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NCT Number: NCT06364579

Patient Reported Outcomes (PROs) in Anal Cancer Patient Treated by Intensity Modulated Radiotherapy (IMRT).

Radiochemotherapy is the standard treatment for neoplasms of the anal canal with excellent rates of local control and preservation of the anal sphincter. However, patients may experience a deterioration of quality of life related to sequelae of the treatment particularly at intestinal, anal sphincter and sexual level. Few studies to date have documented patient-reported outcomes (PROs) in this area. The aim of this observational study is to verify the quality of life (QOL) of the patients by means of self-completed questionnaires.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fondazione Policlinico Universitario A. Gemelli IRCCS

Rome, Lazio, 00168, Italy

Location status: Recruiting

Location contact

Stefania Mandrida

CONTACT

+390630155701

Stefania Manfrida, MD

CONTACT

[email protected]

+3900630154434

Stefania Manfrida, MD

PRINCIPAL_INVESTIGATOR

About this study

In recent times, the focus on collecting patient-reported outcomes (PROs) has increased in healthcare. The Food and Drug Administration defines PROs as a -measurement of any aspect of a health status of the patient that comes directly from the patient-. These includes disease symptoms, functional aspects and quality of life (QOL). The collection of PROs, combined with physician-assessed toxicity, is constantly being incorporated into clinical practice and studies to provide a more holistic picture of the impact of treatment on patients and prove useful for planning future interventions. Although the use of PROs has now become the standard for measuring quality of life of patients there are still few studies on the self-reported long-term QOL of anal cancer patients and on disease or therapy related symptoms that affect QOL. Therefore, the EORTC (European Organisation for Research and Treatment of Cancer) has recently developed the specific Quality of Life Questionnaire for anal cancer (QLQ-AN27) module to explore typical symptoms of anal cancer and its therapy. In this study, the QLQ-AN27 questionnaire will be administered together with the EORTC Quality of Life 30 (QLQ 30) in patients with anal cancer who have undergone radio-chemotherapy. The questionnaire may be administered before treatment, after treatment and during follow-ups until completion of the fifth year. This is an observational study both retrospective and prospective.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Eastern Cooperative Oncology Group (ECOG) 0-3
  • minimum 18 years old
  • squamous cell carcinoma of the anal canal
  • low burden of metastatic disease at diagnosis
  • indication for radiochemotherapy treatment
  • informed consent

Exclusion criteria

  • age under 18 years
  • Eastern Cooperative Oncology Group (ECOG) higher than 3
  • metastatic disease at diagnosis not amenable to radiochemotherapy treatment

Treatment and study plan

Primary outcomes

  1. QOL analysis

    Time frame: 60 months from the last enrolled patient (january 2026)

    Analysis of quality of life (QOL) by administration of PRO questionnaires to patients with cancer of the anus treated with IMRT radiochemotherapy.

Secondary outcomes

  1. Overall survival (OS)

    Time frame: time 0, end of treatment, 6 month post treatment, 1 year follow-up, 2 years follow-up, 3 years follow-up, 4 years follow-up, 5 years follow-up

    Absence of death from any cause.

  2. Colostomy Free Survival (CFS)

    Time frame: time 0, end of treatment, 6 month post treatment, 1 year follow-up, 2 years follow-up, 3 years follow-up, 4 years follow-up, 5 years follow-up

    Being alive without a temporary or permanent ileostomy or colostomy

  3. Loco-Regional Recurrence (LRR)

    Time frame: time 0, end of treatment, 6 month post treatment, 1 year follow-up, 2 years follow-up, 3 years follow-up, 4 years follow-up, 5 years follow-up

    Presence of disease progression inside the target volume of radiation therapy

  4. Disease-Free Survival (DFS)

    Time frame: time 0, end of treatment, 6 month post treatment, 1 year follow-up, 2 years follow-up, 3 years follow-up, 4 years follow-up, 5 years follow-up

    The time from last treatment to cancer recurrence or death from any cause

  5. Acute toxicity

    Time frame: during treatment, end of treatment

    Acute toxicity caused by chemoradiation according to CTCAE v. 5.0

  6. Late toxicity

    Time frame: 6 month post treatment ,1 year follow-up, 2 years follow-up, 3 years follow-up, 4 years follow-up, 5 years follow-up

    Late toxicity caused by chemoradiation according to CTCAE v. 5.0

Study contacts

Contact information is provided by the study sponsor or research team.

Stefania Manfrida

CONTACT

[email protected]

+390630155701

Stefania Manfrida, MD

CONTACT

[email protected]

0039 0630154434

Sponsors and collaborators

Lead sponsor

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Other

Registry information

Acronym: PROACT

Important dates

Study start
2024
Primary completion
2027
Study completion
2031
First posted
Apr 15, 2024
Registry last updated
Aug 26, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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