Neoadjuvant Hypofractionated Stereotactic Body Radiation Therapy Prior to Surgery for Hepatocellular Carcinoma: a Feasibility Study. (KARCHER-1)
Primary Purpose
Hepatocellular Carcinoma
Status
Recruiting
Phase
Phase 1
Locations
France
Study Type
Interventional
Intervention
Surgery with Neoadjuvant stereotactic body radiation therapy
Sponsored by
About this trial
This is an interventional treatment trial for Hepatocellular Carcinoma focused on measuring Hepatocellular carcinoma, Stereotactic body radiation therapy, Hepatectomy, Neoadjuvant therapy, Drop-out
Eligibility Criteria
Inclusion Criteria:
- Biopsy-proven hepatocellular carcinoma or EASL/AASLD criteria
- Single nodule, 3 to 8 cm of largest diameter
- Hepatocellular carcinoma eligible for conventional liver resection with curative intent (R0), without preoperative portal vein embolization
Exclusion Criteria:
- Performance status > 2
- Severe comorbidity with contraindication for either surgery or radiation therapy
- Decompensated liver cirrhosis (Child-Pugh B or C)
- Neoplastic portal vein thrombosis or extra-hepatic metastases
- Previous anticancer therapy within the last 5 years
Sites / Locations
- Hop Claude Huriez Chu LilleRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Experimental group
Arm Description
Outcomes
Primary Outcome Measures
Drop-out rate
Drop-out rate: proportion of patients in whom surgical resection cannot be achieved, due to (at least one of the following reasons):
serious adverse events related to radiation therapy (especially liver decompensation);
disease progression while receiving radiation therapy or awaiting surgery;
patient's death.
Secondary Outcome Measures
Intraoperative number of packed red blood cells transfused (if any).
Toxicity of radiation therapy using the National Cancer Institute CTCAE v.5.0 criteria
Duration of surgery.
Volume of intraoperative blood loss
Quality of life by EORTC QLQ-C30
Intraoperative adverse events
Postoperative severe and overall morbidity rate
defined using the Comprehensive Complication Index and graded with the Dindo-Clavien score
Postoperative mortality rate.
Correlation between radiological observations on preoperative imaging and pathological features on surgical specimen (like percentage of tumor necrosis).
Actuarial overall survival and disease-free survival.
Full Information
NCT ID
NCT04587739
First Posted
October 13, 2020
Last Updated
July 4, 2022
Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France
1. Study Identification
Unique Protocol Identification Number
NCT04587739
Brief Title
Neoadjuvant Hypofractionated Stereotactic Body Radiation Therapy Prior to Surgery for Hepatocellular Carcinoma: a Feasibility Study.
Acronym
KARCHER-1
Official Title
A Pilot Study on the Feasibility and Tolerance of Neoadjuvant Hypofractionated, Stereotactic Body Radiation Therapy Prior to Surgical Resection of Uninodular Hepatocellular Carcinoma.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 31, 2021 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
January 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Lille
Collaborators
Ministry of Health, France
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Hepatocellular carcinoma (HCC) is the fifth more common cancer in the world, with high mortality rates, due to the low number of patients who are eligible for therapy with curative intent, like surgical resection. Moreover, surgical resection is associated with a high risk of tumor recurrence, because of the tumor seeding through microscopic intrahepatic vessels that surround the tumor, the so-called "microvascular invasion".
To adequately deal with this phenomenon, the surgeon has to perform either an 'anatomical' liver resection, which remove not only the tumor but also the whole corresponding vascular network, or a 'tumorectomy' with resection margins of at least 2 cm. Unfortunately, these principles cannot always be achieved due to underlying liver cirrhosis that is present in more than 80% of patients.
Stereotactic body radiation therapy (SBRT) has been proven to efficiently necrotize or stabilize HCC nodules when surgery is not possible. Our hypothesis is that pre-treatment with SBRT prior to surgical resection of HCC might improve the results through the destruction of possible seeding in the peritumoral environment.
