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Table 2 The clinical characteristics of low-risk postmolar GTN

From: The effect of prophylactic chemotherapy on treatment outcome of postmolar gestational trophoblastic neoplasia

Variables*

Control (n = 72)

P-chem (n = 24)

P value

Interval from HM to GTN (days)

44 (11–2555)

69 (14–300)

0.001

Largest dimension of tumor (cm)

   

 < 3

40 (56%)

4 (17%)

0.181

 ≥ 3

23 (32%)

6 (25%)

 

Number of metastases

0 (0–9)

0 (0–9)

0.054

hCG before first-line chemotherapy (IU/L)

4503.5 (5.3–514,972.0)

415.8 (10.7–44,808.0)

0.000

FIGO stage

   

 I

22 (31%)

11 (46%)

0.414

 II

1 (1%)

0 (0%)

 

 III

49 (68%)

13 (54%)

 

WHO risk score

2 (0–6)

2 (0–6)

0.208

First-line chemotherapy agent

   

 Methotrexate

69 (96%)

13 (54%)

0.000

 Actinomycin D

3 (4%)

8 (33%)

 

 5-Fluorouracil

0 (0%)

3 (13%)

 

Resistant to first-line drug

29 (40%)

10 (42%)

0.904

Resistant to first-line MTX

26 (38%)

5 (38%)

0.066

Resistant to second-line drug

6 (21%)

2 (20%)

1.000

Resistant to single-agent drug

8 (11%)

4 (17%)

0.487

Chemotherapy cycles to hCG normalization

4 (1–9)

3 (1–7)

0.157

Total chemotherapy cycles

6 (1–12)

6 (3–11)

0.508

  1. P-chem prophylactic chemotherapy, HM hydatidiform mole, GTN gestational trophoblastic neoplasia
  2. *Continuous variables are reported as medians(range), and categorical variables are reported as raw numbers with proportions