Cutaneous Squamous Cell Carcinoma Clinical Trial
Official title:
Investigation "in Vitro" of New Strategies Alternative to Surgery Against Cutaneous Squamous Cell Carcinoma: Topical Chemotherapy Followed by Superficial Radiotherapy.
The gold treatment for local invasive cutaneous squamous cell carcinoma is surgical excision. Nevertheless, surgery is not always an option as a consequence of the age and/or the health status of the patient. One of the objectives of this study is to assess the effects of cisplatin concomitantly with a subsequent low-energy X-rays irradiation in vitro. In order to enhance the effectiveness of this combined treatment, the temporal fractionation of the platinated compound is expected to be performed.
Cutaneous squamous cell carcinoma (cSCC) accounts for the 20% of the most common skin
malignancies, i.e. the non-melanoma skin cancer. cSCC is considered one public health
problem because of the high costs of its treatment as cSCC are increasing due to a higher
sun exposure, as well as more efficient dermatological examinations. In addition, this kind
of skin cancer is characterized by a relatively high risk of metastasis.
The gold standard treatment for local invasive cSCC is based on the surgical excision,
leading to a 5-years control rate in low-risk patients of 96%. Nevertheless, surgery for
local invasive cSCC is not always an option as a consequence of the age and/or the poor
health status of the patient. Therefore, ionizing radiation is used as either primary or
adjuvant therapy against cSCC in elderly patients or when surgery would be extremely
invasive. Although radiotherapy seem to be a promising option, it needs to be improved in
order to damage locally the tumor area, thus avoiding damaging secondary effects on healthy
tissues. Typical skin radiation sources are based on superficial, orthovoltage X-rays (XR)
beams, as well as electron-beam therapy.
In particular, irradiations of local invasive cSCC by using a superficial XR source at
kilovoltage (kV) energy permit a local dose deposition within the tumor volume, with a
significant smaller penetration capacity with respect to the higher-energy XR sources.
Therefore, kV XR sources become a perfect tool for the treatment of superficial lesions,
such as the cSCC. The combination of these keV-energy photons with metallic atoms localized
in the tumor would enhance the dose deposited locally in the target, improving thus the
therapeutic index of the treatment. Among all the chemotherapeutic options available,
platinum-based agents, such as cis-diamminedichloroplatinum (II) (cisplatin or cisPt) has
become an essential anti-cancer drug with a substantial therapeutic impact against the most
carcinomas-like tumors.
The distortion of the structure of the DNA duplex, converts cisPt in a highly toxic agent
per se because of its influence on DNA replication, apoptotic death, and inhibition of the
major nuclear repair pathway of cisPt-DNA adducts and radiation-induced DNA breaks. However,
dose administration is a key limitation due to the high toxicity of this agent. It is for
this reason that the lowest cisPt concentration was used in this study, and the expected
effectiveness of cisPt on a cSCC cells were enhanced with a subsequent low-energy XR
irradiation in an attempt to explore some new therapeutic strategies against local invasive
cSCC.
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Observational Model: Case Control, Time Perspective: Cross-Sectional
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