Anatomical Resection VS. Nonanatomical Resection for Colorectal Liver Metastases With Gene Mutation or Right-sidedness

Sponsor
Fudan University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05881746
Collaborator
(none)
176
1
2
60
2.9

Study Details

Study Description

Brief Summary

In this study, colorectal cancer patients with initially resectable liver-only metastases, as prospectively confirmed by a local multidisciplinary team (MDT) according to predefined criteria, will be tested for RAS and BRAF tumor mutation status. Patients with gene mutant or right-sidedness will be randomised between anatomical resection (AR) or nonanatomical resection (NAR). The primary end-point is the relapse-free survival.

Condition or Disease Intervention/Treatment Phase
  • Procedure: anatomical liver resection
  • Procedure: nonanatomical liver resection
N/A

Detailed Description

This study is a prospective, single-center, randomized control trial. The major including criteria are (1) Histologically confirmed colorectal cancer initially resectable liver-only metastases ; (2) patient has the opportunity to perform either anatomical resection (AR) or nonanatomical resection (NAR) surgery; (3) the number of metastasis is 1-3; (4) KRAS/NRAS/BRAF mutation or right-sidedness. Patients will be randomised between AR or NAR. Patients will be stratified for gene mutation and right-sidedness.

Based upon the segmental anatomy of the liver according to Couinaud system, AR is defined as the resection of one or more complete hepatic segments in our study, including bisegmentectomy, right hemihepatectomy, left hemihepatectomy, extended right hemihepatectomy, extended left hemihepatectomy, single segmentectomy, caudate lobectomy, or a combination thereof. NAR, also called as wedge resection, is defined as the resection of the tumor with a margin of normal parenchyma regardless of the hepatic anatomy.

The primary end-point is the relapse-free survival. The secondary end-points are postoperative complication, postoperative mortality, hospital length of stay, and overall survival.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
176 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Anatomical Resection Versus Nonanatomical Resection for Colorectal Liver Metastases Patients With Gene Mutation or Right-sidedness: The ARCLAMP Randomized Controlled Trial
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jul 1, 2026
Anticipated Study Completion Date :
Jul 1, 2028

Arms and Interventions

Arm Intervention/Treatment
Experimental: anatomical resection group

Based upon the segmental anatomy of the liver according to Couinaud system, anatomical resection (AR) is defined as the resection of one or more complete hepatic segments in our study, including bisegmentectomy, right hemihepatectomy, left hemihepatectomy, extended right hemihepatectomy, extended left hemihepatectomy, single segmentectomy, caudate lobectomy, or a combination thereof.

Procedure: anatomical liver resection
Based upon the segmental anatomy of the liver according to Couinaud system, anatomical resection (AR) was defined as resection of 1 or more complete hepatic segments in our study, including bisegmentectomy, right hemihepatectomy, left hemihepatectomy, extended right hemihepatectomy, extended left hemihepatectomy, single segmentectomy, caudate lobectomy, or a combination of these.

Active Comparator: nonanatomical resection group

nonanatomical resection (NAR), also called as wedge resection, is defined as the resection of the tumor with a margin of normal parenchyma regardless of the hepatic anatomy.

Procedure: nonanatomical liver resection
Nonanatomical resection(NAR), known as wedge resection, was defined as resection of the tumor with a margin of normal parenchyma without regard to hepatic anatomy.

Outcome Measures

Primary Outcome Measures

  1. relapse-free survival [3 years]

    The relapse-free survival (PFS) was defined as the period from the start of initial liver resection to the date of tumor relapse or death

Secondary Outcome Measures

  1. overall survival [5 years]

    The overall survival (OS) was defined as the period from the start of initial liver resection until death from any cause, at which point the data was censored.

  2. postoperative hospital stay [30 days post operatively]

    The postoperative hospital stay is defined as the number of date from the first day after operation to discharge.

  3. postoperative complication [After surgery during one month]

    Patients will be evaluated for surgical morbidity during 1 month. Postoperative morbidity will be scored according 'Clavien-Dindo Grade'.

  4. postoperative mortality [After surgery during 90 days]

    any death occured within 90 days after the last resection of primary and metastatic lesions

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age ≥ 18 and ≤ 75 years;

  2. Histological proof of colorectal adenocarcinoma;

  3. Resectable colorectal liver metastasis without detectable extrahepatic distant metastatic disease (determined by a local MDT);

  4. Suitable for anatomical or nonanatomical liver resection (determined by a local MDT);

  5. Number of metastasis is 1 to 3;

  6. KRAS/NRAS/BRAF mutation or right-sidedness;

  7. Performance Status (ECOG) 0~1;

  8. Adequate hematological function: Neutrophils≥1.5 x109/l and platelet count≥100 x109/l; Hb ≥9g/dl (within 1 week prior to randomization);

  9. Adequate liver and renal function: total bilirubin ≤2.0 mg/dl, serum transaminases ≤ 5x upper limit of normal(ULN), and serum creatinine ≤ 1.5x ULN and creatinine clearance ≥ 30 ml/min;

  10. Written informed consent.

Exclusion Criteria:
  1. Previous systemic treatment for metastatic disease;

  2. Previous surgery for metastatic disease;

  3. Extrahepatic metastases;

  4. Unresectable primary tumor;

  5. Major cardiovascular events (myocardial infarction, severe/unstable angina, congestive heart failure, CVA) within 12 months before randomisation;

  6. Second primary malignancy within the past 5 years;

  7. Acute or subacute intestinal obstruction;

  8. Drug or alcohol abuse;

  9. No legal capacity or limited legal capacity;

  10. Pregnant or lactating women.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Zhongshan hospital Shanghai Shanghai China 200032

Sponsors and Collaborators

  • Fudan University

Investigators

  • Principal Investigator: Jianmin Xu, MD, Fudan University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xu jianmin, Director of the Department of Colorectal Surgery, Fudan University
ClinicalTrials.gov Identifier:
NCT05881746
Other Study ID Numbers:
  • ARCLAMP
First Posted:
May 31, 2023
Last Update Posted:
May 31, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 31, 2023