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Time to response in patients with advanced anaplastic lymphoma kinase (ALK)-positive non-small-cell lung cancer (NSCLC) receiving alectinib in the phase ii NP28673 and NP28761 studies

Journal
Lung Cancer: Targets and Therapy
Journal Volume
10
Pages
125-130
Date Issued
2019
Author(s)
Gadgeel S
Shaw A.T
Barlesi F
Crino L
CHIH-HSIN YANG 
Dingemans A.-M
Kim D.-W
Marinis F
Schulz M
Liu S
Gupta R
Smoljanovic V
Ou S.-H.I.
DOI
10.2147/LCTT.S209231
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85075088528&doi=10.2147%2fLCTT.S209231&partnerID=40&md5=924fe75f23480729fba0dfea7cfcfdaa
https://scholars.lib.ntu.edu.tw/handle/123456789/494903
Abstract
Introduction: Alectinib is a highly selective and potent ALK inhibitor, approved for the treatment of patients with metastatic ALK+ NSCLC based on results from the Phase II global NP28673 (NCT01801111) and North American NP28761 (NCT01871805) studies. Methods: This exploratory analysis of two Phase II studies of alectinib (NP28673/ NP28761) investigated time to systemic response (TTR) and time to central nervous system (CNS) response (TTCR) in patients with previously treated advanced anaplastic lymphoma kinase fusion gene-positive (ALK+) non-small-cell lung cancer. Patients (n=225) received 600 mg oral alectinib twice daily and had scans every 6/8 weeks (NP28673/NP28761). Results: For NP28673 and NP28761, respectively: median follow-up was 21.3 months/17.0 months; most responders (72.6%/82.9%) responded by the first disease assessment; median TTR was 8 weeks (95% confidence interval [CI]: 8.00–8.14)/6 weeks (95% CI: 5.86–6.14); median TTCR in responders with measurable baseline CNS disease was 8 weeks (95% CI: 7.86–10.29)/6 weeks (95% CI: 5.71–not evaluable). Similar results were observed regardless of measurable/non-measurable disease. Discussion: These data suggest that alectinib achieves a rapid response in patients, both systemically and in the CNS. ? 2019 Gadgeel et al.
Subjects
Alectinib; Non-small-cell lung cancer; NP28673; NP28761; Time to response
SDGs

[SDGs]SDG3

Other Subjects
alectinib; anaplastic lymphoma kinase; advanced cancer; ALK gene; Article; cancer patient; central nervous system metastasis; clinical assessment; controlled study; drug efficacy; exploratory research; follow up; human; major clinical study; multicenter study (topic); non small cell lung cancer; phase 2 clinical trial (topic); radiodiagnosis; time to central nervous system response; treatment response time
Publisher
Dove Medical Press Ltd.
Type
journal article

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