Table 3.
Name of Hormone | Formulation Name and Dose | Observation Time | Study Model | Results | References |
---|---|---|---|---|---|
Aromatase Inhibitor | Anastrozole (1 mg/day), exemestane (25 mg/day)-1 patient, letrozole (2.5 mg/day) | 29.2 months | Patients with uterine sarcoma (4 patients with ESS, endometrial stromal sarcoma, and 3 patients with LMS) | Effective in the treatment of endometrial stromal sarcomas | [117] |
Progesterone | Medroxy progesterone acetate (36 patients; 44%) or megestrol acetate(28 patients; 35%), progestins | 24weeks | 81 patients | When disease recurs, carcinoma extending beyond the uterus is rare in patients reported with well-differentiated endometrial adenocarcinoma who undergo treatment with a progestational agent | [123] |
Estrogen, progestin, aromatase inhibitors |
ERT, tamoxifen, progestins, aromatase inhibitors | 4 to 164 months | 800 patients | MPA and letrozole, in particular, are highly effective and lead to sustained disease control in most cases | [120] |
Progestin, Aromatase inhibitors |
Megestrol acetate (MA), Aromatase inhibitor (letrozole) |
4+ to 252+ months (median 48+ months). | 11 patients | Hormonal treatment for measurable residual or recurrent low-grade ESS has a high response rate and should be considered as the treatment of choice for patients in which recurrent disease cannot easily be eliminated | [122] |
Exogenous or endogenous estrogen and progestins | Megestrol acetate 160 mg, progestins | 100 months (range, 2–258) |
22 patients | ERT was detrimental in patients with low-grade endometrial stromal sarcoma, but progestin therapy should be routinely considered for adjuvant therapy and for the treatment of recurrent endometrial stromal sarcomas | [124] |
Progesterone | Medroxy progesterone acetate (MPA) | Dosing period 64 months (range 28–92 months) but follow-up period was 117 months | 13 patients | MPA therapy might be considered as a therapeutic option for residual or recurrent low-grade ESS and perhaps chosen as a first-line therapy | [125] |
Aromatase | Aromatase inhibitors used were letrozole (in 74% of patients), anastrozole (21%), and exemestane (6%) | Between 1998 and 2008 | 40 patients | Aromatase inhibitors achieved objective response in only 9%. Progression free survival was longer among patients with ER and/or PR positive tumors than among patients with ER and PR negative tumors | [126] |
GnRH agonist | GnRH agonist, leuprolide acetate, adriamycin, cisplatin, ifosfamide etc. | 15 months | A patient with menorrhagia, dysmenorrhea, and an enlarged uterus | GnRH therapy mask the symptoms of leiomyosarcomas, e.g., rapidly enlarging uterine mass, pelvic pain, uterovaginal bleeding | [133] |
Progestin and aromatase | Three cycles of BEP (bleomycin, etoposide, cisplatin), anastrozole and megestrol acetate | 2 years | 48-year-old woman was diagnosed with stage I endometrial stroma sarcoma | Endometrial stromal sarcoma with sex-cord stromal component may be hormonally functional and can be cured by treating with progestin and aromatase inhibitor | [127] |
Estrogen, progesterone | Megestrol acetate and tamoxifen | 6 months | A 22-year-old nullipara | 1 year after the last curettage, there is no evidence of disease | [130] |
Estrogen, progesterone | Combinations of megestrol acetate (160 mg/day), tamoxifen (30 mg/day), and GnRHa | 6 months | 9 patients with clinically diagnosed endometrial adenocarcinoma stage IA, grade 1 | Of the 9 patients, 8 (88.9%) achieved complete remission after hormone therapy. All nine patients have been alive without evidence of disease | [129] |
Estrogen, progesterone, (GnRHa) |
Megestrol (1-month), tamoxifen (20 mg/day) and depot leuprolide acetate subcutaneous injection (3.75 mg/month) | 6-months | A 36-year-old nulliparous woman | This case report signals a warning that negative clinical investigations are not reassuring for a relapsing endometrial adenocarcinoma failing conservative hormonal treatment | [131] |
Estrogen, progestin | 500 mg of oral medroxyprogesterone for 6 months, twice weekly | 9 months (range, 3–18 months) | 2 women | The quarterly interval for D&Cs was satisfactory with medroxyprogesterone treatment, and the patients’ desire not to undergo hysterectomy was met | [132] |