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nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)

Background: The standard therapy for advanced stage non-small cell lung cancer (NSCLC) with no actionable gene alterations is a platinum-based chemotherapy doublet and immune checkpoint blocker (ICB), either concurrently or sequentially, followed by docetaxel at the time of tumor progression. Howeve...

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Autores principales: Morgensztern, Daniel, Dols, Manuel Cobo, Ponce Aix, Santiago, Postmus, Pieter E., Bennouna, Jaafar, Fischer, Jürgen R., Juan-Vidal, Oscar, Stewart, David J., Ardizzoni, Andrea, Bhore, Rafia, Wolfsteiner, Marianne, Reck, Martin, Talbot, Denis, Govindan, Ramaswamy, Ong, Teng Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906015/
https://www.ncbi.nlm.nih.gov/pubmed/33643895
http://dx.doi.org/10.3389/fonc.2020.569715
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author Morgensztern, Daniel
Dols, Manuel Cobo
Ponce Aix, Santiago
Postmus, Pieter E.
Bennouna, Jaafar
Fischer, Jürgen R.
Juan-Vidal, Oscar
Stewart, David J.
Ardizzoni, Andrea
Bhore, Rafia
Wolfsteiner, Marianne
Reck, Martin
Talbot, Denis
Govindan, Ramaswamy
Ong, Teng Jin
author_facet Morgensztern, Daniel
Dols, Manuel Cobo
Ponce Aix, Santiago
Postmus, Pieter E.
Bennouna, Jaafar
Fischer, Jürgen R.
Juan-Vidal, Oscar
Stewart, David J.
Ardizzoni, Andrea
Bhore, Rafia
Wolfsteiner, Marianne
Reck, Martin
Talbot, Denis
Govindan, Ramaswamy
Ong, Teng Jin
author_sort Morgensztern, Daniel
collection PubMed
description Background: The standard therapy for advanced stage non-small cell lung cancer (NSCLC) with no actionable gene alterations is a platinum-based chemotherapy doublet and immune checkpoint blocker (ICB), either concurrently or sequentially, followed by docetaxel at the time of tumor progression. However, more effective treatments are needed. We evaluated the nab-paclitaxel and durvalumab combination in patients with previously treated advanced stage NSCLC. Methods: Patients with advanced stage NSCLC previously treated with one line of platinum-based doublet with or without an ICB and no activating EGFR mutations or ALK translocations received nab-paclitaxel 100 mg/m(2) (days 1 and 8) plus durvalumab 1,125 mg (day 15) every 21 days. The primary endpoint was progression-free survival (PFS). Key secondary endpoints included overall survival (OS) and safety. Results: Between February 2016 and December 2016, 79 patients were enrolled. The median age was 63 years. Most patients were males (68.4%), had non-squamous histology (69.6%), and had no prior ICB treatment (88.6%). The median PFS was 4.5 months; median OS was 10.1 months. A post hoc analysis of survival by prior ICB treatment revealed a median PFS and OS of 4.4 and 9.9 months, respectively, in ICB-naive patients and 6.9 months and not estimable, respectively, in patients previously treated with ICB. The most common treatment-emergent adverse events were asthenia (46.2%) and diarrhea (34.6%); four treatment-related deaths (5.1%) occurred. Conclusions: The nab-paclitaxel and durvalumab combination is feasible and demonstrated antitumor activity without new safety signals. Additional studies using taxanes and ICB in patients with previously treated NSCLC are warranted. Clinical Trial Registration: ClinicalTrials.gov registration (NCT02250326). EudraCT number: 2014-001105-41
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spelling pubmed-79060152021-02-26 nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+) Morgensztern, Daniel Dols, Manuel Cobo Ponce Aix, Santiago Postmus, Pieter E. Bennouna, Jaafar Fischer, Jürgen R. Juan-Vidal, Oscar Stewart, David J. Ardizzoni, Andrea Bhore, Rafia Wolfsteiner, Marianne Reck, Martin Talbot, Denis Govindan, Ramaswamy Ong, Teng Jin Front Oncol Oncology Background: The standard therapy for advanced stage non-small cell lung cancer (NSCLC) with no actionable gene alterations is a platinum-based chemotherapy doublet and immune checkpoint blocker (ICB), either concurrently or sequentially, followed by docetaxel at the time of tumor progression. However, more effective treatments are needed. We evaluated the nab-paclitaxel and durvalumab combination in patients with previously treated advanced stage NSCLC. Methods: Patients with advanced stage NSCLC previously treated with one line of platinum-based doublet with or without an ICB and no activating EGFR mutations or ALK translocations received nab-paclitaxel 100 mg/m(2) (days 1 and 8) plus durvalumab 1,125 mg (day 15) every 21 days. The primary endpoint was progression-free survival (PFS). Key secondary endpoints included overall survival (OS) and safety. Results: Between February 2016 and December 2016, 79 patients were enrolled. The median age was 63 years. Most patients were males (68.4%), had non-squamous histology (69.6%), and had no prior ICB treatment (88.6%). The median PFS was 4.5 months; median OS was 10.1 months. A post hoc analysis of survival by prior ICB treatment revealed a median PFS and OS of 4.4 and 9.9 months, respectively, in ICB-naive patients and 6.9 months and not estimable, respectively, in patients previously treated with ICB. The most common treatment-emergent adverse events were asthenia (46.2%) and diarrhea (34.6%); four treatment-related deaths (5.1%) occurred. Conclusions: The nab-paclitaxel and durvalumab combination is feasible and demonstrated antitumor activity without new safety signals. Additional studies using taxanes and ICB in patients with previously treated NSCLC are warranted. Clinical Trial Registration: ClinicalTrials.gov registration (NCT02250326). EudraCT number: 2014-001105-41 Frontiers Media S.A. 2021-02-11 /pmc/articles/PMC7906015/ /pubmed/33643895 http://dx.doi.org/10.3389/fonc.2020.569715 Text en Copyright © 2021 Morgensztern, Dols, Ponce Aix, Postmus, Bennouna, Fischer, Juan-Vidal, Stewart, Ardizzoni, Bhore, Wolfsteiner, Reck, Talbot, Govindan and Ong. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Morgensztern, Daniel
Dols, Manuel Cobo
Ponce Aix, Santiago
Postmus, Pieter E.
Bennouna, Jaafar
Fischer, Jürgen R.
Juan-Vidal, Oscar
Stewart, David J.
Ardizzoni, Andrea
Bhore, Rafia
Wolfsteiner, Marianne
Reck, Martin
Talbot, Denis
Govindan, Ramaswamy
Ong, Teng Jin
nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)
title nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)
title_full nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)
title_fullStr nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)
title_full_unstemmed nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)
title_short nab-Paclitaxel Plus Durvalumab in Patients With Previously Treated Advanced Stage Non-small Cell Lung Cancer (ABOUND.2L+)
title_sort nab-paclitaxel plus durvalumab in patients with previously treated advanced stage non-small cell lung cancer (abound.2l+)
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7906015/
https://www.ncbi.nlm.nih.gov/pubmed/33643895
http://dx.doi.org/10.3389/fonc.2020.569715
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