DGMed ECT Portal
TR EN

Safety Profile, Contraindications and Regulation

The safety profile of electrochemotherapy follows from its local character: because systemic drug doses are low, systemic adverse effects are limited, while the expected local reactions at the treatment site are pronounced. The tables below summarise the pattern reported in the clinical series within the corpus.

This page is not medical advice. The information below is a synthesis of the literature; per-patient decisions on contraindications, dosing and monitoring rest on the current summary of product characteristics, the device instructions for use and the physician’s clinical judgement. Tracking cumulative drug dose is the responsibility of the treating institution.

Reported Adverse Events

Most local reactions are part of the treatment response and are read as the expected course rather than complications

EventFrequencyMechanismManagement
Muscle contraction during deliveryExpectedMuscle and nerve stimulation by the pulsesAnaesthesia and, where needed, neuromuscular blockade; choice of pulse frequency
Pain at the treatment siteCommonTissue stimulation and post-procedural inflammationAnalgesia plan; pain may persist for days in some patients
Erythema, oedema and superficial necrosisCommon / expectedResponse of the treated tissueWound care; usually heals by epithelialisation within weeks
Hyper- or depigmentationCommonMelanocyte involvementThe cosmetic outcome should be discussed with the patient beforehand
Ulceration and delayed healingUncommonTreatment of large volumes or irradiated tissueHealing may be markedly prolonged in previously irradiated fields
ArrhythmiaUncommonPulses coinciding with the vulnerable cardiac periodECG synchronisation for applications near the heart
Bleomycin-related pulmonary toxicityRare but seriousCumulative bleomycin doseLifetime cumulative dose tracking; careful assessment in patients with lung disease
Hypersensitivity reactionRareDrug-relatedHistory taking and readiness to intervene

Contraindications and Cautions

ConditionNature
Known hypersensitivity to the agent usedAbsolute
For bleomycin: the lifetime cumulative dose limit has been reachedAbsolute
Severe renal impairment (bleomycin is renally excreted)Relative, requires dose adjustment
Clinically significant pulmonary fibrosis or advanced lung diseaseRelative
Pregnancy and breastfeedingAbsolute
Uncontrolled arrhythmia, or a pacemaker/ICD near the treatment siteRelative, cardiology assessment
Active, uncontrolled infection at the treatment siteRelative

Bleomycin and Cumulative Dose

The most serious dose-dependent toxicity of bleomycin is pulmonary fibrosis, and risk rises with lifetime cumulative dose. Single-session doses in electrochemotherapy are low compared with systemic chemotherapy regimens, but repeated sessions and the patient’s prior bleomycin exposure must be assessed together.

Risk factors include advanced age, renal impairment, pre-existing lung disease, prior thoracic radiotherapy and exposure to high oxygen concentrations. Limiting the oxygen concentration in any future anaesthesia may therefore become relevant in patients who have received bleomycin, and this should be recorded prominently in the patient’s file.

Regulatory Framework

Electrochemotherapy is a defined interventional procedure in many countries, but device and drug approvals are separate processes

DocumentScopeNature
NICE IPG446 (2013, United Kingdom)Electrochemotherapy for skin metastases and primary skin cancerInterventional procedure guidance; use under standard clinical governance
NICE IPG478 (2014, United Kingdom)Primary basal cell and squamous cell carcinomaInterventional procedure guidance
ESOPE (2006, updated 2018)Standard operating procedures for cutaneous tumoursA European multicentre consensus document; a practice standard, not binding regulation
National regulationsVary by countryDevice CE/FDA status, off-label drug use and reimbursement conditions must each be assessed separately

Safety Considerations Specific to IRE-ECT

Irreversible electroporation has a different safety profile from RE-ECT. Because high-voltage pulses cause severe muscle contraction, general anaesthesia with deep neuromuscular blockade is standard. ECG synchronisation is used routinely to keep pulses out of the vulnerable cardiac period.

For deep organ applications, electrodes are placed under imaging guidance, which brings procedure-specific risks along the needle tract such as bleeding, pancreatitis or bile leak. Preservation of vascular and ductal structures is the reason the method is chosen for adjacent tumours, but that preservation is not absolute: reports of thrombosis and stricture exist in the literature.