Your browser doesn't support javascript.
loading
Treatment Patterns and Resource Use After Osimertinib Discontinuation in Patients with EGFR + Metastatic NSCLC.
Marrett, Elizabeth; Kwong, Winghan Jacqueline; Song, Jinlin; Manceur, Ameur; Sendhill, Selvam; Wu, Eric.
Afiliação
  • Marrett E; Health Economic and Outcomes Research, Daiichi Sankyo, Inc., 211 Mount Airy Road, Basking Ridge, NJ, 07920, USA. elizabeth.marrett@daiichisankyo.com.
  • Kwong WJ; Health Economic and Outcomes Research, Daiichi Sankyo, Inc., 211 Mount Airy Road, Basking Ridge, NJ, 07920, USA.
  • Song J; Analysis Group, Los Angeles, CA, USA.
  • Manceur A; Analysis Group, Montréal, QB, Canada.
  • Sendhill S; Analysis Group, Los Angeles, CA, USA.
  • Wu E; Analysis Group, Boston, MA, USA.
Oncol Ther ; 12(3): 549-563, 2024 Sep.
Article em En | MEDLINE | ID: mdl-39080178
ABSTRACT

INTRODUCTION:

Current treatment guidelines for patients with epidermal growth factor receptor (EGFR)-mutated metastatic non-small cell lung cancer (mNSCLC) recommend EGFR tyrosine kinase inhibitors (TKIs) as the standard of care for first-line treatment, with third-generation osimertinib the preferred choice. However, most patients develop resistance to targeted therapy, and subsequent systemic chemotherapy is recommended. The aim of this study was to characterize the subsequent line of therapy (LOT) following osimertinib in patients with EGFR-mNSCLC.

METHODS:

Medical and pharmacy claims of adults who initiated a subsequent LOT (index) after initial osimertinib discontinuation between November 2015 and September 2019 were analyzed retrospectively.

RESULTS:

A total of 135 patients met the inclusion criteria. After metastatic diagnosis, 22.2% and 49.6% of patients were treated with osimertinib in the first and second line, respectively. After osimertinib discontinuation, most patients were treated with a platinum-based chemotherapy regimen (57%), of which 40.3% included immuno-oncology therapy. Reuse or continuation of EGFR TKIs was also common (24%). Overall, the median time to treatment discontinuation for the index LOT was 2.4 months. Proportions of patients with ≥ 1 inpatient or emergency department visit were 31.9% and 35.6%, respectively.

CONCLUSIONS:

The duration of the LOT following osimertinib was short and associated with tolerability issues underscoring a high unmet need for new therapies to address EGFR TKI resistance.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article