DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more



Fluorouracil, Leucovorin, and Oxaliplatin With or Without Bevacizumab in Treating Patients Who Have Undergone Surgery for Stage II or Stage III Colon Cancer

Information source: National Cancer Institute (NCI)
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Adenocarcinoma of the Colon; Stage IIA Colon Cancer; Stage IIB Colon Cancer; Stage IIC Colon Cancer; Stage IIIA Colon Cancer; Stage IIIB Colon Cancer; Stage IIIC Colon Cancer

Intervention: oxaliplatin (Drug); leucovorin calcium (Drug); fluorouracil (Drug); bevacizumab (Biological)

Phase: Phase 3

Status: Completed

Sponsored by: National Cancer Institute (NCI)

Official(s) and/or principal investigator(s):
Carmen Allegra, Principal Investigator, Affiliation: NSABP Foundation Inc

Summary

This randomized phase III trial is studying giving oxaliplatin, leucovorin, and fluorouracil together with bevacizumab to see how well it works compared to oxaliplatin, leucovorin, and fluorouracil alone in treating patients who have undergone surgery for stage II or stage III colon cancer. Drugs used in chemotherapy, such as oxaliplatin, leucovorin, and fluorouracil, work in different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as bevacizumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Bevacizumab may also stop the growth of tumor cells by stopping blood flow to the tumor. Giving chemotherapy together with bevacizumab may kill more tumor cells. It is not yet known whether treatment with oxaliplatin, leucovorin, and fluorouracil is more effective with or without bevacizumab in treating patients who have undergone surgery for colon cancer.

Clinical Details

Official title: A Phase III Clinical Trial Comparing Infusional 5-Fluorouracil (5-FU), Leucovorin, and Oxaliplatin (mFOLFOX6) Every Two Weeks With Bevacizumab to the Same Regimen Without Bevacizumab for the Treatment of Patients With Resected Stages II and III Carcinoma of the Colon

Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Primary outcome: Disease-free Survival

Secondary outcome:

Survival as Assessed by Death From Any Cause

Proteinuria After Completion of Bevacizumab

Proteinuria With Clinical Sequelae

The Risk Factors for Development of Proteinuria

As Measured by Blood Pressure and Antihypertensive Medication Hypertension

Delayed Vascular Events Such as Myocardial Infarction, Central Nervous System (CNS) Ischemia, and Thrombosis in Patients Receiving Chemotherapy + Bevacizumab

Ovarian Function in Premenopausal Women as Measured by Serum Ovarian Function Test

Bevacizumab Immunogenicity and Post-treatment Serum Levels of Bevacizumab in Patients Receiving Bevacizumab

Detailed description: PRIMARY OBJECTIVES: I. To compare the relative efficacy of mFOLFOX6 + bevacizumab with that of mFOLFOX6 alone in prolonging disease-free survival (DFS). SECONDARY OBJECTIVES: I. To compare the relative efficacy of mFOLFOX6 + bevacizumab with that of mFOLFOX6 alone in prolonging survival (S). TERTIARY OBJECTIVES: I. To assess the persistence of proteinuria following the discontinuation of bevacizumab. II. To correlate the development of proteinuria with clinical sequelae. III. To evaluate the risk factors for development of proteinuria. IV. To determine the effect of discontinuation of bevacizumab on hypertension. V. To estimate the incidence of delayed vascular events such as myocardia infarction, CNS ischemia, and thrombosis in patients receiving chemotherapy + bevacizumab. VI. To assess the effect of bevacizumab on ovarian function in premenopausal women. VII. To assess the incidence rate of immunogenicity and examine post-treatment serum levels of bevacizumab in patients receiving bevacizumab. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. ARM I: Patients receive adjuvant chemotherapy comprising concurrent oxaliplatin and leucovorin calcium IV over 2 hours on day 1. Patients also receive adjuvant fluorouracil IV over 2-4 minutes on day 1 followed by fluorouracil IV continuously over 46 hours on days 1 and 2. Treatment repeats every 14 days for 12 courses in the absence of disease progression or unacceptable toxicity. ARM II: Patients receive bevacizumab IV over 30-90 minutes on day 1. Patients also receive adjuvant oxaliplatin, leucovorin calcium, and fluorouracil as in arm I. Treatment repeats every 14 days for 12 courses in the absence of disease progression or unacceptable toxicity. After completion of adjuvant chemotherapy, patients continue to receive bevacizumab alone every 14 days for 6 months in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Patients must consent to be in the study and must have signed and dated an IRB

approved consent form conforming to federal and institutional guidelines

- Randomization must occur during the three-week interval beginning on postoperative

day 29 and ending on postoperative day 50

- The distal extent of the tumor must be >= 12 cm from the anal verge on endoscopy; if

the patient is not a candidate for endoscopy, then the distal extent of the tumor must be >= 12 cm from the anal verge as determined by surgical examination

- The patient must have had an en bloc complete gross resection of tumor (curative

resection) by open laparotomy or laparoscopically-assisted colectomy; patients who have had a two-stage surgical procedure, to first provide a decompressive colostomy and then in a later procedure to have the definitive surgical resection, are eligible

- Patients must have histologically confirmed adenocarcinoma of the colon that meets

one of the criteria below:

