Therapeutic sequencing in the era of first-line immune checkpoint inhibitor combinations, a novel challenge in patients with metastatic clear-cell renal cell carcinoma.

Carcinome rénal Deuxième ligne Immune checkpoint Inhibiteurs de points Inhibiteurs de tyrosine Metastatic clear-cell Second line Tyrosine kinase de contrôle immunitaires inhibitors kinase renal cell carcinoma à cellules claires

Journal

Bulletin du cancer
ISSN: 1769-6917
Titre abrégé: Bull Cancer
Pays: France
ID NLM: 0072416

Informations de publication

Date de publication:
May 2022
Historique:
entrez: 27 6 2022
pubmed: 28 6 2022
medline: 30 6 2022
Statut: ppublish

Résumé

Immune checkpoint inhibitor combinations have reshaped the treatment landscape of metastatic clear-cell renal cell carcinoma. As four regimens are now approved in the first-line setting, including nivolumab plus ipilimumab in intermediate and poor-risk patients, and pembrolizumab plus lenvatinib, nivolumab plus cabozantinib and pembrolizumab plus axitinib in all-comers, the choice of subsequent therapies is becoming a novel challenge for physicians. Such choices now rely on several compounds used as monotherapy which have demonstrated sustained activity after previous immune checkpoint or tyrosine kinase inhibitors. Future strategies may lie in novel targets, including hypoxia-inducible factor inhibitors, as well as further exploration of combinations in more advanced settings. Here we review the current evidence regarding treatment activity after immune checkpoint inhibitor combinations, the underlying biological and clinical challenges that may impact patient selection and the optimal sequencing strategies for clinical practice.

Identifiants

pubmed: 35760468
pii: S0007-4551(22)00236-3
doi: 10.1016/S0007-4551(22)00236-3
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0
Nivolumab 31YO63LBSN
Sunitinib V99T50803M

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2S31-2S38

Informations de copyright

Copyright © 2022 Elsevier Masson SAS. Tous droits réservés.

Auteurs

Ronan Flippot (R)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France. Electronic address: ronan.flippot@gustaveroussy.fr.

Violaine Gorgeu (V)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Marc Pujalte (M)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Emeline Colomba (E)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Carolina Alves (C)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Luigi Cerbone (L)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Lucia Carril (L)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Lisa Derosa (L)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Bernard Escudier (B)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

Laurence Albigès (L)

Department of Cancer Medicine, Gustave Roussy, Paris Saclay University, Villejuif, France.

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Classifications MeSH