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Towards an Understanding of Barriers and Delays in the Diagnosis of Anal Cancer

Towards an Understanding of Barriers and Delays in the Diagnosis of Anal Cancer

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07455942
Acronym
FRACAS
Enrollment
300
Registered
2026-03-06
Start date
2026-03-30
Completion date
2028-12-31
Last updated
2026-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Squamous Cell Carcinoma of the Anal Canal, HPV-induced Cancer

Brief summary

This study examines care pathways in 300 patients with anal squamous cell carcinoma to identify barriers and delays in diagnosis, assess the impact of screening and access to care, and improve awareness, screening practices, and early diagnosis.

Detailed description

This situational analysis will make it possible to identify barriers and delays in diagnosis, to assess waiting times for access to consultations, and to evaluate the existence of potential fast-track diagnostic pathways. It will analyze the proportion of cancers diagnosed through screening as well as the proportion of eligible patients who did not benefit from screening. Assessing patient reluctance, the impact of socio-economic conditions, and patients' knowledge of the link between HPV and anal cancer will help better target public information efforts. Ultimately, the aim of the study is to improve care pathways in order to enhance public and healthcare professional awareness and promote earlier diagnosis.

Interventions

Completion of a self-administered questionnaire by the patient to collect information about their care journey, any difficulties or hesitations, as well as their knowledge of the link between papillomavirus and cancer.

Sponsors

Centre Hospitalier Intercommunal Creteil
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Male or female ≥ 18 years 2. Histologically proven invasive or microinvasive squamous cell carcinoma of the anus 3. Having read and understood the information letter provided, either: i. After disclosure of the diagnosis, or ii. At the latest 6 months after initiation of treatment (surgical excision, radiotherapy, or chemoradiotherapy) 4. Affiliated with a social security system

Exclusion criteria

1. Refusal to participate in the protocol 2. Other histological types: lymphoma, adenocarcinoma, neuroendocrine tumor, etc. 3. Time since treatment initiation greater than 6 months 4. Protected persons (pregnant women, breastfeeding women, individuals under guardianship or curators, minors, persons deprived of liberty, or persons unable to express informed consent).

Design outcomes

Primary

MeasureTime frameDescription
First symptom(s) and the histological diagnosisAt the inclusionTime between the first symptom(s) and the histological diagnosis of anal squamous cell carcinoma.

Secondary

MeasureTime frameDescription
Primary tumor, regional nodes, metastasis (TNM) ) stage comparisonAt the inclusionComparison of diagnostic stages and patient pathways according to whether or not they underwent scr
Assessment of Deprivation and Health Inequalities for Health Examination Centers, FrenchAt the inclusionFrench public-health index used to assess an individual's level of social and material deprivation based on living conditions, financial situation, social support, and access to healthcare. It helps identify social health inequalities and adapt medical care accordingly. \[0 to 100\], The higher the score → the greater the level of deprivation.
Link between HPV and anal cancerAt the inclusionProportion of patients aware of the link between HPV and anal cancer
Performing a rectal examination at the first consultationAt the inclusionAssess the proportion of patients who underwent a clinical examination with rectal examination at the first consultation

Contacts

CONTACTISABELLE ETIENNEY
ietienney@hopital-dcss.org(0)1 44 64 20 16 51

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026