Improved treatment outcome of pembrolizumab in patients with nonsmall cell lung cancer and chronic obstructive pulmonary disease.

Abstract

Emerging immune profiling data suggest a higher sensitivity to immune checkpoint inhibitors (ICIs) in nonsmall cell lung cancer (NSCLC) patients with chronic obstructive pulmonary disease (COPD), compared to those without COPD. This study aimed to investigate the clinical impact of COPD on the treatment response to ICIs in a large number of patients with NSCLC. In total, 133 patients with spirometry test results were retrospectively identified among those who received palliative pembrolizumab for NSCLC. COPD was defined as pre-bronchodilator forced expiratory volume in 1 s/forced vital capacity <0.7. Overall survival (OS), progression-free survival (PFS), and objective response rate were analyzed according to the presence of COPD. Spirometry-based COPD was present in 59 (44%) patients. Patients with COPD had better OS (hazard ratio [HR] for death, 0.45; 95% confidence interval [CI], 0.26-0.78) and PFS (HR for disease progression or death, 0.50; 95% CI, 0.31-0.79) than those without COPD. These associations persisted after adjusting for potential confounders including smoking history. The response rate was also higher in patients with COPD than in those without COPD (38.2% vs. 20.5%, p = 0.028). Spirometry-defined COPD was associated with a significantly longer OS and PFS in patients with NSCLC treated with palliative pembrolizumab. Identifying coexisting COPD could predict favorable treatment outcomes in patients with NSCLC treated with pembrolizumab.

• Authors: Sun Hye Shin, Hye Yun Park, Yunjoo Im, Hyun Ae Jung, Jong-Mu Sun, Jin Seok Ahn, Myung-Ju Ahn, Keunchil Park, Ho Yun Lee, Se-Hoon Lee
• Journal: International journal of cancer (Int J Cancer) Vol. 145 Issue 9 Pg. 2433-2439 (11 01 2019) ISSN: 1097-0215 [Electronic] United States
• PMID: 30807641 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2019 UICC.

Chemical References

• Antibodies, Monoclonal, Humanized
• pembrolizumab

Topics

• Aged
• Antibodies, Monoclonal, Humanized (therapeutic use)
• Carcinoma, Non-Small-Cell Lung (drug therapy)
• Disease Progression
• Female
• Forced Expiratory Volume (drug effects)
• Humans
• Lung (drug effects)
• Lung Neoplasms (drug therapy)
• Male
• Middle Aged
• Proportional Hazards Models
• Pulmonary Disease, Chronic Obstructive (drug therapy)
• Retrospective Studies
• Risk Factors
• Spirometry (methods)
• Treatment Outcome
• Vital Capacity