Department of Medical Oncology, Institut Jules Bordet and l'Université Libre de Bruxelles, Boulevard de Waterloo 121, 1000 Brussels, Belgium.
Breast Cancer Res Treat. 2012 May;133(1):387-91. doi: 10.1007/s10549-012-1996-6. Epub 2012 Feb 26.
Only few case reports describe the pregnancy course and outcome of breast cancer patients, who were under treatment with trastuzumab at the time of conception or who have completed trastuzumab therapy before becoming pregnant. The HERA trial is a large phase III randomized clinical trial in which patients with early HER2-positive breast cancer were randomized to receive 1 or 2 years of trastuzumab or observation following completion of primary chemotherapy. To examine the effect of trastuzumab on pregnancy outcome, we report all pregnancy events that occurred until March 2010 in patients enrolled in the study. For the sake of this analysis, patients were assigned to three groups: (1) pregnancy occurring during and up to 3 months after trastuzumab exposure (group 1); (2) pregnancy occurring >3 months of last trastuzumab dose (group 2); and (3) pregnancy occurring in patients without prior exposure to trastuzumab (group 3). Sixteen, 45 and 9 pregnancies took place in groups 1, 2, and 3, respectively. 25 and 16% of patients in groups 1 and 2 experienced spontaneous abortion, the former being higher than figures reported in the general population. However, short-term fetal outcome appeared normal across the three groups. Only 2 congenital anomalies were reported, one in group 2 and one in group 3. No congenital anomalies were reported in those exposed to trastuzumab in utero. This is the first report from a large randomized trial assessing the effect of trastuzumab on pregnancy course and outcome. Based on our results, trastuzumab does not appear to affect fetal outcome in patients who manage to complete their pregnancy. We are currently initiating a collaboration to collect similar data from the other large adjuvant trastuzumab trials to confirm these findings.
仅有少数病例报告描述了在受孕时正在接受曲妥珠单抗治疗或在怀孕前已完成曲妥珠单抗治疗的乳腺癌患者的妊娠过程和结局。HERA 试验是一项大型 III 期随机临床试验,其中早期 HER2 阳性乳腺癌患者被随机分配接受 1 或 2 年的曲妥珠单抗治疗或在完成主要化疗后进行观察。为了研究曲妥珠单抗对妊娠结局的影响,我们报告了截至 2010 年 3 月在该研究中入组的患者发生的所有妊娠事件。为了进行这项分析,患者被分为三组:(1)在曲妥珠单抗暴露期间和暴露后 3 个月内发生的妊娠(组 1);(2)在最后一次曲妥珠单抗剂量 >3 个月后发生的妊娠(组 2);(3)在无先前曲妥珠单抗暴露的患者中发生的妊娠(组 3)。分别有 16、45 和 9 例妊娠发生在组 1、2 和 3 中。组 1 和 2 中分别有 25%和 16%的患者发生自然流产,前者高于一般人群的报告数字。然而,三组的短期胎儿结局似乎正常。仅报告了 2 例先天性异常,其中 1 例发生在组 2,1 例发生在组 3。在子宫内暴露于曲妥珠单抗的患者中未报告先天性异常。这是第一项从大型随机试验中评估曲妥珠单抗对妊娠过程和结局影响的报告。基于我们的结果,曲妥珠单抗似乎不会影响设法完成妊娠的患者的胎儿结局。我们目前正在发起合作,从其他大型辅助曲妥珠单抗试验中收集类似数据,以确认这些发现。