Cyberknife Radiosurgery Boost for Hilar Cholangiocarcinoma (Klatskin Tumor)

Cholangiocarcinoma Clinical Trial

Official title:

Phase I Dose Escalation Trial of External Beam Radiation and Cyberknife Radiosurgery Boost With Concurrent Capecitabine for Hilar Cholangiocarcinoma (Klatskin Tumor)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00630890
• Other study ID #: 07455
• Status: Terminated
• Phase: Phase 1
• First received: February 28, 2008
• Last updated: September 9, 2015
• Start date: October 2007
• Est. completion date: December 2008

Study information

• Verified date: September 2015
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to test the safety of giving external beam radiation, followed by a Cyberknife radiosurgery boost at different dose levels, together with a chemotherapy drug called capecitabine. The dose of Cyberknife radiosurgery boost will be made higher slowly in this protocol. Patients with hilar cholangiocarcinoma (Klatskin tumor), which is not amenable for surgical removal, are eligible.

The hypothesis is that highly focused high dose radiation delivered using Cyberknife in conjunction with traditional radiation and chemotherapy can improve outcome in this patient population.

Description:

This is a dose escalation study which will escalate the dose of Cyberknife radiosurgery boost after external beam radiation of 45 Gy with concurrent capecitabine. The three dose levels are 4 Gy x5, 5 Gy x5 and 6 Gy x 5, with 3 patients at each dose level. Dose-limiting toxicity (DLT) is defined as acute grade 3 liver or intestinal toxicity or any acute grade 4 toxicity. If one patient experienced a DLT at a particular dose level, the cohort should be expanded to 6 patients. The maximum tolerated dose (MTD) is defined as the dose level below that which results in DLT in 2 or more of the 6 patients in each cohort. At least 5 patients should be enrolled in the cohort of 6 Gy x 5 even if none of the first 3 experienced DLT, as a means of added verification of dose tolerance, at this upper limit of dose for this study.

The patient population includes any patients who have unresectable hilar cholangiocarcinoma without any prior history of radiation. We anticipate accruing 1 patient every 2 months; therefore, we estimate that it will require approximately 22 months to accrue 11 patients if no DLT is experienced by any patients requiring expansion of the cohorts.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 11
• Est. completion date: December 2008
• Est. primary completion date: December 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age eighteen years or older

• Histological defined unresectable cholangiocarcinoma of hilar region of the liver

• Patients should have evaluable disease on one or more imaging modalities (CT scan, MRI, and/or PET) since this will be necessary for radiation treatment planning. However, because the borders of these tumors are sometimes difficult to define precisely, measurable disease is not required (see Section 9.1 for definitions of evaluable and measurable disease).

• The maximum tumor dimension should be less than 6 cm.

• Patients with pathologically enlarged perihepatic regional lymph nodes are allowed.

• Prior surgical resection is allowed if there is gross disease remaining

• Adjuvant chemotherapy is allowed at least 1 month after completion of radiation therapy if any grade 3 or higher toxicity has resolved

• Percutaneous biliary drains and biliary stents are allowed

• Performance status of ECOG 0-1 (see Appendix I)

• Life expectancy greater than 6 months

• Subject must have normal organ and marrow functions as defined below

• leukocytes >3,000/mcL

• absolute neutrophil count >1,500/mcL

• platelets >100,000/mcL

• total bilirubin <2.5 X institutional upper limit of normal

• AST(SGOT)/ALT(SGPT) <2.5 X institutional upper limit of normal

• creatinine within normal institutional limits OR

• creatinine clearance >60 mL/min/1.73 m2 for patients with creatinine levels above institutional normal.

• PT/PTT within normal institutional limits

• Gold marker seeds (1 to 3) are required to be placed in or around the primary tumor by an interventional radiologist

• Ability to give written informed consent and willingness to comply with the requirements of the protocol

• Women of child-bearing potential must agree to use an effective method of birth control during treatment and for six months after receiving their last dose of treatment

Exclusion Criteria:

• Patients who have had prior chemotherapy

• Patients who have had external beam radiation to the region of liver hilar previously.

• Patients receiving any other investigational agents

• Patients with known metastases

• History of allergic reactions attributed to compounds of similar chemical or biologic composition to capecitabine.

• 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 who are not candidates for gold marker seeds placement due to position of the tumor or co-existing medical condition.

• Pregnant or lactating women and women of child-bearing potential who are not using an effective method of birth control

• Any condition that compromises compliance with the objectives and procedures of this protocol, as judged by the principal investigator

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Biliary Tract Cancer
• Biliary Tract Neoplasms
• Cholangiocarcinoma
• Klatskin Tumor
• Klatskin's Tumor

Intervention

Radiation:
• External beam radiation and Cyberknife radiosurgery boost and capecitabine
External Beam Radiation to 45 Gy Stereotactic Body Radiotherapy with Cyberknife to 20 Gy in 5 fractions dose escalation to 25 Gy in 5 fractions, and then 30 Gy in 5 fractions Capecitabine 825 mg/m2 q12 hours taken orally 5 days per week

Locations

Country	Name	City	State
United States	University of California San Francisco	San Francisco	California

Sponsors (1)

Lead Sponsor	Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To evaluate acute toxicities		3 months for acute toxicities	Yes
Primary	To determine the maximal tolerated dose of the Cyberknife radiosurgery boost		3 months for acute toxicities	Yes
Secondary	To assess local and regional control		two years	Yes
Secondary	To evaluate radiographic response		two years	Yes
Secondary	To assess delayed and long-term toxicities		two years	Yes
Secondary	To estimate disease specific and overall survival		two years	Yes