Retrospective Observational Study of ALK-Inhibitor Therapy Sequencing and Outcomes in Patients with ALK-Positive Non-small Cell Lung Cancer

被引:14
作者
Waterhouse, David M. [1 ]
Espirito, Janet L. [2 ]
Chioda, Marc D. [3 ]
Baidoo, Bismark [2 ]
Mardekian, Jack [3 ]
Robert, Nicholas J. [2 ]
Masters, Elizabeth T. [3 ]
机构
[1] US Oncol Network, Oncol Hematol Care, 5053 Wooster Rd, Cincinnati, OH 45226 USA
[2] McKesson Life Sci, 10101 Woodloch Forest, The Woodlands, TX 77380 USA
[3] Pfizer Inc, 235 E 42nd St, New York, NY 10017 USA
关键词
CRIZOTINIB; CHEMOTHERAPY; CERITINIB;
D O I
10.1007/s40801-020-00207-6
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BackgroundData are sparse concerning the sequential use of multiple anaplastic lymphoma kinase (ALK) inhibitors for ALK-positive locally advanced or metastatic non-small cell lung cancer (NSCLC).ObjectiveThis study investigated sequencing and outcomes among patients receiving multiple ALK inhibitors.Patients and MethodsThis was a retrospective observational cohort study of adult patients with ALK-positive NSCLC treated with available first- and second-generation ALK inhibitors from 1 September 2011 to 31 December 2017. Duration of therapy (DOT) and overall survival (OS) were assessed with the Kaplan-Meier method. A multivariable linear regression analysis was performed to assess if DOT with a preceding ALK inhibitor was predictive of DOT for subsequent ALK inhibitor treatments.ResultsA total of 410 patients were analyzed: 57% received 1 ALK inhibitor; 35%, 2 ALK inhibitors; and 8%, 3-4 ALK inhibitors. Among those receiving>1 ALK inhibitor (n=177), 60% received a crizotinib-led sequence and 39% an alectinib-led sequence. Nearly 60% of the overall population received chemotherapy prior to their first ALK inhibitor. Median OS for the study population was 28 months, 15 months in patients who received 1 ALK inhibitor, 42 months in patients who received 2 ALK inhibitors, and 56 months in patients who received 3-4 ALK inhibitors. Longer DOT of the first ALK inhibitor was associated with increased DOT of the second (p<0.0001), and longer DOT of the second ALK inhibitor was associated with increased DOT of the third (p<0.0001).ConclusionsThis study provides initial information on real-world treatment patterns following the introduction of new ALK inhibitors, and supports the use of sequential ALK therapies.
引用
收藏
页码:261 / 269
页数:9
相关论文
共 24 条
[1]  
Adult Treatment Editorial Board, 2019, PDQ NONSM CELL LUNG
[2]   Progression-free survival (PFS) from a phase I study of crizotinib (PF-02341066) in patients with ALK-positive non-small cell lung cancer (NSCLC). [J].
Camidge, D. R. ;
Bang, Y. ;
Kwak, E. L. ;
Shaw, A. T. ;
Iafrate, A. J. ;
Maki, R. G. ;
Solomon, B. J. ;
Ou, S. I. ;
Salgia, R. ;
Wilner, K. D. ;
Costa, D. B. ;
Shapiro, G. ;
LoRusso, P. ;
Stephenson, P. ;
Tang, Y. ;
Ruffner, K. ;
Clark, J. W. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (15)
[3]   Updated efficacy and safety data from the global phase III ALEX study of alectinib (ALC) vs crizotinib (CZ) in untreated advanced ALK plus NSCLC. [J].
Camidge, D. Ross ;
Peters, Solange ;
Mok, Tony ;
Gadgeel, Shirish M. ;
Cheema, Parneet K. ;
Pavlakis, Nick ;
De Marinis, Filippo ;
Stroyakovskiy, Daniil L. ;
Cho, Byoung Chul ;
Zhang, Li ;
Moro-Sibilot, Denis ;
Zeaiter, Ali Hassan ;
Mitry, Emmanuel ;
Balas, Bogdana ;
Mueller, Barbara ;
Shaw, Alice .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
[4]  
Clinicaltrials.gov, **NON-TRADITIONAL**
[5]  
Clinicaltrials.gov, STUD IORL VERS CRIZ
[6]   Initial phase II results with crizotinib in advanced ALK-positive non-small cell lung cancer (NSCLC): PROFILE 1005 [J].
Crino, L. ;
Kim, D. ;
Riely, G. J. ;
Janne, P. A. ;
Blackhall, F. H. ;
Camidge, D. R. ;
Hirsh, V. ;
Mok, T. ;
Solomon, B. J. ;
Park, K. ;
Gadgeel, S. M. ;
Martins, R. ;
Han, J. ;
De Pas, T. M. ;
Bottomley, A. ;
Polli, A. ;
Petersen, J. ;
Tassell, V. R. ;
Shaw, A. T. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (15)
[7]   ALK-rearrangement in non-small-cell lung cancer (NSCLC) [J].
Du, Xue ;
Shao, Yun ;
Qin, Hai-Feng ;
Tai, Yan-Hong ;
Gao, Hong-Jun .
THORACIC CANCER, 2018, 9 (04) :423-430
[8]  
Jemal A, 2010, CA-CANCER J CLIN, V60, P277, DOI [10.3322/caac.21254, 10.3322/caac.20073]
[9]   FDA Approval Summary: Crizotinib for the Treatment of Metastatic Non-Small Cell Lung Cancer With Anaplastic Lymphoma Kinase Rearrangements [J].
Kazandjian, Dickran ;
Blumenthal, Gideon M. ;
Chen, Huan-Yu ;
He, Kun ;
Patel, Mona ;
Justice, Robert ;
Keegan, Patricia ;
Pazdur, Richard .
ONCOLOGIST, 2014, 19 (10) :E5-E11
[10]   FDA Approval: Ceritinib for the Treatment of Metastatic Anaplastic Lymphoma Kinase-Positive Non-Small Cell Lung Cancer [J].
Khozin, Sean ;
Blumenthal, Gideon M. ;
Zhang, Lijun ;
Tang, Shenghui ;
Brower, Margaret ;
Fox, Emily ;
Helms, Whitney ;
Leong, Ruby ;
Song, Pengfei ;
Pan, Yuzhuo ;
Liu, Qi ;
Zhao, Ping ;
Zhao, Hong ;
Lu, Donghao ;
Tang, Zhe ;
Al Hakim, Ali ;
Boyd, Karen ;
Keegan, Patricia ;
Justice, Robert ;
Pazdur, Richard .
CLINICAL CANCER RESEARCH, 2015, 21 (11) :2436-2439