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Clinical Trials/NCT00052559
NCT00052559
Completed
Phase 1

A Phase I Study Of The Antiangiogenic Agent Bevacizumab In Combination With 5-Fluourouracil And External Beam Radiation Therapy In Rectal Cancer

National Cancer Institute (NCI)2 sites in 1 country32 target enrollmentAugust 2002

Overview

Phase
Phase 1
Intervention
bevacizumab
Conditions
Adenocarcinoma of the Rectum
Sponsor
National Cancer Institute (NCI)
Enrollment
32
Locations
2
Primary Endpoint
Maximum tolerated dose of bevacizumab when administered concurrently with 5-fluorouracil (5-FU) and external beam radiation therapy (EBRT) in patients with cT3 and T4 rectal cancer prior to surgery
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This phase I trial is studying the side effects and best dose of bevacizumab when given together with fluorouracil and external-beam radiation therapy in treating patients with stage II or stage III rectal cancer. Monoclonal antibodies, such as bevacizumab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or deliver cancer-killing substances to them. Drugs used in chemotherapy work in different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining monoclonal antibody therapy with chemotherapy and radiation therapy may kill more tumor cells.

Detailed Description

PRIMARY OBJECTIVES: I. To determine the maximum tolerated dose (MTD) of a vascular endothelial growth factor (VEGF) neutralizing antibody, bevacizumab, when administered concurrently with 5-fluorouracil (5-FU) and external beam radiation therapy (EBRT) in patients with clinical stage T3 or T4 rectal cancer prior to surgery. II. To obtain preliminary data of the pathological response rate after preoperative therapy. III. To obtain preliminary data regarding progression free survival, local control, and overall survival. IV. To obtain preliminary data of the changes in the angiogenic profile of rectal cancer induced by this therapy. OUTLINE: This is a multicenter, dose-escalation study of bevacizumab. Patients receive bevacizumab IV over 30-90 minutes on day 1 (courses 1-4). Beginning with course 2, patients also receive fluorouracil IV continuously on days 1-14 and undergo external beam radiotherapy on days 1-5 and 8-12. Treatment repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo surgery 7 weeks after completion of chemoradiotherapy. Cohorts of 6 patients receive escalating doses of bevacizumab until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, 20 additional patients are treated at the MTD. Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually for 2 years.

Registry
clinicaltrials.gov
Start Date
August 2002
End Date
April 2003
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Histologically confirmed primary adenocarcinoma of the rectum that begins within 15 cm of the anal verge as determined by sigmoidoscopy and/or colonoscopy
  • Clinical T3 or T4 tumors as determined by the following features:
  • Tethered or fixed tumor on physical exam
  • cT3, cT4, or N+ disease must be confirmed by an endorectal ultrasound or surface coil MRI
  • There must be no evidence of metastatic disease as confirmed by physical examination, chest radiograph, and abdominal/pelvic CT scan
  • ECOG performance status 0, 1, 2 (Karnofsky \>= 70%)
  • Life expectancy of greater than 2 years
  • Leukocytes \>= 3,000/ul
  • Absolute neutrophil count \>= 1,500/ul
  • Platelets \>= 100,000/ul

Exclusion Criteria

  • Patients with a "concurrently active" second malignancy other than non- melanoma skin cancers or in situ cervical cancer are excluded; patients are not considered to have a "concurrently active" malignancy if they have completed therapy and considered by their physician to be at less than 30% risk of relapse at a minimum of 5 years after all therapy
  • Prior Treatment:
  • No prior treatment for this malignancy
  • No prior history of pelvic irradiation
  • No prior history of 5-FU-based therapy for any malignancy
  • No prior treatment with bevacizumab
  • Patients must not be receiving any other investigational agents
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition bevacizumab or other agents used in study
  • Bevacizumab - Specific exclusion criteria:
  • History or evidence upon physical examination of CNS disease (e.g., primary brain tumor, seizures not controlled with standard medical therapy, any brain metastases, or history of stroke

Arms & Interventions

Treatment (bevacizumab, fluorouracil, radiation therapy)

Patients receive bevacizumab IV over 30-90 minutes on day 1 (courses 1-4). Beginning with course 2, patients also receive fluorouracil IV continuously on days 1-14 and undergo external beam radiotherapy on days 1-5 and 8-12. Treatment repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo surgery 7 weeks after completion of chemoradiotherapy. Cohorts of 6 patients receive escalating doses of bevacizumab until the MTD is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, 20 additional patients are treated at the MTD.

Intervention: bevacizumab

Treatment (bevacizumab, fluorouracil, radiation therapy)

Patients receive bevacizumab IV over 30-90 minutes on day 1 (courses 1-4). Beginning with course 2, patients also receive fluorouracil IV continuously on days 1-14 and undergo external beam radiotherapy on days 1-5 and 8-12. Treatment repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo surgery 7 weeks after completion of chemoradiotherapy. Cohorts of 6 patients receive escalating doses of bevacizumab until the MTD is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, 20 additional patients are treated at the MTD.

Intervention: fluorouracil

Treatment (bevacizumab, fluorouracil, radiation therapy)

Patients receive bevacizumab IV over 30-90 minutes on day 1 (courses 1-4). Beginning with course 2, patients also receive fluorouracil IV continuously on days 1-14 and undergo external beam radiotherapy on days 1-5 and 8-12. Treatment repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo surgery 7 weeks after completion of chemoradiotherapy. Cohorts of 6 patients receive escalating doses of bevacizumab until the MTD is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, 20 additional patients are treated at the MTD.

Intervention: external beam radiation therapy

Treatment (bevacizumab, fluorouracil, radiation therapy)

Patients receive bevacizumab IV over 30-90 minutes on day 1 (courses 1-4). Beginning with course 2, patients also receive fluorouracil IV continuously on days 1-14 and undergo external beam radiotherapy on days 1-5 and 8-12. Treatment repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo surgery 7 weeks after completion of chemoradiotherapy. Cohorts of 6 patients receive escalating doses of bevacizumab until the MTD is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, 20 additional patients are treated at the MTD.

Intervention: therapeutic conventional surgery

Treatment (bevacizumab, fluorouracil, radiation therapy)

Patients receive bevacizumab IV over 30-90 minutes on day 1 (courses 1-4). Beginning with course 2, patients also receive fluorouracil IV continuously on days 1-14 and undergo external beam radiotherapy on days 1-5 and 8-12. Treatment repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity. Patients undergo surgery 7 weeks after completion of chemoradiotherapy. Cohorts of 6 patients receive escalating doses of bevacizumab until the MTD is determined. The MTD is defined as the dose preceding that at which at least 2 of 6 patients experience dose-limiting toxicity. Once the MTD is determined, 20 additional patients are treated at the MTD.

Intervention: laboratory biomarker analysis

Outcomes

Primary Outcomes

Maximum tolerated dose of bevacizumab when administered concurrently with 5-fluorouracil (5-FU) and external beam radiation therapy (EBRT) in patients with cT3 and T4 rectal cancer prior to surgery

Time Frame: 29 days

Secondary Outcomes

  • Overall survival(Up to 5 years)
  • Pathological response rate after preoperative bevacizumab, 5-FU, EBRT, and surgery(Up to 5 years)
  • Progression-free survival(From protocol entry until documented progression of disease or death from any cause, assessed up to 5 years)
  • Local control(Up to 5 years)

Study Sites (2)

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