Biomarker Testing, Treatment, and Outcomes in Patients With Advanced/Metastatic Non-Small Cell Lung Cancer Using a Real-World Database

被引:7
作者
Bhandari, Naleen Raj [1 ,3 ]
Hess, Lisa M. [1 ]
He, Dan [2 ]
Peterson, Patrick [1 ]
机构
[1] Eli Lilly & Co, Indianapolis, IN 46285 USA
[2] Syneos Hlth, Morrisville, NC USA
[3] Eli Lilly & Co, Lilly Corp Ctr, Indianapolis, IN 46285 USA
来源
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK | 2023年 / 21卷 / 09期
关键词
OPEN-LABEL; 1ST-LINE TREATMENT; CHEMOTHERAPY; CRIZOTINIB; MULTICENTER; THERAPIES; ERLOTINIB;
D O I
10.6004/jnccn.2023.7039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Little is known about the impact of up-front biomarker testing on long-term outcomes in patients with advanced or meta-static non-small cell lung cancer (a/mNSCLC). This study compared overall survival (OS) by biomarker testing status and by receipt of guideline-concordant therapy in a large real-world cohort of patients with a/mNSCLC in the United States. Patients and Methods: This ret-rospective study used an a/mNSCLC database derived from real -world electronic healthcare records. Patients diagnosed with nonsqua-mous a/mNSCLC who initiated first-line therapy on or after January 1, 2015, were included. We describe the testing of patients for action-able biomarkers and whether they subsequently received guideline-recommended first-line treatment. OS was defined as the number of months from the initiation of first-line therapy to the date of death or end of follow-up, and was described using Kaplan-Meier analysis. Mul-tivariable Cox proportional hazard modeling was conducted to com-pare OS between groups adjusting for baseline covariates; adjusted hazard ratios (HRs) were reported. Results: A total of 21,572 patients with a median age of 69 years (IQR, 61-76 years) and follow-up of 9.5 months (IQR, 3.5-21.5 months) were included. Among patients in the database, 88% had a record of receiving testing for at least 1 bio-marker at any time, and 69% of these patients received testing before or at the start of first-line treatment. The adjusted hazard of death was 30% higher in patients who never (vs ever) received biomarker testing in the database (HR, 1.30; 95% CI, 1.24-1.37), and 12% higher in pa-tients who did not receive (vs did receive) biomarker testing before or at the start of first-line treatment (HR, 1.12; 95% CI, 1.08-1.16). The ad-justed hazard of death was 25% higher in patients who did not receive guideline-concordant first-line treatment (vs those who did) after having a biomarker-positive disease (HR, 1.25; 95% CI, 1.13-1.40). Conclusions: Findings suggest that receipt of first-line treatment that is concordant with biomarker testing results and treatment guidelines is associated with improved survival outcomes in patients with a/mNSCLC in the United States.
引用
收藏
页码:934 / +
页数:13
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