Combination chemotherapy for high-risk gestational trophoblastic tumour

被引:14
|
作者
Deng, Linyu [2 ,3 ]
Yan, Xue [4 ]
Zhang, Jing [5 ]
Wu, Taixiang [1 ]
机构
[1] Sichuan Univ, W China Hosp, Chinese EBM Ctr, Chinese Cochrane Ctr, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, W China Hosp, Natl Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, W China Hosp, Ctr Canc, Chengdu 610041, Sichuan, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Med, Xian 710049, Peoples R China
[5] Sichuan Univ, W China Univ Hosp 2, Dept Obstet & Gynecol, Chengdu 610041, Sichuan, Peoples R China
关键词
HYDATIDIFORM MOLE; INTERMEDIATE TROPHOBLAST; DISEASE; METHOTREXATE; MANAGEMENT; PREGNANCY;
D O I
10.1002/14651858.CD005196.pub3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Gestational trophoblastic disease (GTD) includes gestational trophoblastic tumour and hydatidiform mole. Many women of reproductive age are affected by this disease although its incidence differs by geographical location. A number of chemotherapy regimens are used for treating the disease, such as methotrexate, actinomycin D and cyclophosphamide (MAC), methotrexate, actinomycin D, cyclophosphamide, doxorubicin, melphalan, hydroxyurea and vincristine (CHAMOC), etoposide, methotrexate and actinomycin (EMA) plus cyclophosphamide and vincristine (CO) (EMA-CO), etoposide, methotrexate and actinomycin (EMA) plus etoposide and cisplatin(EP) (EMA-EP). The efficacy of these drugs has not been systematically reviewed. Objectives To determine the efficacy and safety of combination chemotherapy in treating high-risk GTT. Search strategy Electronic searches of Cochrane Central Register of Controlled Trials (CENTRAL) (Issue 2, 2008), MEDLINE, EMB and CBM, May 2008. Four journals were handsearched and other searching methods were used for identifying more studies. Selection criteria The review included randomised controlled trials (RCTs) or quasi-RCTs of combination chemotherapy for treating high-risk GTT. Patients with placental-site trophoblastic tumour (PSTT), who had received chemotherapy in the previous two weeks, or patients with chemotherapy intolerance were excluded. Data collection and analysis Two investigators independently collected data using a data extraction form. Meta-analysis was not performed and the review was conducted as a narrative review. Main results One study with 42 participants was included in this review. It indicated that a MAC regimen was better than a CHAMOCA regimen for high-risk GTT because of lower toxicity. The quality of the study was unclear. Authors' conclusions The methodological limitations of the included study prevent any firm conclusions about the best combination chemotherapy regimen for high-risk GTT. High quality studies are required.
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页数:17
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