options. The response rate was 87%, with a median local progression-free survival of 12.0 months and an overall survival of 29.3 months. Notably, the lesion’s vascular pattern on pre-procedural imaging was the strongest predictor of initial response, aiding patient selection. Prior immunotherapy exposure was the only predictor of shorter progression-free survival, likely related to sequencing rather than to ECT itself. This provides a local option in a primarily palliative setting.
CIRSE Insider: Why did you choose to present your findings at ECIO 2026?
Xhepa: ECIO is the natural home for this kind of research. It brings the interventional oncology community together at the very level where early clinical evidence is tested and, if it holds up, put into practice. That is what percutaneous ECT needs to move beyond a handful of expert centres.
CIRSE Insider: Anything else you’d like to mention?
Xhepa: None of this would have been possible without the entire IO team at Gustave Roussy. My thanks also go to CIRSE and the ECIO Scientific Committee for their recognition. Evidence for percutaneous ECT still largely relies on retrospective, single-centre cohorts. To define its proper place in an increasingly personalized treatment algorithm for soft tissue and bone metastases, spinal cord compression, vascular malformations, and beyond, we need prospective, randomized studies. That is the next step worth supporting.