New endpoints in adrenocortical carcinoma studies: a mini review.


Journal

Endocrine
ISSN: 1559-0100
Titre abrégé: Endocrine
Pays: United States
ID NLM: 9434444

Informations de publication

Date de publication:
09 2022
Historique:
received: 28 04 2022
accepted: 25 06 2022
pubmed: 24 7 2022
medline: 20 8 2022
entrez: 23 7 2022
Statut: ppublish

Résumé

Adrenocortical carcinoma (ACC) is a very rare and aggressive malignant disease. Therefore, overall survival (OS) has long been considered as the best endpoint. Yet, a unique endpoint is not optimal to take into account the heterogeneity in tumor profile and the diversification of therapeutic option. The purpose of this mini review was to describe endpoints used in the past, present and future in the field of ACC. Pubmed and Clinicaltrial.gov were used to identify relevant studies. Before year 2000 only three endpoints were regularly used: OS, recurrence-free survival (RFS) and response rate. These endpoints were used because ACC was seen as a homogeneous diseases with a high recurrence rate and low rate of long-term survival. Since 2000; along with the apparition of new class of drug, progression-free survival (PFS) has been more and more used. Other endpoints as "time to chemotherapy" or "Progression-free survival 2" were used to evaluate multimodal therapies or treatment with a delayed action. Finally, there is a hope that in the near future, quality of life along with other patient-reported outcomes may be used more frequently. While OS and PFS are currently the most used endpoints in ACC, new endpoints are needed to better take into account the challenges offered by different situations and treatment strategies.

Identifiants

pubmed: 35869971
doi: 10.1007/s12020-022-03128-2
pii: 10.1007/s12020-022-03128-2
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

419-424

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Matthieu Faron (M)

Department de Chirurgie Oncologique, Gustave Roussy Cancer Campus, Villejuif, France. Matthieu.faron@gustaveroussy.fr.
INSERM 1018, Equipe Oncostat, Université Paris Saclay, Gif-sur-Yvette, France. Matthieu.faron@gustaveroussy.fr.

Livia Lamartina (L)

Service d'oncologie Endocrinienne, Département d'imagerie, Gustave Roussy, Villejuif, France.

Segolene Hescot (S)

Service de Médecine Nucléaire, Institute Curie, Saint-Cloud, France.

Sophie Moog (S)

Service d'oncologie Endocrinienne, Département d'imagerie, Gustave Roussy, Villejuif, France.

Frederic Deschamps (F)

Service de Radiologie Interventionelle, Gustave Roussy Cancer Campus, Villejuif, France.

Charles Roux (C)

Service de Radiologie Interventionelle, Gustave Roussy Cancer Campus, Villejuif, France.

Rosella Libe (R)

Coordinator of the INCA-COMETE Network, Gustave Roussy Cancer Campus, Villejuif, France.
Service d'Endocrinologie, Cochin Hospital, Paris, France.

Jerome Durand-Labrunie (J)

Service de d'onco-radiothérapie, Gustave Roussy Cancer Campus, Villejuif, France.

Abir Al Ghuzlan (A)

Service d'anatomopathologie, Gustave Roussy Cancer Campus, Villejuif, France.

Julien Hadoux (J)

Service d'oncologie Endocrinienne, Département d'imagerie, Gustave Roussy, Villejuif, France.

Eric Baudin (E)

Service d'oncologie Endocrinienne, Département d'imagerie, Gustave Roussy, Villejuif, France.

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