Radiation Therapy and Fluorouracil With or Without Combination Chemotherapy Followed by Surgery in Treating Patients With Stage II or Stage III Rectal Cancer
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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.
Condition | Intervention | Phase |
---|---|---|
Colorectal Cancer |
Drug: fluorouracil Drug: leucovorin calcium Drug: oxaliplatin Procedure: conventional surgery Radiation: radiation therapy Other: laboratory biomarker analysis Genetic: DNA analysis Genetic: polymerase chain reaction Other: immunohistochemistry staining method |
Phase 2 |
Study Type: | Interventional |
Study Design: | Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
Official Title: | Timing of Rectal Cancer Response to Chemoradiation |
- Rate of pathologic complete response [ Time Frame: Determined at the time of surgery ] [ Designated as safety issue: No ]
- Effect of different chemoradiation-to-surgery intervals on rate of pathologic complete response and surgical difficulty. [ Time Frame: Measured at the time of surgery ] [ Designated as safety issue: No ]
- Effect of different chemoradiation-to-surgery intervals on postoperative complications [ Time Frame: 30 days after surgery ] [ Designated as safety issue: No ]
Estimated Enrollment: | 248 |
Study Start Date: | August 2008 |
Estimated Primary Completion Date: | December 2017 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
Experimental: Group 1 (Closed to Enrollment)
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..
|
Drug: fluorouracil
Given IV
Procedure: conventional surgery
Patients undergo surgery
Radiation: radiation therapy
Patients undergo radiotherapy
Other: laboratory biomarker analysis
Correlative studies
Genetic: DNA analysis
Correlative studies
Genetic: polymerase chain reaction
Correlative studies
Other Name: PCR
Other: immunohistochemistry staining method
Correlative studies
Other Name: immunohistochemistry
|
Experimental: Group 2 (Closed to Enrollment)
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.
|
Drug: fluorouracil
Given IV
Drug: leucovorin calcium
Given IV
Drug: oxaliplatin
Given IV
Procedure: conventional surgery
Patients undergo surgery
Radiation: radiation therapy
Patients undergo radiotherapy
Other: laboratory biomarker analysis
Correlative studies
Genetic: DNA analysis
Correlative studies
Genetic: polymerase chain reaction
Correlative studies
Other Name: PCR
Other: immunohistochemistry staining method
Correlative studies
Other Name: immunohistochemistry
|
Experimental: Group 3 (chemotherapy, FOLFOX, conventional surgery)
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.
|
Drug: fluorouracil
Given IV
Drug: leucovorin calcium
Given IV
Drug: oxaliplatin
Given IV
Procedure: conventional surgery
Patients undergo surgery
Radiation: radiation therapy
Patients undergo radiotherapy
Other: laboratory biomarker analysis
Correlative studies
Genetic: DNA analysis
Correlative studies
Genetic: polymerase chain reaction
Correlative studies
Other Name: PCR
Other: immunohistochemistry staining method
Correlative studies
Other Name: immunohistochemistry
|
Experimental: Group 4 (chemotherapy, FOLFOX, conventional surgery)
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.
