Ferrigno Guajardo Ana S, Vaca-Cartagena Bryan F, Mayer Erica L, Bousrih Chayma, Oluchi Oke, Saura Cristina, Peccatori Fedro, Muñoz-Montaño Wendy, Cabrera-Garcia Alvaro, Lambertini Matteo, Corrales Luis, Becerril-Gaitan Andrea, Sella Tal, Newman Alexandra Bili, Pistilli Barbara, Martinez Ashley, Ortiz Carolina, Joval-Ramentol Laia, Scarfone Giovanna, Buonomo Barbara, Lara-Medina Fernando, Sanchez Jacqueline, Arecco Luca, Ramos-Esquivel Allan, Susnjar Snezana, Morgan Gilberto, Villarreal-Garza Cynthia, Azim Hatem A
Department of Medicine, Yale University School of Medicine, New Haven, CT, USA.
Breast Cancer Center, Hospital Zambrano Hellion, Tecnologico de Monterrey, San Pedro Garza Garcia, Mexico.
J Natl Cancer Inst. 2024 Feb 8;116(2):239-248. doi: 10.1093/jnci/djad219.
The addition of taxanes to anthracycline-based chemotherapy is considered standard of care in the treatment of breast cancer. However, there are insufficient data regarding the safety of taxanes during pregnancy. The aim of this study was to describe the incidence of obstetric and neonatal adverse events associated with the use of taxane-containing chemotherapy regimens for the treatment of breast cancer during pregnancy.
This is a multicenter, international cohort study of breast cancer patients treated with taxanes during pregnancy. A descriptive analysis was undertaken to synthetize available data.
A total of 103 patients were included, most of whom were treated with paclitaxel and anthracyclines given in sequence during gestation (90.1%). The median gestational age at taxane initiation was 28 weeks (range = 12-37 weeks). Grade 3-4 adverse events were reported in 7 of 103 (6.8%) patients. The most common reported obstetric complications were intrauterine growth restriction (n = 8 of 94, 8.5%) and preterm premature rupture of membranes (n = 5 of 94, 5.3%). The live birth rate was 92 of 94 (97.9%), and the median gestational age at delivery was 37 weeks (range = 32-40 weeks). Admission to an intensive care unit was reported in 14 of 88 (15.9%) neonates, and 17 of 70 (24.3%) live births resulted in small for gestational age neonates. Congenital malformations were reported in 2 of 93 (2.2%).
Obstetric and neonatal outcomes after taxane exposure during pregnancy were generally favorable and did not seem to differ from those reported in the literature with standard anthracycline-based regimens. This study supports the use of taxanes during gestation when clinically indicated.
在基于蒽环类药物的化疗中添加紫杉烷被认为是乳腺癌治疗的标准疗法。然而,关于紫杉烷在孕期安全性的数据不足。本研究的目的是描述与孕期使用含紫杉烷化疗方案治疗乳腺癌相关的产科和新生儿不良事件的发生率。
这是一项对孕期接受紫杉烷治疗的乳腺癌患者进行的多中心国际队列研究。进行描述性分析以综合现有数据。
共纳入103例患者,其中大多数在妊娠期依次接受紫杉醇和蒽环类药物治疗(90.1%)。开始使用紫杉烷时的中位孕周为28周(范围 = 12 - 37周)。103例患者中有7例(6.8%)报告了3 - 4级不良事件。报告的最常见产科并发症是宫内生长受限(94例中有8例,8.5%)和胎膜早破(94例中有5例,5.3%)。94例中有92例(97.9%)活产,分娩时的中位孕周为37周(范围 = 32 - 40周)。88例新生儿中有14例(15.9%)报告入住重症监护病房,70例活产中有17例(24.3%)为小于胎龄儿。93例中有2例(2.2%)报告有先天性畸形。
孕期接触紫杉烷后的产科和新生儿结局总体良好,似乎与文献中基于标准蒽环类药物方案报告的结局无差异。本研究支持在临床指征明确时在孕期使用紫杉烷。