First report of successful pregnancies after treatment with alpelisib for PIK3CA-related overgrowth spectrum

IF 4.6 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Gabriel Morin, Antoine Fraissenon, Caroline Chopinet, Estelle Balducci, Sophie Kaltenbach, Patrick Villarese, Vahid Asnafi, Laurent Guibaud, Guillaume Canaud
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引用次数: 0

Abstract

Alpelisib is a selective PI3Kα inhibitor approved for treating PIK3CA-related overgrowth spectrum (PROS), a group of rare malformation disorders. Given that PI3Kα is a ubiquitous protein involved in cell proliferation, understanding the long-term impact of alpelisib on fertility is of critical importance. Here, we report the favorable outcomes of three pregnancies in PROS patients after prolonged treatment with alpelisib. Although disease progression was observed in all three patients during pregnancy, vascular malformations remained sensitive to alpelisib without evidence of secondary resistance upon resuming treatment. In conclusion, we provide the first evidence that alpelisib does not appear to affect fertility in female patients with PROS.
首次报道用alpelisib治疗pik3ca相关过度生长谱后成功怀孕。
Alpelisib是一种选择性PI3Kα抑制剂,被批准用于治疗pik3ca相关过度生长谱(PROS),这是一组罕见的畸形疾病。鉴于PI3Kα是一种普遍存在的参与细胞增殖的蛋白,了解alpelisib对生育的长期影响至关重要。在这里,我们报告了三例妊娠的PROS患者在接受alpelisib长期治疗后的良好结果。虽然所有3例患者在妊娠期间均观察到疾病进展,但血管畸形对alpelisib仍然敏感,在恢复治疗后没有出现继发耐药的证据。总之,我们提供了第一个证据,证明alpelisib似乎不会影响女性pro患者的生育能力。
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
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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