Survival Disparities in Black Patients With EGFR-mutated Non-small-cell Lung Cancer

被引:12
|
作者
Cheng, Haiying [1 ]
Hosgood, H. Dean [2 ]
Deng, Lei [3 ]
Ye, Kenny [2 ]
Su, Christopher [4 ]
Sharma, Janaki [1 ]
Yang, Yuanquan [5 ]
Halmos, Balazs [1 ]
Perez-Soler, Roman [1 ]
机构
[1] Albert Einstein Coll Med, Dept Med Oncol, Montefiore Med Ctr, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Jacobi Med Ctr, Dept Med, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Dept Med, Montefiore Med Ctr, Bronx, NY 10461 USA
[5] Roswell Park Comprehens Canc Ctr, Dept Med, Buffalo, NY USA
基金
美国国家卫生研究院;
关键词
Black patients; EGFR; Lung cancer; Survival; Uncommon EGFR mutations; GROWTH-FACTOR RECEPTOR; AFRICAN-AMERICANS; ETHNIC DISPARITIES; UNITED-STATES; MUTATIONS; FREQUENCY; ERLOTINIB; RACE; PREVALENCE; DIVERSITY;
D O I
10.1016/j.cllc.2019.07.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Non-small-cell lung cancer (NSCLC) harboring epidermal growth factor receptor (EGFR) mutation is a distinct molecular subgroup with effective targeted therapy. In our study of 2773 patients, the survival was similar between races among EGFR wild-type NSCLC; h owever, black patients with EGFR-mutant NSCLC had inferior survival compared with their non-black counterparts. More tailored management for this population is warranted. Background: Little is known about the difference between black and non-black patients with epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC), particularly regarding survival. We thus characterized the EGFR expression profile, clinical characteristics, and survival outcome in these patients. Patient and Methods: We reviewed the cancer registry and patient charts at a New York-Bronx network (n = 2773) treating a large population of minority patients, for non-squamous NSCLC (n = 1986) diagnosed between 2009 and 2015. Survival was adjusted for smoking, gender, age, weight, and stage. Results: The EGFR mutation rate was 15% (98/652) in tested patients (black, 14%; non-black, 16%). There was no significant difference between the 2 cohorts with respect to age at diagnosis, gender, presenting stages, and socioeconomic status. On the other hand, weight was noted to be heavier in black patients with EGFR-mutated NSCLC than their non-black counterparts (P =.012). After adjusting for gender, age, smoking status, weight, and stage, the multivariate analysis revealed no racial disparity in survival among patients with wild-type EGFR (P =.774); However, among patients with EGFR-mutated NSCLC, black patients had shorter survival in comparison with non-black patients (P = .001), with 2-year survival rates being 33% versus 61%, respectively. Such shorter survival was also observed among EGFR-inhibitor treated patients with common EGFR mutations (P =.040). Conclusions: To our knowledge, this is the first report of inferior survival among black patients with NSCLC with EGFR mutations, relative to non-black patients. The survival disparities suggest the need of more tailored management for this patient population.
引用
收藏
页码:177 / 185
页数:9
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