Paclitaxel-bevacizumab combination in advanced non-squamous non-small-cell lung cancer (NSCLC): AVATAX, a retrospective multicentric study.

NSCLC bevacizumab chemotherapy immunotherapy non-small cell lung cancer paclitaxel

Journal

Therapeutic advances in medical oncology
ISSN: 1758-8340
Titre abrégé: Ther Adv Med Oncol
Pays: England
ID NLM: 101510808

Informations de publication

Date de publication:
2022
Historique:
received: 27 02 2022
accepted: 21 04 2022
entrez: 13 6 2022
pubmed: 14 6 2022
medline: 14 6 2022
Statut: epublish

Résumé

Compared with docetaxel, the phase-III trial, ULTIMATE, showed a significant improvement of progression-free survival (PFS) with paclitaxel-bevacizumab combination (PB) as second- or third-line treatment in advanced non-small cell lung cancer (NSCLC). With the increase of immunotherapy treatment in first-line settings, the optimal treatment after first-line failure must be redefined. This multicentric retrospective study identified all advanced NSCLC patients treated with PB as second-line therapy and beyond. The main efficacy outcomes assessed were objective response rate (ORR), disease control rate (DCR), PFS, and overall survival (OS). The adverse events were reported according to Common Terminology Criteria for Adverse Events (CTCAE). From January 2010 to February 2020, 314 patients in 16 centers received the PB combination. Most patients were male (55%), with a median age of 60 years (19-82), 95% had adenocarcinoma, 27% had a performance status ⩾2, 45% had brain metastases at the time of inclusion. They mostly received the PB combination either in second (20%) or in third-line (39%), and 28% were treated just after ICI failure. ORR and DCR were 40% and 77%, respectively; median PFS and OS were 5.7 [interquartile range (IQR): 3.2-9.6] and 10.8 [IQR: 5.3-19.6] months, respectively. All grade adverse events concerned 82% of patients, including 53% asthenia and 39% neurotoxicity, and 25% of patients continued monotherapy (mostly with bevacizumab) alone due to toxicity. Median PFS for patients treated after ICI failure (ICI+) was significantly superior compared with those not previously treated with ICI (ICI-): 7.0 [IQR: 4.2-11.0] PB combination as second-line treatment or beyond for advanced non-squamous NSCLC had acceptable toxicity and a clinically relevant efficacy and is an option as salvage treatment for these patients, more particularly after ICI progression.

Identifiants

pubmed: 35694190
doi: 10.1177/17588359221099399
pii: 10.1177_17588359221099399
pmc: PMC9174558
doi:

Types de publication

Journal Article

Langues

eng

Pagination

17588359221099399

Informations de copyright

© The Author(s), 2022.

Déclaration de conflit d'intérêts

Conflict of interest statement: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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Auteurs

Geoffroy Bilger (G)

Centre Hospitalier Universitaire de Grenoble, 38700 Grenoble, France. Oncology, Grenoble University Hospital, Grenoble, France.

Anne-Claire Toffart (AC)

Centre Hospitalier Universitaire de Grenoble, Grenoble, FranceOncology, Grenoble University Hospital, Grenoble, France.

Marie Darrason (M)

Service de Pneumologie Aigue Spécialisée et Cancérologie Thoracique, Hôpital Lyon-Sud, CHU Lyon, Pierre-Bénite, France.

Michaël Duruisseaux (M)

URCOT, Institut de Cancérologie des Hospices Civils de Lyon, Lyon, France.

Lucie Ulmer (L)

Thoracic Oncology Department, Hospital Albert Calmette, Lille, France.

Pascal Wang (P)

Thoracic Oncology, APHP, Paris, France.

Etienne Giroux Leprieur (EG)

APHP Hopital Ambroise Pare and Universite Paris-Saclay, Boulogne-Billancourt, France.

Nicolas Girard (N)

Institut Curie, Paris, France.

Marie Ange Massiani (MA)

Oncology Hospital Rene Huguenin, Saint-Cloud, France.

Paul Bore (P)

Thoracic Oncology Department, Hospital Morvan, Brest, France.

Renaud Descourt (R)

Thoracic Oncology Department, Hospital Morvan, Brest, France.

Julian Pinsolle (J)

Unité de pneumologie, Centre Hospitalier Métropole Savoie, Chambéry, France.

Solene Valery (S)

Thoracic Oncology, APHP, Paris, France.

Isabelle Monnet (I)

Pneumology Department, CHI Creteil, Creteil, France.

Aurélie Swalduz (A)

Department of Thoracic Oncology, Centre Léon Bérard, Lyon, France.

Claire Tissot (C)

Pneumology Department, Institut de Cancérologie de la Loire Lucien Neuwirth, Saint-Priest-en-Jarez, France.

Pierre Fournel (P)

Service d'Oncologie Médicale, Institut de Cancérologie, CHU de Saint-Etienne, Saint-Etienne Cedex 2, France.

Anne Baranzelli (A)

Unité de pneumologie, Centre Hospitalier Métropole Savoie, Chambéry, France.

Alexis B Cortot (AB)

Thoracic Oncology Department, Hospital Albert Calmette, Lille, France.

Chantal Decroisette (C)

CH Annecy Genevois, Epagny Metz-Tessy, France.

Classifications MeSH