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Economic burden in patients with ALK plus non-small cell lung cancer, with or without brain metastases, receiving second-line anaplastic lymphoma kinase (ALK) inhibitors
被引:11
|作者:
Lin, Huamao M.
[1
]
Pan, Xiaoyun
[1
]
Hou, Peijie
[1
]
Huang, Hui
[1
]
Wu, Yanyu
[1
]
Ren, Kaili
[1
]
Jahanzeb, Mohammad
[2
]
机构:
[1] Millennium Pharmaceut Inc, Global Outcomes Res, 40 Landsdowne St, Cambridge, MA 02139 USA
[2] Florida Precis Oncol, Boca Raton, FL USA
关键词:
Non-small cell lung cancer;
anaplastic lymphoma kinase positive;
treatment pattern;
healthcare cost;
brain metastasis;
EML4-ALK FUSION GENE;
TREATMENT PATTERNS;
OPEN-LABEL;
CRIZOTINIB;
CHEMOTHERAPY;
ALECTINIB;
CERITINIB;
SURVIVAL;
IMPACT;
EGFR;
D O I:
10.1080/13696998.2020.1762620
中图分类号:
F [经济];
学科分类号:
02 ;
摘要:
Aims: To describe the real-world economic burden of patients with anaplastic lymphoma kinase-positive (ALK+) non-small cell lung cancer (NSCLC) treated with post-crizotinib, second-line ALK inhibitor therapy. Materials and methods: Retrospective analysis using data from US Optum: Clinformatics Data Mart administrative claims database. Adult patients with ALK + NSCLC treated with ceritinib or alectinib as second-line ALK inhibitors between 1 January 2011 and 30 September 2017 were included. Healthcare costs and resource utilization for up to 1 year of therapy were calculated on a per-patient-per-month (PPPM) basis and stratified by presence or absence of brain metastases (BM). Multivariate regression analysis was performed to identify factors associated with costs. Top ten cost drivers of non-inpatient procedure costs were recorded. Results: One hundred and twelve patients received second-line ALK inhibitors. Total mean PPPM healthcare costs were $23,984 for all patients receiving up to 1 year of post-crizotinib, second-line ALK inhibitor therapy. Total mean PPPM costs for patients with BM on or prior to post-crizotinib, second-line ALK inhibitor therapy were 1.37-times as high as those for patients without BM (p = 0.0406). Mean PPPM outpatient visits and inpatient hospitalization stays were higher for patients with BM versus no BM. The main cost drivers for non-inpatient procedures were radiation therapy, medications, and diagnostic radiology. Limitations: Analyses did not include newer ALK-directed therapies. BM development after the index date (defined as the date of the first claim for a second-line ALK inhibitor) may have been misclassified as non-BM. Findings may not be generalizable to patients with no health insurance coverage. Conclusions: Treatment of patients with ALK + NSCLC with ceritinib or alectinib as post-crizotinib, second-line ALK inhibitor therapy represents a high economic burden. Healthcare costs and resource utilization were significantly higher for patients with ALK + NSCLC with BM versus no BM.
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页码:894 / 901
页数:8
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