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Cited 34 time in webofscience Cited 39 time in scopus
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Pazopanib maintenance after first-line etoposide and platinum chemotherapy in patients with extensive disease small-cell lung cancer: a multicentre, randomised, placebo-controlled Phase II study (KCSG-LU12-07)open access

Authors
Sun, Jong-MuLee, Ki HyeongKim, Bong-SeogKim, Hoon-GuMin, Young JooYi, Seong YoonYun, Hwan JungJung, Sin-HoLee, Se-HoonAhn, Jin SeokPark, KeunchilAhn, Myung-Ju
Issue Date
6-Mar-2018
Publisher
NATURE PUBLISHING GROUP
Keywords
small-cell lung cancer; pazopanib; maintenance therapy
Citation
BRITISH JOURNAL OF CANCER, v.118, no.5, pp 648 - 653
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
BRITISH JOURNAL OF CANCER
Volume
118
Number
5
Start Page
648
End Page
653
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/11817
DOI
10.1038/bjc.2017.465
ISSN
0007-0920
1532-1827
Abstract
Background: We investigated whether pazopanib maintenance following first-line chemotherapy would improve survival in patients with extensive disease small-cell lung cancer (ED-SCLC). Methods: This study is a randomised, placebo-controlled, phase II study that enroled ED-SCLC patients who had not progressed after four cycles of etoposide plus platinum therapy. Eligible patients were randomly assigned (1 : 1 ratio) to either placebo or pazopanib 800mg per day until progression or unacceptable toxicity. The primary end point was progression-free survival (PFS). Results: 97 patients were enroled and randomly assigned; 2 patients did not receive study drugs. In total, 95 patients received maintenance therapy (pazopanib, n = 48; placebo, n = 47) and were included in the analyses. Grade 3 toxicities for pazopanib maintenance were thrombocytopenia (10.4%, including one case with grade 4 toxicity), liver enzyme elevation (10.4%), fatigue (6.3%), and hypertension (6.3%). Median PFS was 3.7 months for pazopanib maintenance and 1.8 months for placebo (hazard ratio 0.44, 95% confidence interval: 0.29-0.69, P<0.0001). Conclusions: Pazopanib maintenance significantly prolonged PFS in patients with ED-SCLC. Given the toxicity profiles, however, relevant biomarkers to select patients for benefit from pazopanib should be further investigated.
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