Nanoparticle Albumin-bound Paclitaxel Plus Carboplatin Induction Followed by Nanoparticle Albumin-bound Paclitaxel Maintenance in Squamous Non-Small-cell Lung Cancer (ABOUND.sqm): A Phase III Randomized Clinical Trial.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
01 2021
Historique:
received: 15 05 2020
revised: 26 08 2020
accepted: 04 09 2020
pubmed: 25 10 2020
medline: 15 12 2021
entrez: 24 10 2020
Statut: ppublish

Résumé

We evaluated maintenance nanoparticle albumin-bound (nab) paclitaxel in the treatment of advanced squamous non-small-cell lung cancer. Patients with treatment-naive squamous non-small-cell lung cancer received four 21-day cycles of nab-paclitaxel 100 mg/m Overall, 420 patients had received induction therapy; 202 (nab-paclitaxel plus BSC, 136; BSC, 66) had received maintenance therapy. Enrollment was discontinued after a preplanned interim futility analysis (patients could remain in the study at the investigator's discretion). The median PFS was 3.12 months for nab-paclitaxel plus BSC and 2.60 months for BSC; the difference was not statistically significant (hazard ratio [HR], 0.85; 95% confidence interval [CI], 0.61-1.19; P = .36). The median OS (median follow-up, 24.2 months) was 17.18 months for nab-paclitaxel plus BSC and 12.16 months for BSC (HR, 0.70; 95% CI, 0.48-1.02; nominal P = .07). An updated analysis (median follow-up, 28.4 months) revealed a median OS of 17.61 months for nab-paclitaxel plus BSC and 12.16 months for BSC (HR, 0.68; 95% CI, 0.47-0.98; nominal P = .037). The most frequent grade 3 and 4 treatment-emergent adverse events for the entire study were neutropenia (53.1% [nab-paclitaxel plus BSC] vs. 50.0% [BSC]) and anemia (33.1% [nab-paclitaxel plus BSC] vs. 32.3% [BSC]). Only peripheral neuropathy had occurred in ≥ 5% of patients during maintenance therapy (13.1%; nab-paclitaxel plus BSC). The results of the ABOUND.sqm did not meet the primary endpoint of PFS. An updated OS analysis revealed a trend favoring nab-paclitaxel plus BSC.

Sections du résumé

BACKGROUND
We evaluated maintenance nanoparticle albumin-bound (nab) paclitaxel in the treatment of advanced squamous non-small-cell lung cancer.
PATIENTS AND METHODS
Patients with treatment-naive squamous non-small-cell lung cancer received four 21-day cycles of nab-paclitaxel 100 mg/m
RESULTS
Overall, 420 patients had received induction therapy; 202 (nab-paclitaxel plus BSC, 136; BSC, 66) had received maintenance therapy. Enrollment was discontinued after a preplanned interim futility analysis (patients could remain in the study at the investigator's discretion). The median PFS was 3.12 months for nab-paclitaxel plus BSC and 2.60 months for BSC; the difference was not statistically significant (hazard ratio [HR], 0.85; 95% confidence interval [CI], 0.61-1.19; P = .36). The median OS (median follow-up, 24.2 months) was 17.18 months for nab-paclitaxel plus BSC and 12.16 months for BSC (HR, 0.70; 95% CI, 0.48-1.02; nominal P = .07). An updated analysis (median follow-up, 28.4 months) revealed a median OS of 17.61 months for nab-paclitaxel plus BSC and 12.16 months for BSC (HR, 0.68; 95% CI, 0.47-0.98; nominal P = .037). The most frequent grade 3 and 4 treatment-emergent adverse events for the entire study were neutropenia (53.1% [nab-paclitaxel plus BSC] vs. 50.0% [BSC]) and anemia (33.1% [nab-paclitaxel plus BSC] vs. 32.3% [BSC]). Only peripheral neuropathy had occurred in ≥ 5% of patients during maintenance therapy (13.1%; nab-paclitaxel plus BSC).
CONCLUSIONS
The results of the ABOUND.sqm did not meet the primary endpoint of PFS. An updated OS analysis revealed a trend favoring nab-paclitaxel plus BSC.

Identifiants

pubmed: 33097414
pii: S1525-7304(20)30270-9
doi: 10.1016/j.cllc.2020.09.007
pii:
doi:

Substances chimiques

130-nm albumin-bound paclitaxel 0
Albumins 0
Carboplatin BG3F62OND5
Paclitaxel P88XT4IS4D

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6-15.e4

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

David R Spigel (DR)

Sarah Cannon Research Institute, Nashville, TN. Electronic address: dspigel@tnonc.com.

Robert M Jotte (RM)

Rocky Mountain Cancer Centers, Denver, CO.

Santiago Ponce Aix (SP)

Unidad de Investigación Clínica de Cáncer Pulmón H12O-CNIO, Madrid, Spain.

Laurent Gressot (L)

North Cypress Cancer Center, Cypress, TX.

Daniel Morgensztern (D)

Washington University School of Medicine, St. Louis, MO.

Michael McCleod (M)

Florida Cancer Specialists, Fort Myers, FL.

Mark A Socinski (MA)

AdventHealth Cancer Institute, Orlando, FL.

Davey Daniel (D)

Tennessee Oncology, Chattanooga, TN.

Oscar Juan-Vidal (O)

Hospital Universitari i Politécnic La Fe, Valencia, Spain.

Kathryn F Mileham (KF)

Levine Cancer Institute, Atrium Health, Charlotte, NC.

Howard West (H)

Swedish Cancer Institute, Seattle, WA.

Ray Page (R)

The Center for Cancer and Blood Disorders, Fort Worth, TX.

Niels Reinmuth (N)

Asklepios Fachkliniken München-Gauting, Gauting, Germany.

Jeanna Knoble (J)

The Mark H. Zangmeister Center, Columbus, OH.

Tianlei Chen (T)

Bristol Myers Squibb, Summit, NJ.

Rafia Bhore (R)

Bristol Myers Squibb, Summit, NJ.

Marianne Wolfsteiner (M)

PRA Health Sciences, Lenexa, KS.

Teng Jin Ong (TJ)

Bristol Myers Squibb, Summit, NJ.

Cesare Gridelli (C)

S.G. Moscati Hospital, Avellino, Italy.

Michael Thomas (M)

Internistische Onkologie der Thoraxtumoren, Thoraxklinik im Universitätsklinikum Heidelberg, Translational Lung Research Center Heidelberg, Heidelberg, Germany.

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Classifications MeSH