Second-line treatment and prognostic factors in neuroendocrine carcinoma: the RBNEC study.


Journal

Endocrine-related cancer
ISSN: 1479-6821
Titre abrégé: Endocr Relat Cancer
Pays: England
ID NLM: 9436481

Informations de publication

Date de publication:
01 10 2022
Historique:
received: 30 05 2022
accepted: 29 06 2022
pubmed: 4 8 2022
medline: 19 8 2022
entrez: 3 8 2022
Statut: epublish

Résumé

Neuroendocrine carcinomas (NEC) are aggressive malignant diseases. Etoposide-based rechallenge (EBR) and the prognostic role of RB transcriptional corepressor 1 (RB1) status in second-line chemotherapy (2L) have not been studied. The objectives of this study were to report the results of 2L including EBR as well as prognostic factors in a national retrospective multicentre study. NEC patients treated with 2L and further, with tissue samples available, were included. RB1 status and morphological classification were reviewed centrally. Among the 121 NEC patients (40% female, median age 61 years) included, there were 73 small-cell NEC (60%), 34 large-cell NEC (28%) and 14 NEC (not otherwise specified, 12%). Primary sites were lung (39%), gastroenteropancreatic (36%), other (13%) and unknown (12%). Median Ki-67 index was 80%. Median progression-free survival (PFS) and overall survival (OS) under 2L were 2.1 and 6.2 months, respectively. No difference was observed between patients who received an 'adenocarcinoma-like' or a 'neuroendocrine-like' 2L or according to the RB1 status. Thoracic NEC primary was the only adverse prognostic factor for OS. EBR, administered to 31 patients, resulted in a 62% disease control rate with a median PFS and OS of 3.2 and 11.7 months, respectively. In the 94 patients with a relapse-free interval of ≥3 months after first-line platinum-etoposide chemotherapy, the median OS was 12 months in patients who received EBR as compared to 5.9 months in patients who did not (P = 0.043). EBR could be the best 2L option for patient with initial response to first-line platinum-etoposide lasting at least 3 months. RB1 status does not provide prognostic information in this setting.

Identifiants

pubmed: 35920609
doi: 10.1530/ERC-22-0102
doi:

Substances chimiques

Platinum 49DFR088MY
Etoposide 6PLQ3CP4P3

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

569-580

Auteurs

Julien Hadoux (J)

Oncologie Endocrinienne, Département d'Imagerie, Gustave Roussy, Villejuif, France.

Thomas Walter (T)

Service d'Oncologie, ENETS Centre of Excellence, Hospices Civils de Lyon et Université de Lyon, Lyon, France.

Christina Kanaan (C)

Service de Pathologie, Département de Biologie et Pathologie Médicale, Gustave Roussy, Villejuif, France.

Ségolène Hescot (S)

Département d'Oncologie, Institut Curie, Paris, France.

Vincent Hautefeuille (V)

Service d'Hépato-gastro-entérologie et Cancérologie Digestive, CHU Amiens Picardie, Amiens, France.

Marine Perrier (M)

Département d'Hépato-gastro-entérologie, CHU de Reims, Reims, France.

Igor Tauveron (I)

Service d'Endocrinologie, Diabétologie et Maladies Métaboliques, CHU Clermont-Ferrand, Clermont-Ferrand, France.
Laboratoire GReD, Université Clermont Auvergne, Clermont-Ferrand, France.

Sandrine Laboureau (S)

Département d'Endocrinologie-Diabétologie-Nutrition, CHU d'Angers, Angers Cedex 9, France.

Christine Do Cao (C)

CHU de Lille, Service d'Endocrinologie, Lille, France.

Caroline Petorin (C)

CHU Clermont-Ferrand, Service de Chirurgie Digestive et Hépatobiliaire, Clermont-Ferrand, France.

Odile Blanchet (O)

CRB, CHU d'Angers, Angers Cedex 9, France.

Matthieu Faron (M)

Département de Chirurgie, Gustave Roussy, Villejuif, France.

Emmanuelle Leteurtre (E)

CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, Université de Lille, CNRS, Inserm, CHU Lille, UMR9020-U1277, Lille, France.

Marie-Christine Rousselet (MC)

Département de Pathologie, CHU d'Angers, Angers Cedex 9, France.

Juliette Joubert Zakeyh (J)

Laboratoire d'Anatomie Pathologique, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Aude Marchal (A)

Service d'Anatomo-Pathologie, CHU Reims, Reims, France.

Denis Chatelain (D)

Service d'Anatomo-Pathologie, CHU Amiens, Amiens, France.

Clément Beaulaton (C)

Service d'Anatomo-Pathologie, Institut Curie, Paris, France.

Valérie Hervieu (V)

Service d'Anatomo-Pathologie, ENETS Centre of Excellence, Hospices Civils de Lyon et Université de Lyon, Lyon, France.

Catherine Lombard-Bohas (C)

Service d'Oncologie, ENETS Centre of Excellence, Hospices Civils de Lyon et Université de Lyon, Lyon, France.

Michel Ducreux (M)

Service d'Oncologie Digestive, Département de Médecine, Gustave Roussy, Villejuif, France.
Faculté de Médecine, Université Paris Saclay, Le Kremlin-Bicêtre, France.

Jean-Yves Scoazec (JY)

Service de Pathologie, Département de Biologie et Pathologie Médicale, Gustave Roussy, Villejuif, France.
Faculté de Médecine, Université Paris Saclay, Le Kremlin-Bicêtre, France.

Eric Baudin (E)

Oncologie Endocrinienne, Département d'Imagerie, Gustave Roussy, Villejuif, France.

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Classifications MeSH