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Pulse actinomycin D as first-line treatment of low-risk post-molar non-choriocarcinoma gestational trophoblastic neoplasia
被引:12
|作者:
Li, Lei
[1
]
Wan, Xirun
[1
]
Feng, Fengzhi
[1
]
Ren, Tong
[1
]
Yang, Junjun
[1
]
Zhao, Jun
[1
]
Jiang, Fang
[1
]
Xiang, Yang
[1
]
机构:
[1] Beijing Union Med Coll Hosp, Peking Union Med Coll, Dept Obstet & Gynecol, Shuaifuyuan 1, Beijing 100730, Peoples R China
来源:
BMC CANCER
|
2018年
/
18卷
关键词:
Actinomycin D;
Gestational trophoblastic neoplasia;
Transvaginal ultrasound;
beta-hCG;
AGENT METHOTREXATE CHEMOTHERAPY;
WEEKLY INTRAMUSCULAR METHOTREXATE;
FOLINIC ACID;
TREATMENT OUTCOMES;
RESISTANCE;
TUMORS;
WOMEN;
CLASSIFICATION;
DACTINOMYCIN;
MANAGEMENT;
D O I:
10.1186/s12885-018-4512-5
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Little data exists predicting the resistance to actinomycin D (Act-D) single-agent for gestational trophoblastic neoplasia (GTN). The objective was to determine the overall success of pulse Act-D and the factors predictive of resistance to pulse Act-D in the treatment of low-risk, non-choriocarcinoma post-molar GTN. Methods: From January 2013 to October 2016, according to the FIGO criteria for the diagnosis of post-molar disease and the FIGO risk-factor scoring system for GTN, a total of 135 patients with post-molar non-choriocarcinoma GTN who were chemotherapy-naive with a FIGO score < 7 were treated with single-agent pulse Act-D as a first-line regimen, in Peking Union Medical College Hospital. The pulse Act-D regimen is defined as 1.25 mg/m(2) (max 2 mg) IV push every other week. All patients were followed until May 2017. Epidemiological and clinical data were compared between patients with remission and resistance to Act-D to determine predictive factors by univariate and multivariate analysis. Results: Ninety-six of 135 patients (71.1%) achieved complete remission after first-line chemotherapy of pulse Act-D. In multivariate analysis, existing invasive uterine lesions observed by pre-chemotherapy transvaginal ultrasound (odds ratio [OR] 7.5, 95% confidence intervals [CI] 2.7-20.8), FIGO score >= 5 (OR 15.2, 95% CI 1.5-156.1) and pre-chemotherapy levels of beta-hCG >= 4000 IU/L (OR 3.1, 95% CI 1.2-8.3) were independent high-risk factors predicting resistance to pulse Act-D as single-agent chemotherapy. During follow-up, no relapse, treatment-associated serious adverse events, or death occurred. Conclusions: As first-line chemotherapy, pulse Act-D was effective and tolerable for patients with low-risk post-molar non-choriocarcinoma. Existing invasive uterine lesions observed by pre-chemotherapy transvaginal ultrasound, a FIGO score >= 5, and pre-chemotherapy levels of beta-hCG >= 4000 IU/L were independent factors for resistance to pulse Act-D.
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