Radiotherapy With Chemotherapy as Neoadjuvant Therapy of Resectable and Borderline Resectable Pancreas Cancer

University of Virginia

Status and phase: Unknown; Phase 2

Conditions: Pancreatic Cancer

Treatments: Radiation: Standard Dose Acclerated Fraction Radiotherapy; Drug: Capecitabine

Study type: Interventional

Funder types: Other

Identifiers

NCT01333332

15050

Details and patient eligibility

About

The purpose of this study is to determine safety and to obtain preliminary estimates of the rate of major pathologic response of neoadjuvant accelerated fraction, standard dose radiation given with chemotherapy in patients with locally advanced pancreas cancer.

Enrollment: 35 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

1. Clinically staged I-III, pathologically confirmed adenocarcinoma of the pancreas. Mixed (e.g. adeno-squamous, neuroendocrine features) and/or poorly differentiated carcinomas are eligible as long as the carcinoma is not a predominantly neuroendocrine carcinoma. Cancers must be deemed by multidisciplinary assessment at UVA to be either

   • Resectable

     • No overt evidence of vascular involvement
     • No overt metastatic disease

   • Borderline Resectable, meeting one of the following categories:

     • Local tumor characteristics:

       • Abutment of <180◦ of the superior mesenteric artery and/or celiac axis
       • Abutment or encasement of a short segment hepatic artery
       • Involvement of the portal vein or superior mesenteric vein amenable to vascular reconstruction

     • Concern for extra pancreatic metastatic disease

       • indeterminant nodule on imaging
       • Pathologically confirmed N1

     • Borderline performance status or medical comorbidities as determined by investigators to be concerning for patient's ability to tolerate pancreatic resection

   • Patients with overtly unresectable disease are ineligible

2. No prior therapy for pancreatic cancer, including surgery, radiation, or chemotherapy

3. ≥18 years of age

4. Able to provide informed consent and comply with study procedures

5. Concurrent therapy with warfarin is permitted, but INR must be checked weekly

6. Concurrent therapy with phenytoin is permitted, but phenytoin levels must be checked weekly.

7. Concurrent therapy with CYP2C9 substrates is permitted but discouraged. Patients taking fluoxetine, glipizide, losartan, voriconazole, or other CYP2C9 substrates should consider switching to an alternative medication if feasible. (see Appendix 11.3 for a list of CYP2C9 substrates).

8. Adequate organ function:

   • Hematologic

     • ANC ≥ 1.5 x 10^9 cells/liter
     • Plts ≥ 100,000 x 10^9 cells/liter

   • Hepatic

     • Total bilirubin ≤ 5 fold the upper limits of normal for laboratory if due to biliary obstruction secondary to disease. For patients with total bilirubin 3-5 times the upper limit, attempt to relieve biliary obstruction is required
     • AST/ALT ≤ 5 fold the upper limits of normal for laboratory

   • Renal

     • Creatinine clearance as measured by Cockcroft-Gault (APPENDIX) of >30 mL/min.
     • Patients with creatinine clearance of 30-50 mL/min require 25% reduction of capecitabine dose.

Exclusion:

1. No pregnant or lactating women. Women of child bearing age must have a negative pregnancy test within seven days of beginning therapy and agree to use reliable contraception for the duration of the study period.
2. No comorbid condition which is deemed by the investigator to have a life expectancy of less than 6 months
3. No other malignancy diagnosed within the past 5 years, excepting all in situ cancers and invasive nonmelanomatous skin cancers.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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35 participants in 1 patient group

Capecitabine, Radiation

Experimental group

Treatment:

Radiation: Standard Dose Acclerated Fraction Radiotherapy

Drug: Capecitabine