Pancreatic Cancer |
|
|
Clinical Trial: Surgery Followed by Radiation Therapy and Chemotherapy in Treating Patients With Cancer of the Pancreas
This study is no longer recruiting patients.
Purpose
RATIONALE: Surgery to remove the pancreas, some of the small intestine, and lymph nodes may be more effective treatment for cancer of the pancreas than surgery to remove the pancreas and some of the small intestine alone. Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining surgery, radiation therapy, and chemotherapy may be an effective treatment for cancer of the pancreas.
PURPOSE: Randomized phase III trial to compare the effectiveness of surgery to remove the pancreas and a portion of the small intestine with or without removing lymph nodes, followed by radiation therapy and chemotherapy, in treating patients with cancer of the pancreas.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| stage I pancreatic cancer stage II pancreatic cancer stage III pancreatic cancer adenocarcinoma of the pancreas | Drug: fluorouracil Drug: leucovorin calcium Procedure: chemotherapy Procedure: conventional surgery Procedure: radiation therapy Procedure: surgery | Phase III |
MedlinePlus related topics: Pancreatic Cancer
Study Type: Interventional
Study Design: Treatment
Official Title: Phase III Randomized Study of Pancreatoduodenectomy With or Without Extended Lymphadenectomy Followed by Chemoradiation Therapy for Resectable Pancreatic Adenocarcinoma
OBJECTIVES:
- Assess the overall survival of patients with resectable ductal pancreatic adenocarcinoma undergoing extended versus standard pancreatoduodenectomy.
OUTLINE: Patients are randomized to undergo standard pancreatoduodenectomy (PD) or PD with extended lymph node resection after an exploratory laparotomy.
Patients receive adjuvant chemoradiation therapy 4-6 weeks after surgery, if no metastases are evident. Radiation therapy is given every week for 5 weeks. Fluorouracil/leucovorin calcium is administered by rapid IV push daily within 2 hours of radiation on days 1-4 of week 1 and days 29-31 of week 5.
Patients are followed every 4 months for the first year, then every 6 months for the next 2 years.
PROJECTED ACCRUAL: 50 patients will be accrued per group for a total of 100 patients.
Eligibility
Ages Eligible for Study: 18 Years and above, Genders Eligible for Study: Both
Criteria
DISEASE CHARACTERISTICS:
- Histologically or cytologically proven adenocarcinoma of the exocrine pancreas excluding periampullary cancer
- Resectable malignancy must be located in a region that can be encompassed by a radiation port of 20 x 20 cm
- No evidence of extranodal metastatic disease
PATIENT CHARACTERISTICS: Age:
- 18 and over
Performance status:
- ECOG 0-2
Life expectancy:
- Not specified
Hematopoietic:
- WBC at least 3500/mm^3
- Platelet count at least 100,000/mm^3
Hepatic:
- Not specified
Renal:
- Bilateral renal function as demonstrated by excretory urogram (IVP) or abdominal CT scan with contrast OR
- Greater than 2/3 of one functioning kidney must be shielded during radiation therapy
Other:
- Must have adequate oral nutrition (greater than 1200 calories daily)
- Greater than 5 years since prior malignancy except:
- Squamous cell skin cancer
- Basal cell skin cancer
- In situ cervical cancer
- Not pregnant or lactating
- Patients of reproductive potential must use effective birth control
- No cystic neoplasms of the pancreas
- No islet cell, periampullary or cholangiocarcinoma
- No Federal Medical Center inmates
PRIOR CONCURRENT THERAPY: Biologic therapy:
- Not specified
Chemotherapy:
- No prior chemotherapy for this disease
Endocrine therapy:
- Not specified
Radiotherapy:
- No prior radiation therapy for this disease
- No prior radiation therapy to the abdomen
Surgery:
- Celiotomy and standardized exploration for resectability required
Location Information
Randall K. Pearson, MD, Study Chair, Mayo Clinic Cancer Center
More Information
Clinical trial summary from the National Cancer Institute's PDQ® database
Record last reviewed: December 2003
Last Updated: October 13, 2004
Record first received: November 1, 1999
ClinicalTrials.gov Identifier: NCT00003049
Health Authority: Unspecified
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005

Not Signed In -


