In initially metastatic rectal carcinoma, a neo-adjuvant multi-drug chemotherapy is usually performed, followed by a pelvic chemoradiation. The surgical indications on both metastases and the pelvic site are then discussed: in the case where a complete (or near-complete) response (CR) of the rectal tumor is observed (10 to 40%), the local surgery may be omitted or poned ("wait-and-see") in a sphincter-sparing strategy, in order to minimize or avoid the surgical morbidity, to focus on metastatic disease by the continuation of chemotherapy, and to preserve a better quality of life. After 8 weeks of induction chemotherapy (mFolfox6 regimen, 4 cycles), the aim of our study is to optimize the chemoradiation step on the distal rectal tumor, thanks to Intensity-Modulated Radiotherapy (IMRT) with simultaneous integrated boost (SIB) (Phase-1 part of the study), concomitantly with oral capecitabine. According to a Fibonacci dose-escalation scheme, 3 radiation dose-levels are defined, up to the definition of the maximal tolerated dose (MTD), requiring the inclusion of a maximum of 20 patients. Further patients will be included at the recommended dose for phase-2 (RDP2) in a two-step phase-2 study, considering simultaneously as principal objective at 12 months, both the efficacy (local CR rate in the range of 10 to 25%) and the tolerance (pelvic radiation disease: grade 3-4 toxicities in the range of 30 to 10%). Overall 65 patients will be included in the phase-2 study at the RDP2 dose.
The study population has metastatic rectal cancer. After obtaining informed consent and if they fulfil all of the criteria for inclusion, patients will be included. After 8 weeks of induction chemotherapy with FOLFOX, patients perform an imaging assessment. Then they are treated by radiotherapy with an oral Xeloda At the end of irradiation, patients realize on other Imaging assessment. Patients are then followed for 2 years
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
It's a dose escalation of radiation (IMRT), during 5 to 7 weeks, 5 days per week. Concomitantly, patient have oral chemotherapy (capecitabin)
Institut de Cancérologie de l'Ouest
Angers, France
maximum tolerated radiation dose (MTD) delivered by IMRT with SIB, in combination with oral capecitabine, for initially metastatic, low and middle rectal cancer after 4 induction cycles of mFolfox6 regimen.
MTD = dose level -1 after at least 2 patients with DLT to upper level
Time frame: 84 months
Local Progression-free survival at 12 months,
% patient with Local Progression at CT scan, 12 months after inclusion
Time frame: 12 months after inclusion
Toxicity profile of the chemoradiation step for NCI.CTC grade 3-4 local toxicities due to "Pelvic Radiation Disease"
% patient with \>= grade 3 toxicity (NCI.CTC AE)
Time frame: 84 months
To evaluate quality of Life
EORTC-QLQC-30
Time frame: 84 months
To evaluate quality of Life
QLQ-CR29
Time frame: 84 months
Overall survival at 2 years
Overall survival is defined as the delay between the date of inclusion and the date of end of study
Time frame: 24 months after inclusion
The usefulness of surgery
The surgical decision within 12 months after the end of radiochemotherapy will be recovered
Time frame: 12 months after the end of radiochemotherapy
The prognostic value of PET
The interest of PET to define the volume in radiotherapy
Time frame: 108 months
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