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低危型妊娠滋养细胞肿瘤患者采用单药肌内注射甲氨蝶呤联合口服亚叶酸治疗的结局。

The outcome of patients with low risk gestational trophoblastic neoplasia treated with single agent intramuscular methotrexate and oral folinic acid.

机构信息

Sheffield Centre for Trophoblastic Disease, Weston Park Hospital, Cancer Research-UK/Yorkshire Cancer Research Sheffield Cancer Research Centre, Sheffield, UK.

出版信息

Eur J Cancer. 2013 Oct;49(15):3184-90. doi: 10.1016/j.ejca.2013.06.004. Epub 2013 Jul 16.

Abstract

BACKGROUND

Gestational trophoblastic neoplasia (GTN) persisting despite local treatment requires chemotherapy. In 2000, the revised International Federation of Gynaecology and Obstetrics (FIGO)/World Health Organisation (WHO) staging system was introduced, classifying patients as at 'low' or 'high' risk for resistance to single agent treatment.

PATIENTS AND METHODS

We have evaluated the complete response rates of patients with low risk GTN treated with 2 weekly intramuscular (IM) methotrexate 50mg four doses days 1, 3, 5, 7 and oral folinic acid 15 mg days 2, 4, 6, 8 (MTX/FA). Patient data between January 2000 and December 2011 were collated and the relationships between FIGO/WHO risk score and outcomes evaluated.

RESULTS

Two hundred and eighty nine patients were treated with single agent IM MTX/FA and assessed for treatment response. 29/36 (81%) patients with a FIGO/WHO total score of 6 developed resistance to MTX/FA compared with 87/253 (34%) patients with a score of 0-5 (p ≤ 0.0001). Significantly higher rates of resistance were found for patients with an hCG level of >100,000 iu/l compared to an hCG level of <100,000 iu/l (84% versus 34% p ≤ 0.0001). All patients were eventually cured with chemotherapy or surgical salvage.

CONCLUSIONS

Patients with low risk GTN that have a FIGO/WHO score of 6 or hCG level of >100,000 iu/l have high rates of resistance to MTX/FA and require further treatment. Revision of the FIGO/WHO scoring system may be appropriate to enable selection of more effective first line chemotherapy.

摘要

背景

尽管进行了局部治疗,但仍存在妊娠滋养细胞肿瘤(GTN)需要化疗。2000 年,修订后的国际妇产科联合会(FIGO)/世界卫生组织(WHO)分期系统引入,将患者分为对单一药物治疗具有“低”或“高”耐药风险的类别。

患者和方法

我们评估了低风险 GTN 患者接受每周 2 次肌内(IM)甲氨蝶呤 50mg 四剂(第 1、3、5 和 7 天)和口服亚叶酸 15mg(第 2、4、6 和 8 天)(MTX/FA)治疗的完全缓解率。收集了 2000 年 1 月至 2011 年 12 月期间的数据,并评估了 FIGO/WHO 风险评分与结局之间的关系。

结果

289 例患者接受了单药 IM MTX/FA 治疗并评估了治疗反应。36 例(81%)FIGO/WHO 总评分 6 的患者对 MTX/FA 产生耐药,而 253 例(34%)评分 0-5 的患者中耐药的患者为 87 例(p≤0.0001)。hCG 水平>100,000iu/l 的患者耐药率明显高于 hCG 水平<100,000iu/l 的患者(84%比 34%,p≤0.0001)。所有患者最终均通过化疗或手术挽救治愈。

结论

FIGO/WHO 评分 6 或 hCG 水平>100,000iu/l 的低危 GTN 患者对 MTX/FA 耐药率高,需要进一步治疗。FIGO/WHO 评分系统的修订可能有助于选择更有效的一线化疗药物。

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