Efficacy of administration sequence: Sacituzumab Govitecan and Trastuzumab Deruxtecan in HER2-low metastatic breast cancer.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
25 Jun 2024
Historique:
received: 31 03 2024
accepted: 13 06 2024
revised: 11 06 2024
medline: 26 6 2024
pubmed: 26 6 2024
entrez: 25 6 2024
Statut: aheadofprint

Résumé

Current guidelines recommend that patients with HER2-low metastatic breast cancer (MBC) receive sequentially two antibody-drug conjugates (ADCs): Sacituzumab Govitecan (SG) and Trastuzumab Deruxtecan (T-DXd), despite a similar payload. However, the effectiveness of one after another is unknown. ADC-Low is a multicentre, retrospective study evaluating the efficacy of SG and T-DXd, one after another, with or without intermediary lines of chemotherapy, in patients with HER2-low MBC. One hundred and seventy-nine patients were included: the majority with HR-negative tumours received SG first (ADC1) (n = 100/108) while most with HR-positive tumours received T-DXd first (n = 56/71). Median progression-free survival 2 was short: 2.7 months (95% CI: 2.4-3.3) in the whole population, respectively, 3.1 (95% CI: 2.6-3.6) and 2.2 months (95% CI: 1.9-2.7) for patients receiving T-DXd or SG second (ADC2). Intermediary lines of chemotherapy between ADC1 and ADC2 had no impact. Primary resistance to ADC2 occurred in 54.4% of patients. Certain patients showed initial response to ADC2. Clinical benefit of sequentially administered SG and T-DXd is limited for most patients. Nevertheless, a subset of patients might benefit-on the short term-from a second ADC. Additional studies are needed to identify patients who could benefit from two ADCs with similar payloads.

Sections du résumé

BACKGROUND BACKGROUND
Current guidelines recommend that patients with HER2-low metastatic breast cancer (MBC) receive sequentially two antibody-drug conjugates (ADCs): Sacituzumab Govitecan (SG) and Trastuzumab Deruxtecan (T-DXd), despite a similar payload. However, the effectiveness of one after another is unknown.
METHODS METHODS
ADC-Low is a multicentre, retrospective study evaluating the efficacy of SG and T-DXd, one after another, with or without intermediary lines of chemotherapy, in patients with HER2-low MBC.
RESULTS RESULTS
One hundred and seventy-nine patients were included: the majority with HR-negative tumours received SG first (ADC1) (n = 100/108) while most with HR-positive tumours received T-DXd first (n = 56/71). Median progression-free survival 2 was short: 2.7 months (95% CI: 2.4-3.3) in the whole population, respectively, 3.1 (95% CI: 2.6-3.6) and 2.2 months (95% CI: 1.9-2.7) for patients receiving T-DXd or SG second (ADC2). Intermediary lines of chemotherapy between ADC1 and ADC2 had no impact. Primary resistance to ADC2 occurred in 54.4% of patients. Certain patients showed initial response to ADC2.
CONCLUSIONS CONCLUSIONS
Clinical benefit of sequentially administered SG and T-DXd is limited for most patients. Nevertheless, a subset of patients might benefit-on the short term-from a second ADC. Additional studies are needed to identify patients who could benefit from two ADCs with similar payloads.

Identifiants

pubmed: 38918555
doi: 10.1038/s41416-024-02766-9
pii: 10.1038/s41416-024-02766-9
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer Nature Limited.

Références

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Auteurs

F Poumeaud (F)

Department of Medical Oncology, Oncopole Claudius Regaud, IUCT-O, Toulouse, France. poumeaud.francois@iuct-oncopole.fr.

M Morisseau (M)

Biostatistics & Health Data Science Unit, Oncopole Claudius Regaud IUCT-O, Toulouse, France.

L Cabel (L)

Department of Medical Oncology, Institut Curie, Paris, France.

A Gonçalves (A)

Aix-Marseille University, CNRS, INSERM, Institut Paoli-Calmettes, Department of Medical Oncology, CRCM, Marseille, France.

C Rivier (C)

Department of Medical Oncology, Centre Léon Bérard, Cancer Research Center of Lyon (UMR Inserm 1052 - CNRS 5286), Lyon, France.

