Trial Search Results
Phase II Gemcitabine + Fractionated Stereotactic Radiotherapy for Unresectable Pancreatic Adenocarcinoma
This multi-institutional trial aims to evaluate the potential benefit and side effects of adding fractionated stereotactic body radiotherapy/surgery (SBRT) before and after chemotherapy with gemcitabine for locally advanced pancreatic cancer.
Stanford is currently not accepting patients for this trial.
Collaborator: Johns Hopkins University
- Device: CyberKnife based stereotactic radiotherapy
- Drug: Gemcitabine
- Drug: Fludeoxyglucose (18F) (FDG)
3.1.1 Histologically confirmed adenocarcinoma of the pancreas.
3.1.2 Unresectable disease as determined by a pancreatic cancer surgeon and assessment at a
GI oncology tumor board (JHU - Johns Hopkins University, SU - Stanford University, or MSKCC
- Memorial Sloan Kettering Cancer Center).
3.1.3 Up to 3 weeks of gemcitabine chemotherapy is allowed prior to SBRT.
3.1.4 Pancreatic tumors must be less than 7.5 cm in greatest axial dimension (or <1000 cc
in volume) at the time of treatment planning.
3.1.5 No prior upper abdominal or liver radiation therapy.
3.1.6 No chemotherapy within 2 weeks of radiotherapy, or chemotherapy within parameters set
by Investigator for each institution.
3.1.7 Age >=18 years.
3.1.8 No infections requiring systemic antibiotic treatment.
3.1.9 Karnofsky >= 70% (see Appendix III).
3.1.10 Patients must have acceptable organ and marrow function as defined below (within 1
month prior to radiotherapy):
- leukocytes: >=3,000/microliter (uL)
- absolute neutrophil count: >=1,500uL
- platelets: >=100,000/uL
- total bilirubin: within 1.5 times (1.5X) normal institutional limits
- AST (aspartate aminotransferase)(SGOT -Serum glutamic oxaloacetic
transaminase)/ALT(alanine aminotransferase)(SGPT-serum glutamic-pyruvic transaminase):
<=2.5 X institutional upper limit of normal
- creatinine: within normal institutional limits
- creatinine clearance: >=60 mL/min/1.73 m^2 for patients with creatinine levels above
3.1.11 The effects of radiation on the developing human fetus at recommended therapeutic
doses can result in death of the fetus. If a woman is of child-bearing potential, a
negative urine or serum pregnancy test must be demonstrated prior to treatment. Women of
childbearing potential and men must agree to use adequate contraception (hormonal or
barrier method of birth control; abstinence) for the duration of study participation and
for up to 4 weeks following the study. Should a woman become pregnant or suspect she is
pregnant while participating in this study, she should inform her treating physician
3.1.12 Ability to understand and the willingness to sign a written informed consent
3.1.13 Life expectancy > 6 months
3.2.1 Patients who have had prior radiotherapy to the upper abdomen.
3.2.2 Patients receiving more than 1 cycle of gemcitabine chemotherapy or other therapy
prior to SBRT.
3.2.3 Children are excluded because pancreatic tumors rarely occur in this age group.
Furthermore, treatment requires a great deal of patient cooperation including the ability
to lie still for several hours in an isolated room.
3.2.4 No laboratory personnel will be included.
3.2.5 Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with study
3.2.6 Any concurrent malignancy other than non-melanoma skin cancer, non-invasive bladder
cancer, or carcinoma in situ of the cervix. Patients with a previous malignancy without
evidence of disease for > 5 years will be allowed to enter the trial.
3.2.7 Pregnant and breastfeeding women are excluded. Women of child-bearing potential who
are unwilling or unable to use an acceptable method of birth control to avoid pregnancy for
the entire study period and for up to 4 weeks after the study are excluded. This applies to
any woman who has experienced menarche and who has not undergone successful surgical
sterilization or is not postmenopausal (defined as amenorrhea for at least 12 consecutive
months, or women on hormone replacement therapy with serum FSH (follicle stimulating
hormone) levels greater than 35 IU/mL (international units/milliliter). A negative urine or
serum pregnancy test must be obtained within 72 hours prior to the start of study
medication in all women of childbearing potential. Male subjects must also agree to use
effective contraception for the same period as above.
Ages Eligible for Study
18 Years - N/A
Genders Eligible for Study