妊娠滋养细胞疾病的治疗结果,来自沙特阿拉伯的经验。

Muhammad Farooq Latif, Faisal Azam, Syed Hammad Hassan Tirmazy, Nedal Bukhari
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引用次数: 0

摘要

背景:本研究旨在评估诊断为妊娠滋养细胞瘤(GTN)患者的人绒毛膜促性腺激素(HCG)水平正常化所需的治疗结果和化疗时间,包括良性和恶性形式的条件。方法:本回顾性研究纳入2016年1月至2022年5月在单一肿瘤诊所接受化疗的GTD患者。临床资料从患者的电子记录中收集。结果:研究期间,共有24例诊断为GTD的患者接受了化疗,中位年龄32岁(范围:18-51岁)。肌注甲氨蝶呤是20例(83%)低风险疾病的主要单药化疗方案,而EMA-CO方案是3例(13%)高风险疾病的主要联合化疗方案。化疗周期的中位数为2(范围:1-16),人绒毛膜促性腺激素(HCG)正常化所需的中位数持续时间为4周(范围:1-16)。大约一半的患者(n=10, 47.5%)过渡到二线联合化疗,中位正常化持续时间为4个月。4名患者(40%)随后接受了EMA-CO方案的三线联合化疗。11例患者(47%)接受一线治疗获得初步完全缓解,10例患者(43%)需要二线化疗,4例患者(17%)需要三线EMACO化疗。在24名患者中,22名患者完全缓解,2名患者目前正在接受治疗。结论:所有患者化疗均获得完全缓解。实现HCG正常化的中位化疗时间为4周,相当于2个周期。值得注意的是,在一线和二线单药化疗后,只有4例患者需要三线化疗。
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TREATMENT OUTCOMES OF GESTATIONAL TROPHOBLASTIC DISEASE, EXPERIENCE FROM SAUDI ARABIA.

Background: This research aims to assess the treatment outcomes and chemotherapy duration required for the normalization of Human chorionic gonadotropin (HCG) levels in patients diagnosed with Gestational Trophoblastic Neoplasia (GTN), encompassing both benign and malignant forms of the condition.

Methods: This retrospective study included GTD patients treated with chemotherapy in a single oncology clinic from January 2016 to May 2022. Clinical data were gathered from electronic records of the patients.

Results: During the study period, a total of 24 patients diagnosed with GTD underwent chemotherapy, with a median age of 32 years (range: 18-51). Intramuscular Methotrexate was the primary single-agent chemotherapy utilized in 20 cases (83%) for low-risk disease, while the EMA-CO regimen was the predominant combination chemotherapy employed in 3 cases (13%) for high-risk disease. The median number of chemotherapy cycles administered was 2 (range: 1-16), with a median duration of 4 weeks (range: 1-16) required for Human chorionic gonadotropin (HCG) normalization. Approximately half of the patients (n=10, 47.5%) transitioned to second-line combination chemotherapy, with a median normalization duration of 4 months. Four patients (40%) subsequently received third-line combination chemotherapy using the EMA-CO regimen. Initial complete response was achieved in 11 patients (47%) with first-line treatment, while 10 patients (43%) required second-line chemotherapy and 4 patients (17%) necessitated third-line EMACO chemotherapy. Of the 24 patients, 22 achieved complete response, while 2 patients are currently undergoing treatment.

Conclusions: All patients successfully attained complete response with chemotherapy. The median duration of chemotherapy for achieving normalization of HCG was 4 weeks, equivalent to 2 cycles. Notably, only 4 patients necessitated third-line chemotherapy following single-agent chemotherapy in the first and second lines.

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