Horne Andrew W, Tong Stephen, Moakes Catherine A, Middleton Lee J, Duncan W Colin, Mol Ben W, Whitaker Lucy H R, Jurkovic Davor, Coomarasamy Arri, Nunes Natalie, Holland Tom, Clarke Fiona, Doust Ann M, Daniels Jane P
MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, UK.
Department of Obstetrics and Gynaecology, University of Melbourne, Melbourne, VIC, Australia.
Lancet. 2023 Feb 25;401(10377):655-663. doi: 10.1016/S0140-6736(22)02478-3. Epub 2023 Feb 1.
Tubal ectopic pregnancies can cause substantial morbidity or even death. Current treatment is with methotrexate or surgery. Methotrexate treatment fails in approximately 30% of women who subsequently require rescue surgery. Gefitinib, an epidermal growth factor receptor inhibitor, might improve the effects of methotrexate. We assessed the efficacy of oral gefitinib with methotrexate, versus methotrexate alone, to treat tubal ectopic pregnancy.
We performed a multicentre, randomised, double-blind, placebo-controlled trial across 50 UK hospitals. Participants diagnosed with tubal ectopic pregnancy were administered a single dose of intramuscular methotrexate (50 mg/m) and randomised (1:1 ratio) to 7 days of additional oral gefitinib (250 mg daily) or placebo. The primary outcome, analysed by intention to treat, was surgical intervention to resolve the ectopic pregnancy. Secondary outcomes included time to resolution of ectopic pregnancy and serious adverse events. This trial is registered at the ISRCTN registry, ISCRTN 67795930.
Between Nov 2, 2016, and Oct 6, 2021, 328 participants were allocated to methotrexate and gefitinib (n=165) or methotrexate and placebo (n=163). Three participants in the placebo group withdrew. Surgical intervention occurred in 50 (30%) of 165 participants in the gefitinib group and in 47 (29%) of 160 participants in the placebo group (adjusted risk ratio 1·15, 95% CI 0·85 to 1·58; adjusted risk difference -0·01, 95% CI -0·10 to 0·09; p=0·37). Without surgical intervention, median time to resolution was 28·0 days in the gefitinib group and 28·0 days in the placebo group (subdistribution hazard ratio 1·03, 95% CI 0·75 to 1·40). Serious adverse events occurred in five (3%) of 165 participants in the gefitinib group and in six (4%) of 162 participants in the placebo group. Diarrhoea and rash were more common in the gefitinib group.
In women with a tubal ectopic pregnancy, adding oral gefitinib to parenteral methotrexate does not offer clinical benefit over methotrexate and increases minor adverse reactions.
National Institute of Health Research.
输卵管异位妊娠可导致严重发病甚至死亡。目前的治疗方法是使用甲氨蝶呤或手术。约30%接受甲氨蝶呤治疗的女性治疗失败,随后需要进行挽救性手术。吉非替尼是一种表皮生长因子受体抑制剂,可能会提高甲氨蝶呤的疗效。我们评估了口服吉非替尼联合甲氨蝶呤与单用甲氨蝶呤治疗输卵管异位妊娠的疗效。
我们在英国50家医院进行了一项多中心、随机、双盲、安慰剂对照试验。诊断为输卵管异位妊娠的参与者接受单剂量肌内注射甲氨蝶呤(50 mg/m),并按1:1比例随机分为两组,分别额外口服吉非替尼7天(每日250 mg)或安慰剂。按意向性分析的主要结局是为解决异位妊娠而进行的手术干预。次要结局包括异位妊娠消退时间和严重不良事件。本试验已在国际标准随机对照试验编号注册库注册,编号为ISRCTN 67795930。
在2016年11月2日至2021年10月6日期间,328名参与者被分配至甲氨蝶呤联合吉非替尼组(n = 165)或甲氨蝶呤联合安慰剂组(n = 163)。安慰剂组有3名参与者退出。吉非替尼组165名参与者中有50名(30%)进行了手术干预,安慰剂组160名参与者中有47名(29%)进行了手术干预(调整风险比1.15,95%置信区间0.85至1.58;调整风险差 -0.01,95%置信区间 -0.10至0.09;p = 0.37)。在未进行手术干预的情况下,吉非替尼组的中位消退时间为28.0天,安慰剂组为28.0天(亚组分布风险比1.03,95%置信区间0.75至1.40)。吉非替尼组165名参与者中有5名(3%)发生严重不良事件,安慰剂组162名参与者中有6名(4%)发生严重不良事件。腹泻和皮疹在吉非替尼组中更常见。
对于输卵管异位妊娠女性,在胃肠外使用甲氨蝶呤基础上加用口服吉非替尼相比单用甲氨蝶呤并无临床益处,且会增加轻微不良反应。
英国国家卫生研究院。