Overview

This trial is active, not recruiting.

Condition colorectal cancer
Treatments fluorouracil, leucovorin calcium, oxaliplatin, conventional surgery, radiation therapy, laboratory biomarker analysis, dna analysis, polymerase chain reaction, immunohistochemistry staining method
Phase phase 2
Sponsor Memorial Sloan Kettering Cancer Center
Collaborator National Cancer Institute (NCI)
Start date August 2008
End date December 2017
Trial size 248 participants
Trial identifier NCT00335816, CDR0000458059, CHNMC-07182, P30CA033572, R01CA090559, UCSF-03451, UCSF-H44287-23127-03, UMN-2003UC036, mskcc 12-201

Summary

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as fluorouracil, oxaliplatin, and leucovorin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Fluorouracil may also make tumor cells more sensitive to radiation therapy. Leucovorin calcium may protect normal cells from the side effects of chemotherapy, and it may help fluorouracil work better by making tumor cells more sensitive to the drug. Giving radiation therapy together with chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed.

PURPOSE: This phase II trial is studying how well giving radiation therapy together with fluorouracil with or without combination therapy works in treating patients who are undergoing surgery for stage II or stage III rectal cancer.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Intervention model parallel assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
All patients undergo chemoradiation therapy comprising radiation therapy once daily 5 days a week for 5 weeks and fluorouracil intravenously continuously over 24 hours 7 days a week for 6 weeks. Patients undergo standard surgical resection after completion of chemoradiation therapy..
fluorouracil
Given IV
conventional surgery
Patients undergo surgery
radiation therapy
Patients undergo radiotherapy
laboratory biomarker analysis
Correlative studies
dna analysis
Correlative studies
polymerase chain reaction PCR
Correlative studies
immunohistochemistry staining method immunohistochemistry
Correlative studies
(Experimental)
All patients undergo chemoradiation therapy comprising radiation therapy once daily 5 days a week for 5 weeks and fluorouracil IV continuously over 24 hours 7 days a week for 6 weeks. Beginning 4 weeks after completion of chemoradiation therapy, patients receive modified FOLFOX-6 chemotherapy comprising oxaliplatin IV over 2 hours and leucovorin calcium IV over 2 hours on day 1 and fluorouracil IV continuously over 46 hours on days 1-2. Treatment repeats every 14 days for 2 courses. After the last week of post-radiation chemotherapy, patients undergo standard surgical resection.
fluorouracil
Given IV
leucovorin calcium
Given IV
oxaliplatin
Given IV
conventional surgery
Patients undergo surgery
radiation therapy
Patients undergo radiotherapy
laboratory biomarker analysis
Correlative studies
dna analysis
Correlative studies
polymerase chain reaction PCR
Correlative studies
immunohistochemistry staining method immunohistochemistry
Correlative studies
(Experimental)
All patients undergo chemoradiation therapy comprising radiation therapy once daily 5 days a week for 5 weeks and fluorouracil IV continuously over 24 hours 7 days a week for 6 weeks. Beginning 4 weeks after completion of chemoradiation therapy, patients receive modified FOLFOX-6 chemotherapy as in group II. Treatment repeats every 14 days for 4 courses. After the last week of post-radiation chemotherapy, patients undergo standard surgical resection.
fluorouracil
Given IV
leucovorin calcium
Given IV
oxaliplatin
Given IV
conventional surgery
Patients undergo surgery
radiation therapy
Patients undergo radiotherapy
laboratory biomarker analysis
Correlative studies
dna analysis
Correlative studies
polymerase chain reaction PCR
Correlative studies
immunohistochemistry staining method immunohistochemistry
Correlative studies
(Experimental)
All patients undergo chemoradiation therapy comprising radiation therapy once daily 5 days a week for 5 weeks and fluorouracil IV continuously over 24 hours 7 days a week for 6 weeks. Beginning 4 weeks after completion of chemoradiation therapy, patients receive modified FOLFOX-6 chemotherapy as in group II. Treatment repeats every 14 days for 6 courses. After the last week of post- radiation chemotherapy, patients undergo standard surgical resection. Patients then receive 3 additional courses of FOLFOX-6 chemotherapy or other chemotherapy off study as directed by the physician.
fluorouracil
Given IV
leucovorin calcium
Given IV
oxaliplatin
Given IV
conventional surgery
Patients undergo surgery
radiation therapy
Patients undergo radiotherapy
laboratory biomarker analysis
Correlative studies
dna analysis
Correlative studies
polymerase chain reaction PCR
Correlative studies
immunohistochemistry staining method immunohistochemistry
Correlative studies

Primary Outcomes

Measure
Rate of pathologic complete response
time frame: Determined at the time of surgery
Effect of different chemoradiation-to-surgery intervals on rate of pathologic complete response and surgical difficulty.
time frame: Measured at the time of surgery
Effect of different chemoradiation-to-surgery intervals on postoperative complications
time frame: 30 days after surgery

