Head Neck Cancer Clinical Trial
Official title:
Calcium Electroporation for Head and Neck Cancer
In a phase I protocol to primarily investigate the safety of using calcium combined with electroporation on recurrent head and neck cancers. Secondly, to evaluate tumour response on PET/MRI (positron emission tomography/magnetic resonance imaging), clinical evaluation, biopsies. Thirdly, to evaluate the effect of calcium electroporation compared to electrochemotherapy as well as the patients life-of-quality through questionnaires, EORTC QLQ C-30 and H&N35 (european organisation for research and treatment of cancer).
Calcium electroporation. Electroporation is a technique that facilitates the transport of
molecules across the cell membrane by using electric pulses. The electric field applied to
the cell membrane creates a temporary destabilization. As the electric capacity of the
membrane is exceeded, cracks are formed in the membrane and the molecules are free to
diffuse into the cytosol of the cell. The process is reversible and the cell membrane is
stabilized in a matter of minutes. While the cell membrane is permeable there is an
increased influx of Ca2+ into the cell. Calcium influx may be further improved by combining
calcium together with electroporation; this is called calcium electroporation.
In vivo studies have shown that when enhancing the extracellular calcium concentration
before applying electroporation, a larger Ca2+ influx occurs. The large Ca2+ influx can lead
to a reduction in ATP (adenosine triphosphate) levels and cell death. A fall in ATP levels
is seen for two reasons: First, an increase in intracellular Ca2+ leads to a higher activity
of the Ca2+-ATPase and Na+/K+-ATPase. Secondly, the high concentration of Ca2+ leads to loss
of the electrochemical gradient in the mitochondrial membrane, which causes mitochondrial
collapse. Upon collapse of the mitochondria, the cell can no longer produce ATP. Overall,
the increased consumption and decreased production of ATP leads to lover ATP levels.
Combined with other cellular processes such as activation of lipases and proteases, the cell
will eventually die.
Trials objectives.
1. Primary outcome. Evaluating the safety measures of using calcium electroporation on
mucosal head and neck cancer. This is done by continuously evaluating pain by VAS-score
(visual analogue scale) and side effects by Common Terminology Criteria for Adverse
Events (CTCAE) registration into Adverse Events (AE) and Serious Adverse Events (SAE).
The safety of using calcium intratumourally is also evaluated by measurement of Ca2+ in
blood samples after treatment.
2. Secondary outcome. Evaluation of response by imaging: PET-MRI, Clinical photography,
Biopsies from tumour site The subjects subjective evaluation of the treatment and post
treatment period is evaluated through Quality of life questionnaires, EORTC QLQ-C30 and
H&N35: two different questionnaires both validated for head and neck cancer patients.
3. Tertiary outcome. The response to treatment will be compared to the results from our
current trial, where we use electrochemotherapy on mucosal head and neck tumours. The
comparison will be between imaging response, VAS score and results from questionnaires
(EORTC QLQ-C30 and H&N35).
Trial design. This is a phase I, interventional, clinical trial for the safety of calcium
electroporation on mucosal head and neck tumours. Subjects will have relapsed or primary
head and neck cancer. Treatment is intended as palliative and not curative. All subjects
will be offered standard treatment with surgery and radiotherapy before enrolment to the
trial, if possible. There is no scheduled control group, meaning that all eligible patients
will be offered treatment.
Electroporation and anaesthesia. The treatment is performed under general anaesthesia
because the localization of head and neck tumours complicates treatment under local
anaesthetic. After the patient is anaesthetized, the tumour area will be injected with
calcium. After administration of calcium electrodes are inserted into the tumour and
electrical pulses are generated and documented using a Cliniporator (IGEA, Capri, Italy).
Overall operating time/anaesthesia time will be 1-2 hours and expected hospital stay of 3
days. Treatment is intended as a once-only treatment but measurable response on evaluation
scans combined with continued cancer activity in the treated area can result in another
treatment session.
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