BReak Interval Delayed Surgery for Gastrointestinal Extraperitoneal Rectal Cancer (BRIDGE)

Institute of Hospitalization and Scientific Care (IRCCS)

Status: Unknown

Conditions: Rectal Cancer

Treatments: Diagnostic Test: Repetition of Re-staging

Study type: Interventional

Funder types: Other

Identifiers

NCT03581344

1908

Details and patient eligibility

About

This is a randomized multicentric clinical trial in patients affected by resectable rectal cancer, cT2N1-2, cT3N0-2, MRF -, aiming to evaluate the impact of the interval between chemoradiotherapy and surgery on the pathological response.

Patients will undergo a neoadjuvant chemoradiotherapy treatment and those achieving a major or complete clinical and instrumental response will then be randomized and submitted to surgery with two options: the first group will be operated after an interval of 9-11 weeks, while the second will undergo surgery at 13-16 weeks, after a further clinical and instrumental re-evaluation 11-12 weeks after the end of chemoradiotherapy.

Full description

The proposed study is a randomized multicentric phase III study. The Patients included in the study will undergo a chemoradiotherapy neoadjuvant treatment.

Patients will undergo a clinical-instrumental restaging at 7-8 weeks and will be randomized in two groups in case of major or complete response:

1. Surgery 9-11 weeks after the end of neoadjuvant treatment
2. Second clinical and instrumental re-evaluation after 11-12 weeks and then surgery 13-16 weeks after the end of chemoradiotherapy.

Only patients who underwent preoperative chemoradiotherapy and achieved a complete or major response at the clinical-instrumental restaging 7-8 weeks after the end of neoadjuvant treatment will be included in the study.

The control arm of the BRIDGE-1 study is represented by patients undergoing surgery 9-11 weeks after the end of chemoradiotherapy, whose major/complete response has to be assessed with clinical-instrumental exams to be performed 7-8 weeks after the end of chemoradiotherapy.

The experimental arm of the the BRIDGE-1 study is represented by patients undergoing surgery 13-16 weeks after the end of chemoradiotherapy, showing a major/complete response at the clinical-instrumental exams to be performed 7-8 weeks after the end of chemoradiotherapy. These patients will undergo a new clinical and instrumental evaluation, 11-12 weeks after the end of neoadjuvant chemoradiotherapy treatment, prior to be submitted to the delayed surgical procedure.

Patients will be recruited in the two different arms, according to a randomized assignment, realized through an electronic table, in order to assure the efficacy of this study. Patients will be divided according to gender, age, stage and tumour site (low, medium and high) in each centre.

When a patient will be assigned to a specific arm, the randomization procedure will recruit a similar patient in the other arm.

CLINICAL STAGING AND RESTAGING EVALUATION TNM clinical and pathological stages are reported according to the American Joint Committee on Cancer 7th Edition, adenocarcinoma histological grading according to WHO classification.

Staging and baseline clinical evaluation

1. Patient history
2. Digital rectal examination
3. Recto-colonoscopy + biopsy (in case of impossibility to perform colonoscopy due to stenosing lesion, rectoscopy + biopsy and double-contrast barium enema or colon CT or colonoscopy within 6 months from surgery are suggested)
4. Pelvic MRI for loco-regional staging
5. CT of the thorax and abdomen for distant metastases staging
6. PET-CT (optional)
7. CEA test
8. Quality of Life (QoL) questionnaires compilation

Restaging at 7-8 weeks

1. Digital rectal examination
2. Pelvic MRI
3. PET-CT if performed during staging
4. Rectoscopy (in case of major/complete response)
5. CEA test
6. Quality of Life (QoL) questionnaires compilation

7.3 Restaging at 11-12 weeks (for patients randomized in the delayed surgery arm)

1. Digital rectal examination
2. Pelvic MRI
3. PET-CT if previously performed
4. Rectoscopy
5. CEA test

As secondary outcomes, acute and late toxicities, quality of life, bowel function, rectal continence and sexual activity will be evaluated in this study.

PREOPERATIVE CHEMORADIOTHERAPY TREATMENT Chemoradiotherapy treatment schedule considers a total radiotherapy dose of 55 Gy in 5 weeks, delivered with a 3D concomitant boost or Intensity Modulated Radiation Therapy (IMRT) Simultaneous Integrated Boost (SIB) technique.

Concomitant chemotherapy considers administration of Capecitabine for the whole radiotherapy course.

