Gillespie A M, Lorigan P C, Radstone C R, Waterhouse J C, Coleman R E, Hancock B W
Sheffield Supraregional Trophoblastic Disease Screening and Treatment Centre, Yorkshire Cancer Research Campaign Department of Clinical Oncology, Weston Park Hospital, UK.
Br J Cancer. 1997;76(10):1382-6. doi: 10.1038/bjc.1997.564.
The Sheffield Trophoblastic Disease Centre treats about 25 patients with persistent trophoblastic disease each year. A total of 75% of patients are classified as low risk according to the Charing Cross Hospital prognostic scoring system and receive methotrexate (MTX) 50 mg, i.m., on days 1, 3, 5, 7 with folinic acid 7.5 mg orally 24 h after each methotrexate injection. There is a 7-day rest between treatment cycles. Remission is achieved in 85% of cases. Approximately 20% of patients experienced pleuritic chest pain and dyspnoea. We have evaluated prospectively lung function in 16 low-risk patients receiving methotrexate. All patients had pulmonary function tests [spirometry-forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), peak expiratory flow rate (PEFR), and transfer factor - TLCO, kCO] performed before and after completed treatment. A mean of 7.5 cycles of MTX were administered (range 4-11). There was a significant reduction in the mean TLCO (mean pre/post 8.15/7.38 mmol min-1 kPa-1, P = 0.01), but there were no other statistically significant changes. Three patients experienced respiratory symptoms and were found to have a 39%, 28%, and 11% reduction in TLCO from baseline, improving on follow up to pretreatment levels. Low-dose MTX is an effective therapy but may cause troublesome pulmonary toxicity.
谢菲尔德滋养细胞疾病中心每年治疗约25例持续性滋养细胞疾病患者。根据查令十字医院预后评分系统,共有75%的患者被归类为低风险,并在第1、3、5、7天接受50毫克甲氨蝶呤(MTX)肌肉注射,每次甲氨蝶呤注射后24小时口服7.5毫克亚叶酸。治疗周期之间休息7天。85%的病例实现缓解。约20%的患者出现胸膜炎性胸痛和呼吸困难。我们前瞻性地评估了16例接受甲氨蝶呤治疗的低风险患者的肺功能。所有患者在完成治疗前后均进行了肺功能测试[肺活量测定——1秒用力呼气量(FEV1)、用力肺活量(FVC)、呼气峰值流速(PEFR)和转运因子——TLCO、kCO]。平均给予7.5个周期的MTX(范围4 - 11个周期)。平均TLCO有显著降低(平均治疗前/后为8.15/7.38 mmol min-1 kPa-1,P = 0.01),但没有其他具有统计学意义的变化。3例患者出现呼吸道症状,发现TLCO较基线水平分别降低了39%、28%和11%,随访时恢复到治疗前水平。低剂量MTX是一种有效的治疗方法,但可能会引起麻烦的肺毒性。