AMR B: HPV positive ctDNA guided imaging in follow-up
Diagnostic TestBlood samples in follow-up positive for ctDNA leads to an extra PET-CT scan to detect early treatment failure
NCT Number: NCT05572801
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Department of Oncology Herlev and Gentofte Hospital, Herlev, Capital Region of Denmark, Denmark
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
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Blood samples in follow-up positive for ctDNA leads to an extra PET-CT scan to detect early treatment failure
Time frame: after 2 years
Disease free survival 2 years from end of therapy
Time frame: after 5 years
Lead time between ctDNA detected and CT verified recurrences
Time frame: after 5 years
Rate of succesful salvage surgery
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
Time frame: after 5 years
Disease free survival at 5 years follow-up
Time frame: after 5 years
The rate of distant failures
Time frame: 5 years
Overall survival from beginning of treatment to death of any cause
Time frame: 5 years
Explorative analysis of total circulating free DNA (cfDNA)
Time frame: 5 years
Analysis of ctDNA in HPV negative cases
Time frame: after 2 and 5 years
Acute toxicity (CTCAE 5.0)
Time frame: after 2 and 5 years
Late toxicity (CTCAE 5.0)
Time frame: after 2 and 5 years
Health related quality of life (EORTC QLQ-ANL27)
Contact information is provided by the study sponsor or research team.
Karen-Lise G Spindler, Professor
CONTACT
Louise V Laursen, Secretary
CONTACT
Aarhus University Hospital
Other
NOAC9 - A Phase II Randomised Nordic Anal Cancer Group Study on Circulating Tumor DNA Guided Follow-Up
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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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