Gestational choriocarcinoma

妊娠绒毛膜癌
  • 文章类型: Journal Article
    目的:探讨临床病理特征,预后因素,治疗,临床反应,和妊娠绒毛膜癌(GCC)的结局。
    方法:对1992年至2020年在土耳其两个转诊中心诊断并治疗GCC的13例患者的临床病理和生存数据进行了回顾性回顾。
    结果:患者的中位年龄为36岁(范围,27-54岁),七个≤39岁。9例(69.2%)的先期妊娠是一个术语,风险评分≥7/11(84.6%)。根据国际妇产科联合会2009年分期,八个病例处于第一阶段,第二阶段是第三阶段,第三阶段。除了一个病人,所有其他人都接受了联合化疗(CT),其中两人也接受了放射治疗。化学抗性在50%(6/12)发展,其中4例接受了二线CT检查。总体完全缓解率为69.2%。四名患者死于化疗耐药和疾病进展,他们都是先期怀孕,高分≥7分,并有转移。
    结论:GCC是妊娠滋养细胞肿瘤的一种独特亚型,在预后不良方面与其他人不同,早期转移的频繁趋势,和对治疗的抵抗力。为了能够达到最有效的治疗和预后,应开发基于组织病理学的风险模型。
    OBJECTIVE: To investigate the clinicopathological features, prognostic factors, treatment, clinical response, and outcome of gestational choriocarcinoma (GCC).
    METHODS: A retrospective review was made of the clinicopathological and survival data of 13 patients who were diagnosed and treated for GCC in two referral centers in Turkey between 1992 and 2020.
    RESULTS: The median age of patients was 36 years (range, 27-54 years), and seven were ≤39 years. The antecedent pregnancy was a term in nine (69.2%) cases, and the risk score was ≥7 in 11 (84.6%). According to the International Federation of Gynecology and Obstetrics 2009 staging, eight cases were in stage I, two in stage III, and three in stage IV. With the exception of one patient, all the others received combination chemotherapy (CT), and two of those were also treated with radiotherapy. Chemoresistance developed in 50% (6/12), and second-line CT was given to four of these. The overall complete response rate was 69.2%. Four patients died of chemoresistance and disease progression, all of them were with antecedent-term pregnancy, had high scores ≥7, and had metastases.
    CONCLUSIONS: GCC is a unique subtype of gestational trophoblastic neoplasia, which differs from others in terms of poor prognosis, a frequent tendency to early metastasis, and resistance to treatment. To be able to achieve the most efficient therapy and prognosis, histopathology-based risk models should be developed.
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  • 文章类型: Journal Article
    目的:确定在第1、3、5和7天肌内给予甲氨蝶呤50mg和在第2、4、6和8天口服亚叶酸15mg的单药化疗(IMMTX/FA)是否是低危妊娠绒毛膜癌患者的有效治疗方案。
    方法:从2000年1月至2011年12月,在Sheffield和CharingCross超区域滋养细胞疾病中心搜索电子数据库以确定妊娠绒毛膜癌患者。对FIGO评分为0-6的低风险患者的临床记录进行回顾性审查,以评估治疗结果和随后的复发。
    结果:65例患者被确定为低风险绒毛膜癌。在不需要化疗的24例患者中,血清hCG水平正常化(19例经组织学证实,4个高度可疑的组织学和1个临床诊断)。在23例经组织学证实的绒毛膜癌患者中,8(35%)对IMMTX/FA有持续的完全反应,没有复发。FIGO评分为6的患者和1例FIGOIII期转移性疾病患者均对IMMTX/FA产生耐药性,需要进一步治疗。尽管出现了耐药性或复发,但所有患者均通过后续治疗成功挽救。
    结论:并非所有的低风险绒毛膜癌患者在分期前都进行了初步干预,如手术切除或子宫排空需要化疗,提供hCG水平继续下降到正常。低风险(FIGO0-5)患者最初应接受IMMTX/FA,因为其低毒性,门诊用药及疗效合理。FIGO评分为6或FIGOIII期疾病的患者应在IMMTX/FA和联合化疗之间做出明智的选择。
    OBJECTIVE: To determine whether single agent chemotherapy with intramuscular methotrexate 50mg administered on days 1, 3, 5, and 7 and oral folinic acid 15mg administered on days 2, 4, 6, and 8 in 2 weekly cycles (IM MTX/FA) is an effective treatment regimen for patients with low risk gestational choriocarcinoma.
    METHODS: Electronic databases were searched to identify patients with gestational choriocarcinoma at the Sheffield and Charing Cross supra-regional trophoblastic disease centres from January 2000 to December 2011. Clinical notes of low risk patients with FIGO score 0-6 were retrospectively reviewed to assess treatment outcomes and subsequent relapse.
    RESULTS: 65 patients were identified with low risk choriocarcinoma. Serum hCG levels normalised in 24 patients without the requirement of chemotherapy (19 with histological confirmation, 4 highly suspicious histology and 1 clinical diagnosis). Of 23 patients with histologically confirmed choriocarcinoma, 8 (35%) had a sustained complete response to IM MTX/FA and did not relapse. Both patients with FIGO score 6, and 1 patient with FIGO stage III metastatic disease developed resistance to IM MTX/FA and required further treatment. Despite the development of drug resistance or relapse all patients were successfully salvaged by subsequent treatments.
    CONCLUSIONS: Not all patients with low risk choriocarcinoma that have had primary intervention prior to staging, such as surgical resection or uterine evacuation will require chemotherapy, providing hCG levels continue to decline to normal. Low risk (FIGO 0-5) patients should initially receive IM MTX/FA due to its low toxicity, outpatient administration and reasonable efficacy. Patients with FIGO score 6 or FIGO stage III disease should make an informed choice between IM MTX/FA and combination chemotherapy.
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