Stereotactic Body Radiation Therapy for Unresectable Perihilar Cholangiocarcinoma

Klatskin Tumor Clinical Trial

— STRONG  

Official title:

A Pilot Study to Determine the Feasibility of Stereotactic Body Radiation Therapy Following Chemotherapy for Unresectable Perihilar Cholangiocarcinoma. "The STRONG Trial"

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03307538
• Other study ID #: NL 60588.078.17
• Status: Completed
• Phase: N/A
• Start date: November 6, 2017
• Est. completion date: June 30, 2020

Study information

• Verified date: January 2021
• Source: Erasmus Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Rationale: For patients with perihilar cholangiocarcinoma, surgery is the only treatment modality that can result in cure. Unfortunately, in the majority of these patients the tumors are found to be unresectable at presentation due to local invasive tumor growth or the presence of distal metastases. For patients with unresectable cholangiocarcinoma palliative chemotherapy is the standard treatment yielding an estimated median overall survival of 12-15.2 months. There is no evidence from randomized trials that support the routine use of stereotactic body radiation therapy (SBRT) for cholangiocarcinoma. However, small and most often retrospective studies combining chemotherapy with SBRT showed promising results with overall survival reaching up to 33-35 months. Based upon these observations, the investigators designed a local feasibility trial with SBRT after chemotherapy in patients with unresectable perihilar cholangiocarcinoma in order to try to confirm the observed tolerability of adding SBRT to standard chemotherapy. The expected time to include the required patients for this pilot study will be one year. Objective: To assess feasibility of SBRT as add on treatment after standard chemotherapy. Study design: Local feasibility trial. Study population: Patients diagnosed with perihilar cholangiocarcinoma, 18 years of age or older, T1-4 N0-1 M0 (AJCC 7th Edition), after completion of standard chemotherapy. Exclusion criteria are local tumor growth into either stomach, colon, duodenum, pancreas or abdominal wall. Sample size will be 6 patients. Intervention: SBRT will be delivered in 15 fractions of 3 to 4.5Gy after 8 cycles of chemotherapy. In case of toxicity causing premature termination of systemic treatment, the patient can still proceed to SBRT. Main study parameters/endpoints: The primary endpoint of this study is feasibility measured by radiotherapy induced toxicity according to CTC v4.0.3. Secondary endpoints will be: - Quality of life - Local progression - Progression free survival - Overall survival - Cellular radiosensitivity.

Description:

For patients with perihilar cholangiocarcinoma, surgery is the only treatment modality that can result in cure. Unfortunately, in the majority of these patients the tumors are found to be unresectable at presentation due to local invasive tumor growth or the presence of distant metastases. For these patients palliative chemotherapy is the standard treatment yielding an estimated median overall survival of 12-15.2 months. There is no evidence from randomized trials that supports the routine use of stereotactic body radiation therapy (SBRT) for unresectable cholangiocarcinoma. However, small and most often retrospective studies combining chemotherapy with SBRT showed promising results with overall survival reaching up to 33-35 months. This pilot study is designed as a first step to confirm and extend these findings. Up to six patients diagnosed with unresectable perihilar cholangiocarcinoma will be treated with standard chemotherapy followed by SBRT in order to assess possible severe side effects of the treatment. As part of this research, patients will be followed with CT- or MRI-scan and blood tests exams until progression. In addition to this clinical evaluation, the investigators will also work towards developing a predictive assay for radiotherapy response of both normal and tumor tissue by establishing normal tissue and tumor organoids and determining several key parameters for their response to ionizing radiation treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: June 30, 2020
• Est. primary completion date: March 30, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion criteria:

In order to be eligible to participate in this study, a subject must be discussed in a

multidisciplinary liver tumor board and should meet all of the following criteria:

• Patients diagnosed with perihilar cholangiocarcinoma according to the criteria of the

Mayo Clinic, Rochester:

• Positive or strongly suspicious intraluminal brush or biopsy or,
• A radiographic malignant appearing stricture plus either:
• CA 19-9>100 U/ml in the absence of acute bacterial cholangitis, or
• polysomy on FISH, or
• a well-defined mass on cross sectional imaging.
• One tumor mass
• Unresectable tumor
• Finished chemotherapy treatment with Gemcitabine and Cisplatin, preferably 8 cycles. If less cycles are given, patients are still eligible for this study.
• T1-T4 (AJCC staging 7th edition), before chemotherapy
• N0-N1 (AJCC staging 7th edition), radiologically or pathologically suspect, before chemotherapy
• Measurable disease to be selected as a target on CT/MRI-scan, according to RECIST criteria, after chemotherapy within 6 weeks prior to inclusion
• Tumor visibility on CT
• If liver cirrhosis is present, it should be well compensated, with Child-Pugh grade A.
• Age = 18 years
• ECOG performance status 0-1
• Bilirubin =1.5 times normal value, AST/ALT =5 times ULN, within 6 weeks prior to inclusion
• Platelets = 50x10E9/ l, Leukocytes > 1.5x10E9/l, Hb > 6 mmol/l, within 6 weeks prior to inclusion
• Written informed consent, after chemotherapy
• Willing and able to comply to the follow-up schedule
• Able to start SBRT within 12 weeks after completion of chemotherapy.

Exclusion criteria:

• Eligibility for resection
• Prior surgery or transplantation
• Multifocal tumor
• Tumor extension in stomach, colon, duodenum, pancreas or abdominal wall.
• N2, (AJCC staging 7th edition), radiologically or pathologically suspect, before chemotherapy
• Distant metastases
• Progression (local or distant) during or after chemotherapy Ascites
• Previous radiotherapy to the liver
• Current pregnancy

Related Conditions & MeSH terms

• Cholangiocarcinoma
• Klatskin Tumor

Intervention

Radiation:
• Stereotactic body radiation therapy
15 fractions of 3-4,5 Gy (risk-adapted)

Locations

Country	Name	City	State
Netherlands	Erasmus MC	Rotterdam	Zuid Holland

Sponsors (1)

Lead Sponsor	Collaborator
Erasmus Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Acute toxicity	Limiting toxicity will be defined as more than one patient with grade 4 hepatobiliary toxicity related to study procedures, or more than one patient with grade 3 gastrointestinal toxicity related to study procedures, occurring in the period up to 3 months after the last SBRT administration.	3 months
Secondary	Quality of life	Assessed by means of the EORTC QLQ-C30 questionnaire	2 years
Secondary	Quality of life	Assessed by means of the EORTC QLQ-BIL21 questionnaire	2 years
Secondary	Quality of life	Assessed by means of the EuroQoL-5D questionnaire	2 years
Secondary	Local progression	Measured on CT	2 years
Secondary	Local progression	Measured on MRI	2 years
Secondary	Progression free survival	Time from treatment to progression measured on CT	2 years
Secondary	Overall survival		2 years
Secondary	Cellular radiosensitivity	A predictive assay will be developed for radiotherapy response of both normal and tumor tissue by establishing normal tissue and tumor organoids and determining several key parameters for their response to ionizing radiation treatment.	2 years