Anal CancerNCT05835947
Anal Cancer Risk In Women
An observational study of Anal Cancer and Human Papilloma Virus, run by Imperial College London at 2 sites in United Kingdom.
Trial summary
This is a retrospective cross-sectional study involving the analysis of Cancer Registry Data. As part of this study, cancer registration data collated by the National Cancer Registration and Analysis Service (NCRAS; the national cancer registry in England), via NHS Digital data access request service (DARS), will be… Read more about this study
- Who is it for?
- Ages 25 to 100 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Anal Cancer, Human Papilloma Virus, Anal Intraepithelial Neoplasia
- What is being tested?
- Dual Pathology
- How many people
- 200 participants
- Where
- 2 sitesUnited Kingdom
- Study dates
- 1 Sep 2022to 1 Oct 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 25 to 100 years
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Study population: Women in England affected by both an anal and a genital HSILs/SCCs between 2001-2019.
Who may be able to join
- Women aged 25-90+ years of age.
- 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:
- vaginal cancer and/ or HSIL
- vulvar cancer and/or HSIL
Show all 11Show fewer
- cervical cancer and/or HSIL
- vaginal and vulvar cancer and/or HSIL
- vaginal and cervical cancer and/or HSIL
- vulvar and cervical cancer and/or HSIL
- vaginal, cervical and vulvar cancer and/or HSIL
Who cannot join
- Men with a diagnosis of anal HSIL and/or SCC.
- 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.
Trial locations and contacts
2 sites in 1 country.
United Kingdom2 sites, 2 recruiting
- Recruiting
Imperial College London- Chelsea and Westminster NHS Foundation Trust
London, SW10 9NH
Micol Lupi, 020 3315 8000 ext. 4469, m.lupi22@imperial.ac.uk
Christos Kontovounisios, 020 3315 8000 ext. 4469, c.kontovounisios@imperial.ac.uk
- Recruiting
Imperial College London- Chelsea and Westminster NHS Foundation Trust
London, SW10 9NH
Micol Lupi, 020 3315 8000, m.lupi22@imperial.ac.uk
About this study
Official title: The Role of Early Detection and Treatment of Anal Intraepithelial Neoplasia in the Prevention of Anal Squamous Cell Carcinoma in Women: Establishing the Disease Burden in Women With Genital Cancer
This is a retrospective cross-sectional study involving the analysis of Cancer Registry Data. As part of this study, cancer registration data collated by the National Cancer Registration and Analysis Service (NCRAS; the national cancer registry in England), via NHS Digital data access request service (DARS), will be analysed on all female patients aged between 25-90+ years in England with a registered diagnosis of anal and vaginal and/or vulvar and/or cervical cancer and/or high grade squamous intraepithelial lesions (HSIL) between 2001 and 2019. For these patients information on age at diagnosis, ethnicity, deprivation, performance status, stage of the cancer at diagnosis, the date of each diagnosis, the treatment received for the diagnosis and the route to diagnosis, will be analysed. Additionally, the total number of women/year (between 1995 and 2019), in England, aged between 25-90+ years with a diagnosis of anal, vulvar, vaginal and cervical cancer as well as their respective HSILs will be requested. Together this data will be used to establish the incidence of anal cancer and HSIL in women with genital cancers and/or HSILs, the progression timelines between the different pathologies, as well as identify relevant sociodemographic risk factors in this patient group.
Read the detailed description
Hypothesis: Women with genital HSILs/SCCs have an increased risk of anal HSIL/SCC regardless of whether they have received treatment for their genital condition and would benefit from surveillance and treatment of anal HSIL in the prevention of ASCC.
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:
- Month, Year of each diagnosis.
- Age at each diagnosis.
- Cancer stage (for each cancer): 1, 2, 3, 4, not known, other, unstageable disease.
- Performance status at each diagnosis: 1,2,3,4, not known.
- Treatments received (for each diagnosis): Surgery, Chemotherapy, Radiotherapy.
- 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.
- Route to Diagnosis (for each diagnosis): Emergency Presentation, GP referral, Inpatient Elective, Other Outpatient, Screening, Two Week Wait, Unknown.
- 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:
- Asses the risk of anal HSIL and SCC in women with genital HSILs and/or SCC in England.
- Investigate the sociodemographic risk profile of women developing multizonal anogenital HPV driven high-risk pathologies.
- 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:
- The risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England.
- The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors (ethnicity, age, social deprivation).
- 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
- Anal Cancer, Human Papilloma Virus, Anal Intraepithelial Neoplasia, Genital Neoplasm, Genital Cancer
- Being tested
- Dual Pathology
- Medical subject headings
- Anus Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dual PathologyOther
Women with both genital HSIL/SCC and Anal HSIL/SCC
What is being measured
The primary outcome is the main question the study is designed to answer.
The incidence of anal HSIL and cancer in women with genital HSIL and/cancer in England
as above
Measured: 2001- 2019
Secondary outcomes (3)
he risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England
as above
Measured: 2001-2019
The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors.
as above
Measured: 2001-2019
The amount of time in years and months between the diagnosis of genital HSIL/SCC and anal HSIL/SCC
as above
Measured: 2001-2019
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Apr 2023
- Study start1 Sep 2022
- Primary completion1 Jan 2024 (estimated)
- Study completion1 Oct 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Anal CancerStudies of the same condition, open and under way.
