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Clinical Trials/NCT01051284
NCT01051284CompletedPhase 1

A Pilot Study of Full Dose Gemcitabine and Hypofractionated Stereotactic Radiosurgery in the Treatment of Unresectable Pancreatic Cancer

Georgetown University1 site in 1 country14 target enrollmentStarted: November 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 1
Status
Completed
Enrollment
14
Locations
1
Primary Endpoint
To demonstrate that radiation treatments can be reproduced as determined by evaluation of the prescription isodose curves

Study Overview

Brief Summary

People with pancreatic cancer that cannot be cured by surgery are being asked to participate in this study.

The purpose of this study is to test the ability of the radiation oncologists to administer Cyberknife therapy along with Gemcitabine chemotherapy for patients with pancreatic cancer. Radiation and Gemcitabine are both effective at killing cancer cells but they generally cannot be given at the same time. Cyberknife therapy is highly focused radiation that is being used extensively at Georgetown University and around the United States to treat a number of cancers. It is believed that because Cyberknife is so highly focused it can be given safely with regular doses of chemotherapy to attack cancer cells in two ways at the same time.

This research is being done because it is not known if using Cyberknife with chemotherapy will be a safe way to treat pancreatic cancer.

Detailed Description

This is a single arm, open-label pilot study of Cyberknife plus Gemcitabine in 10 patients with locally advanced pancreatic cancer who have not received prior local or systemic therapy for their pancreatic cancer.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Histologically proven unresectable, non-metastatic pancreatic adenocarcinoma with measurable or evaluable disease and without involvement of the duodenum
  • •Performance Status 0-2
  • •No prior anticancer therapy for pancreatic adenocarcinoma
  • •No prior anticancer therapy of any kind within the last 5 years
  • •Adequate hepatic, bone marrow, and renal function
  • •Life expectance of > 12 weeks
  • •Women of childbearing potential must have a negative serum pregnancy test

Exclusion Criteria

  • •Duodenal involvement of pancreatic cancer
  • •Metastatic cancer
  • •Active severe infection, or known chronic infection with HIV, hepatitis B virus, or hepatitis C virus
  • •Cardiovascular disease including unstable angina, therapy for life-threatening ventricular arrhythmia, myocardial infarction, stroke, or congestive heart failure within the last 6 months
  • •Life-threatening visceral disease or other severe concurrent disease
  • •Pregnant or breastfeeding
  • •Anticipated patient survival under 3 months
  • •Another active malignancy within the past 5 years except for cervical cancer in situ, in situ carcinoma of the bladder or non-melanoma carcinoma of the skin.

Arms & Interventions

Cyberknofe and Gemcitabine

Experimental

Cyberknife radiation and 6 cycles Gemcitabine

Intervention: Cyberknife radiation and gemcitabine (Radiation)

Outcomes

Primary Outcomes

To demonstrate that radiation treatments can be reproduced as determined by evaluation of the prescription isodose curves

Time Frame: 10 days

Secondary Outcomes

  • Acute and late toxicity as determined by patient self-reporting instruments that assess gastrointestinal side effects(6 months)
  • Quality of life as determined by patient self-reporting instruments(6 months)
  • Acute stomach/duodenal mucosa injury as assessed by upper endoscopy(one month)
  • Late stomach/duodenal mucosa injury as assessed by upper endoscopy(6 months)
  • Feasibility of integrating metabolomic analysis into the evaluation of patients with unresectable pancreatic cancer undergoing chemotherapy and radiation therapy measured by the ability to collect tumor specimens(6 months)
  • The feasibility of measuring pancreatic cancer stem cell populations by analysis of fine needle aspirate specimens(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Michael J Pishvaian

Assistant Professor

Georgetown University

Study Sites (1)

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