Value of Precision Medicine in AdvancedNon-SmallCell Lung Cancer:Real-WorldOutcomes Associated with the Use of Companion Diagnostics

被引:22
作者
John, Ani [1 ]
Shah, Roma A. [1 ]
Wong, William B. [2 ]
Schneider, Charles E. [3 ]
Alexander, Marliese [4 ,5 ]
机构
[1] Roche Diagnost Informat Solut, 4300 Hacienda Dr, Pleasanton, CA 94588 USA
[2] Genentech Inc, San Francisco, CA 94080 USA
[3] Roche Sequencing Solut, Pleasanton, CA USA
[4] Peter MacCallum Canc Ctr, Pharm Dept, Melbourne, Vic, Australia
[5] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic, Australia
关键词
Real-world; Survival; Mortality; Advanced non-small cell lung cancer; Companion diagnostic testing; PERSONALIZED MEDICINE; SELECTION; SURVIVAL;
D O I
10.1634/theoncologist.2019-0864
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Companion diagnostic (CDx) testing for patients with advanced non-small cell lung cancer (aNSCLC) identifies patients more likely to benefit from biomarker-driven treatments. Methods Patients with nonsquamous cell (non-Sq) aNSCLC from the Flatiron Health database (diagnosed January 1, 2011-May 31, 2018) who had CDx testing were compared with those who had no reported evidence of testing. The association between CDx testing and overall survival was evaluated by unadjusted and adjusted Cox proportional hazards regression models. Logistic regression analysis identified characteristics associated with CDx testing. The revised modified Lung Cancer Prognostic Index and other factors identified a priori were included in the adjusted models. Results A total of 17,555 patients with non-Sq aNSCLC (CDx,n= 14,732; no CDx,n= 2,823) with mean +/- SD age of 67.2 +/- 10.0 years were included. Most were insured (91.7%) and white (67.1%). Asian patients and those who were never-smokers were more likely to undergo CDx testing. Those with CDx testing lived longer than those without (median [95% confidence interval (CI)] survival, 13.04 [12.62-13.40] vs. 6.01 [5.72-6.24] months) and had a decreased mortality risk (adjusted hazard ratio [95% CI], 0.72 [0.69-0.76]). A survival advantage was also seen for patients with CDx testing who received biomarker-driven first-line therapy. Conclusion Patients with non-Sq aNSCLC who had CDx testing had a greater survival benefit than those without, supporting broader use of CDx testing in routine clinical practice to identify patients more likely to benefit from precision medicine. Implications for Practice Companion diagnostic (CDx) testing coupled with biomarker-driven treatment offers a greater survival benefit for patients with advanced non-small cell lung cancer (aNSCLC). In this study, patients with nonsquamous aNSCLC from Flatiron Health, a large, real-world oncology database, with CDx testing had a reduced mortality risk and lived longer than patients without reported evidence of CDx testing; those who received biomarker-driven therapy as their first line of treatment were likely to survive three times longer than those who did not. These results demonstrate the clinical utility of CDx testing as the first step in treating nonsquamous aNSCLC in real-world clinical practice.
引用
收藏
页码:E1743 / E1752
页数:10
相关论文
共 35 条
[1]   Lung cancer prognostic index: a risk score to predict overall survival after the diagnosis of non-small-cell lung cancer [J].
Alexander, Marliese ;
Wolfe, Rory ;
Ball, David ;
Conron, Matthew ;
Stirling, Robert G. ;
Solomon, Benjamin ;
MacManus, Michael ;
Officer, Ann ;
Karnam, Sameer ;
Burbury, Kate ;
Evans, Sue M. .
BRITISH JOURNAL OF CANCER, 2017, 117 (05) :744-751
[2]  
American Cancer Society, 2025, Cervical Cancer Survival Rates
[3]  
[Anonymous], LUNG CANC 101 TYP ST
[4]  
[Anonymous], International Classification of Diseases, Ninth Revision
[5]  
[Anonymous], SEER Cancer Statistics Review, 1975-2015
[6]  
[Anonymous], COMM CANC TYP
[7]  
ClinicalTrials.gov, 2019, MER NONSM CELL LUNG
[8]  
ClinicalTrials.gov, 2019, CAB PAT RET FUS POS
[9]  
ClinicalTrials.gov, 2019, TRIAL TRAM PON PAT K
[10]   Development and Validation of a High-Quality Composite Real-World Mortality Endpoint [J].
Curtis, Melissa D. ;
Griffith, Sandra D. ;
Tucker, Melisa ;
Taylor, Michael D. ;
Capra, William B. ;
Carrigan, Gillis ;
Holzman, Ben ;
Torres, Aracelis Z. ;
You, Paul ;
Arnieri, Brandon ;
Abernethy, Amy P. .
HEALTH SERVICES RESEARCH, 2018, 53 (06) :4460-4476