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Trial · NCT07913113

Liver Transplantation Versus Conventional Medical Therapy for Low-Grade GEP-NET With Liver Metastases

NCT07913113, Enrolling by invitation, Chiyi Chen

3 sourcestrials-2026-11-12-0.4.0

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ConductScience Library. Liver Transplantation Versus Conventional Medical Therapy for Low-Grade GEP-NET With Liver Metastases. Trials, record NCT07913113. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07913113

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Liver Transplantation Versus Conventional Medical Therapy for Low-Grade GEP-NET With Liver Metastases
NCT number
NCT07913113
Status
Enrolling by invitation
Enrollment
100 participants, estimated
Lead sponsor
Chiyi Chen
Conditions
Neuroendocrine Tumors
Interventions
Liver Transplantation
First posted
2026-11-03
Last updated
2026-11-03

Source ClinicalTrials.gov

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
Primary5-Year Overall SurvivalUp to 5 years after enrollmentTime from enrollment to death from any cause, assessed up to 5 years after enrollment. OS will be estimated by the Kaplan-Meier method and compared between groups using the log-rank test.
SecondaryOverall Survival Rate at 1 Year1 year after enrollmentPercentage of participants alive at 1 year after enrollment, estimated by the Kaplan-Meier method.
SecondaryOverall Survival Rate at 3 Years3 years after enrollmentPercentage of participants alive at 3 years after enrollment, estimated by the Kaplan-Meier method.
SecondaryProgression-Free SurvivalUp to 5 years after enrollmentTime from enrollment to radiological progression (per RECIST 1.1) or death from any cause, whichever occurs first, assessed in the conventional medical therapy group.
SecondaryPost-transplant Disease-Free SurvivalUp to 5 years after liver transplantationTime from liver transplantation to first radiological recurrence or death from any cause, whichever occurs first, assessed in the liver transplantation group.
SecondaryRecurrence Pattern After Liver TransplantationUp to 5 years after liver transplantationAnatomic pattern of first recurrence, categorized as intrahepatic (graft) recurrence or extrahepatic recurrence.
SecondaryTreatment-Related Adverse EventsUp to 5 years after enrollment
Percentage of participants experiencing treatment-emergent adverse events, graded by severity according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0, including post-transplant surgical complications, graft-related events, and systemic drug toxicities.
SecondaryQuality of Life Assessed by the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ-C30) Global Health Status/Quality of Life ScoreBaseline, 6 months, 1 year, and annually thereafter up to 5 yearsThe EORTC QLQ-C30 global health status/quality of life subscale score ranges from 0 to 100, with higher scores indicating better quality of life.
SecondaryTotal Direct Medical CostsUp to 5 years after enrollmentTotal direct medical costs attributable to the treatment course, including surgery, hospitalization, systemic therapy, and management of adverse events, reported in Chinese Yuan (CNY).
SecondaryExploratory Prognostic Value of Ki-67 Proliferation IndexBaseline
Ki-67 proliferation index (percentage of positively stained tumor cell nuclei) assessed by immunohistochemistry on tumor tissue; ranges from 0% to 100%, with higher values indicating higher proliferative activity.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release
trials-2026-11-12-0.4.0
Release manifest SHA-256
0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture
2026-11-12
Results copy, AACT
2026-03-23
NIH clinical studies file
2026-11-13

Source ClinicalTrials.gov

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07913113

GET https://conductscience.org/api/trials/v1/NCT07913113/registered