Clinical Trial

Study of SIB-IMRT in Combination With 5-FU and Mitomycin-C Among Patients With Locally Advanced Anal Canal Cancer: Efficacy, Safety and Quality of Life

Study acronym: CANAL-IMRT-01
Active, Not Recruiting Phase 2
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Summary
Anal canal carcinoma (ACC) represents 1.2% of digestive cancers. Its incidence is increasing. As epidermoid ACC (95% of ACC) are particularly sensitive to radio and chemotherapy, concomitant radio-chemotherapy is the standard treatment of locally advanced ACC, with proven efficacy on locoregional control, anal sphincter preservation, progression-free survival and complete response rate higher than 80%. Nevertheless, conventional radiotherapy frequently induces significant non-haematological toxicities requiring treatment interruptions. Thus, treatment usually includes a chemotherapy (5-Fluorouracil and Mitomycine-C) and 25 fractions of 1.8 Gy followed by a planned 1-week (or more) interruption and a boost, for a total 54-60 Gy radiation dose over 9 weeks. Considering the numerous anatomic pelvic structures, ACC has become a localisation of interest for Intensity-Modulated Radiation Therapy (IMRT) associated with less toxicity. However, IMRT induces grade≥3 cutaneous toxicities requiring irradiation breaks. Dose escalade did not show its interest: 60 Grays remains the standard. Assuming the deleterious effect of increased overall treatment time on local control and survival in head-and-neck and cervical cancers and the epidermoid histology of ACC, the benefit of no irradiation break on ACC tumour control is of interest. IMRT offers the possibility to deliver different doses to different target volumes simultaneously by altered fractionation schedule like SIB-IMRT (simultaneously integrated boost-IMRT). Several SIB-IMRT schedules have been retrospectively evaluated. Similar results were observed with moderate doses and schedules delivering higher doses with short interruptions. Nevertheless, standard SIB-IMRT schedule in ACC still not exist.
Protocol Amendment History 14 amendments
This ClinicalTrials.gov record has been amended 14 times since 2016-03-02; most recent amendment 2025-09-17.
Status change: Recruiting → Active, Not Recruiting 2022-12-07
Status change: Active, Not Recruiting → Recruiting 2021-10-19
Status change: Recruiting → Active, Not Recruiting 2021-06-25
Status change: Suspended → Recruiting 2018-01-02
Status change: Recruiting → Suspended 2017-07-27
Trial Details
NCT Number NCT02701088
Lead Sponsor Centre Francois Baclesse
Collaborators: Accuray Incorporated
Conditions Locally Advanced Anal Canal Cancer
Enrollment 71 participants
Start Date 2015-12
Primary Completion 2021-06-25 (estimated)
Study Completion 2025-12 (estimated)
Updated on ClinicalTrials.gov 2025-09-22