- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07704216
Peritumoral MRE Stiffness for Predicting Resection Margin Status and Recurrence in Liver Cancer
10. juli 2026 opdateret af: Second Affiliated Hospital of Xi'an Jiaotong University
A Prospective Study on the Association Between Peritumoral Elasticity Measured by Three-Dimensional Magnetic Resonance Elastography and Pathological Resection Margin Status and Postoperative Recurrence in Patients With Liver Cancer
Microscopic residual tumor at the resection margin is a critical risk factor for recurrence in patients undergoing hepatectomy for liver cancer, yet current detection relies solely on postoperative pathological examination of the resected specimen, which reflects only the removed tissue rather than the actual remnant liver in the patient.
How to non-invasively detect residual tumor at the resection margin of the remnant liver after surgery remains an important unresolved problem in the surgical management of liver cancer.
We hypothesize that tissue stiffness at the resection margin of the remnant liver, measured by postoperative three-dimensional magnetic resonance elastography (3D-MRE), may reflect microscopic residual tumor and may therefore correlate with pathological resection margin status and be predictive of postoperative tumor recurrence.
This study aims to prospectively evaluate the diagnostic performance of postoperative 3D-MRE in detecting residual tumor at the resection margin, using pathological resection margin status as the reference standard, and to further assess its value in predicting tumor recurrence in patients undergoing hepatectomy for liver cancer.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Undersøgelsestype
Observationel
Tilmelding (Anslået)
150
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Kai Qu
- Telefonnummer: +8613609117104
- E-mail: qukai001@xjtu.edu.cn
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
This study will enroll adult patients with primary or metastatic liver cancer, including hepatocellular carcinoma, intrahepatic cholangiocarcinoma, or liver metastases (e.g., from colorectal cancer), who undergo curative-intent hepatectomy at the Second Affiliated Hospital of Xi'an Jiaotong University.
Eligible patients will undergo postoperative 3D-MRE examination of the remnant liver and be followed to assess pathological resection margin status and subsequent tumor recurrence.
Patients will be consecutively recruited from the hepatobiliary surgery department of the study center.
Beskrivelse
Inclusion Criteria:
- Age 18-80 years
- Pathologically confirmed diagnosis of hepatocellular carcinoma, intrahepatic cholangiocarcinoma, or liver metastasis (e.g., from colorectal cancer)
- Underwent curative-intent hepatectomy with available postoperative pathological resection margin assessment
- Child-Pugh class A or B liver function (for patients with primary liver cancer)
- Able to undergo 3D-MRE examination at postoperative day 7-14
- Provision of signed and dated informed consent
Exclusion Criteria:
- Contraindication to MRI (e.g., non-MRI-compatible implants, severe claustrophobia)
- Palliative or non-curative surgery (R2 resection)
- Presence of unresectable extrahepatic disease at the time of surgery
- Reoperation or unplanned return to surgery within 14 days after the initial hepatectomy
- Severe postoperative complications precluding MRI examination at postoperative day 7-14 (e.g., unstable vital signs, need for intensive care)
- Death within 14 days after surgery from non-tumor-related causes
- Prior history of liver resection or liver transplantation
- Pregnant or breastfeeding women
- Anticipated poor compliance with postoperative MRE examination or follow-up
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Diagnostic performance of postoperative 3D-MRE for detecting residual tumor at the resection margin
Tidsramme: Postoperative day 7-14
|
Sensitivity, specificity, and area under the receiver operating characteristic curve (AUC) of 3D-MRE-derived stiffness parameters at the resection margin of the remnant liver, compared with pathological resection margin status (R0 vs. R1) of the surgical specimen as the reference standard.
|
Postoperative day 7-14
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Recurrence-Free Survival (RFS)
Tidsramme: Up to 2 years after surgery
|
Time from surgery to radiologically or pathologically confirmed tumor recurrence, or last follow-up if no recurrence occurs
|
Up to 2 years after surgery
|
|
Overall Survival (OS)
Tidsramme: Up to 2 years after surgery
|
Time from surgery to death from any cause
|
Up to 2 years after surgery
|
|
Correlation between 3D-MRE parameters at the resection margin and time to recurrence
Tidsramme: Postoperative day 7-14 (MRE); up to 2 years (recurrence follow-up)
|
Association between quantitative 3D-MRE parameters (e.g., stiffness, damping ratio) measured at postoperative day 7-14 and subsequent time to tumor recurrence
|
Postoperative day 7-14 (MRE); up to 2 years (recurrence follow-up)
|
|
Recurrence pattern (local vs. distant intrahepatic vs. extrahepatic)
Tidsramme: Up to 2 years after surgery
|
Classification of recurrence site and pattern based on imaging follow-up
|
Up to 2 years after surgery
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
1. august 2026
Primær færdiggørelse (Anslået)
1. oktober 2029
Studieafslutning (Anslået)
1. oktober 2031
Datoer for studieregistrering
Først indsendt
10. juli 2026
Først indsendt, der opfyldte QC-kriterier
10. juli 2026
Først opslået (Faktiske)
15. juli 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. juli 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. juli 2026
Sidst verificeret
1. juli 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- XJTUSAH-MRE-002
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