The Association of Immune-Related Adverse Events with the Efficacy of Atezolizumab in Previously Treated Advanced Non-Small-Cell Lung Cancer Patients: A Single-Center Experience.
Filip MarkovicMihailo StjepanovicNatalija SamardžićMilica KontićPublished in: Cancers (2024)
Immune checkpoint inhibitors (ICIs) are pivotal in managing metastatic non-oncogene addicted non-small-cell lung cancer (NSCLC). They have unique toxicities known as immune-related adverse events (irAEs). Previous studies have linked irAEs during atezolizumab-based first-line treatments in advanced NSCLC with improved outcomes. This study explored the association between irAEs and the efficacy of atezolizumab in advanced NSCLC patients who had previously received platinum-based chemotherapy. The study involved 105 advanced NSCLC patients who received atezolizumab monotherapy after progressing on at least one line of platinum-based chemotherapy from a single academic institution in Serbia. Data were obtained from a hospital lung cancer registry. Among the participants, 63.8% were male, with the majority being current (53.3%) or former smokers (37.1%). About half had a good performance status (ECOG PS 0-1) at the start of atezolizumab treatment. irAEs occurred in 23 patients (21.9%). The median progression-free survival (mPFS) was significantly longer for patients with irAEs (13.03 months) compared to those without (3.4 months) (HR 0.365 [95% CI, 0.195-0.681], p = 0.002). irAEs and ECOG PS 0-1 were predictors of longer mPFS, with irAEs being more common in patients with good performance status ( p = 0.01). irAEs were linked to improved mPFS in NSCLC patients treated with atezolizumab after multiple lines of platinum-based chemotherapy.
Keyphrases
- small cell lung cancer
- advanced non small cell lung cancer
- free survival
- end stage renal disease
- brain metastases
- newly diagnosed
- squamous cell carcinoma
- healthcare
- chronic kidney disease
- ejection fraction
- emergency department
- randomized controlled trial
- prognostic factors
- mesenchymal stem cells
- stem cells
- clinical trial
- epidermal growth factor receptor
- peritoneal dialysis
- study protocol
- metabolic syndrome
- open label
- adipose tissue
- bone marrow
- cell therapy
- replacement therapy
- double blind