Table 2.
All hormone related clinical trials in this review
| First author (year) |
Drug | Dose | Study design | Median treatment duration (months) |
Number of patients |
Sex | Median age (years) |
Primary outcome |
|---|---|---|---|---|---|---|---|---|
| Markwalder (1985) [47] | Tamoxifen | 10 mg orally t.i.d | Prospective cohort; pilot study | 12 | 6‡ | 5 F; 1 M | 71.5 | 4 assessed; 1 non-specific response; 2 stable; 1 progressed |
| Goodwin (1993) [48] | Tamoxifen | 40 mg b.i.d. for 4 days then 10 mg orally b.i.d | Prospective cohort; phase II | 31 | 21‡ | 14 F; 7 M | 58 | 1 partial response; 2 minor response; 6 stable; 10 progressed |
| Grunberg (1990) [50] | Megestrol acetate | 40–80 mg orally q.i.d | Prospective cohort | 5 | 9 | 5 F; 4 M | 40 | 2 stable; 7 progressed |
| Grunberg (2006) [51] | Mifepristone 14-day course of dexamethasone 1 mg | 200 mg q.d. orally | Prospective cohort | 35 | 28 | 19 F; 9 M | 56 | 5 minor response; 3 clinical without radiographic improvement; 2 progressed |
| Touat (2014) [52] | Mifepristone | 200 mg q.d. orally | Case series | 60 | 3 | 3 F | 54 | 100% had > 20% volume reduction |
| Ji (2015) [42] | Mifepristone | 200 mg b.i.d. or placebo orally | Randomized phase III clinical trial | Placebo 11[6-18]; mifepristone 10[7–13]+ | 164 | 116 F; 48 M | 57 | HR 1.02 95%CI[0.72, 1.48] Adjusted P = 0.9 |
Cohort statistics includes patients that were not included in the trial aggregated by publishing author
Failure free survival