NCT06934018

Brief Summary

The main objective of this study was to evaluate the effect of surgical margin width on the prognosis of patients with hepatic oligometastasis of colorectal cancer by statistical 1-year intrahepatic recurrence-free survival rate (ihRFSrate). The secondary objective of the study was to evaluate the effect of surgical margin width on long-term survival and total recurrence of colorectal cancer in patients with hepatohepatic metastasis by statistical overall survival time (OS) and relapse-free survival time (RFS), and to evaluate the safety of wide margin surgery compared with narrow margin surgery in patients with Cromitis during perioperative period. This was a single-center, prospective, randomized controlled clinical study to evaluate the effects of surgical margin width on 1-year intrahepatic relapse-free survival, relapse-free survival time, overall survival time, and perioperative safety in patients with hepatic oligometastasis of colorectal cancer. Subjects will undergo radical resection of liver tumors and will be randomly assigned to a wide margin group (≥7mm) or narrow margin group (\<7mm) using stratified randomization, stratified by primary lesion site (right colon vs left colon/rectum). The margin width was the narrowest margin distance measured in fresh specimens. After radical liver tumor resection, subjects were pretreated regularly Follow-up evaluation.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
140

participants targeted

Target at P50-P75 for not_applicable

Timeline
24mo left

Started Apr 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress35%
Apr 2025Apr 2028

First Submitted

Initial submission to the registry

April 9, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

April 18, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

April 21, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 7, 2026

Completed
2.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2028

Expected
Last Updated

May 6, 2025

Status Verified

May 1, 2025

Enrollment Period

12 months

First QC Date

April 9, 2025

Last Update Submit

May 2, 2025

Conditions

Keywords

Liver metastasis of colorectal cancer

Outcome Measures

Primary Outcomes (1)

  • Intrahepatic recurrence-free survival at 1 year(ihRFS rate)

    Refers to the percentage of subjects in this group who received intrahepatic imaging diagnosis of recurrence or death from any cause from surgery to 1 year after surgery.

    From liver tumor resection to 1 year after surgery

Secondary Outcomes (3)

  • Recurrence free survival time(RFS)

    12 months

  • Overall survival time(OS)

    24 months

  • Perioperative safety

    Patient 90 days after hepatectomy

Study Arms (2)

Experimental group

EXPERIMENTAL

The surgical margin width was greater than or equal to 7mm

Procedure: Surgery and procedure

Control group

EXPERIMENTAL

The surgical margin width was less than 7mm

Procedure: Surgery and procedure

Interventions

According to the "Chinese Guidelines for the Diagnosis and Comprehensive Treatment of Liver metastases of Colorectal Cancer (2023 edition)", R0 resection of metastatic tumors is satisfied, and the objective is to preserve sufficient functional liver tissue, and the surgical margin width is less than 7mm

Control group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Male or female patients, age ≥18 years;
  • ECOG Physical condition score :0-1 score;
  • Liver biopsy pathologic diagnosis or clinical history combined with laboratory examination and imaging findings can be used to diagnose colorectal cancer in liver;
  • The primary lesion of colorectal cancer has been resected or can be resected 4-6 weeks after hepatectomy;
  • The number of liver metastases was less than or equal to 5;
  • There was no extrahepatic metastases or the metastases were radically resected;
  • Preoperative assessment (based on enhanced CT or MRI image AI segmentation combined with three-dimensional reconstruction of hepatic parenchymal blood vessels) enables radical (R0) resection of hepatic oligometastases, and wide surgical margin (the narrowest incisal margin of fresh specimens surgically removed is greater than or equal to 7mm) can be achieved technically, and the incisal margin width is not affected by the intrahepatic vasculature;
  • Good liver reserve function (preoperative Child-Pugh grade A liver function, estimated remaining liver volume ≥30%);
  • Preoperative examinations do not show clear surgical contraindications;
  • Volunteer to participate in this study and sign the informed consent;
  • The compliance was good, and the family members were willing to cooperate with the follow-up;

You may not qualify if:

  • There are still untreated extra-hepatic metastases;
  • Staging hepatectomy is planned, such as PVE combined with hepatectomy, ALPPS, etc;
  • The number of liver metastases before chemotherapy was more than 5;
  • Complicated with portal vein tumor thrombus or hepatic vein invasion;
  • Concurrent with other uncured malignancies or with other primary malignancies for less than 5 years;
  • Expected survival time ≤6 months;
  • Those who have a history of psychotropic substance abuse and are unable to abstain or have mental disorders;
  • Have a history of immunodeficiency or other acquired or congenital immunodeficiency diseases; Or have an autoimmune disease;
  • According to the study, there are serious concomitant diseases that endanger the patient's safety or interfere with the patient's completion of the study;
  • Patients or family members could not understand the conditions and goals of the study;

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, 200062, China

RECRUITING

Related Publications (4)

  • Weichselbaum RR, Hellman S. Oligometastases revisited. Nat Rev Clin Oncol. 2011 Jun;8(6):378-82. doi: 10.1038/nrclinonc.2011.44. Epub 2011 Mar 22.

    PMID: 21423255BACKGROUND
  • Su YM, Liu W, Yan XL, Wang LJ, Liu M, Wang HW, Jin KM, Bao Q, Wang K, Li J, Xu D, Xing BC. Five-year survival post hepatectomy for colorectal liver metastases in a real-world Chinese cohort: Recurrence patterns and prediction for potential cure. Cancer Med. 2023 Apr;12(8):9559-9569. doi: 10.1002/cam4.5732. Epub 2023 Feb 27.

    PMID: 36846977BACKGROUND
  • Laroche S, Scatton O, Charlotte F, Bachet JB, Lim C, Fuks D, Goumard C. Prognosis of a Heterogeneous TRG Pathological Response to Neoadjuvant Chemotherapy in Patients who Undergo Resection for Colorectal Liver Metastases. Ann Surg Oncol. 2024 Jul;31(7):4436-4444. doi: 10.1245/s10434-024-15196-x. Epub 2024 Mar 28.

    PMID: 38549003BACKGROUND
  • Guckenberger M, Lievens Y, Bouma AB, Collette L, Dekker A, deSouza NM, Dingemans AC, Fournier B, Hurkmans C, Lecouvet FE, Meattini I, Mendez Romero A, Ricardi U, Russell NS, Schanne DH, Scorsetti M, Tombal B, Verellen D, Verfaillie C, Ost P. Characterisation and classification of oligometastatic disease: a European Society for Radiotherapy and Oncology and European Organisation for Research and Treatment of Cancer consensus recommendation. Lancet Oncol. 2020 Jan;21(1):e18-e28. doi: 10.1016/S1470-2045(19)30718-1.

    PMID: 31908301BACKGROUND

MeSH Terms

Conditions

NeoplasmsRecurrenceNeoplasm Metastasis

Interventions

Surgical Procedures, Operative

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsNeoplastic Processes

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
MD,PhD

Study Record Dates

First Submitted

April 9, 2025

First Posted

April 18, 2025

Study Start

April 21, 2025

Primary Completion

April 7, 2026

Study Completion (Estimated)

April 30, 2028

Last Updated

May 6, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations