Vulvar Cancer Clinical Trials

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Use of Electrochemotherapy in Women With Vulvar Cancer

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This phase I/II interventional study evaluates the effectiveness and safety of electrochemotherapy (ECT) as neoadjuvant treatment for local recurrence of vulvar cancer. Electrochemotherapy combines intravenous administration of bleomycin with delivery of electric pulses to the tumor area, increasing drug uptake into cancer cells. The main goal is to assess tumor response and reduce the need for mutilating surgical procedures, thereby improving quality of life in women with recurrent vulvar cancer. Participants will be followed prospectively and treatment outcomes will be evaluated using RECIST criteria and adverse events using CTCAE v5.0.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Local recurrence of vulvar cancer

• Age ≥ 18 years

• Expected life expectancy \> 3 months

• Karnofsky performance status ≥ 70 or WHO performance status ≤ 2

• At least 2 weeks since last treatment

• Ability to understand the procedure and possible adverse effects

• Ability to provide written informed consent

• Patient discussed at multidisciplinary tumor board before enrollment

• Fit for anesthesia

Locations
Other Locations
Slovenia
Institute of Oncology Ljubljana
RECRUITING
Ljubljana
Contact Information
Primary
Sebastjan Merlo, MD
smerlo@onko-i.si
+38615879490
Time Frame
Start Date: 2021-09-01
Estimated Completion Date: 2026-08-31
Participants
Target number of participants: 13
Treatments
Experimental: Electrochemotherapy (ECT) Treatment Arm
Women with recurrent vulvar cancer receive electrochemotherapy using intravenous bleomycin followed by electric pulse delivery to tumor lesions according to ESOPE standard operating procedures. Tumor response is assessed using RECIST criteria and safety is monitored using CTCAE v5.0.
Related Therapeutic Areas
Sponsors
Leads: Institute of Oncology Ljubljana

This content was sourced from clinicaltrials.gov

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