O Trédan (O)

Department of Medical Oncology, Centre Léon Bérard, Cancer Research Center of Lyon (UMR Inserm 1052 - CNRS 5286), Lyon, France.

E Volant (E)

Department of Medical Oncology, Institut de cancérologie de l'Ouest, Saint-Herblain, France.

J-S Frenel (JS)

Department of Medical Oncology, Institut de cancérologie de l'Ouest, Saint-Herblain, France.

S Ladoire (S)

Department of Medical Oncology, Centre Georges-François Leclerc, INSERM U1231, Dijon, France.

W Jacot (W)

Department of Medical Oncology, Institut du Cancer de Montpellier, Montpellier University, INSERM U1194, Montpellier, France.

M Jamelot (M)

Department of Medical Oncology and Cellular Therapy, Faculté de médecine Sorbonne Université, Hôpital Tenon, Paris, France.

H Foka Tichoue (H)

Department of Medical Oncology, Hôpital de la Pitié-Salpêtrière, Institut Universitaire de Cancérologie AP-HP, Sorbonne Université, Paris, France.

A Patsouris (A)

Department of Medical Oncology, Institut de Cancérologie de l'Ouest Pays de la Loire, Angers, France.

L Teixeira (L)

Department of Medical Oncology, INSERM U976, Université de Paris Cité, Hopital Saint Louis, Paris, France.

F-C Bidard (FC)

Department of Medical Oncology, Institut Curie, Saint-Cloud, France.
Versailles Saint-Quentin University, Paris Saclay, Saint-Cloud, France.

D Loirat (D)

Department of Medical Oncology, Institut Curie, Paris, France.

M Brunet (M)

Clinical Trials Department - Breast Cancers, Institut Bergonié, Bordeaux, France.

C Levy (C)

Department of Medical Oncology, Centre François Baclesse, Caen, France.

C Bailleux (C)

Department of Medical Oncology, Centre Antoine Lacassagne, Nice, France.

B Cabarrou (B)

Biostatistics & Health Data Science Unit, Oncopole Claudius Regaud IUCT-O, Toulouse, France.

A Deleuze (A)

Department of Medical Oncology, Centre Eugène Marquis, Rennes, France.

L Uwer (L)

Department of Medical Oncology, Institut de Cancérologie de Lorraine, Nancy, France.

E Deluche (E)

Department of Medical Oncology, Centre Hospitalier Universitaire de Limoges, Limoges, France.

T Grellety (T)

Department of Medical Oncology, Centre Hospitalier de la côte basque, Bayonne, France.

C Franchet (C)

Department of Pathology, Oncopole Claudius Regaud, IUCT-O, Toulouse, France.

F Fiteni (F)

Department of Medical Oncology, University Hospital, Nimes, France.
UMR INSERM IDESP-Desbrest Institute of Epidemiology and Public Health, University of Montpellier, Montpellier, France.

H Bischoff (H)

Department of Medical Oncology, Institut de Cancérologie de Strasbourg Europe, Strasbourg, France.

R Vion (R)

Department of Medical Oncology, Centre Henri Becquerel, Rouen, France.

M Pagliuca (M)

University Paris-Saclay, Gustave Roussy, INSERM U981, Molecular Predictors and New Targets in Oncology, Villejuif, France.
Division of Breast Medical Oncology, Instituto Nazionale Tumori - IRCCS - Fondazione G. Pascale, Napoli, Italia.

B Verret (B)

Departmentof Medical Oncology, Institut Gustave Roussy, Paris, France.

S Bécourt (S)

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

T Reverdy (T)

Department of Medical Oncology, Institut de Cancérologie des Hospices Civils de Lyon (IC-HCL), Université Lyon 1, Lyon, France.

A de Nonneville (A)

Aix-Marseille University, CNRS, INSERM, Institut Paoli-Calmettes, Department of Medical Oncology, CRCM, Marseille, France.

F Dalenc (F)

Department of Medical Oncology, Oncopole Claudius Regaud, IUCT-O, Toulouse, France.

Classifications MeSH