Treatment strategies for thymic carcinoma in a real-life setting. Insights from the RYTHMIC network.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
02 2022
Historique:
received: 09 07 2021
revised: 31 10 2021
accepted: 28 11 2021
pubmed: 30 12 2021
medline: 22 4 2022
entrez: 29 12 2021
Statut: ppublish

Résumé

Thymic carcinomas are aggressive and difficult to treat a subset of thymic epithelial tumours that represent a heterogeneous group of rare intrathoracic malignancies. The treatment strategy of thymic carcinomas is based on whether surgical resection may be achieved, which represents the most significant favourable prognostic factor on survival. For this study, we took advantage of the unique prospective Réseau tumeurs THYMiques et Cancer (RYTHMIC) database to describe baseline characteristics, analyse treatment strategies in light of existing guidelines and provide landmark patient outcomes data with regards to response and survival of patients in a real-life clinical practice setting. Inclusion criteria for this analysis were the following: (1) histologically-confirmed thymic carcinomas - excluding neuroendocrine tumours-after pathological review by the RYTHMIC pathology panel, (2) discussion of the case at the RYTHMIC multidisciplinary tumour board, (3) at least one active treatment modality. A total of 213 patients were analysed. Overall, 60 (28%) patients were considered as surgical candidates upfront, 91 (43%) patients received primary chemotherapy, and 62 (29%) patients received exclusive chemotherapy. Median overall survival (OS) was 49.2 months (IC95%: 34.8-63.6); OS was significantly longer in patients with a lower stage at diagnosis (p < 0.001), who were operated on upfront, as opposed to patients who received primary or exclusive chemotherapy (p < 0.001). Surgery, conducted upfront or after primary chemotherapy, was significantly associated with more prolonged OS (p < 0.001); complete resection and postoperative radiotherapy were also predictors of better outcome (p = 0.018 and p = 0.051, respectively). Our cohort is the first to analyse in-depth outcomes and treatment strategies in a prospective cohort of consecutive patients with thymic carcinoma. While we confirm the major prognostic impact of surgery, our data highlight the need for optimised multidisciplinary management and innovative therapies as the survival of patients remains limited.

Sections du résumé

BACKGROUND
Thymic carcinomas are aggressive and difficult to treat a subset of thymic epithelial tumours that represent a heterogeneous group of rare intrathoracic malignancies. The treatment strategy of thymic carcinomas is based on whether surgical resection may be achieved, which represents the most significant favourable prognostic factor on survival. For this study, we took advantage of the unique prospective Réseau tumeurs THYMiques et Cancer (RYTHMIC) database to describe baseline characteristics, analyse treatment strategies in light of existing guidelines and provide landmark patient outcomes data with regards to response and survival of patients in a real-life clinical practice setting.
METHODS
Inclusion criteria for this analysis were the following: (1) histologically-confirmed thymic carcinomas - excluding neuroendocrine tumours-after pathological review by the RYTHMIC pathology panel, (2) discussion of the case at the RYTHMIC multidisciplinary tumour board, (3) at least one active treatment modality.
RESULTS
A total of 213 patients were analysed. Overall, 60 (28%) patients were considered as surgical candidates upfront, 91 (43%) patients received primary chemotherapy, and 62 (29%) patients received exclusive chemotherapy. Median overall survival (OS) was 49.2 months (IC95%: 34.8-63.6); OS was significantly longer in patients with a lower stage at diagnosis (p < 0.001), who were operated on upfront, as opposed to patients who received primary or exclusive chemotherapy (p < 0.001). Surgery, conducted upfront or after primary chemotherapy, was significantly associated with more prolonged OS (p < 0.001); complete resection and postoperative radiotherapy were also predictors of better outcome (p = 0.018 and p = 0.051, respectively).
CONCLUSIONS
Our cohort is the first to analyse in-depth outcomes and treatment strategies in a prospective cohort of consecutive patients with thymic carcinoma. While we confirm the major prognostic impact of surgery, our data highlight the need for optimised multidisciplinary management and innovative therapies as the survival of patients remains limited.

Identifiants

pubmed: 34965496
pii: S0959-8049(21)01247-8
doi: 10.1016/j.ejca.2021.11.028
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

118-127

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement N. Girard reports grants and personal fees from BMS, grants and personal fees from MSD, grants and personal fees from Pfizer, during the conduct of the study. Other authors have nothing to disclose.

Auteurs

Arthur Petat (A)

Respiratory Medicine Department, Hospices Civils de Lyon, Lyon, France; University of Lyon, University Claude Bernard Lyon 1, Lyon, France.

Eric Dansin (E)

Medical Oncology Department, Centre Oscar Lambret, Lille, France.

Fabien Calcagno (F)

Medical Oncology Department, University Hospital, Besançon, France.

Laurent Greillier (L)

Multidisciplinary Oncology and Therapeutic Innovations Department, Hôpital Nord, APHM, Aix Marseille Univ, INSERM, CNRS, CRCM, Marseille, France.

Eric Pichon (E)

Respiratory Medicine Department, University Hospital, Tours, France.

Mallorie Kerjouan (M)

Respiratory Medicine Department, University Hospital, Rennes, France.

Christelle Clement-Duchene (C)

Medical Oncology Department, Cancer Institute, Nancy, France.

Bertrand Mennecier (B)

Respiratory Medicine Department, University Hospital, Strasbourg, France.

Virginie Westeel (V)

Respiratory Medicine Department, University Hospital, Besançon, France.

François Thillays (F)

Radiation Oncology Department, Institut de Cancérologie de l'Ouest, Nantes, France.

Xavier Quantin (X)

Respiratory Medicine Department, Montpellier Cancer Institute, Montpellier, France.

Youssef Oulkhouir (Y)

Respiratory Medicine Department, University Hospital, Caen, France.

Luc Thiberville (L)

Respiratory Medicine Department, University Hospital, Rouen, France.

Charles Ricordel (C)

Respiratory Medicine Department, University Hospital, Rennes, France.

Vincent Thomas De Montpreville (V)

Pathology Department, Marie Lannelongue Center, Le Plessis Robinson, France.

Lara Chalabreysse (L)

Pathology Department, Hospices Civils de Lyon, Lyon, France.

Véronique Hofman (V)

Pathology Department, University Hospital, Nice, France.

Thierry Molina (T)

Pathology Department, Necker Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.

Pierre Fournel (P)

Medical Oncology Department, Institut de Cancérologie de la Loire, Saint-Etienne, France.

Laurence Bigay Game (L)

Respiratory Medicine Department, University Hospital, Toulouse, France.

Benjamin Besse (B)

Medical Oncology Department, Gustave Roussy, Villejuif, France.

Nicolas Girard (N)

Institut Curie, Institut du Thorax Curie Montsouris, Paris, France. Electronic address: nicolas.girard2@curie.fr.

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Classifications MeSH