Please use this identifier to cite or link to this item: https://ninho.inca.gov.br/jspui/handle/123456789/4791
Title: Challenges in the diagnosis and treatment of gestational trophoblastic neoplasia worldwide
Authors: Melo, Andreia Cristina de
Braga, Antonio
Mora, Paulo Alexandre Ribeiro
Rodrigues, Angélica Nogueira
Amim Junior, Joffre
Rezende Filho, Jorge
Seckl, Michael
Keywords: Diagnóstico
Diagnosis
Gravidez
Pregnancy
Neoplasias
Neoplasms
Doença Trofoblástica Gestacional
Gestational Trophoblastic Disease
Issue Date: 2019
Publisher: World J Clin Oncol
Citation: MELO, Andreia Cristina de et al. Challenges in the diagnosis and treatment of gestational trophoblastic neoplasia worldwide. World J Clin Oncol, v. 10, n. 2, p. 28-37, feb. 2019.
Abstract: Gestational trophoblastic neoplasia (GTN) is a rare tumor that originates from pregnancy that includes invasive mole, choriocarcinoma (CCA), placental site trophoblastic tumor and epithelioid trophoblastic tumor (PSTT/ETT). GTN presents different degrees of proliferation, invasion and dissemination, but, if treated in reference centers, has high cure rates, even in multi-metastatic cases. The diagnosis of GTN following a hydatidiform molar pregnancy is made according to the International Federation of Gynecology and Obstetrics (FIGO) 2000 criteria: four or more plateaued human chorionic gonadotropin (hCG) concentrations over three weeks; rise in hCG for three consecutive weekly measurements over at least a period of 2 weeks or more; and an elevated but falling hCG concentrations six or more months after molar evacuation. However, the latter reason for treatment is no longer used by many centers. In addition, GTN is diagnosed with a pathological diagnosis of CCA or PSTT/ETT. For staging after a molar pregnancy, FIGO recommends pelvic-transvaginal Doppler ultrasound and chest X-ray. In cases of pulmonary metastases with more than 1 cm, the screening should be complemented with chest computed tomography and brain magnetic resonance image. Single agent chemotherapy, usually Methotrexate (MTX) or Actinomycin-D (Act-D), can cure about 70% of patients with FIGO/World Health Organization (WHO) prognosis risk score ≤ 6 (low risk), reserving multiple agent chemotherapy, such as EMA/CO (Etoposide, MTX, Act-D, Cyclophosphamide and Oncovin) for cases with FIGO/WHO prognosis risk score ≥ 7 (high risk) that is often metastatic. Best overall cure rates for low and high risk disease is close to 100% and > 95%, respectively. The management of PSTT/ETT differs and cure rates tend to be a bit lower. The early diagnosis of this disease and the appropriate treatment avoid maternal death, allow the healing and maintenance of the reproductive potential of these women.
Description: p. 28-37. : il. p&b.
URI: http://sr-vmlxaph03:8080/jspui/handle/123456789/4791
ISSN: 2218-4333
Appears in Collections:Artigos de Periódicos da área de Ginecologia



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