|
Drug: fluorouracil
Given IV
Drug: leucovorin calcium
Given IV
Drug: oxaliplatin
Given IV
Procedure: conventional surgery
Patients undergo surgery
Radiation: radiation therapy
Patients undergo radiotherapy
Other: laboratory biomarker analysis
Correlative studies
Genetic: DNA analysis
Correlative studies
Genetic: polymerase chain reaction
Correlative studies
Other Name: PCR
Other: immunohistochemistry staining method
Correlative studies
Other Name: immunohistochemistry
|
Detailed 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.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
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
United States, California | |
Cancer Care Center at John Muir Health - Concord Campus | Recruiting |
Concord, California, United States, 94524-4110 | |
Contact: Clinical Trials Office - Cancer Care Center at John Muir Healt 925-674-2580 | |
City of Hope Medical Center | Recruiting |
Duarte, California, United States, 91010-3000 | |
Contact: City of Hope Medical Center 800-826-4673 | |
Chao Family Comprehensive Cancer Center at University of California Irvine Medical Center | Recruiting |
Orange, California, United States, 92868 | |
Contact: Clinical Trials Office - Chao Family Comprehensive Cancer Cent 877-827-8839 ucstudy@uci.edu | |
St. Joseph Hospital Regional Cancer Center - Orange | Recruiting |
Orange, California, United States, 92868-3849 | |
Contact: Theodore Coutsoftides, MD 714-532-2544 | |
UCSF Helen Diller Family Comprehensive Cancer Center | Recruiting |
San Francisco, California, United States, 94115 | |
Contact: Clinical Trials Office - UCSF Helen Diller Family Comprehensi 877-827-3222 | |
United States, District of Columbia | |
Washington Cancer Institute at Washington Hospital Center | Recruiting |
Washington, District of Columbia, United States, 20010 | |
Contact: Clinical Trials Office - Washington Cancer Institute 202-877-8839 | |
United States, Florida | |
H. Lee Moffitt Cancer Center and Research Institute at University of South Florida | Recruiting |
Tampa, Florida, United States, 33612-9497 | |
Contact: Clinical Trials Office - H. Lee Moffitt Cancer Center and Rese 800-456-7121 canceranswers@moffitt.org | |
United States, Illinois | |
University of Chicago Cancer Research Center | Recruiting |
Chicago, Illinois, United States, 60637-1470 | |
Contact: Clinical Trials Office - University of Chicago Cancer Research 773-834-7424 | |
United States, Minnesota | |
Masonic Cancer Center at University of Minnesota | Recruiting |
Minneapolis, Minnesota, United States, 55455 | |
Contact: Clinical Trials Office - Masonic Cancer Center at University o 612-624-2620 | |
United States, Missouri | |
Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis | Recruiting |
Saint Louis, Missouri, United States, 63110 | |
Contact: Stephen Hunt, MD 314-454-7204 | |
United States, Nebraska | |
Colon and Rectal Surgery, Incorporated | Recruiting |
Omaha, Nebraska, United States, 68114 | |
Contact: Charles A. Ternent, MD 402-343-1122 | |
United States, Ohio | |
Cleveland Clinic Taussig Cancer Center | Recruiting |
Cleveland, Ohio, United States, 44195 | |
Contact: Clinical Trials Office - Cleveland Clinic Taussig Cancer Cente 866-223-8100 | |
United States, Oregon | |
Knight Cancer Institute at Oregon Health and Science University | Recruiting |
Portland, Oregon, United States, 97239-3098 | |
Contact: Clinical Trials Office - Knight Cancer Institute at Oregon Hea 503-494-1080 trials@ohsu.edu | |
United States, Vermont | |
Vermont Cancer Center at University of Vermont | Recruiting |
Burlington, Vermont, United States, 05405-0110 | |
Contact: Clinical Trials Office - Vermont Cancer Center at University o 802-656-2178 | |
Canada, Alberta | |
Tom Baker Cancer Centre - Calgary | Suspended |
Calgary, Alberta, Canada, T2N 4N2 |
Study Chair: | Julian Sanchez, MD | City of Hope Medical Center |
Additional Information:
No publications provided by City of Hope Medical Center
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | City of Hope Medical Center |
ClinicalTrials.gov Identifier: | NCT00335816 History of Changes |
Other Study ID Numbers: | 07182, P30CA033572, CHNMC-07182, UCSF-H44287-23127-03, UMN-2003UC036, UCSF-03451, CDR0000458059, R01CA090559 |
Study First Received: | June 8, 2006 |
Last Updated: | July 3, 2012 |
Health Authority: | United States: Institutional Review Board |
Keywords provided by City of Hope Medical Center:
stage II rectal cancer stage III rectal cancer adenocarcinoma of the rectum |
Additional relevant MeSH terms:
Rectal Neoplasms Colorectal Neoplasms Intestinal Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Neoplasms Digestive System Diseases Gastrointestinal Diseases Intestinal Diseases Rectal Diseases Colonic Diseases Fluorouracil Oxaliplatin Leucovorin |
Levoleucovorin Antimetabolites Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Antimetabolites, Antineoplastic Antineoplastic Agents Therapeutic Uses Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Vitamin B Complex Vitamins Micronutrients Growth Substances Antidotes |
ClinicalTrials.gov processed this record on October 16, 2012