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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02697084
Other study ID # 2014/54
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 2014
Est. completion date October 2021

Study information

Verified date July 2021
Source Centre Antoine Lacassagne
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anal canal cancer is a relatively rare disease, representing 1.2% of digestive cancers and 6% of anorectal cancers. Incidence is less than 1/100 000 of the general population. However, the incidence has increased considerably over the past three decades. The main risk factors are HPV infections and smoking. Initial treatment comprises radiochemotherapy or radiotherapy alone, according to the patient's tumor stage and tolerance of chemotherapy. The choice of the most appropriate treatment strategy will condition the patient's prognosis. Consequently, early assessment of the initial extension of the tumor, its therapeutic response and relapses constitute determining factors in the management of the disease Despite the good results obtained, persistent disease is observed in 30% of cases and abdominal-pelvic salvage amputation can then prove effective in cases of local or loco-regional relapse. The great majority of relapses occur within 2 years after treatment. Reported prognostic survival factors are the T stage, size inferior or superior to 4 cm and inguinal or pelvic lymph node involvement. The rules for follow-up are not substantiated by high levels of proof. Follow-up focuses principally on the clinical examination although the type and frequency of the paraclinical examinations are not backed by any consensus.


Description:

Post-treatment 18-FDG PET scan at 2 months can prove useful to predict locoregional or metastatic recurrence in patients treated by radiochemotherapy or radiotherapy in the anal canal cancer setting. There appear to be an FDG intensity variable and a metabolic response criterion enabling establishment of two groups of patients: low recurrence risk versus high recurrence risk at 2 years.


Recruitment information / eligibility

Status Recruiting
Enrollment 110
Est. completion date October 2021
Est. primary completion date September 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Consecutive inclusion of incident cases of anal canal cancer between November 2014 and May 2018. These patients are volunteers and have signed informed consent. Exclusion Criteria: - Presence of a nother cancer and specific treatment (chemotherapy, radiotherapy). Follow-up impossible during two years or more. Refusal to submit to initial or post-treatment PET/CT.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
anal cancer
Anal cancer patients with TEP TDM

Locations

Country Name City State
France Centre Antoine Lacassagne Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Antoine Lacassagne

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary time of disease-free survival 3 years
Secondary best metabolic response measurement variable: SUVmax 3 years
Secondary best metabolic response measurement variable: SUVmean 3 years
Secondary best metabolic response measurement variable: SUL peak 3 years
Secondary best metabolic response measurement variable: Metabolic Total Volume (MTV) 3 years
Secondary best metabolic response measurement variable: Total Lesion Glycolysis (TLG) 3 years
Secondary best treatment response criterion: SUV or metabolic volume threshold 3 years
Secondary best treatment response criterion: ratio (SUV or metabolic volume) 3 years
Secondary best treatment response criterion: complete or partial metabolic response according to EORTC or PERCIST criteria 3 years
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