Survival of Asian Females With Advanced Lung Cancer in the Era of Tyrosine Kinase Inhibitor Therapy

被引:3
|
作者
Becker, Daniel J. [1 ,2 ]
Wisnivesky, Juan P. [3 ]
Grossbard, Michael L. [2 ]
Chachoua, Abraham [2 ]
Camidge, D. Ross [4 ]
Levy, Benjamin P. [3 ]
机构
[1] Vet Affairs New York Harbor Healthcare Syst, Sect Hematol Oncol, Manhattan Campus, New York, NY USA
[2] NYU, Sch Med, Dept Med, 423 West 23rd St,Mailbox 111, New York, NY 10010 USA
[3] Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA
[4] Univ Colorado, Sch Med, Dept Med, Aurora, CO USA
关键词
Epidermal growth factor receptor; Ethnic disparities; Outcome research; SEER; TKIs; 1ST-LINE TREATMENT; EGFR MUTATIONS; OPEN-LABEL; PHASE-III; CHEMOTHERAPY; ADENOCARCINOMA; GEFITINIB; ERLOTINIB; AFATINIB; IMPACT;
D O I
10.1016/j.cllc.2016.08.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It has been difficult to prove a survival advantage for epidermal growth factor receptor (EGFR) inhibitors in lung cancer patients with EGFR mutations. Among 38,381 patients, we found that the introduction of EGFR inhibitors was associated with a survival increase among Asian female patients that was not matched by non-Asian male patients. Our study adds population-based data to support that the use of EGFR inhibitors extends lives. Introduction: We examined the effect of access to epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) therapy on survival for Asian female (AF) EGFR mutation-enriched patients with advanced lung adenocarcinoma. Materials and Methods: We used the Surveillance Epidemiology and End Results database to study patients with stage IV lung adenocarcinoma diagnosed from 1998 to 2012. We compared survival (lung cancer-specific survival [LCSS] and overall survival) between AFs and non-Asian males (NAMs), an EGFR mutation-enriched and EGFR mutation-unenriched population, respectively, with a diagnosis in the pre-EGFR TKI (1998-2004) and EGFR TKI (20052012) eras. We used Cox proportional hazards models to examine the interaction of access to TKI treatment and EGFR enrichment status. Results: Among 3029 AF and 35,352 NAM patients, we found that LCSS was best for AFs with a diagnosis in the TKI era (median, 14 months), followed by AFs with a diagnosis in the pre-TKI era (median, 8 months), NAMs with a diagnosis in the TKI era (median, 5 months), and NAMs with a diagnosis in the pre-TKI era (median, 4 months; log-rank P < .0001). In a multivariable model, the effect of a diagnosis in the TKI era on survival was greater for AFs than for NAMs (LCSS, P = .0020; overall survival, P = .0007). A lung cancer diagnosis in the TKI era was associated with an overall mortality decrease of 26% for AFs (hazard ratio, 0.740; 95% confidence interval, 0.682-0.80) and 15.9% for NAMs (hazard ratio, 0.841; 95% confidence interval, 0.822-0.860). Conclusions: We found increased survival for lung adenocarcinoma diagnoses made after widespread access to EGFR TKIs, with the greatest increase among AF patients enriched for EGFR mutations. The present analysis eliminated the effect of crossover, which has complicated assessments of the survival advantage in EGFR TKI randomized trials.
引用
收藏
页码:E35 / E40
页数:6
相关论文
共 50 条
  • [1] The epidermal growth factor receptor-tyrosine kinase inhibitor era has changed the causes of death of patients with advanced non-small-cell lung cancer
    Wu, Wen-Shuo
    Chen, Yuh-Min
    Tsai, Chun-Ming
    Shih, Jen-Fu
    Lee, Yu-Chin
    Perng, Reury-Perng
    Whang-Peng, Jacqueline
    JOURNAL OF THE CHINESE MEDICAL ASSOCIATION, 2013, 76 (12) : 682 - 685
  • [2] Epidermal growth factor receptor tyrosine kinase inhibitors in advanced nonsmall cell lung cancer: what is the preferred first-line therapy?