- More trials run by Imperial College LondonThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 200 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Imperial College London
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05835947
- Sponsor's protocol ID
- 315094
- Status last verified
- Apr 2023
- First submitted
- 19 Apr 2023
- Last updated
- 28 Apr 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Request to NHS digital is for de-personalised data. Researchers will not have access to individual participant data.
Study at a glance
From the registry record, last updated by the sponsor on 28 Apr 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Role of Early Detection and Treatment of Anal Intraepithelial Neoplasia in the Prevention of Anal Squamous Cell Carcinoma in Women: Establishing the Disease Burden in Women With Genital Cancer
- ClinicalTrials.gov ID
- NCT05835947
- Acronym / sponsor ID
- 315094
- Conditions
- Anal Cancer, Human Papilloma Virus, Anal Intraepithelial Neoplasia, Genital Neoplasm, Genital Cancer
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 200 participants (estimated)
- Lead sponsor
- Imperial College LondonUniversity, hospital or other
- Study start
- 1 Sep 2022 (actual)
- Primary completion
- 1 Jan 2024 (estimated)
- Study completion
- 1 Oct 2024 (estimated)
- First posted
- 28 Apr 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a retrospective cross-sectional study involving the analysis of Cancer Registry Data. As part of this study, cancer registration data collated by the National Cancer Registration and Analysis Service (NCRAS; the national cancer registry in England), via NHS Digital data access request service (DARS), will be analysed on all female patients aged between 25-90+ years in England with a registered diagnosis of anal and vaginal and/or vulvar and/or cervical cancer and/or high grade squamous intraepithelial lesions (HSIL) between 2001 and 2019. For these patients information on age at diagnosis, ethnicity, deprivation, performance status, stage of the cancer at diagnosis, the date of each diagnosis, the treatment received for the diagnosis and the route to diagnosis, will be analysed. Additionally, the total number of women/year (between 1995 and 2019), in England, aged between 25-90+ years with a diagnosis of anal, vulvar, vaginal and cervical cancer as well as their respective HSILs will be requested. Together this data will be used to establish the incidence of anal cancer and HSIL in women with genital cancers and/or HSILs, the progression timelines between the different pathologies, as well as identify relevant sociodemographic risk factors in this patient group.
Detailed description
Hypothesis: Women with genital HSILs/SCCs have an increased risk of anal HSIL/SCC regardless of whether they have received treatment for their genital condition and would benefit from surveillance and treatment of anal HSIL in the prevention of ASCC.
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:
- Month, Year of each diagnosis.
- Age at each diagnosis.
- Cancer stage (for each cancer): 1, 2, 3, 4, not known, other, unstageable disease.
- Performance status at each diagnosis: 1,2,3,4, not known.
- Treatments received (for each diagnosis): Surgery, Chemotherapy, Radiotherapy.
- 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.
- Route to Diagnosis (for each diagnosis): Emergency Presentation, GP referral, Inpatient Elective, Other Outpatient, Screening, Two Week Wait, Unknown.
- 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:
- Asses the risk of anal HSIL and SCC in women with genital HSILs and/or SCC in England.
- Investigate the sociodemographic risk profile of women developing multizonal anogenital HPV driven high-risk pathologies.
- 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:
- The risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England.
- The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors (ethnicity, age, social deprivation).
- 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.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
Who may qualify
- Ages
- 25 to 100 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Women in England affected by both an anal and a genital HSILs/SCCs between 2001-2019.
Key inclusion criteria (11 listed)
- Women aged 25-90+ years of age.
- 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:
Key exclusion criteria (4 listed)
- Men with a diagnosis of anal HSIL and/or SCC.
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dual PathologyWomen with both genital HSIL/SCC and Anal HSIL/SCC | Other | – |
Primary outcome
The incidence of anal HSIL and cancer in women with genital HSIL and/cancer in England
Time frame: 2001- 2019
as above
3 secondary outcomes
he risk of anal HSIL and/or SCC in women with genital HSILs and/or SCC in England
Time frame: 2001-2019
The relationship between the incidence of multizonal anogenital disease and specific sociodemographic risk factors.
Time frame: 2001-2019
The amount of time in years and months between the diagnosis of genital HSIL/SCC and anal HSIL/SCC
Time frame: 2001-2019
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Apr 2023.
- Individual participant dataSharing planned: No. Request to NHS digital is for de-personalised data. Researchers will not have access to individual participant data.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Imperial College London- Chelsea and Westminster NHS Foundation Trust
London, United Kingdom
Imperial College London- Chelsea and Westminster NHS Foundation Trust
London, United Kingdom
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Anal Cancer and Human Papilloma Virus, run by Imperial College London at 2 sites in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 11 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 28 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The incidence of anal HSIL and cancer in women with genital HSIL and/cancer in England (time frame: 2001- 2019). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Apr 2023.