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-Mu; Lee, Ki Hyeong; Kim, Bong-Seog; Kim, Hoon-Gu; Min, Young Joo; Yi, Seong Yoon; Yun, Hwan Jung; Jung, Sin-Ho; Lee, Se-Hoon; Ahn, Jin Seok; Park, Keunchil; Ahn, 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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