Efficacy and safety of LY01005 versus goserelin implant in Chinese patients with prostate cancer: A multicenter, randomized, open-label, phase III, non-inferiority trial.
- Author:
Chengyuan GU
1
;
Zengjun WANG
2
;
Tianxin LIN
3
;
Zhiyu LIU
4
;
Weiqing HAN
5
;
Xuhui ZHANG
6
;
Chao LIANG
2
;
Hao LIU
3
;
Yang YU
4
;
Zhenzhou XU
5
;
Shuang LIU
6
;
Jingen WANG
7
;
Linghua JIA
7
;
Xin YAO
8
;
Wenfeng LIAO
8
;
Cheng FU
9
;
Zhaohui TAN
10
;
Guohua HE
11
;
Guoxi ZHU
12
;
Rui FAN
13
;
Wenzeng YANG
14
;
Xin CHEN
15
;
Zhizhong LIU
16
;
Liqiang ZHONG
17
;
Benkang SHI
18
;
Degang DING
19
;
Shubo CHEN
20
;
Junli WEI
20
;
Xudong YAO
21
;
Ming CHEN
22
;
Zhanpeng LU
23
;
Qun XIE
24
;
Zhiquan HU
25
;
Yinhuai WANG
26
;
Hongqian GUO
27
;
Tiwu FAN
28
;
Zhaozhao LIANG
29
;
Peng CHEN
30
;
Wei WANG
31
;
Tao XU
32
;
Chunsheng LI
33
;
Jinchun XING
34
;
Hong LIAO
35
;
Dalin HE
36
;
Zhibin WU
37
;
Jiandi YU
38
;
Zhongwen FENG
39
;
Mengxiang YANG
40
;
Qifeng DOU
41
;
Quan ZENG
42
;
Yuanwei LI
43
;
Xin GOU
44
;
Guangchen ZHOU
45
;
Xiaofeng WANG
46
;
Rujian ZHU
47
;
Zhonghua ZHANG
48
;
Bo ZHANG
49
;
Wanlong TAN
50
;
Xueling QU
51
;
Hongliang SUN
51
;
Tianyi GAN
51
;
Dingwei YE
1
Author Information
- Publication Type:Multicenter Study
- MeSH: Humans; Male; Antineoplastic Agents, Hormonal/therapeutic use*; East Asian People; Gonadotropin-Releasing Hormone/agonists*; Goserelin/therapeutic use*; Prostate-Specific Antigen; Prostatic Neoplasms/drug therapy*; Testosterone
- From: Chinese Medical Journal 2023;136(10):1207-1215
- CountryChina
- Language:English
-
Abstract:
BACKGROUND:LY01005 (Goserelin acetate sustained-release microsphere injection) is a modified gonadotropin-releasing hormone (GnRH) agonist injected monthly. This phase III trial study aimed to evaluated the efficacy and safety of LY01005 in Chinese patients with prostate cancer.
METHODS:We conducted a randomized controlled, open-label, non-inferiority trial across 49 sites in China. This study included 290 patients with prostate cancer who received either LY01005 or goserelin implants every 28 days for three injections. The primary efficacy endpoints were the percentage of patients with testosterone suppression ≤50 ng/dL at day 29 and the cumulative probability of testosterone ≤50 ng/dL from day 29 to 85. Non-inferiority was prespecified at a margin of -10%. Secondary endpoints included significant castration (≤20 ng/dL), testosterone surge within 72 h following repeated dosing, and changes in luteinizing hormone, follicle-stimulating hormone, and prostate specific antigen levels.
RESULTS:On day 29, in the LY01005 and goserelin implant groups, testosterone concentrations fell below medical-castration levels in 99.3% (142/143) and 100% (140/140) of patients, respectively, with a difference of -0.7% (95% confidence interval [CI], -3.9% to 2.0%) between the two groups. The cumulative probabilities of maintaining castration from days 29 to 85 were 99.3% and 97.8%, respectively, with a between-group difference of 1.5% (95% CI, -1.3% to 4.4%). Both results met the criterion for non-inferiority. Secondary endpoints were similar between groups. Both treatments were well-tolerated. LY01005 was associated with fewer injection-site reactions than the goserelin implant (0% vs . 1.4% [2/145]).
CONCLUSION:LY01005 is as effective as goserelin implants in reducing testosterone to castration levels, with a similar safety profile.
TRIAL REGISTRATION:ClinicalTrials.gov, NCT04563936.