    Roeper, Julia
    Griesinger, Frank
    CURRENT OPINION IN ONCOLOGY, 2019, 31 (01) : 1 - 7
  • [3] Association of EGFR Tyrosine Kinase Inhibitor Treatment With Progression-Free Survival Among Taiwanese Patients With Advanced Lung Adenocarcinoma and EGFR Mutation
    Chen, Po-Yen
    Wang, Chin-Chou
    Hsu, Chien-Ning
    Chen, Chung-Yu
    FRONTIERS IN PHARMACOLOGY, 2021, 12
  • [4] A radiomics-based deep learning approach to predict progression free-survival after tyrosine kinase inhibitor therapy in non-small cell lung cancer
    Lu, Chia-Feng
    Liao, Chien-Yi
    Chao, Heng-Sheng
    Chiu, Hwa-Yen
    Wang, Ting-Wei
    Lee, Yen
    Chen, Jyun-Ru
    Shiao, Tsu-Hui
    Chen, Yuh-Min
    Wu, Yu-Te
    CANCER IMAGING, 2023, 23 (01)
  • [5] Dacomitinib in lung cancer: a "lost generation" EGFR tyrosine-kinase inhibitor from a bygone era?
    Ou, Sai-Hong Ignatius
    Soo, Ross A.
    DRUG DESIGN DEVELOPMENT AND THERAPY, 2015, 9 : 5641 - 5653
  • [6] The Frequency of EGFR Mutation in Lung Adenocarcinoma and the Efficacy of Tyrosine Kinase Inhibitor Therapy in a Hungarian Cohort of Patients
    Sarosi, Veronika
    Baliko, Zoltan
    Smuk, Gabor
    Laszlo, Terezia
    Szabo, Mariann
    Ruzsics, Istvan
    Mezosi, Emese
    PATHOLOGY & ONCOLOGY RESEARCH, 2016, 22 (04) : 755 - 761
  • [7] Radiation recall pneumonitis induced by epidermal growth factor receptor-tyrosine kinase inhibitor in patients with advanced nonsmall-cell lung cancer
    Chiang, Chi-Lu
    Chen, Yi-Wei
    Wu, Mei-Han
    Huang, Hsu-Ching
    Tsai, Chun-Ming
    Chiu, Chao-Hua
    JOURNAL OF THE CHINESE MEDICAL ASSOCIATION, 2016, 79 (05) : 248 - 255
  • [8] Survival analysis of patients with advanced non-small cell lung cancer receiving tyrosine kinase inhibitor (TKI) treatment: A multi-center retrospective study
    Shi, Qingming
    Guan, Maojing
    Wang, Yong
    Xu, Congjing
    Tang, Lei
    Fu, Wenhua
    Bi, Minghong
    Sun, Xiang
    Gu, Kangsheng
    Pang, Dongsheng
    THORACIC CANCER, 2018, 9 (02) : 278 - 283
  • [9] Which tyrosine kinase inhibitor should be recommended as initial treatment for non-small cell lung cancer patients with EGFR mutations?
    Tartarone, Alfredo
    Lerose, Rosa
    Lazzari, Chiara
    Gregorc, Vanesa
    Aieta, Michele
    MEDICAL ONCOLOGY, 2014, 31 (08)
  • [10] Clinical modes of EGFR tyrosine kinase inhibitor failure and subsequent management in advanced non-small cell lung cancer
    Yang, Jin-Ji
    Chen, Hua-Jun
    Yan, Hong-Hong
    Zhang, Xu-Chao
    Zhou, Qing
    Su, Jian
    Wang, Zhen
    Xu, Chong-Rui
    Huang, Yi-Sheng
    Wang, Bin-Chao
    Yang, Xue-Ning
    Zhong, Wen-Zhao
    Nie, Qiang
    Liao, Ri-Qiang
    Jiang, Ben-Yuan
    Dong, Song
    Wu, Yi-Long
    LUNG CANCER, 2013, 79 (01) : 33 - 39