- Stage II carcinoma (T3,4 N0 M0); the tumor invades through the muscularis

propria into the subserosa or into non-peritonealized pericolic or perirectal tissues (T3); or directly invades other organs or structures, and/or perforates visceral peritoneum (T4)

- Stage III carcinoma (any T N1,2 M0); the tumor has invaded to any depth, with

involvement of regional lymph nodes

- Patients with T4 tumors that have involved an adjacent structure (e. g., bladder,

small intestine, ovary, etc.) by direct extension from the primary tumor are eligible if all of the following conditions are met:

- All or a portion of the adjacent structure was removed en bloc with the primary

tumor

- In the opinion of the surgeon, all grossly visible tumor was completely resected

("curative resection")

- Histologic evaluation by the pathologist confirms the margins of the resected

specimen are not involved by malignant cells; and

- Local radiation therapy will not be utilized

- Patients with more than one synchronous primary colon tumor are eligible; (staging

classification will be based on the more advanced primary tumor)

- Patients must have an ECOG performance status of 0 or 1

- At the time of randomization, postoperative absolute granulocyte count (AGC) must be

>= 1500/mm^3 (or < 1500/mm^3, if in the opinion of the investigator, this represents an ethnic or racial variation of normal)

- At the time of randomization, the postoperative platelet count must be >=

100,000/mm^3

- Bilirubin must be =< ULN for the lab unless the patient has a chronic grade 1

bilirubin elevation due to Gilbert's disease or similar syndrome due to slow conjugation of bilirubin

- Alkaline phosphatase must be < 2. 5 x ULN for the lab

- AST must be < 1. 5 x ULN for the lab

- If AST is > ULN, serologic testing for hepatitis B and C must be performed and

results must be negative

- Serum creatinine =< 1. 5 x ULN for the lab

- Urine protein/creatinine (UPC) ratio of < 1. 0; patients with a UPC ratio >= 1. 0 must

undergo a 24-hour urine collection, which must be an adequate collection and must demonstrate < 1 gm of protein in the 24-hour urine collection in order to participate in the study

- Patients with prior malignancies, including colorectal cancers, are eligible if they

have been disease-free for >= 5 years and are deemed by their physician to be at low risk for recurrence; patients with squamous or basal cell carcinoma of the skin, melanoma in situ, carcinoma in situ of the cervix, or carcinoma in situ of the colon or rectum that have been effectively treated are eligible, even if these conditions were diagnosed within 5 years prior to randomization Exclusion Criteria:

- Patients < 18 years old

- Colon tumor other than adenocarcinoma, i. e., sarcoma, lymphoma, carcinoid, etc

- Rectal tumors, i. e. a tumor located < 12 cm from the anal verge on endoscopy, or by

surgical exam if the patient is not a candidate for endoscopy

- Isolated, distant, or non-contiguous intra-abdominal metastases, even if resected

- Any systemic or radiation therapy initiated for this malignancy

- Any significant bleeding that is not related to the primary colon tumor within 6

months before study entry

- Serious or non-healing wound, skin ulcers, or bone fracture

- Gastroduodenal ulcer(s) determined by endoscopy to be active

- Invasive procedures defined as follows:

- Major surgical procedure, open biopsy, or significant traumatic injury within 28

days prior to randomization

- Anticipation of need for major surgical procedures during the course of the

study

- Core biopsy or other minor procedure, excluding placement of a vascular access

device, within 7 days prior to randomization

- Uncontrolled blood pressure defined as > 150/90 mmHg

- History of TIA or CVA

- History of arterial thrombotic event within 12 months before study entry

- Symptomatic peripheral vascular disease

- PT/INR > 1. 5, unless the patient is on therapeutic doses of warfarin. If so, the

following criteria must be met for enrollment:

- The subject must have an in-range INR (usually between 2 and 3) on a stable dose

of warfarin

- The subject must not have active bleeding or a pathological condition that is

associated with a high-risk of bleeding

- Concomitant halogenated antiviral agents

- Clinically significant peripheral neuropathy at the time of randomization (defined in

the NCI Common Terminology Criteria for Adverse Events Version 3. 0 [CTCAE v3. 0] as grade 2 or greater neurosensory or neuromotor toxicity)

- Non-malignant systemic disease (cardiovascular, renal, hepatic, etc.) that would

preclude any of the study therapy drugs; specifically excluded are the following cardiac conditions:

- New York Heart Association Class III or IV cardiac disease

- History of myocardial infarction within 12 months before study entry

- Unstable angina within 12 months before study entry; and

- Symptomatic arrhythmia

- History of chronic or persistent viral hepatitis or other chronic liver disease

- Pregnancy or lactation at the time of proposed randomization; eligible patients of

reproductive potential (both sexes) must agree to use adequate contraceptive methods during study therapy and for at least 3 months after the completion of bevacizumab

- Psychiatric or addictive disorders or other conditions that, in the opinion of the

investigator, would preclude the patient from meeting the study requirements

Locations and Contacts

National Surgical Adjuvant Breast and Bowel Project, Pittsburgh, Pennsylvania 15212-5234, United States
Additional Information

Starting date: September 2004
Last updated: May 16, 2014

Page last updated: August 23, 2015

-- advertisement -- The American Red Cross
 
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2017