Chemotherapy for high-risk gestational trophoblastic tumors

被引:0
|
作者
Richard, S. [1 ]
Baste-Rotllan, N. [1 ]
Soares, D. G. [1 ]
Selle, F. [1 ,2 ]
Khalil, A. [1 ]
Gligorov, J. [1 ,2 ]
Avenin, D. [1 ]
Provent, S. [1 ]
Lotz, J. -P. [1 ,2 ]
机构
[1] Hop Tenon, AP HP, Serv Oncol Med & Therapie Cellulaire, APREC Alliance Rech Cancerol, F-75970 Paris 20, France
[2] Univ Paris 06, F-75005 Paris, France
关键词
Gestational trophoblastic neoplasia; High-Risk patients; Chemotherapy; Methotrexate; Cisplatin; Etoposide; Brain metastases; HIGH-DOSE CHEMOTHERAPY; COMBINATION CHEMOTHERAPY; GROWTH-FACTOR; ETOPOSIDE; DISEASE; CISPLATIN; NEOPLASIA; METHOTREXATE; VINCRISTINE; EMA/CO;
D O I
10.1007/s10269-014-2402-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Primary therapy for high-risk gestational trophoblastic neoplasia (GTN) includes a multi-agent, methotrexate-based regimen, named EMA/CO. In France, the guidelines recommend the use of either a platinum-based protocol when methotrexate is contra-indicated or a highdose EMA/CO once brain metastases are diagnosed. For patients who are resistant to the initial therapy, different salvage approaches have been developed or adapted from treatments already used for germ cell tumors. Currently, the most frequently used protocol is a combination of etoposide and platinum-based therapy (EMA/EP). In the EMA/EP protocol, etoposide and cisplatin are used in place of cyclophosphamide and vincristine (CO in the EMA/CO regimen) with the goal of reversing resistance mechanisms of previously used drugs. Although, new approaches for improving the management of high-risk patients who are resistant or refractory to the initial therapy are now available, new molecules are still awaited to optimize patient's care.
引用
收藏
页码:291 / 299
页数:9
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