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Trial Title:
Immunohistochemical Expression of Excision Repair Cross Complementation Group 1 (ERCC1) in Laryngeal Squamous Cell Carcinoma and Its Correlation With Response to Radiotherapy.
NCT ID:
NCT05832593
Condition:
Laryngeal Squamous Cell Carcinoma
Conditions: Official terms:
Carcinoma
Carcinoma, Squamous Cell
Squamous Cell Carcinoma of Head and Neck
Study type:
Observational
Overall status:
Not yet recruiting
Study design:
Time perspective:
Cross-Sectional
Intervention:
Intervention type:
Other
Intervention name:
Immunohistochemistry
Description:
Immunohistochemical expression of ERCC1
Arm group label:
Group 1
Arm group label:
Group 2
Summary:
1. Determine the correlation between immunohistochemical expression of ERCC1 in
laryngeal cancer cells with clinico-pathological variables.
2. Assess the correlation between ERCC1 expression and response to radiotherapy.
Detailed description:
The global burden of laryngeal cancer increased during the past 3 decades. A total number
of 210,606 new cases of laryngeal cancer have been diagnosed in 2017 (2.76 new cases per
100,000 inhabitants) worldwide, with a prevalence of 1.09 million cases (14.33 cases per
100,000 inhabitants), accounting for as many as 126,471 deaths (1.66 per 100,000
inhabitants). The incidence and prevalence have both increased by 12.0% and 23.8%,
respectively during the past 3 decades, whilst mortality has declined by approximately 5
%.
In Egypt, laryngeal cancer represents 5.7% of all body malignancies and 38.7% of the head
and neck malignancies.
Squamous cell carcinoma is the most common histologic variant and accounts for 85-95% of
all malignant tumors of the larynx. According to World Health Organization it is the
second most common malignancy of the upper aerodigestive tract. It occurs more in people
above 40 years of age and more common in males.
The larger number of laryngeal cancer cases originate from the glottic region (i.e.,
approximately two-third), followed by the supraglottic area (about 30%), whilst
trans-glottic and purely subglottic tumors are generally less frequent.
Excision repair cross-complementation group 1 (ERCC1) is a key DNA repair gene in the
nucleotide excision repair pathway which is activated in the repair of intra- and
interstrand DNA crosslink.
Ionizing radiation (IR) acts directly or indirectly to cause various forms of
deoxyribonucleic acid (DNA) damage in cells. DNA damage repair is initiated after the
cell is genetically damaged. Nucleotide-excision repair (NER) is one of the ways of DNA
repair. ERCC1 is a structure-specific endonuclease that cut DNA at
single-stranded/double-stranded junctions with a specific polarity.
There is some clinical evidence suggesting that ERCC1 status (ERCC1 mRNA expression,
ERCC1 protein expression, and ERCC1 polymorphisms) is associated with platinum-based
therapy efficacy in some kinds of cancers.
In a previous meta-analysis, ERCC1 protein low expression status detected by
immunohistochemical methods significantly correlated with higher response to
platinum-based chemotherapy in ovarian cancers.
Another meta-analysis evaluated non-small cell lung cancer patients treated with
platinum-based chemoradiation showed that both low tumoral mRNA and protein levels were
associated with a better response rate and overall patient survival.
In head and neck squamous cell carcinomas, the available studies have a conflict in
results. Of six studies evaluating the relation between ERCC1 status and outcomes of head
and neck cancer patients, three showed positive and another three were with negative
results.
Criteria for eligibility:
Study pop:
patients with laryngeal squamous cell carcinoma that will be treated with radiotherapy.
Sampling method:
Non-Probability Sample
Criteria:
Inclusion Criteria:
- Stage: All stages of laryngeal squamous cell carcinoma.
- Grade: Both high and low grades.
- Patients treated with radiotherapy.
- Normal laryngeal tissue as a control.
Exclusion Criteria:
- • Patients with deficient clinical data.
- Patients treated with chemotherapy
Gender:
All
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Start date:
May 1, 2023
Completion date:
January 2025
Lead sponsor:
Agency:
Assiut University
Agency class:
Other
Source:
Assiut University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05832593