Treatment for low-risk gestational trophoblastic disease: Comparison of single-agent methotrexate, dactinomycin and combination regimens
| Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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| Data(s) |
19/10/2012
19/10/2012
2008
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| Resumo |
Objectives. To compare the efficacy of three different standard chemotherapy regimens for low-risk gestational trophoblastic disease according to the FIGO staging system in a single-institute setting. Methods. From 1980 until 2002, we retrospectively reviewed 108 cases with low-risk persistent gestational trophoblastic disease who were treated with first-line chemotherapy. Patients were divided in three groups according to chemotherapy regimen: patients treated with methotrexate (MTX group; n=42), patients treated with dactinomycin (ACT group; n=42) and patients treated with methotrexate and dactinomycin in combination (MACT group; n=24). We compared the number of chemotherapy courses for achieving remission, the duration of treatment, the adverse side effects, the efficacy of the treatment and the need for performing a hysterectomy among the groups Results. The complete remission rates were 69%, 61.4% and 79.1% for methotrexate (MTX), dactinomycin (ACT) and the combination regimen (MACT) treated groups, respectively (p=0.7). The duration of the treatment and the number of chemotherapy courses were similar among the groups (p = 0.2 and p = 0.4, respectively). Adverse side effects rate was reported to be 62.5% in the MACT group, 28.6% in the MTX group and 19.1% in the ACT group (p=0.0003). Second-line chemotherapy was indicated for 30 patients. Hysterectomy was performed in 21 patients overall, and there was no difference among the groups (P=0.6). Conclusion. Our analysis indicates that single-agent chemotherapy regimens are as effective as combination chemotherapy for low-risk gestational trophoblastic disease. Dactinomycin is a less toxic drug and might offer the best cost-effective treatment option. Methotrexate must be considered as the regimen of choice for low resource areas because of the feasibility of its administration. (c) 2007 Elsevier Inc. All rights reserved. |
| Identificador |
GYNECOLOGIC ONCOLOGY, v.108, n.1, p.149-153, 2008 0090-8258 http://producao.usp.br/handle/BDPI/24577 10.1016/j.ygyno.2007.09.006 |
| Idioma(s) |
eng |
| Publicador |
ACADEMIC PRESS INC ELSEVIER SCIENCE |
| Relação |
Gynecologic Oncology |
| Direitos |
restrictedAccess Copyright ACADEMIC PRESS INC ELSEVIER SCIENCE |
| Palavras-Chave | #human chorionic gonadotrophin #gestational trophoblastic disease #chemotherapy #FACTOR SCORING SYSTEM #ACTINOMYCIN-D #ONCOLOGY-GROUP #FOLINIC ACID #TUMORS #CHEMOTHERAPY #NEOPLASIA #THERAPY #WOMEN #MANAGEMENT #Oncology #Obstetrics & Gynecology |
| Tipo |
article original article publishedVersion |