Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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