- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07629193
Liver Transplant for Hepatocellular Carcinoma (TH-CHC)
This research focuses on analysing data collected as part of your usual care. Currently, the eligibility of patients with hepatocellular carcinoma for liver transplantation is based on the calculation of scores. These scores mainly take into account the volume of the tumour measured by imaging, one or more blood markers and the patient's general condition.
However, these scores do not take into account:
- the concept of downstaging (i.e. the prior reduction of tumour volume through locoregional or systemic treatments, which subsequently allows access to LT), which is becoming increasingly widespread
- the dynamics of hepatocellular carcinoma (tumour recurrence while waiting on the transplant list, administration of wait-and-see treatments)
- certain anatomopathological parameters (such as the macro-trabecular subtype of HCC).
The aim of our study is to develop a new score incorporating these factors in order to identify patients with hepatocellular carcinoma who could truly benefit from a liver transplant.
To answer the question posed in the research, data will be collected from 402 people who received a liver transplant for hepatocellular carcinoma at three hospitals in the Paris region between 1 January 2018 and 31 December 2023, and from 160 people at two international hospitals in Canada and Belgium.
Studieoversikt
Status
Detaljert beskrivelse
Hepatocellular carcinoma (HCC) is a major public health problem. It is the fifth most common cancer and the third leading cause of cancer death worldwide. Its prevalence continues to increase and mortality associated with HCC remains high, unlike the overall cancer mortality rate. Liver transplantation (LT) remains the only curative treatment option that addresses both the tumour disease and the underlying liver disease. However, this approach presents a major challenge: the occurrence of tumour recurrence after LT, which is highly morbid. Rigorous selection for LT of candidates with HCC is essential and is currently based on standardised scores, such as AFP, Milan or Up to Seven scores, which take into account tumour volume and the patient's general condition prior to LT.
The recent arrival of immunotherapy in the management of advanced HCC has opened up new prospects for LT. In particular, the question arises as to whether LT should be offered to patients initially diagnosed with advanced HCC who have benefited from downstaging treatments, including immunotherapy.
At the same time, due to the shortage of transplants, waiting times on the LT list are getting longer in some countries and patients are increasingly receiving expectant management for their HCC. They are exposed to the risk of HCC progression or recurrence while on the list, ruling out any possibility of subsequent LT. Certain histological subtypes of HCC, particularly macrotrabecular HCC, have recently been identified as being associated with a poor prognosis, but little data is available on the risk of recurrence of these HCCs after LT raising questions about the relevance of LT for these patients.
Finally, the impact of the choice of immunosuppression on the risk of HCC recurrence after LT remains largely unexplored.
Main objective:
In accordance with TRIPOD recommendations (40), the objective is to improve the predictive scores for LT failure in patients with HCC by analysing biological, clinical, imaging and anatomopathological parameters at enrolment. This score will also include the number and type of HCC recurrences, as well as the associated expectant management. The objective is to determine the threshold of predictive score for achieving a probability of LT failure in patients of less than 20%.
Secondary objectives:
- To study overall survival and recurrence-free survival in patients with a selection score with a previously identified LT failure target (defined as removal from the LT list or recurrence after LT) <20%.
- To compare the performance of different selection scores for LT eligibility (AFP score, Milan score, Up-to-Seven, newly identified score) on LT failure rate, overall survival and recurrence-free survival in patients with HCC.
- To assess the impact of HCC recurrence and watchful waiting on TH failure rate, overall survival and recurrence-free survival in HCC patients on the LT list.
- To assess the impact of HCC subtypes, particularly macro-trabecular HCC, on LT failure rates, overall survival and recurrence-free survival in patients on the LT waiting list.
- To assess the impact of underlying liver disease etiology and the presence of portal hypertension on LT failure rates, overall survival and recurrence-free survival in patients on the LT waiting list.
- To assess the impact of modulating immunosuppressive therapy on the risk of recurrence and the occurrence of rejection in patients transplanted for HCC.
Studietype
Registrering (Antatt)
Kontakter og plasseringer
Studiekontakt
- Navn: Manon Allaire, MD
- Telefonnummer: +33 1 42 16 10 34
- E-post: manon.allaire@aphp.fr
Studer Kontakt Backup
- Navn: Héloïse Giudicelli, MD
- E-post: heloise.giudicelli@gmail.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Prøvetakingsmetode
Studiepopulasjon
We will retrospectively include patients who underwent LT for HCC between 1 January 2018 and 31 December 2023 in the Paris, Montreal and Brussels centres.
The derivation cohort will include patients from the AP-HP, while the validation cohort will include patients from the centres in Montreal and Brussels.
Beskrivelse
Inclusion Criteria
- Adults (≥18 years).
- Underwent LT for HCC between January 1, 2018 and December 31, 2023.
Exclusion Criteria
- No evidence of HCC (imaging or histology).
- LT performed for another intrahepatic tumor other than HCC.
- The patient's objection to the use of their data.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Failure of liver transplantation (LT)
Tidsramme: Up to 7 years after LT
|
Failure of LT is defined as the occurrence of one of the following events: (i) removal from the transplant waiting list, (ii) recurrence of HCC post-LT, or (iii) death.
|
Up to 7 years after LT
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Overall survival
Tidsramme: Up to 7 years after LT
|
Up to 7 years after LT
|
|
Recurrence-free survival
Tidsramme: Up to 7 years after LT
|
Up to 7 years after LT
|
|
Occurrence of acute cellular rejection
Tidsramme: Up to 7 years after LT
|
Up to 7 years after LT
|
|
Correlation of LT failure rate, overall survival and recurrence-free survival with biological, clinical, imaging and anatomopathological parameters (macro-trabecular subtype) at enrolment and on the day of LT
Tidsramme: Up to 7 years after LT
|
Up to 7 years after LT
|
Samarbeidspartnere og etterforskere
Etterforskere
- Studiestol: Manon Allaire, MD, Assistance Publique - Hôpitaux de Paris
- Studieleder: Héloïse Giudicelli, MD, Sorbonne University, Paris, France
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- APHP251223
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .