Actively Recruiting

Age: 18Years +
All Genders
ID05328765

ACTION HIV: A Global Record of Patients With Anal Squamous Cell Carcinoma With and Without HIV Infection

Led by Latin American Cooperative Oncology Group · Updated on 2025-03-07

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting an observational study to understand prognostic and predictive factors affecting patients with anal squamous cell carcinoma (CCA), both with and without HIV infection. The study seeks to describe patient profiles worldwide, including factors such as CD4 counts, duration of HIV infection, viral load, AIDS diagnosis, geographic treatment regions, clinical staging, medication interactions, comorbidities, use and duration of highly active antiretroviral therapy (HAART), and radiotherapy types. It aims to compare clinical outcomes between patients living with HIV and those without. Participants include patients diagnosed with anal squamous cell carcinoma, with or without HIV infection. The study groups are divided based on HIV status. Data collected will reflect real-world treatment modalities, including conventional 3D radiotherapy versus Intensity Modulated Radiotherapy (IMRT), and responses to specific chemotherapy regimens. There are no interventional treatments assigned by the study, as this is an observational record. Participants will be followed to assess key outcomes such as median disease-free survival over three years, complete clinical response at six months, and overall survival from treatment start to death from any cause within three years. Researchers will gather data on treatment details, clinical staging, medication use, and other health factors. The study aims to provide comprehensive insights into how HIV status and related factors influence anal cancer treatment outcomes and survival over time.

CONDITIONS

Brief Title

A Global Record of Patients With Anal Squamous Cell Carcinoma With and Without HIV Infection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years of age or older
  • Confirmed histological diagnosis of anal canal squamous cell carcinoma, including basaloid subtype
  • Have undergone serological test for HIV infection
  • Any clinical stage of anal squamous cell carcinoma
Not Eligible

You will not qualify if you...

  • Lack of data on treatments and clinical outcomes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

Duration - Up to 3 years

Participants who have confirmed anal squamous cell carcinoma with or without HIV infection are observed to collect data on disease progression and clinical outcomes.

Visits as per routine care and data collection schedules

Trial Site Locations

Total: 1 location

1

A.C. Camargo Cancer Center

São Paulo, Brazil, 01509-001

Actively Recruiting

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Research Team

V

Viviane Horn de Melo

L

Laura Voelcker

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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