Given the novelty of this therapeutic strategy, it is necessary to verify its feasibility and safety, prior to test its efficacy in patients with HCC. The KARCHeR-1 study aims at making sure that preoperative SBRT would not result in important delays or serious adverse events such as to cancel the planned surgical resection, in patients who otherwise could have benefited from it. This issue is commonly called 'drop-out'. Thirty patients are expected to be included in the KARCHeR-1 study, which would be in favor of continuing to evaluate this therapeutic strategy if less than 3 drop-outs occur, and would be immediately discontinued if 3 drop-outs occur. Other outcomes will also been studied, like intraoperative issues, postoperative morbi-mortality, pathological features on the surgical specimen and its correlation with preoperative imaging, and finally, tumor recurrence and survival.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatocellular Carcinoma
Keywords
Hepatocellular carcinoma, Stereotactic body radiation therapy, Hepatectomy, Neoadjuvant therapy, Drop-out
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental group
Arm Type
Experimental
Intervention Type
Combination Product
Intervention Name(s)
Surgery with Neoadjuvant stereotactic body radiation therapy
Intervention Description
Stereotactic hypofractionated robotic radiation therapy (24-45 Gy / 3 fractions) followed after 4-6 weeks by conventional hepatectomy (either anatomical liver resection, or non-anatomical liver resection with intention to achieve a minimal 2 cm margin).
Primary Outcome Measure Information:
Title
Drop-out rate
Description
Drop-out rate: proportion of patients in whom surgical resection cannot be achieved, due to (at least one of the following reasons):
serious adverse events related to radiation therapy (especially liver decompensation);
disease progression while receiving radiation therapy or awaiting surgery;
patient's death.
Time Frame
Five months after the inclusion of the last participating patient
Secondary Outcome Measure Information:
Title
Intraoperative number of packed red blood cells transfused (if any).
Time Frame
Postoperative 90 days
Title
Toxicity of radiation therapy using the National Cancer Institute CTCAE v.5.0 criteria
Time Frame
Postoperative 90 days
Title
Duration of surgery.
Time Frame
Postoperative 90 days
Title
Volume of intraoperative blood loss
Time Frame
Postoperative 90 days
Title
Quality of life by EORTC QLQ-C30
Time Frame
between before and after stereotactic radiotherapy
Title
Intraoperative adverse events
Time Frame
Postoperative 90 days
Title
Postoperative severe and overall morbidity rate
Description
defined using the Comprehensive Complication Index and graded with the Dindo-Clavien score
Time Frame
Postoperative 90 days
Title
Postoperative mortality rate.
Time Frame
Postoperative 90 days
Title
Correlation between radiological observations on preoperative imaging and pathological features on surgical specimen (like percentage of tumor necrosis).
Time Frame
Postoperative day 30.
Title
Actuarial overall survival and disease-free survival.
Time Frame
Postoperative 24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Biopsy-proven hepatocellular carcinoma or EASL/AASLD criteria
Single nodule, 3 to 8 cm of largest diameter
Hepatocellular carcinoma eligible for conventional liver resection with curative intent (R0), without preoperative portal vein embolization
Exclusion Criteria:
Performance status > 2
Severe comorbidity with contraindication for either surgery or radiation therapy
Decompensated liver cirrhosis (Child-Pugh B or C)
Neoplastic portal vein thrombosis or extra-hepatic metastases
Previous anticancer therapy within the last 5 years
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emmanuel Boleslawski, MD,PhD
Phone
320444260
Ext
+33
Email
emmanuel.boleslawski@chru-lille.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emmanuel Boleslawski, MD,PhD
Organizational Affiliation
University Hospital, Lille
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hop Claude Huriez Chu Lille
City
Lille
ZIP/Postal Code
59037
Country
France
Individual Site Status
Recruiting
Facility Contact:
Phone
0320445962
12. IPD Sharing Statement
Learn more about this trial
Neoadjuvant Hypofractionated Stereotactic Body Radiation Therapy Prior to Surgery for Hepatocellular Carcinoma: a Feasibility Study.
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