Microwave Ablation Combined With Chemotherapy for Colorectal Liver Metastases: a Multicenter Cohort Study
Primary Purpose
Colorectal Carcinoma, Chemotherapy, Liver Metastases
Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Chemotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Colorectal Carcinoma focused on measuring Microwave Ablation, Colorectal liver metastasis
Eligibility Criteria
Inclusion Criteria:
- 1) Aged between 18 and 80, WHO physical status score < level 2
- 2) Histologically confirmed colorectal cancer, liver metastasis (≤4), maximum diameter ≤4cm;
- 3) Patients without extrahepatic metastasis;
- 4) If the primary tumor has been resected or has metastasized at the same time, the multidisciplinary panel determines that the primary tumor can be resected and resected within one month after ablation;
- 5) No other chemotherapy experience except anti-tumor treatment for the primary cancer;
6) The main organs function normally, that is, they meet the following standards:
- Blood routine examination: HB≥90 g/L; The ANC acuity 1.5 x 109 / L; PLT 60 x 109 / L or higher;
- Biochemical examination: ALB ≥29g/L; ALT and AST < 3 uln; 1.5 ULN TBIL or less; Creatinine 1.5 or less ULN.
Exclusion Criteria:
- 1) A history of other malignant tumors in the past 5 years;
- 2) Cardiovascular diseases with significant clinical symptoms (uncontrolled congestive heart failure, angina pectoris, hypertension, arrhythmia);
- 3) Persons with coagulation disorders;
- 4) Combined with active infection;
- 5) Those with any contraindications related to chemotherapy;
- 6) Pregnant or lactating women;
- 7) A history of substance abuse and mental illness;
- 8) The investigator believes that there are any other factors that are not suitable for inclusion or affect the subject's participation in the study.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Experimental
Arm Label
Only MWA
MWA combined with perioperative chemotherapy
MWA combined with postoperative chemotherapy
Arm Description
Only preform MWA, chemotherapy isn't necessary
MWA combined with perioperative chemotherapy. Chemotherapy was preformed before MWA and after MWA
MWA combined with perioperative chemotherapy. Chemotherapy was preformed after MWA
Outcomes
Primary Outcome Measures
DFS
From the beginning of randomization to the time of disease recurrence or death due to disease progression
Secondary Outcome Measures
OS
Time from randomization to death from any cause.
ORR
Proportion of patients whose tumors shrink to a certain extent and remain constant for a certain period of time, including cases of complete response (CR) and partial response (PR).
LTP
From the beginning of randomization to the time of disease progression or death.
CSS
After treatment, death caused by tumor was considered as the end point, and the proportion of patients still alive after several years of follow-up accounted for the total number of follow-up patients.
Tumor reactivity assessment
Tumor reactivity assessment by mRECIST
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04562727
Brief Title
Microwave Ablation Combined With Chemotherapy for Colorectal Liver Metastases: a Multicenter Cohort Study
Official Title
Microwave Ablation Combined With Chemotherapy for Colorectal Liver Metastases: a Multicenter Cohort Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2021 (Anticipated)
Primary Completion Date
August 1, 2022 (Anticipated)
Study Completion Date
September 1, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ping Liang
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
Colorectal cancer is the second deadliest malignant tumor worldwide, and liver is the most common site of hematogenic metastasis of Colorectal cancer. Surgery is an effective treatment for colorectal cancer with liver metastasis, however, only 10%-20% of patients with liver metastasis are feasible for radical surgical resection. Many single-center retrospective studies have demonstrated that thermal ablation for liver metastases is comparable to surgery. Chemotherapy can kill the microscopic cancer foci of the liver. The timing of ablation-related chemotherapeutic administration still needs to be explained.
The purpose of this study was to compare the clinical efficacy of thermal ablation or combined with perioperative chemotherapy and postoperative chemotherapy in the treatment of colorectal cancer with liver metastasis.
Detailed Description
Colorectal cancer is the second deadliest malignant tumor worldwide, and liver is the most common site of hematogenic metastasis of Colorectal cancer. Surgery is an effective treatment for colorectal cancer with liver metastasis, however, only 10%-20% of patients with liver metastasis are feasible for radical surgical resection.
In the early 1990s, radiofrequency ablation (RFA) was first applied in the treatment of liver metastases. In the late 1990s and early 2000s, microwave ablation (MWA), irreversible electroporation (IRE) and other technologies emerged. Today, with the continuous improvement of ablation techniques, many single-center retrospective studies have demonstrated that thermal ablation for liver metastases is comparable to surgery. Currently, institutions have conducted multi-center randomized controlled trials to compare the outcomes of the two treatment approaches. The expert consensus of tumor ablation therapy has confirmed that the ablation technique has the advantages of minimally invasive, well tolerated and low complications, and has been widely used in the treatment of solid tumors. In the treatment of liver metastases, it also has the advantage of not being limited by residual liver volume.
