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.
引用
收藏
页码:894 / 901
页数:8
相关论文
共 50 条
  • [1] DURATION OF TREATMENT AND ECONOMIC BURDEN IN PATIENTS WITH ANAPLASTIC LYMPHOMA KINASE POSITIVE (ALK plus ) NON-SMALL CELL LUNG CANCER (NSCLC) RECEIVING SECOND-LINE ALK INHIBITORS
    Lin, H. M.
    Hou, P.
    Huang, H.
    Desai, A.
    Jahanzeb, M.
    VALUE IN HEALTH, 2018, 21 : S17 - S17
  • [2] Economic burden in patients with anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC), with or without brain metastases, receiving first-line ALK inhibitors
    Wu, Yanyu
    Ren, Kaili
    Wan, Yin
    Lin, Huamao M.
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2023, 29 (06) : 1418 - 1427
  • [3] Economic burden of brain metastases in patients with anaplastic lymphoma kinase positive (ALK plus ) non-small cell lung
    Lin, Huamao Mark
    Pan, Lucy
    Hou, Peijie
    Huang, Hui
    Desai, Avinash
    Jahanzeb, Mohammad
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (30)
  • [4] Anaplastic lymphoma kinase (ALK) inhibitors for second-line therapy of non-small cell lung cancer
    Berghmans, Thierry
    Remmelink, Myriam
    Awada, Ahmad
    LUNG CANCER-TARGETS AND THERAPY, 2012, 3 : 91 - 99
  • [5] ECONOMIC BURDEN OF BRAIN METASTASES IN PATIENTS WITH ALK plus NON-SMALL CELL LUNG CANCER IN CHINA
    Xiao, F.
    Peng, X.
    Li, R.
    Luan, L.
    Le, H.
    Dong, P.
    VALUE IN HEALTH, 2024, 27 (12) : S99 - S99
  • [6] Outcomes of first, second, and third-generation anaplastic lymphoma kinase (ALK) inhibitors in non-small cell lung cancer brain metastases (NSCLCBM).
    Tatineni, Vineeth
    O'Shea, Patrick Joseph
    Rauf, Yasmeen
    Jia, Xuefei
    Murphy, Erin Sennett
    Chao, Samuel T.
    Suh, John H.
    Peereboom, David M.
    Ahluwalia, Manmeet Singh
    JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (15)
  • [7] EVALUATION OF ANAPLASTIC LYMPHOMA KINASE (ALK) INHIBITOR BRIGATINIB [AP26113] IN PATIENTS (PTS) WITH ALK plus NON-SMALL CELL LUNG CANCER (NSCLC) AND BRAIN METASTASES
    Kerstein, D.
    Gettinger, S.
    Gold, K.
    Langer, C. J.
    Shaw, A. T.
    Bazhenova, L. A.
    Salgia, R.
    Dorer, D. J.
    Conlan, M. G.
    Camidge, D. R.
    ANNALS OF ONCOLOGY, 2015, 26
  • [8] Economic evaluation of crizotinib, alectinib, ceritinib, and brigatininb in anaplastic lymphoma kinase positive (ALK plus ) non-small cell lung cancer (NSCLC) as second-line treatment.
    Alkhatib, Nimer S.
    Choi, Briana
    Halawah, Hala
    Calamia, Matthias
    Gulick, Dexter
    Manasrah, AlMothana
    Alkhdour, Odai
    McBride, Ali
    Abraham, Ivo
    JOURNAL OF CLINICAL ONCOLOGY, 2021, 39 (15)
  • [9] Efficacy and Safety of Anaplastic Lymphoma Kinase (ALK) Tyrosine Kinase Inhibitors in ALK-Positive Non-Small Cell Lung Cancer
    Imase, R.
    Endo, S.
    Sasahara, Y.
    Shinmura, T.
    Ozawa, T.
    Majima, H.
    Hara, T.
    Shimada, H.
    Yamauchi, S.
    Sakakibara, Y.
    Kobayashi, A.
    Yamazaki, K.
    Jin, Y.
    Yamanaka, K.
    Matsubara, O.
    JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (11) : S1953 - S1953
  • [10] Brain metastases in patients with ALK plus non-small cell lung cancer: clinical symptoms, treatment patterns and economic burden
    Guerin, Annie
    Sasane, Medha
    Zhang, Jie
    Culver, Kenneth W.
    Dea, Katherine
    Nitulescu, Roy
    Wu, Eric Qiong
    JOURNAL OF MEDICAL ECONOMICS, 2015, 18 (04) : 312 - 322