PMID- 38177082 OWN - NLM STAT- MEDLINE DCOM- 20240123 LR - 20240305 IS - 1097-0223 (Electronic) IS - 0197-3851 (Linking) VI - 44 IP - 1 DP - 2024 Jan TI - Mammalian target of rapamycin inhibitors: A new-possible approach for in-utero medication therapy. PG - 88-98 LID - 10.1002/pd.6492 [doi] AB - The mammalian/mechanistic target of rapamycin (mTOR) is a protein kinase that plays a crucial role in regulating cellular growth, metabolism, and survival. Although there is no absolute contraindication for the use of mTOR inhibitors during pregnancy, the specific fetal effects remain unknown. Available data from the past 2 decades have examined the use of mTOR inhibitors during pregnancy in patients with solid organ transplantation, showing no clear link to fetal complications or structural abnormalities. Recently, a handful of case reports and series have described transplacental therapy of mTOR inhibitors to control symptomatic and complicated pathologies in the fetus. The effect of these agents includes a significant reduction in lesion size in the fetus and a reduced need for mechanical ventilation in neonates. In this context, we delve into the potential of mTOR inhibitors as in-utero therapy for fetal abnormalities, with a primary focus on lymphatic malformation (LM) and cardiac rhabdomyoma (CR). While preliminary reports underscore the efficacy of mTOR inhibitors for the treatment of fetal CR and fetal brain lesions associated with tuberous sclerosis complex, chylothorax, and LMs, additional investigation and clinical trials are essential to comprehensively assess the safety and efficacy of these medications. CI - (c) 2024 John Wiley & Sons Ltd. FAU - Qaderi, Shohra AU - Qaderi S AD - Maternal Fetal Care Center, Division of Fetal Medicine and Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. FAU - Javinani, Ali AU - Javinani A AD - Maternal Fetal Care Center, Division of Fetal Medicine and Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. FAU - Blumenfeld, Yair J AU - Blumenfeld YJ AUID- ORCID: 0000-0002-9440-8175 AD - Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, California, USA. FAU - Krispin, Eyal AU - Krispin E AUID- ORCID: 0000-0001-5859-9528 AD - Maternal Fetal Care Center, Division of Fetal Medicine and Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. FAU - Papanna, Ramesha AU - Papanna R AUID- ORCID: 0000-0002-3801-346X AD - Division of Fetal Intervention, Department of Obstetrics, Gynecology and Reproductive Sciences, McGovern Medical School at UT Health Houston, Houston, Texas, USA. FAU - Chervenak, Frank A AU - Chervenak FA AD - Department of Obstetrics and Gynecology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Lenox Hill Hospital, New York, New York, USA. FAU - Shamshirsaz, Alireza A AU - Shamshirsaz AA AUID- ORCID: 0000-0001-6333-3177 AD - Maternal Fetal Care Center, Division of Fetal Medicine and Surgery, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. LA - eng PT - Journal Article PT - Review DEP - 20240104 PL - England TA - Prenat Diagn JT - Prenatal diagnosis JID - 8106540 RN - W36ZG6FT64 (Sirolimus) RN - 0 (MTOR Inhibitors) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) SB - IM MH - Pregnancy MH - Infant, Newborn MH - Female MH - Humans MH - Sirolimus/therapeutic use MH - MTOR Inhibitors MH - TOR Serine-Threonine Kinases MH - *Tuberous Sclerosis MH - Fetus/metabolism MH - *Rhabdomyoma/drug therapy EDAT- 2024/01/05 00:42 MHDA- 2024/01/23 06:43 CRDT- 2024/01/04 22:42 PHST- 2023/12/04 00:00 [revised] PHST- 2023/09/13 00:00 [received] PHST- 2023/12/04 00:00 [accepted] PHST- 2024/01/23 06:43 [medline] PHST- 2024/01/05 00:42 [pubmed] PHST- 2024/01/04 22:42 [entrez] AID - 10.1002/pd.6492 [doi] PST - ppublish SO - Prenat Diagn. 2024 Jan;44(1):88-98. doi: 10.1002/pd.6492. Epub 2024 Jan 4.