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Persistent trophoblasic gestational disease: retrospective study about 55 cases at the National Institute of Oncology from 2000 to 2008

机译:持续性滋养性妊娠疾病:2000年至2008年美国国立肿瘤研究所约55例病例的回顾性研究

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Abstract Introduction: Persistent trophoblastic disease is curable and chemosensitive with a cure rate of up to 90% even at a metastatic stage. The aim of this retrospective study is to highlight different aspects of epidemiological, clinical, therapeutic treatment of persistent gestational trophoblastic disease (MTGP) in Moroccan patients through a series of 55 cases collected at the National Institute of Oncology between 2000 and 2008.Materials and methods: We collected for each patient, the different epidemiological, clinical and therapeutic features. Results: The mean age was 37.8 years. Clinical aspects were dominated by bleeding and pelvic pain. There were 19 cases of invasive mole and 34 cases of choriocarcinoma. 41.8% had in their antecedents a hydatidiform mole. All patients were evaluable and were graded according to the score of FIGO 2000, 70.9% were found to be at high risk. Treatment consisted of chemotherapy based on methotrexate or cisplatin. The overall survival rate was 81.82% and median survival was 152.2 months (? 9.8 months). Survival according to chemotherapy regimen based or not on platinum showed a statistically significant difference (P = 0.019).Conclusion: Given these data, a first-line chemotherapy based on platinum regimen in high-risk patients could be an effective and tolerable option if there is any contra indication or unavailability of methotrexate. Other prospective trials should evaluate these two options.
机译:摘要简介:持久性滋养细胞疾病可治愈且对化学敏感,即使在转移阶段,治愈率也高达90%。这项回顾性研究的目的是通过2000年至2008年间在美国国家肿瘤研究所收集的一系列55例病例来突出摩洛哥患者持续妊娠滋养细胞疾病(MTGP)的​​流行病学,临床,治疗方法的不同方面。 :我们为每位患者收集了不同的流行病学,临床和治疗特征。结果:平均年龄为37.8岁。临床方面以出血和骨盆疼痛为主。浸润性葡萄胎19例,绒毛膜癌34例。 41.8%的前胎有葡萄胎。所有患者都是可评估的,并根据FIGO 2000的评分进行分级,发现有70.9%的患者处于高风险。治疗包括基于甲氨蝶呤或顺铂的化疗。总体生存率为81.82%,中位生存期为152.2个月(约9.8个月)。结论:根据这些数据,如果存在高风险患者,基于铂方案的一线化疗可能是一种有效且可耐受的方案,存在统计学差异(P = 0.019)。是甲氨蝶呤的任何禁忌症或不可用。其他前瞻性试验应评估这两种选择。

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