Relevance of body mass index as a predictor of systemic therapy outcomes in metastatic melanoma: analysis of the MelBase French cohort data☆
- Creators
- Di Filippo, Y.
- Dalle, S.
- Mortier, L.
- Dereure, O.
- Dalac, S.
- Dutriaux, C.
- Leccia, M.-T.
- Legoupil, D.
- Saiag, P.
- Brunet-Possenti, F.
- Arnnault, J.-P.
- Maubec, E.
- Granel-Brocard, F.
- de Quatrebarbes, J.
- Aubin, F.
- Lesimple, T.
- Beylot-Barry, M.
- Stoebner, P.-E.
- Dupuy, A.
- Stephan, A.
- Grob, J.-J.
- Lefevre, W.
- Oriano, B.
- Allayous, C.
- Lebbé, C.
- Montaudié, H.
- Others:
- Centre Hospitalier Universitaire de Nice (CHU Nice)
- Centre méditerranéen de médecine moléculaire (C3M) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS) ; COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Côte d'Azur (UCA)
- Hospices Civils de Lyon (HCL)
- Centre de Recherche en Cancérologie de Lyon (UNICANCER/CRCL) ; Centre Léon Bérard [Lyon]-Université Claude Bernard Lyon 1 (UCBL) ; Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
- Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)
- Université de Lille
- Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
- Pathogénèse et contrôle des infections chroniques (PCCI) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre Hospitalier Universitaire de Montpellier (CHU Montpellier )
- Service de Dermatologie (CHU de Dijon) ; Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)
- Service de dermatologie [Bordeaux] ; Université Bordeaux Segalen - Bordeaux 2-CHU Bordeaux [Bordeaux]-Hôpital Haut-Lévêque [CHU Bordeaux] ; CHU Bordeaux [Bordeaux]
- CHU Grenoble
- Université Grenoble Alpes (UGA)
- Centre Hospitalier Régional Universitaire de Brest (CHRU Brest)
- Hôpital Ambroise Paré [AP-HP]
- Biomarqueurs et essais cliniques en Cancérologie et Onco-Hématologie (BECCOH) ; Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Université Paris-Saclay
- AP-HP - Hôpital Bichat - Claude Bernard [Paris] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Service de dermatologie [CHU d'Amiens-Picardie] ; CHU Amiens-Picardie
- Service de dermatologie [Avicenne] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Avicenne [AP-HP] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Sorbonne Paris Nord
- Service de Dermatologie et Allergologie [CHRU Nancy] ; Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy)
- Centre Hospitalier Annecy-Genevois [Saint-Julien-en-Genevois]
- Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)
- CRLCC Eugène Marquis (CRLCC)
- Centre Hospitalier Universitaire de Nîmes (CHU Nîmes)
- Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM) ; Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
- Service de Dermatologie [Rennes] = Dermatology [Rennes] ; CHU Pontchaillou [Rennes]
- Service de Dermatologie [CHU Caen] ; Université de Caen Normandie (UNICAEN) ; Normandie Université (NU)-Normandie Université (NU)-CHU Caen ; Normandie Université (NU)-Tumorothèque de Caen Basse-Normandie (TCBN)-Tumorothèque de Caen Basse-Normandie (TCBN)
- Service de dermatologie, vénéreologie et cancérologie cutanée [Hôpital de la Timone - APHM] ; Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)- Hôpital de la Timone [CHU - APHM] (TIMONE)
- Service de Dermatologie [AP-HP Hôpital Saint-Louis] ; Hopital Saint-Louis [AP-HP] (AP-HP) ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
- Immunologie humaine, physiopathologie & immunothérapie (HIPI (UMR_S_976 / U976)) ; Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)
- Centre d'épidémiologie Clinique [Hôtel-Dieu] ; Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Hôpital Hôtel Dieu
Description
Background: The 'obesity paradox' suggests that higher body mass index (BMI) is associated with better survival values in metastatic melanoma patients, especially those receiving targeted and immune checkpoint inhibitor therapy. Higher BMI is also associated with higher incidences of treatment-related adverse events (TRAEs). This study assesses whether BMI is associated with survival outcomes and adverse events in metastatic melanoma patients with systemic therapy.Patients and methods: This multicentric retrospective study, conducted from 1 March 2013 to 29 April 2019, enrolled adults with unresectable stage III or IV melanoma from the French multicentric prospective cohort-MelBase (NCT02828202). Patients with first-line chemotherapy and targeted and immune therapy were included. Underweight people and those with metastatic mucosal or ocular melanoma were excluded. BMI was categorized using the World Health Organization criteria. Co-primary outcomes included the association between BMI and progression-free survival and overall survival, stratified by treatment type, sex, and age. Secondary endpoints were the association of BMI with overall response and TRAEs. Multivariate analyses were carried out.Results: A total of 1214 patients were analyzed. Their median age was 66.0 years (range, 53-75). Male predominance was observed [n = 738 (61%)]. Most patients received immune checkpoint inhibitor therapy (63%), followed by targeted therapy (32%), and had stage M1c disease (60.5%). Obese patients represented 22% of the cohort. The median follow-up duration was 13.5 months (range, 6.0-27.5). In the pooled analysis, no positive or negative association between BMI and progression-free survival (P = 0.88)/overall survival (P = 0.25) was observed, regardless of treatment type, sex, and age. These results were nonsignificant in the univariate and multivariate analyses. The objective response rate, according to BMI category, did not differ significantly regardless of age. TRAEs were not associated with BMI.Conclusion: The observed lack of an association between BMI and survival demonstrates that BMI is not a valuable marker of systemic treatment-related outcomes in metastatic melanoma. Future approaches might focus on the whole-body distribution.
Abstract
International audience
Additional details
- URL
- https://hal.umontpellier.fr/hal-03169422
- URN
- urn:oai:HAL:hal-03169422v1
- Origin repository
- UNICA