Your browser doesn't support javascript.
loading
Q-TWiST analysis of survival benefits with brigatinib versus crizotinib in patients with anaplastic lymphoma kinase-positive non-small cell lung cancer based on results of the ALTA-1L trial.
Garcia Campelo, M R; Wan, Y; Lin, H M; Chen, T; Shen, J; Zhang, P; Camidge, D R.
Affiliation
  • Garcia Campelo MR; Dept. Medical Oncology, Complejo Hospitalario Universitario A Coruña, A Coruña, Spain.
  • Wan Y; Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Lin HM; Takeda Development Center Americas, Inc., Lexington, MA, USA. Electronic address: Mark.Lin@takeda.com.
  • Chen T; Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Shen J; Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Zhang P; Takeda Development Center Americas, Inc., Lexington, MA, USA.
  • Camidge DR; Medical Oncology, University of Colorado Cancer Center Anschutz Cancer Pavilion, Aurora, CO, USA.
Lung Cancer ; 185: 107376, 2023 Nov.
Article in En | MEDLINE | ID: mdl-37722340
ABSTRACT

OBJECTIVES:

The ALTA-1L phase 3 open-label trial demonstrated increased progression-free survival (PFS) with brigatinib versus crizotinib in patients with anaplastic lymphoma kinase-positive (ALK-positive) locally advanced or metastatic non-small cell lung cancer (NSCLC) previously untreated with ALK-targeted therapy. This post-hoc analysis of data from the ALTA-1L trial used the quality-adjusted (QA) time without symptoms of disease or toxicity (Q-TWiST) methodology to compare the QA survival benefit of brigatinib versus crizotinib in this patient population. PATIENTS AND

METHODS:

The Q-TWiST analysis was performed using final (January 29, 2021) individual patient-level blinded independent review committee (BIRC)- and investigator-assessed survival data for brigatinib (n = 137) and crizotinib (n = 138) in adult patients (N = 275) with ALK-positive locally advanced or metastatic NSCLC previously untreated with ALK-targeted therapy. Q-TWiST was compared between the two treatments. Subgroup analyses were performed in patients stratified by various clinicopathological characteristics, including presence or absence of brain metastases at baseline.

RESULTS:

Brigatinib was associated with significantly longer time without symptoms of disease or toxicity (P < 0.001) than crizotinib, with significantly greater Q-TWiST (mean [SE] months BIRC-assessed, 28.2 [1.2] versus 25.1 [1.1], P = 0.045; investigator-assessed, 28.5 [1.2] versus 24.8 [1.1], P = 0.018). Relative gains in Q-TWiST with brigatinib compared to crizotinib were clinically meaningful (BIRC-assessed, 10.4%; investigator-assessed, 12.3%). Patients with brain metastases at baseline receiving brigatinib had significantly greater Q-TWiST (mean [SE] months BIRC-assessed, 29.0 [1.9] versus 19.0 [1.9], P = 0.0001) than those receiving crizotinib.

CONCLUSION:

First-line brigatinib treatment was associated with significant and clinically meaningful gains in Q-TWiST compared to crizotinib in patients with ALK-positive locally advanced or metastatic NSCLC, supporting the results of the ALTA-1L trial and brigatinib as a safe and effective first-line treatment for ALK-positive NSCLC.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Lung Cancer Journal subject: NEOPLASIAS Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Lung Cancer Journal subject: NEOPLASIAS Year: 2023 Document type: Article Affiliation country: