Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
200 participants
OBSERVATIONAL
2022-09-01
2024-10-01
Brief Summary
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Detailed Description
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This is a retrospective observational (cross sectional) study in which de-personalised patient level National Cancer Registration and Analysis Service data via NHS Digital DARS will be requested.
In particular, patient level data for all women in England, between 2001 and 2019, aged 25- 90+ years, with a diagnosis of anal cancer and/or anal HSIL and:
* vaginal SCC and/or HSIL
* vulvar SCC and/or HSIL
* cervical SCC and/or HSIL
* vaginal and vulvar SCC and/or HSIL
* vaginal and cervical SCC and/or HSIL
* vulvar and cervical SCC and/or HSIL
* vaginal, cervical and vulvar SCC and/or HSIL
For these women with synchronous or metachronous anal and genital HSILs or SCCs data will be collected on:
1. Month, Year of each diagnosis.
2. Age at each diagnosis.
3. Cancer stage (for each cancer): 1, 2, 3, 4, not known, other, unstageable disease.
4. Performance status at each diagnosis: 1,2,3,4, not known.
5. Treatments received (for each diagnosis): Surgery, Chemotherapy, Radiotherapy.
6. Ethnicity: British, Irish, Other white, White/ Black Caribbean, White/Black African, White/ Asian, Other Mixed, Indian, Pakistani, Bangladeshi, Other Asian, Black Caribbean, Black African, Other black, Chinese, Other Ethnic, Not Known.
7. Route to Diagnosis (for each diagnosis): Emergency Presentation, GP referral, Inpatient Elective, Other Outpatient, Screening, Two Week Wait, Unknown.
8. Deprivation score: 1 (least deprived), 2, 3, 4, 5 (Most deprived).
In order to establish the incidence of anal cancer in women with genital cancers, data will be requested on the total number of women/year (between 2001 and 2019), in England, aged between 25-90+ years with a diagnosis of:
* Anal cancer
* Anal HSIL
* Vulvar cancer
* Vulvar HSIL
* Vaginal cancer
* Vaginal HSIL
* Cervical cancer
* Cervical HSIL
ICD-10 malignant neoplasm and carcinoma in-situ codes will be used to identify these patients:
* Anal Cancer C21.0. C21.1, C21.8
* Cancer of the Vulva C51.0, C51.1, C51.2, C51.8, C51.9
* Cancer of the Vagina C52.
* Cancer of the Cervix Uteri C53.0, C53.1, C53.8, C53.9
* Anal HSIL D01.3
* Vulval HSIL D07.1
* Vaginal HSIL D07.2
* Cervical HSIL D06.0, D06.1, D06.7, D06.9
Primary Objective:
Establish the incidence of anal HSIL and cancer in women with genital HSILs and/cancers and vice versa in England.
Secondary Objectives:
1. Asses the risk of anal HSIL and SCC in women with genital HSILs and/or SCC in England.
2. Investigate the sociodemographic risk profile of women developing multizonal anogenital HPV driven high-risk pathologies.
3. Establish the timelines between the development of genital HSIL/SCC and anal HSIL/SCC.
Primary Outcome:
The incidence of anal HSIL and cancer in women with genital HSIL and/cancer in England between 2001- 2019.
Secondary Outcomes:
1. The risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England.
2. The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors (ethnicity, age, social deprivation).
3. The amount of time in years and months between the diagnosis of genital HSIL/SCC and anal HSIL/SCC.
Statistics and Data Analysis:
Data will be analysed using SPSS Statistics software. All outcomes extracted from the database will be expressed in categorical fields; therefore, comparisons of outcomes will be analysed using Chi squared or Fisher's Exact Tests. A statistically significant p value for this analysis is defined as p \< 0.05. Incidence will be calculated per 100,000 people per year. Any missing data fields were classified as "unknown" within the database. Missing data will not be excluded from the analysis and "unknown" variables are included with tables and figures to prevent bias.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Interventions
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Dual Pathology
Women with both genital HSIL/SCC and Anal HSIL/SCC
Eligibility Criteria
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Inclusion Criteria
* Women diagnosed with anal cancer and/or HSIL between 2001 and 2019.
* The anogenital cancer must be a squamous cell carcinoma.
* Women with a diagnosis of anal cancer and/or HSIL and:
1. vaginal cancer and/ or HSIL
2. vulvar cancer and/or HSIL
3. cervical cancer and/or HSIL
4. vaginal and vulvar cancer and/or HSIL
5. vaginal and cervical cancer and/or HSIL
6. vulvar and cervical cancer and/or HSIL
7. vaginal, cervical and vulvar cancer and/or HSIL
Exclusion Criteria
* Women aged outside of the 25-90+ years bracket.
* Women diagnosed with anal cancer or HSIL before 2001 and after 2019.
* Women with genital or anal cancer which is not a squamous cell carcinoma.
25 Years
100 Years
FEMALE
Yes
Sponsors
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Imperial College London
OTHER
Responsible Party
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Locations
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Imperial College London- Chelsea and Westminster NHS Foundation Trust
London, , United Kingdom
Imperial College London- Chelsea and Westminster NHS Foundation Trust
London, , United Kingdom
Countries
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Facility Contacts
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Micol Lupi
Role: primary
Christos Kontovounisios
Role: backup
Micol Lupi
Role: primary
Other Identifiers
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315094
Identifier Type: -
Identifier Source: org_study_id