Real-World Efficacy of Nintedanib Plus Docetaxel After Progression on Immune Checkpoint Inhibitors: Results From the Ongoing, Non-interventional VARGADO Study.


Journal

Clinical oncology (Royal College of Radiologists (Great Britain))
ISSN: 1433-2981
Titre abrégé: Clin Oncol (R Coll Radiol)
Pays: England
ID NLM: 9002902

Informations de publication

Date de publication:
07 2022
Historique:
received: 13 05 2021
revised: 09 11 2021
accepted: 13 12 2021
pubmed: 12 1 2022
medline: 16 6 2022
entrez: 11 1 2022
Statut: ppublish

Résumé

To evaluate the efficacy and safety of nintedanib plus docetaxel in patients with advanced adenocarcinoma non-small cell lung cancer (NSCLC) who progressed after chemotherapy and immune checkpoint inhibitor (ICI) therapy. VARGADO (NCT02392455) is an ongoing, prospective, non-interventional, real-world study of nintedanib plus docetaxel after first-line chemotherapy in the routine clinical treatment of patients with locally advanced, metastatic or locally recurrent adenocarcinoma NSCLC. Data were collected during routine visits. We report the results from cohort B (n = 80), who received third-line nintedanib plus docetaxel after first-line chemotherapy and second-line ICI therapy. The median duration of follow-up was 12.4 months. Median progression-free survival from initiation of third-line nintedanib plus docetaxel was 6.4 months (95% confidence interval 4.8, 7.3); median overall survival was 12.1 months (95% confidence interval 9.4, 13.5). The 1-year overall survival rate after initiation of third-line nintedanib plus docetaxel treatment (primary end point) was 52% (95% confidence interval 38.0%, 64.4%). Among 64 patients with a documented response, the objective response rate was 50% (n = 32; one complete response and 31 partial responses) and the disease control rate was 86% (n = 55). There were no new safety signals or unexpected toxicities. Among all treated patients, 74% (n = 59) experienced drug-related adverse events, most commonly (nintedanib-related/docetaxel-related) diarrhoea (34%/24%), a decreased white blood cell count (11%/19%) and nausea (13%/16%). Nintedanib plus docetaxel demonstrated a high response rate and disease stabilisation in the third-line setting after failure of prior chemotherapy and ICI treatment, with a manageable safety profile. These results suggest that nintedanib plus docetaxel represents an efficient treatment option after failure of prior ICIs. The ongoing VARGADO study provides valuable real-world data to inform clinical decision-making regarding treatment sequencing after chemotherapy and ICI failure in patients with adenocarcinoma NSCLC.

Identifiants

pubmed: 35012901
pii: S0936-6555(21)00491-X
doi: 10.1016/j.clon.2021.12.010
pii:
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0
Indoles 0
Docetaxel 15H5577CQD
nintedanib G6HRD2P839

Banques de données

ClinicalTrials.gov
['NCT02392455']

Types de publication

Clinical Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

459-468

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

C Grohé (C)

Department of Pneumology, ELK Berlin, Berlin, Germany. Electronic address: christian.grohe@jsd.de.

W Blau (W)

Department of Internal Medicine IV/V (Hematology/Oncology), University Hospital Giessen, Giessen, Germany.

W Gleiber (W)

Department of Pulmonary Medicine, University Hospital, Goethe University Frankfurt, Frankfurt, Germany.

S Haas (S)

Clinics for Haematology, Oncology and Nephrology, Friedrich-Ebert Hospital, Neumünster, Germany.

S Hammerschmidt (S)

Department of Internal Medicine, Klinikum Chemnitz, Chemnitz, Germany.

S Krüger (S)

Department for Pneumology, Cardiology and Intensive Care Medicine, Florence-Nightingale-Hospital, Düsseldorf, Germany.

H Müller-Huesmann (H)

Brüderkrankenhaus St. Josef Paderborn, Klinik für Hämatologie und Onkologie, Paderborn, Germany.

M Schulze (M)

Praxis Dr. Schulze, Zittau, Germany.

T Wehler (T)

EVK, Evangelisches Krankenhaus Hamm, Hamm, Germany.

J Atz (J)

Boehringer Ingelheim Pharma, Ingelheim, Germany.

R Kaiser (R)

Institute of Pharmacology, Johannes Gutenberg-University Mainz, Mainz, Germany.

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Classifications MeSH