SURGICAL APPROACH Surgery will be performed according to standard techniques using the " open " approach, laparoscopic or robotic, according to surgeon's preference and including both anterior resection of the rectum and abdominoperineal rectal resection with mesorectal total excision (Total Mesorectal Excision, TME).

The possibility of sphincter salvage will be evaluated collectively by the members of the multidisciplinary team at the time of diagnosis, at first re-evaluation and in case of second re-evaluation.

PATHOLOGICAL EVALUATION Resected rectal specimens will undergo gross examination in order to macroscopically evaluate the status of the mesorectal margin.

After marking with indian ink the mesorectal margin, cutting axially the colorectal segment on its anti-mesorectal side and fixating it in formalin, transverse sections of the surgical specimen will be serially cut.

In case of macroscopic evidence of disease, sampling of the most infiltrated area and of the tumoral area with the minimum distance from the mesorectal margin, which will be included, will be performed.

In case of macroscopic absence or in the suspect of residual disease, the initial tumour site will be completely included in the specimen, localizing it from clinical reports with the potential aid of endoscopic tattoos and/or tissue alterations by the treatment (scar retraction or increase of tissue consistency).

In case of negative reports of the first histological sections, each inclusion will undergo three levels of histological section series.

The histopathological evaluation of the response to the therapy will be scored according to the following classifications: Mandard A.M., et al; Washington MK et al/College of American Pathologists; in presence of positive nodes, the Nottingham Rectal Cancer Prognostic Index (NRPI) score will also be used.

ADJUVANT CHEMOTHERAPY The protocol does not establish criteria for the administration of adjuvant systemic treatment.

The single center maintains the discretion to administer postoperative chemotherapy.

FOLLOW-UP The follow-up program recommended in the study is described in the national guidelines in effect.

Patients will undergo a clinical evaluation 1 month after surgery, every third month during the first year and then every sixth month up to the fifth year.

During follow-up visits the following tests will be performed and evaluated :

1. Physical examination and digital rectal exam ;
2. CEA and routine blood chemistry screen ;
3. Colonoscopy (at 1 year, if negative repeat after 3 years, if still negative repeat after 5 years) ;
4. Thoracic-abdominal-pelvic CT 3 months after surgery and then every sixth 6 month for the first 2 years, then annually (unless different clinical indication, i.e. suspicious lesions requiring short-term monitoring), in rotation with abdominal US ;
5. Complete abdominal US, each 6 months for the first 2 years, the annually (unless different clinical indication, i.e. suspicious lesions requiring short-term monitoring), in succession with Thoracic-abdominal-pelvic CT ;
6. Adverse events report (CTCAE v.04)
7. Quality of life (QoL) questionnaires to be filled during first follow up visits and then at 6 and 12 months.

Enrollment: 148 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• ECOG Performance Status 0-1
• Histological confirmation of Adenocarcinoma
• Rectal tumor localized within 12 cm from the internal anal sphincter (IAS)
• Clinical stage cT2N1-2, M0; cT3, N0-N2, M0 and MRF - , EMVI -
• Absence of major comorbidities contraindicating oncological treatments
• Major/complete clinical-instrumental response after CRT treatment
• Informed consent acquisition

Exclusion criteria

• cT4 and/or mesorectal fascia involvement (MRF+) and or EMVI +
• T localized at a distance > 12 cm from the internal anal sphincter (IAS)
• Presence of extramesorectal nodes
• Presence of distant metastases
• Pregnancy or breastfeeding status
• Diagnosis of tumor in other sites treated within the last five years, with the exception of basal cell skin carcinoma or in situ carcinoma of the cervix
• Absolute contraindication to pelvic radiotherapy, chemotherapy and/or surgery
• Contraindication to magnetic resonance imaging and/or endoscopy
• Informed consent absence
• Partial response, "no-change" or disease progression at restaging after 7-8 weeks from CRT end

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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148 participants in 2 patient groups

Control arm

No Intervention group

Description:

Patients undergoing surgery 9-11 weeks after the end of chemoradiotherapy, whose major/complete response has to be assessed with clinical-instrumental exams to be performed 7-8 weeks after the end of chemoradiotherapy.

Experimental arm

Experimental group

Description:

Patients undergoing surgery 13-16 weeks after the end of chemoradiotherapy, (length of surgical interval ) showing a major/complete response at the clinical-instrumental exams to be performed 7-8 weeks after the end of chemoradiotherapy. These patients will undergo a repetition of re-staging (a second clinical and instrumental re-evaluation after 11-12 weeks and then surgery 13-16 weeks after the end of chemoradiotherapy.)

Treatment:

Diagnostic Test: Repetition of Re-staging