Study | Reason for exclusion |
---|---|
Fariba 2016 | A prospective randomised clinical trial comparing intravenous (IV) MTX and IV Act‐D in the treatment of low‐risk gestational trophoblastic neoplasia, invasive mole, and choriocarcinoma. |
Geng 2011 | A retrospective study evaluating characteristics and outcomes for 23 women with high‐risk HM who received prophylactic chemotherapy (5‐FU or dactinomycin). |
Mousavi 2012 | A RCT of 75 patients with low‐risk GTD (FIGO stage I, II, or III disease, a WHO risk score of 6 or less), 50 receiving pulsed actinomycin D and 25 receiving 5‐day methotrexate. |
Uberti 2006 | A retrospective study evaluating a bolus dose of dactinomycin for prevention of persistent GTD in 29 adolescents with high‐risk molar pregnancy compared with a similar control group of 31 adolescents. |
Uberti 2009 | A retrospective study evaluating the effect of a bolus dose of dactinomycin, given 1 hour before ERPC to women with high‐risk HM, on the rate of malignant transformation to GTN. |
5‐FU: 5‐fluorouracil; ERPC: evacuation of retained products of conception; GTD: gestational trophoblastic disease; GTN: gestational trophoblastic neoplasia; HM: hydatidiform mole.