Clinical outcome following stimulation with highly purified hMG or recombinant FSH in patients undergoing IVF: a randomized assessor-blind controlled trial

被引:243
作者
Andersen, Anders Nyboe
Devroey, Paul
Arce, Joan-Carles
机构
[1] Rigshosp, Fertil Clin, DK-2100 Copenhagen, Denmark
[2] Vrije Univ Brussel VIB, Ctr Reprod Med, B-1050 Brussels, Belgium
[3] Ferring Pharmaceut AS, Clin Res & Dev, Copenhagen, Denmark
关键词
embryo quality; highly purified menotrophin; IVF; pregnancy; recombinant FSH;
D O I
10.1093/humrep/del284
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: LH activity may influence treatment response and outcome in IVF cycles. METHODS: A randomized, assessor-blind, multinational trial compared ongoing pregnancy rates (primary end-point) in 731 women undergoing IVF after stimulation with highly purified menotrophin (HP-hMG) (n = 363) or recombinant FSH (rFSH) (n = 368) following a long GnRH agonist protocol. Patients received identical pre- and post-randomization interventions. One or two embryos were transferred on day 3. RESULTS: More oocytes were retrieved (P < 0.001) after rFSH treatment (11.8) compared with HP-hMG treatment (10.0), but a higher proportion developed into top-quality embryos (P = 0.044) with HP-hMG (11.3%) than with rFSH (9.0%). At the end of stimulation, lower estradiol (E-2) (P = 0.031) and higher progesterone (P < 0.001) levels were found with rFSH, even after adjusting for follicular response. The distribution of hypo-, iso- and hyper-echogenic endometrium showed a significant (P = 0.023) shift towards the hyperechogenic pattern after rFSH treatment. The ongoing pregnancy rate per cycle was 27% with HP-hMG and 22% with rFSH [odds ratio (95% confidence interval): 1.25 (0.89-1.75)]. CONCLUSION: Superiority of HP-hMG over rFSH in ongoing pregnancy rate could not be concluded from this study, but non-inferiority was established. Pharmacodynamic differences in follicular development, oocyte/embryo quality, endocrine response and endometrial echogenicity exist between HP-hMG and rFSH preparations, which may be relevant for treatment outcome.
引用
收藏
页码:3217 / 3227
页数:11
相关论文
共 23 条
[1]  
[Anonymous], 2001, CPMP/ICH/364/96
[2]   Resolving methodological and clinical issues in the design of efficacy trials in assisted reproductive technologies: a mini-review [J].
Arce, JC ;
Andersen, AN ;
Collins, J .
HUMAN REPRODUCTION, 2005, 20 (07) :1757-1771
[3]   The human cumulus-oocyte complex gene-expression profile [J].
Assou, Said ;
Anahory, Tal ;
Pantesco, Veronique ;
Le Carrour, Tanguy ;
Pellestor, Franck ;
Klein, Bernard ;
Reyftmann, Lionel ;
Dechaud, Herve ;
De Vos, John ;
Hamamah, Samir .
HUMAN REPRODUCTION, 2006, 21 (07) :1705-1719
[4]   Pitfalls in the design and analysis of efficacy trials in subfertility [J].
Daya, S .
HUMAN REPRODUCTION, 2003, 18 (05) :1005-1009
[5]  
Diedrich K, 2002, FERTIL STERIL, V78, P520
[6]  
*ESHRE, 2006, EUR IVF MON PROGR EI
[7]  
*EUR MED AG, 2000, CPMPEWP48299
[8]  
European Medicines Agency, 2006, GUID CHOIC NON MARG
[9]  
European Medicines Agency, 1998, CPMPICH36396
[10]   New look at endometrial echogenicity: objective computer-assisted measurements predict endometrial receptivity in in vitro fertilization-embryo transfer [J].
Fanchin, R ;
Righini, C ;
Ayoubi, JM ;
Olivennes, F ;
de Ziegler, D ;
Frydman, R .
FERTILITY AND STERILITY, 2000, 74 (02) :274-281