Intestinal Microbiome Modulation With Antibiotics in the Neoadjuvant Treatment of Locally Advanced Rectal Cancer

This is a single-center, phase 2, single-arm clinical trial, compared with a historical control. The intervention consists of the oral administration of metronidazole at a daily dose of 1.500 mg, divided into three 500mg doses taken every 8 hours, during the first seven days of neoadjuvant radiotherapy. Adherence to metronidazole will be monitored by evaluating records on the patient´s daily card, designed by the researchers, and questioning during medical visits. Adverse events related to metronidazole use are uncommon and mainly include gastrointestinal disturbances. Infrequent reactions occur in less than 0,01% of patients. All adverse effects will be carefully monitored by the study team. Patients may discontinue the medication for any following reasons: disease progression, death, adverse event, leading to permanent discontinuation of chemoradiotherapy, medication intolerance, withdrawal of consent by the patient (or legal representative), or the need for new systemic oncological therapy or surgery. The primary objective of the study is to determine the effectiveness of antimicrobial therapy at the start of neoadjuvant treatment in patients with locally advanced rectal adenocarcinoma. The secondary objectives are to evaluate changes in the intestinal bacterial profile through intestinal analyses (16S RNA analysis) in pre- and post-treatment fecal samples, to measure the organ preservation rate, to determine the rate of complete pathological response among operated patients, to monitor the toxicity of neoadjuvant treatment and to calculate the 3-year locoregional recurrence-free survival rate. The primary outcome will be a complete clinical response to neoadjuvant treatment, defined by the absence of detectable residual disease through the following methods: digital rectal examination, rectal endoscopy, and magnetic resonance image. The standard neoadjuvant treatment regimen consists of long-course radiotherapy, with 4.500 cGy fractionated into 25 applications of 180 cGy, and a boost to the primary tumor up to a total dose of 54 Gy, concomitant with fluoropyrimidine. The current practice is to perform the entire neoadjuvant treatment before surgery, which consists of chemoradiotherapy followed by chemotherapy with fluoropyrimidine and oxaliplatin for up to 6 cycles (TNT consolidation), or starting with chemotherapy followed by chemoradiotherapy (TNT induction). The primary outcome will be evaluated between 7 and 10 days after the completion of chemotherapy in TNT consolidation or between 10-12 weeks after the radiotherapy in TNT induction. For patients who were candidates for rectal amputation and achieved complete clinical response after the neoadjuvant treatment, an organ preservation strategy (Watch Wait - WW) will be recommended as the first option. For patients with mid-rectal tumors, where surgery involves sphincter preservation, total mesorectal excision surgery with sphincter preservation will be offered as the first treatment option, regardless of the response pattern. In cases of complete clinical response, the WW strategy will be offered as an alternative to patients who refuse surgery. For the evaluation of adverse events, patients will be seen before the start of the study, within 7 days of the start of chemoradiotherapy, and at the end of the study, during the evaluation of the primary outcome, with a complete clinical examination and routine laboratory tests. Patients who experience intolerable grade 2 or 3 toxicity will have their treatment dose reduced and/ or interrupted, according to routine procedures. All adverse effects will be graded and assessed to determine if they are treatment-related. Since this is a Brazilian-approved drug that is widely used commercially, the investigators do not expect to observe severe adverse events. However, if there is intolerance, dose reduction will not be allowed, but the investigators will recommend discontinuation. Adverse events will be evaluated according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Whenever possible, each adverse event must be evaluated to determine: its severity, its relationship to each study drug, its duration, and actions taken. The investigators will collect pre- and post-intervention stool samples from all patients included in the study to investigate the secondary outcome, which consists of evaluating changes in the intestinal bacteria profile through intestinal analyses (16S RNA analysis) in pre- and post-treatment fecal samples.