TY - JOUR
T1 - Dalpiciclib or placebo plus fulvestrant in hormone receptor-positive and HER2-negative advanced breast cancer
T2 - a randomized, phase 3 trial
AU - DAWNA-1 Study Consortium
AU - Xu, Binghe
AU - Zhang, Qingyuan
AU - Zhang, Pin
AU - Hu, Xichun
AU - Li, Wei
AU - Tong, Zhongsheng
AU - Sun, Tao
AU - Teng, Yuee
AU - Wu, Xinhong
AU - Ouyang, Quchang
AU - Yan, Xi
AU - Cheng, Jing
AU - Liu, Qiang
AU - Feng, Jifeng
AU - Wang, Xiaojia
AU - Yin, Yongmei
AU - Shi, Yanxia
AU - Pan, Yueyin
AU - Wang, Yongsheng
AU - Xie, Weimin
AU - Yan, Min
AU - Liu, Yunjiang
AU - Yan, Ping
AU - Wu, Fei
AU - Zhu, Xiaoyu
AU - Zou, Jianjun
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2021/11
Y1 - 2021/11
N2 - Blockade of the cyclin-dependent kinase 4 and 6 pathway has been shown to be effective in the treatment of hormone receptor-positive advanced breast cancer (ABC). We report the interim results of DAWNA-1 (NCT03927456), a double-blind, randomized, phase 3 trial of dalpiciclib (a new cyclin-dependent kinase 4 and 6 inhibitor) plus fulvestrant in hormone receptor-positive, HER2-negative ABC with disease progression after endocrine therapy. A total of 361 patients were randomized 2:1 to receive dalpiciclib plus fulvestrant or placebo plus fulvestrant. The study met the primary end point, showing significantly prolonged investigator-assessed progression-free survival with dalpiciclib plus fulvestrant versus placebo plus fulvestrant (median = 15.7, 95% confidence interval (CI) = 11.1–not reached versus 7.2, 95% CI = 5.6–9.2 months; hazard ratio = 0.42, 95% CI = 0.31–0.58; one-sided P < 0.0001 (boundary was P ≤ 0.008)). The most common grade 3 or 4 adverse events with dalpiciclib plus fulvestrant were neutropenia (84.2%) and leukopenia (62.1%). The incidence of serious adverse events was 5.8% with dalpiciclib plus fulvestrant versus 6.7% with placebo plus fulvestrant. Our findings support dalpiciclib plus fulvestrant as a new treatment option for pretreated hormone receptor-positive, HER2-negative ABC.
AB - Blockade of the cyclin-dependent kinase 4 and 6 pathway has been shown to be effective in the treatment of hormone receptor-positive advanced breast cancer (ABC). We report the interim results of DAWNA-1 (NCT03927456), a double-blind, randomized, phase 3 trial of dalpiciclib (a new cyclin-dependent kinase 4 and 6 inhibitor) plus fulvestrant in hormone receptor-positive, HER2-negative ABC with disease progression after endocrine therapy. A total of 361 patients were randomized 2:1 to receive dalpiciclib plus fulvestrant or placebo plus fulvestrant. The study met the primary end point, showing significantly prolonged investigator-assessed progression-free survival with dalpiciclib plus fulvestrant versus placebo plus fulvestrant (median = 15.7, 95% confidence interval (CI) = 11.1–not reached versus 7.2, 95% CI = 5.6–9.2 months; hazard ratio = 0.42, 95% CI = 0.31–0.58; one-sided P < 0.0001 (boundary was P ≤ 0.008)). The most common grade 3 or 4 adverse events with dalpiciclib plus fulvestrant were neutropenia (84.2%) and leukopenia (62.1%). The incidence of serious adverse events was 5.8% with dalpiciclib plus fulvestrant versus 6.7% with placebo plus fulvestrant. Our findings support dalpiciclib plus fulvestrant as a new treatment option for pretreated hormone receptor-positive, HER2-negative ABC.
UR - https://www.scopus.com/pages/publications/85118888923
U2 - 10.1038/s41591-021-01562-9
DO - 10.1038/s41591-021-01562-9
M3 - 文章
C2 - 34737452
AN - SCOPUS:85118888923
SN - 1078-8956
VL - 27
SP - 1904
EP - 1909
JO - Nature Medicine
JF - Nature Medicine
IS - 11
ER -