The role of low‐dose methotrexate and folinic acid in gestational trophoblastic tumours (GTT)

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Abstract
Summary. Between 1964 and 1986, 487 patients with gestational trophoblastic tumour (GTT) were treated with methotrexate and folinic acid. The patients comprise two groups: between 1964 and 1974, 126 patients were treated but were not systematically stratified using a prognostic score before the start of treatment. These patients formed part of the 317 women who were analysed to identify a number of prognostic variables (Bagshawe 1976). Retrospective analysis of these 126 patients using these prognostic factors showed that in the true low-risk group 85/88 (96%) are alive while 20/22 (91%) of the medium-risk group and only 5/16 (31%) of the high-risk group are alive. Overall the survival was 110/126 (87%) with a minimum follow-up of 14 years. From 1974 all patients were stratified on admission into prognostic groups. Of the true low-risk patients 347/348 survived (99·7%); 13 patients were underscored and treated as low risk when they should have been treated as medium risk, 12 (92%) of these are alive, but nine (69%) needed to change treatment because of drug resistance. While the overall survival in the 1974–1986 group was 359/361 (99%) with a minimum follow-up of 16 months, the survival in all patients (1964–1986) was 469/487 (96%). Although the survival in these patients is excellent it should be noted that 69/348 (20%) low-risk patients had to change treatment because of the development of drug resistance, and a further 23 (6%) needed to change treatment because of drug-induced toxicity. Low-dose methotrexate and folinic acid given in the schedule described remains the treatment of choice in patients with low-risk GTT because of its effectiveness and minimal short- and long-term toxicity. Patients presenting with medium- and high-risk GTT need to start with combination chemotherapy from the outset to avoid the development of drug resistance.