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| Name | Class |
|---|---|
| Ministry of Health, Brazil | OTHER_GOV |
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Standard therapy for localized rectal cancer includes chemotherapy and radiation therapy, followed by a "recovery" period of 7-12 weeks, surgery and adjuvant chemotherapy for 3-6 months. Even though this protocol achieves high cure rates, many patients need a rectal amputation with placement of definitive colostomies. About 10-20% of patients have a complete clinical response to chemo-radiation and no tumor can be found in the surgical specimen. These patients can be followed with close surveillance and avid surgery. The aim of this study is to evaluate if a strategy including the use of a highly active chemotherapy called "FOLFIRINOX" during the 12 weeks between the end of radiation therapy and evaluation for surgery increases the rates of complete response and, therefore, allows more patients to undergo non-surgical management.
Adult patients with locally advanced rectal cancer who have completed conventional long-course chemo-radiation of 54Gy with capecitabine will be randomized 1:1 to a total neo-adjuvant therapy (TNT) protocol or to a control group. Patients in the TNT arm will receive 4 cycles of interval chemotherapy with FOLFIRINOX (5-FU, irinotecan, oxaliplatin) between the end of chemo-radiation and re-staging and those in the control group will undergo standard post-radiation care during this period. All patients will be re-staged with colonoscopy and pelvic MRI 12 weeks after the end of chemo-radiation. Those with a complete clinical response will be placed under a watch-and-wait protocol with digital rectal examinations every 2 months and pelvic MRI and sigmoidoscopy every 6 months. Those wih residual tumors will undergo resection with total mesorectal excision (TME). Patients with a "near complete response", as defined by a multidisciplinary tumor board, will be re-staged at week 16 or 18 after chemo-radiation before undergoing surgery. Adjuvant chemotherapy will be done following the local standard of care.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Total neoadjuvant therapy (TNT) | Experimental | 4 cycles of mFOLFIRINOX every 14 days:
|
|
| Standard of care | No Intervention | Standard post-radiation care |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Folfirinox | Drug | 5-FU 2400mg/m2; Oxaliplatin 85 mg/m2, Irinotecan 150mg/m2 |
|
| Measure | Description | Time Frame |
|---|---|---|
| cCR + PathCR | Complete clinical response or pathological response | 12 weeks after the end of chemoradiation |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of R0 resection | Rate of tumor resection with negative margins | 12 weeks |
| Rate of organ preservation | Rate of patients who remain colostomy-free |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Diogo Gomes, MD | Contact | +55-11-2151-8056 | diogo.gomes@einstein.br | |
| Leticia Brito, MD | Contact | +55-11-2151-8056 | leticia.brito@einstein.br |
| Name | Affiliation | Role |
|---|---|---|
| Diogo Gomes, MD | Hospital Israelita Albert Einstein | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hospital Municipal Vila Santa Catarina | Recruiting | São Paulo | 04378-500 | Brazil |
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| Label | URL |
|---|---|
| Program of the Brazilian Ministry of Health that us sponsoring the trial | View source |
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| D012004 | Rectal Neoplasms |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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| ID | Term |
|---|---|
| C000627770 | folfirinox |
| C509829 | FOLFOXIRI protocol |
| D005472 | Fluorouracil |
| D000077150 | Oxaliplatin |
| D000077146 | Irinotecan |
| ID | Term |
|---|---|
| D014498 | Uracil |
| D011744 | Pyrimidinones |
| D011743 | Pyrimidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
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Patients will be randomized 1:1 to one of two arms: TNT and conventional therapy (control). Randomization will be stratified by study site and tumor stage (II vs III)
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This is an open-label study
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| 6 months after surgery |
| Overall toxicity | Grade 3-4 toxicities according to CTCAE 4.0 | 12 weeks |
| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |
| D006571 |
| Heterocyclic Compounds |
| D056831 | Coordination Complexes |
| D009930 | Organic Chemicals |
| D002166 | Camptothecin |
| D000470 | Alkaloids |