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Trial · NCT07895732

Personalized Adaptive Radiotherapy for Hepatocellular Carcinoma

NCT07895732, Phase 3, Not yet recruiting, University Health Network, Toronto

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Personalized Adaptive Radiotherapy for Hepatocellular Carcinoma. Trials, record NCT07895732. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07895732

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Trial

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

Title
Personalized Adaptive Radiotherapy for Hepatocellular Carcinoma
NCT number
NCT07895732
Status
Not yet recruiting
Phases
Phase 3
Enrollment
60 participants, estimated
Lead sponsor
University Health Network, Toronto
Conditions
Hepatocellular Carcinoma (HCC)
Interventions
Best Supportive Care (BSC), Personalized ultrafractionated stereotactic adaptive radiation therapy (PULSAR)
First posted
2026-10-26
Last updated
2026-10-26

Source ClinicalTrials.gov

Registered outcomes9

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

ListOutcomeTime frameDescription
PrimaryOverall Survival (OS)5 yearsOverall survival (OS) is defined as the time from randomization to death from any cause. OS will be estimated using the Kaplan-Meier method and compared between both arms using a log-rank test.
SecondaryProgression Free Survival (PFS)From randomization until disease progression, death, or end of follow-up (up to [5 years]).Progressive-free survival (PFS): time to progression or death
SecondaryLesion Progression5 yearsProgression and/or development of new (intrahepatic or extra-hepatic) lesions are defined by RECIST 1.1 criteria after comprehensive clinical examination and radiographic evaluation.
SecondaryLiver Decompensation (Child Pugh)5 yearsAssessed using Child Pugh score where higher scores indicating worse liver function.
SecondaryLiver Decompensation (mALBI)5 yearsModified ALBI (mALBI) score where it ranges from Grade 1 (best liver function) to Grade 3 (worst liver function).
SecondaryPhysician-assessed toxicities5 yearsNational Cancer Institute (NCI) Common Terminology Criteria of Adverse Events (CTCAE) V.6 where higher grades indicate greater severity of toxicity.
SecondaryPatients-reported toxicities5 yearsPatient Reported Outcomes - Common Terminology Criteria of Adverse Events (PRO CTCAE) V.1 where higher scores indicate greater symptom burden and worse patient-reported toxicity.
SecondaryQuality of life (QOL) (FACT-Hep)5 yearsFunctional Assessment of Cancer Therapy - Hepatobiliary (FACT-Hep), with higher scores indicating better health-related quality of life.
SecondaryQuality of life (QOL) (EQ-5D-5L)5 yearsEQ-5D-5L questionnaires, where higher scores indicate better health-related quality of life.

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.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license 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/NCT07895732

GET https://conductscience.org/api/trials/v1/NCT07895732/registered