Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07404605

Electrochemotherapy-Induced Changes in Tumor Microenvironment in Cutaneous Melanoma

Led by Institute of Oncology Ljubljana · Updated on 2026-02-19

150

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Cutaneous melanoma frequently develops cutaneous and subcutaneous metastases, which may cause significant morbidity and negatively affect quality of life. Electrochemotherapy (ECT) is an established local treatment modality for cutaneous and subcutaneous tumor lesions that combines the administration of cytotoxic drugs with the application of electric pulses to increase drug uptake into tumor cells. In addition to its direct cytotoxic effects, electrochemotherapy may induce changes in the tumor microenvironment, including immune cell infiltration, vascular alterations, and other biological responses that could influence tumor control. The aim of this study is to evaluate changes in the tumor microenvironment of cutaneous and subcutaneous melanoma metastases following electrochemotherapy with either intravenous bleomycin or intratumoral cisplatin. Tumor tissue samples collected before and after treatment will be analyzed to characterize microenvironmental changes and to compare treated and untreated lesions. The results of this study may improve understanding of biological effects of electrochemotherapy in melanoma metastases and support further development of treatment strategies.

CONDITIONS

Official Title

Electrochemotherapy-Induced Changes in Tumor Microenvironment in Cutaneous Melanoma

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Histologically confirmed cutaneous melanoma
  • Presence of cutaneous and/or subcutaneous metastases eligible for electrochemotherapy
  • Candidate for electrochemotherapy with intravenous bleomycin or intratumoral cisplatin according to standard clinical practice
  • Ability to provide written informed consent
Not Eligible

You will not qualify if you...

  • Contraindication to electrochemotherapy or study drugs (bleomycin or cisplatin)
  • Pregnancy or breastfeeding
  • Severe comorbidities preventing electrochemotherapy
  • Inability to comply with study procedures

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Institute of Oncology Ljubljana

Ljubljana, Slovenia, 1000

Actively Recruiting

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Research Team

K

Klavdija Korošec

CONTACT

N

Neža Gros

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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