Loco-Regional Therapies in Oligometastatic Adrenocortical Carcinoma.

adrenocortical carcinoma interventional radiology loco-regional treatments oligometastatic prognosis factors

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
31 May 2022
Historique:
received: 20 04 2022
revised: 27 05 2022
accepted: 30 05 2022
entrez: 10 6 2022
pubmed: 11 6 2022
medline: 11 6 2022
Statut: epublish

Résumé

Objective: The recommended first-line treatment for low-tumor-burden ACC (stage IVa ACC) not amenable to radical resection is mitotane in association with loco-regional treatments (LRs). The aim of this study was to determine the patient population that would benefit the most from LR. Materials and methods: This retrospective monocentric expert center chart review study was performed from 2008 to 2021 and included stage IVa patients (≤2 tumoral organs) treated with LR (either radiotherapy, surgery, or interventional radiology). The primary endpoint was disease control (DC). Correlations between DC, time to systemic chemotherapy (TTC), overall survival (OS), and tumor characteristics were analyzed using Kaplan−Meier survival analysis and Cox’s proportional hazards regression model for multivariate analysis. Results: Thirty-four women (57%) and 26 men with a median age of 48.1 years (IQR: 38.3−59.8) were included. One hundred and nine LRs were performed, with a median of 2 (IQR: 1−3) per patient. DC was achieved in 40 out of 60 patients (66.7%). Patients with DC had a significantly longer TTC (HR: 0.27, p < 0.001) and OS (HR: 0.22, p < 0.001). Patients with less than or equal to 5 metastases (HR: 6.15 (95% CI: 1.88−20.0), p = 0.002) or a maximum metastasis diameter below 3 cm had higher rates of DC (HR: 3.78 (95% CI: 1.09−13.14), p = 0.035). Conclusion: stage IVa ACC patients with ≤5 metastases or a maximum metastasis diameter below 3 cm had favorable responses to LR. We propose the name oligometastatic ACC for this subgroup of patients.

Identifiants

pubmed: 35681708
pii: cancers14112730
doi: 10.3390/cancers14112730
pmc: PMC9179919
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Charles Roux (C)

Gustave Roussy, Département de Radiologie Interventionnelle, F-94805 Villejuif, France.

Alice Boileve (A)

Gustave Roussy, Département D'oncologie Endocrinienne, F-94805 Villejuif, France.

Matthieu Faron (M)

Gustave Roussy, Département de Chirurgie, F-94805 Villejuif, France.

Livia Lamartina (L)

Gustave Roussy, Département D'oncologie Endocrinienne, F-94805 Villejuif, France.

Alexandre Delpla (A)

Gustave Roussy, Département de Radiologie Interventionnelle, F-94805 Villejuif, France.

Lambros Tselikas (L)

Gustave Roussy, Département de Radiologie Interventionnelle, F-94805 Villejuif, France.

Jérome Durand-Labrunie (J)

Gustave Roussy, Département de Radiothérapie, F-94805 Villejuif, France.

Segolène Hescot (S)

Institut Curie, Département de Médecine Oncologique, F-75005 Paris, France.

Thierry de Baere (T)

Gustave Roussy, Département de Radiologie Interventionnelle, F-94805 Villejuif, France.

Julien Hadoux (J)

Gustave Roussy, Département D'oncologie Endocrinienne, F-94805 Villejuif, France.

Frederic Deschamps (F)

Gustave Roussy, Département de Radiologie Interventionnelle, F-94805 Villejuif, France.

Eric Baudin (E)

Gustave Roussy, Département D'oncologie Endocrinienne, F-94805 Villejuif, France.

Classifications MeSH