Continuous ovarian stimulation: a proof-of-concept study exploring the uninterrupted use of corifollitropin α in DuoStim cycles for enhanced efficiency and patient convenience (Alicante protocol)

Juan Carlos Castillo M.D., Ph.D. , Ana Fuentes M.D. , Jose Antonio Ortiz M.Sc., Ph.D. , Esther Abellán M.Sc. , Andrea Bernabeu M.D., Ph.D. , Rafael Bernabeu M.D., Ph.D.
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引用次数: 0

Abstract

Objective

To explore the use of weekly continuous dosing of corifollitropin α in DuoStim cycles.

Design

Pilot-matched case-control study.

Setting

Private fertility center.

Patient(s)

Cases were defined as DuoStim cycles performed from November 2022 to May 2023 receiving weekly continuous dosing of corifollitropin α (n = 15). Controls were chosen from a database comprising DuoStim cycles conducted at our institution during the years 2021/2022. Matching was done on a 1-to-1 basis, based on antimüllerian hormone values (±0.4 pmol/L) and age (n = 15).

Intervention(s)

Injections of corifollitropin α once every 8 days, along with uninterrupted oral administration of micronized progesterone 200 mg/d (for luteinizing hormone surge prevention) throughout the follicular and luteal phases for ovarian stimulation. Oocyte retrieval.

Main outcome measure(s)

Total number of cumulus-oocyte complexes and metaphase II oocytes obtained in follicular + luteal phase stimulation. Secondary outcomes evaluated fertilization rates, number of blastocysts, days of stimulation, number of injectables required, and gonadotropin cost.

Result(s)

The study group achieved similar total oocyte and MII yield vs. daily follicle-stimulating hormone protocol (13.3 ± 6.9 vs. 11.8 ± 6.1 and 10.4 ± 6.3 vs. 9.2 ± 4.6, respectively). All secondary outcomes showed no significant differences. The study group experienced a significant reduction of injections to complete a DuoStim cycle (4.5 ± 1.4 vs. 35.2 ± 12.2; mean deviation -30.7; 95% confidence interval, −37.5– to −23.9)].

Conclusion(s)

Corifollitropin α on a weekly basis throughout a DuoStim cycle yields an equivalent number of oocytes as standard daily follicle-stimulating hormone administration while drastically reducing the number of required injections.

Trial registration number

NCT05815719. EudraCT: 2022-003177-32.

持续卵巢刺激:一项概念验证研究,探索在双刺激周期中不间断使用甲型促性腺激素,以提高效率和方便患者(阿利坎特方案)
目的探讨在DuoStim周期中使用每周连续给药的促甲状腺激素α的情况.设计试验性匹配病例对照研究.地点私立生殖中心.患者病例定义为2022年11月至2023年5月期间接受每周连续给药的促甲状腺激素α的DuoStim周期(n = 15)。对照组选自本机构 2021/2022 年进行的 DuoStim 周期数据库。干预措施:在卵泡期和黄体期的整个卵巢刺激过程中,每8天注射一次促性腺激素α,同时不间断地口服微粒化黄体酮200毫克/天(用于预防黄体生成素激增)。主要结果指标:在卵泡期和黄体期刺激中获得的积液-卵母细胞复合体和分裂期 II 卵母细胞总数。次要结果评估受精率、囊胚数量、刺激天数、所需注射剂数量和促性腺激素成本。结果:与每日卵泡刺激素方案相比,研究组获得了相似的卵母细胞和MII总产量(分别为13.3 ± 6.9 vs. 11.8 ± 6.1和10.4 ± 6.3 vs. 9.2 ± 4.6)。所有次要结果均无明显差异。结论:在整个DuoStim周期中,每周使用促卵泡激素α可获得与每天使用标准促卵泡激素相同数量的卵母细胞,同时大大减少了所需的注射次数。EudraCT:2022-003177-32。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
FS Reports
FS Reports Medicine-Embryology
CiteScore
3.50
自引率
0.00%
发文量
78
审稿时长
60 days
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