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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
Ping Liang
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Carcinoma focused on measuring Microwave Ablation, Colorectal liver metastasis

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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:

    1. Blood routine examination: HB≥90 g/L; The ANC acuity 1.5 x 109 / L; PLT 60 x 109 / L or higher;
    2. 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

    First Posted
    September 6, 2020
    Last Updated
    March 3, 2021
    Sponsor
    Ping Liang
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    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

    Learn more about this trial

    Microwave Ablation Combined With Chemotherapy for Colorectal Liver Metastases: a Multicenter Cohort Study

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