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria: - Patients must have an Eastern Cooperative Oncology Group (ECOG) Status of 0 or 1, or comparable Karnofsky performance status - Patients must have histologically confirmed invasive adenocarcinoma of the rectum Distal border of the tumor must be within 12 cm from the anal verge as measured on rigid proctoscopic exam - Patients must have Stage II (uT3-4, uN0) or Stage III (any T, uN1-2) tumors, as confirmed by ERUS or MRI; females with anterior tumors invading the posterior vaginal wall (uT4) and males with anterior tumors that invade the seminal vesicles or adjacent organs (uT4) will also be eligible provided they undergo an extended resection including the organs involved - Patients with high grade obstruction that impedes the ERUS exam are eligible for the study provided they can be staged by MRI - Patients with synchronous or metachronous colorectal cancer are eligible for the study on condition that they are treated for rectal cancer in accordance with the protocol - Patients with the following are NOT allowed on study: - Metastatic disease or other primaries - Locally recurrent rectal cancer - Previously documented history of Familial Adenomatous Polyposis - History of Inflammatory Bowel Disease - History of prior radiation treatments to pelvis - History of clinically significant cardiac disease (i.e., Class 3-4 congestive heart failure, symptomatic coronary artery disease, uncontrolled arrhythmia, and/or myocardial infarction within the previous 6 months - History of uncontrolled seizures or clinically significant central nervous system disorders - History of psychiatric conditions or diminished capacity that could compromise the giving of informed consent, or interfere with study compliance - History of allergy and/or hypersensitivity to 5-fluorouracil (fluorouracil), leucovorin (leucovorin calcium), and/or oxaliplatin - History of difficulty or inability to take or absorb oral medications - Patients must have adequate bone marrow, hepatic and renal function within 7 days prior to registration - White blood cells (WBC) >= 3,000 mm^3 - Absolute neutrophil count (ANC) > 1,500 mm^3 - Hemoglobin > 9.5 mg/dl - Platelet count >= 100,000 mm^3 - Total bilirubin =< 1.5 mg/dl - Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) =< 2.0 times institutional upper limit of normal (ULN) - Alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) =< 2.0 times ULN - Alkaline phosphatase =< 2.0 times ULN - Serum creatinine =< 1.5 times ULN - Patients with hereditary non-polyposis colorectal cancer are eligible for the study provided they meet the rest of the eligibility criteria - Patients who have experienced a prior malignancy should have received potentially curative therapy for that malignancy, and should be cancer-free for at least five years from the date of initial diagnosis (Exceptions: patients treated for basal cell carcinoma, or carcinoma in-situ of the cervix) - Patients of reproductive potential should agree to use an effective method of birth control when undergoing treatments with known or possible mutagenic or teratogenic effects; all female participants of childbearing potential must have a negative urine or serum pregnancy test within two weeks prior to study registration - Patients or the patient's legally acceptable representative must provide written authorization to allow the use and disclosure of protected health information; NOTE: this may be obtained in either the study-specific informed consent or in a separate authorization form and must be obtained from the patient prior to study registration or the initiation of any study-specific procedures

Additional Information

Official title Timing of Rectal Cancer Response to Chemoradiation
Description OBJECTIVES: I. To determine the rate of pathologic complete response to chemoradiation (no evidence of residual tumor in the resected specimen) of Stage II and Stage III rectal cancers that are staged preoperatively by endorectal ultrasound (ERUS) or magnetic resonance imaging (MRI), treated according to a standardized chemoradiation and surgery protocol, and evaluated by a systematic pathologic exam of the surgical specimen. II. To study the effect of different chemoradiation-to-surgery intervals on the rate of pathologic complete response, on surgical difficulty, and on postoperative complications. III. To investigate the feasibility of using sensitive molecular assays to detect tumor cells in the tumor bed and regional lymph nodes of rectal cancer specimens, with or without pathologic complete response to preoperative chemoradiation. OUTLINE: Patients are assigned to 1 of 4 treatment groups. All patients undergo chemoradiation therapy comprising radiation therapy once daily 5 days a week for 5 weeks and fluorouracil intravenously (IV) continuously over 24 hours 7 days a week for 6 weeks. GROUP I (closed to enrollment): Patients undergo standard surgical resection after completion of chemoradiation therapy. GROUP II (closed to enrollment): Beginning 4 weeks after completion of chemoradiation therapy, patients receive modified FOLFOX-6 chemotherapy comprising oxaliplatin IV over 2 hours and leucovorin calcium IV over 2 hours on day 1 and fluorouracil IV continuously over 46 hours on days 1-2. Treatment repeats every 14 days for 2 courses. After the last week of post-radiation chemotherapy, patients undergo standard surgical resection. GROUP III: Beginning 4 weeks after completion of chemoradiation therapy, patients receive modified FOLFOX-6 chemotherapy as in group II. Treatment repeats every 14 days for 4 courses. After the last week of post-radiation chemotherapy, patients undergo standard surgical resection. GROUP IV: Beginning 4 weeks after completion of chemoradiation therapy, patients receive modified FOLFOX-6 chemotherapy as in group II. Treatment repeats every 14 days for 6 courses. After the last week of post- radiation chemotherapy, patients undergo standard surgical resection. In all groups, treatment continues in the absence of disease progression or unacceptable toxicity. A fter completion of study treatment, patients are followed up for 5 years.
Trial information was received from ClinicalTrials.gov and was last updated in October 2015.
Information provided to ClinicalTrials.gov by Memorial Sloan Kettering Cancer Center.