Study To Establish Maximum Tolerated Dose (MTD) of Cyberknife in Patients With Un-Resectable Pancreas Cancer (TL002)

Sponsor

The Cooper Health System (Other)

Overall Status

Terminated

CT.gov ID

NCT02707328

Collaborator

(none)

Enrollment

Location

Arm

34.3

Duration (Months)

0.9

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study is looking at determining the maximum safe dose of CyberKnife when given with chemotherapy for unresectable adenocarcinoma of the pancreas.

Condition or Disease	Intervention/Treatment	Phase
Pancreas Cancer Pancreatic Cancer Adenocarcinoma of the Pancreas Pancreas Adenocarcinoma Pancreatic Adenocarcinoma	Drug: Gemcitabine Drug: nab-paclitaxel Radiation: CyberKnife	Phase 1

Detailed Description

The purpose of this study is to determine the MTD for radiosurgery in the treatment of unresectable pancreas cancer, this MTD can then be used in future phase II or III studies. In terms of starting dose for the phase I study, based on the low toxicity seen in the Moffitt study we feel that 30 Gy in five fractions will be a successful starting dose.

Most of the data in unresectable is derived from patients in the metastatic setting in terms of chemotherapy agents. There have been two major studies that looked at various chemotherapy regimens versus the previous standard of care Gemzar. One study found improved survival with FOLFIRINOX and a second found that the combination of nab-paclitaxel and gemzar were superior to gemzar alone. Thus, the current standard of care for metastatic pancreas cancer (in which a local therapy like radiation has more limited role) is either FOLFIRINOX or gemzar and nab-paclitaxel. While there is some discussion of a randomized study comparing FOLFIRINOX and gemzar combined with nab-paclitaxel such a study has not started as of this time and it is unclear how much interest there would be in accruing to this study. Therefore the exact best chemotherapy regimen for metastatic disease is unclear but is either FOLFIRIONX or gemzar-nab-paclitaxel. The chemotherapy regimens for unresectable cancer are extrapolated from the metastatic setting, per NCCN guidelines any chemotherapy regimen approved for metastatic disease is reasonable to use in unresectable pancreas cancer. Thus for purpose of this study we have chosen one of the two chemotherapy regimens that have shown the best results in the metastatic setting, since there is no way to determine the exact best regimen we have chosen gemzar and nab-paclitaxel since it is felt that this is a less toxic regimen as compared to FOLFIRINOX.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

30 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase I Study To Establish Maximum Tolerated Dose (MTD) of Cyberknife in Patients With Un-Resectable Pancreas Cancer (TL002)

Study Start Date :

Jan 1, 2015

Actual Primary Completion Date :

Nov 10, 2017

Actual Study Completion Date :

Nov 10, 2017

Arms and Interventions

Arm	Intervention/Treatment
Experimental: A Chemotherapy: Gemcitabine 1000 mg/m2 and Abraxane 125 mg/m2 weekly x3 of 28 day cycle Radiation: 20-55 GY over 5 fractions Dosing schedule: 3 cycles of chemotherapy, followed by CyberKnife, followed by 3 additional cycles of chemotherapy.	Drug: Gemcitabine Other Names: gemzar Drug: nab-paclitaxel Other Names: abraxane Radiation: CyberKnife Other Names: cyber knife, CK, Stereotactic radiosurgery

Arm

Intervention/Treatment

Experimental: A

Chemotherapy: Gemcitabine 1000 mg/m2 and Abraxane 125 mg/m2 weekly x3 of 28 day cycle Radiation: 20-55 GY over 5 fractions Dosing schedule: 3 cycles of chemotherapy, followed by CyberKnife, followed by 3 additional cycles of chemotherapy.

Drug: Gemcitabine

Other Names:

gemzar

Drug: nab-paclitaxel

Other Names:

abraxane

Radiation: CyberKnife

Other Names:

cyber knife, CK, Stereotactic radiosurgery

Outcome Measures

Primary Outcome Measures

Maximum tolerable dose [4-7 months]
This study is to evaluate the MTD for Cyberknife when given in conjunction with Gemcitabine and Abraxane.

Secondary Outcome Measures

overall survival [6 months, 1 year, 5 years]
Tumor response per RECIST 1.1 [4 months, 6 months, 1 year]
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 [2 months, 6 months, 1 year]
quality of life [2 months, 4 months, 6 months, 1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Pathologically confirmed adenocarcinoma of the pancreas
Unresectable disease based on the following imaging criteria (table 1)
extrapancreatic extension
tumor involvement of the SMA or celiac axis
evidence of occlusion of the SMV-portal vein confluence
KPS > 50 (ECOG 0-2)
Age >18 years
Women of childbearing age and male participants must practice adequate contraception (hormonal or barrier method of birth control; abstinence) prior to and throughout study treatment.
Life expectancy > 3 months
Ability to understand and the willingness to sign a written informed consent.
Note that patients with metastatic disease are eligible if it is felt that the patients will benefit from local control of the primary disease.
Disease that is measureable or evaluable for response endpoint per RECIST

Exclusion Criteria:

Prior radiotherapy to the upper abdomen
Resectable or borderline resectable pancreas cancer. Note that these patients are eligible for a separate study looking at radiosurgery for borderline resectable pancreas cancer
Severe comorbidity rendering a candidate ineligible for chemotherapy or radiation, 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 requirements.
Patients of childbearing age who are unwilling or unable to practice contraception
Inability to undergo MRI or CT with contrast for treatment planning
Patients may not be receiving any other investigational nor commercial agents with therapeutic intent to treat pancreatic cancer while on this trial. Note that patients can have had previous investigational therapy but cannot have this concurrently with this protocol treatment.