Postoperative tumor recurrence occurred in about 2/3 of the patients with liver stump, mainly due to the residual microscopic cancer foci. Chemotherapy can kill the microscopic cancer foci of the liver. EORTC (40983) confirmed that: compared with surgery alone, perioperative chemotherapy for resectable liver metastases (<4) could benefit patients with PFS and reduce the incidence of tumor progression-related events. EORTC (40004) proved that in the treatment of non-resectable liver metastases (1 ~ 10, with a maximum diameter <4cm), ablation combined with postoperative chemotherapy was superior to chemotherapy alone. E. Tanis et al compared two randomized controlled trials of EORTC for colorectal cancer liver metastasis, namely 40983 (EPOC) and 40004 (CLOCC), and confirmed the treatment of liver metastasis (<3cm) after integration. There was no significant difference in local recurrence rate between the RFA+ postoperative chemotherapy group and the surgery + perioperative chemotherapy group. At the beginning, neoadjuvant chemotherapy was designed to provide surgical resection opportunities for patients who could not be resected with metastatic tumor. Later, it was gradually applied to resectable liver metastasis. Studies on surgical combination with chemotherapy proved that preoperative chemotherapy was no less effective than postoperative chemotherapy for resectable liver metastasis. However, for isolated small metastatic tumors (<3cm), complete tumor response after neoadjuvant chemotherapy should be avoided, leading to the dilemma of inoperable. Studies have reported that ablation combined with preoperative chemotherapy can cause hepatic steatosis and tumor shrinkage, which makes tumor visualization difficult to a certain extent. If the tumor disappeared on imaging, the pathological specimen confirmed that there were still residues, and the tumor could "reappear" during follow-up. Therefore, the timing of ablation-related chemotherapeutic administration still needs to be explained, and there is still a lack of high-quality evidence-based medical evidence at home and abroad.
The purpose of this study was to compare the clinical efficacy of thermal ablation or combined with perioperative chemotherapy and postoperative chemotherapy in the treatment of colon cancer with liver metastasis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Carcinoma, Chemotherapy, Liver Metastases
Keywords
Microwave Ablation, Colorectal liver metastasis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
668 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Only MWA
Arm Type
Experimental
Arm Description
Only preform MWA, chemotherapy isn't necessary
Arm Title
MWA combined with perioperative chemotherapy
Arm Type
Active Comparator
Arm Description
MWA combined with perioperative chemotherapy. Chemotherapy was preformed before MWA and after MWA
Arm Title
MWA combined with postoperative chemotherapy
Arm Type
Experimental
Arm Description
MWA combined with perioperative chemotherapy. Chemotherapy was preformed after MWA
Intervention Type
Drug
Intervention Name(s)
Chemotherapy
Other Intervention Name(s)
preoperative chemotherapy, postoperative chemotherapy
Intervention Description
perioperative chemotherapy or postoperative chemotherapy
Primary Outcome Measure Information:
Title
DFS
Description
From the beginning of randomization to the time of disease recurrence or death due to disease progression
Time Frame
60 months
Secondary Outcome Measure Information:
Title
OS
Description
Time from randomization to death from any cause.
Time Frame
60 months
Title
ORR
Description
Proportion of patients whose tumors shrink to a certain extent and remain constant for a certain period of time, including cases of complete response (CR) and partial response (PR).
Time Frame
60 months
Title
LTP
Description
From the beginning of randomization to the time of disease progression or death.
Time Frame
60 months
Title
CSS
Description
After treatment, death caused by tumor was considered as the end point, and the proportion of patients still alive after several years of follow-up accounted for the total number of follow-up patients.
Time Frame
60 months
Title
Tumor reactivity assessment
Description
Tumor reactivity assessment by mRECIST
Time Frame
60 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
1) Aged between 18 and 80, WHO physical status score < level 2
2) Histologically confirmed colorectal cancer, liver metastasis (≤4), maximum diameter ≤4cm;
3) Patients without extrahepatic metastasis;
4) If the primary tumor has been resected or has metastasized at the same time, the multidisciplinary panel determines that the primary tumor can be resected and resected within one month after ablation;
5) No other chemotherapy experience except anti-tumor treatment for the primary cancer;
6) The main organs function normally, that is, they meet the following standards:
Blood routine examination: HB≥90 g/L; The ANC acuity 1.5 x 109 / L; PLT 60 x 109 / L or higher;
Biochemical examination: ALB ≥29g/L; ALT and AST < 3 uln; 1.5 ULN TBIL or less; Creatinine 1.5 or less ULN.
Exclusion Criteria:
1) A history of other malignant tumors in the past 5 years;
2) Cardiovascular diseases with significant clinical symptoms (uncontrolled congestive heart failure, angina pectoris, hypertension, arrhythmia);
3) Persons with coagulation disorders;
4) Combined with active infection;
5) Those with any contraindications related to chemotherapy;
6) Pregnant or lactating women;
7) A history of substance abuse and mental illness;
8) The investigator believes that there are any other factors that are not suitable for inclusion or affect the subject's participation in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
jianming Li, Dr
Phone
860118810611944
Email
lijianming@ccmu.edu.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Ping Liang, Doctor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ping Liang, Doctor
Organizational Affiliation
Chinese PLA General Hospital
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Microwave Ablation Combined With Chemotherapy for Colorectal Liver Metastases: a Multicenter Cohort Study
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