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NCT Number: NCT05572801

NOAC9 - Circulating Tumor DNA Guided Follow-Up in Anal Cancer

This study investigates if circulating tumor DNA can improve the detection of early treatment failure or recurrence in localized squamous cell carcinoma of the anus (SCCA) after curative chemoradiotherapy thereby increasing the potential for cure. This will be done by comparing the standard follow-up program with ctDNA guided imaging follow-up. Secondly, the aim is to establish early interventions against late morbidities.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Oncology Herlev and Gentofte Hospital, Herlev, Capital Region of Denmark, Denmark

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About this study

Squamous cell carcinoma of the anus (SCCA) is a rare disease with less than 200 new cases in Denmark and Sweden each year and approximately 100 new cases in Norway and Finland but with increasing incidence. Primary treatment is chemo-radiotherapy (CRT) comprising high dose IMRT based radiation therapy with combination chemotherapy of 5-FU and Cisplatin. Overall treatment response is good in small tumors, but less pronounced for high-risk tumors.

In absence of complete pathological response after CRT or local recurrence, patients are evaluated for. salvage surgery. The importance of R0 resection on overall survival has been described in several studies. It is suggested that early detection of treatment failure and recurrences increases the chance of possible curative surgery (R0-resection) and thereby overall survival.

A follow-up program has 3 purposes

  • To detect lack of complete response to primary treatment
  • Early detection of local or distant recurrences
  • Describing and managing late morbidity

Purpose:

The main purpose of this follow-up study is to investigate if circulating tumor tDNA can improve detection of early treatment failure or recurrences thereby assisting in increasing the potential for cure. Secondly, to provide evidence for use of imaging and third objective is to establish early intervention against late morbidities.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with SCCA eligible for definitive (chemo)radiotherapy
  • ≥ 18 of years
  • Written and oral consent

Exclusion criteria

  • Conditions that will contraindicate blood samples
  • Conditions that will contraindicate a PET-CT scan.
  • Potential lack of compliance to standard FU program and study participation.

Treatment and study plan

AMR B: HPV positive ctDNA guided imaging in follow-up

Diagnostic Test

Blood samples in follow-up positive for ctDNA leads to an extra PET-CT scan to detect early treatment failure

Primary outcomes

  1. Disease free survival

    Time frame: after 2 years

    Disease free survival 2 years from end of therapy

Secondary outcomes

  1. Time between ctDNA detected and CT verified recurrences

    Time frame: after 5 years

    Lead time between ctDNA detected and CT verified recurrences

  2. Rate of succesful salvage surgery

    Time frame: after 5 years

    Rate of succesful salvage surgery

  3. Pattern of failure

    Time frame: after 5 years

    Pattern of failure defined as ln-field failures (within GTV-T, GTV-N, CTV or irradiated areas) or out-of-field failures

  4. Disease free survival at 5 years follow-up

    Time frame: after 5 years

    Disease free survival at 5 years follow-up

  5. The rate of distant failures

    Time frame: after 5 years

    The rate of distant failures

  6. Overall survival

    Time frame: 5 years

    Overall survival from beginning of treatment to death of any cause

  7. Explorative analysis of total circulating free DNA (cfDNA)

    Time frame: 5 years

    Explorative analysis of total circulating free DNA (cfDNA)

  8. ctDNA assays for HPV negative cases

    Time frame: 5 years

    Analysis of ctDNA in HPV negative cases

  9. Acute toxicity

    Time frame: after 2 and 5 years

    Acute toxicity (CTCAE 5.0)

  10. Late toxicity

    Time frame: after 2 and 5 years

    Late toxicity (CTCAE 5.0)

  11. Health related quality of life

    Time frame: after 2 and 5 years

    Health related quality of life (EORTC QLQ-ANL27)

Study contacts

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

Karen-Lise G Spindler, Professor

CONTACT

[email protected]

91137244

Louise V Laursen, Secretary

CONTACT

[email protected]

78454979

Sponsors and collaborators

Lead sponsor

Aarhus University Hospital

Other

Collaborators

  • Danish Comprehensive Cancer Center
  • Nordic Cancer Union
  • The regions medicine- and treatment funds

Registry information

Official study title

NOAC9 - A Phase II Randomised Nordic Anal Cancer Group Study on Circulating Tumor DNA Guided Follow-Up

Important dates

Study start
2023
Primary completion
2026
Study completion
2031
First posted
Oct 10, 2022
Registry last updated
Aug 14, 2024

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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