Table 3.
Drugs used in hormonal therapy of meningioma
| Drug name | Drug composition/molecular formula administration | Mechanism of action | Type of study | References | ||||
|---|---|---|---|---|---|---|---|---|
| Hormonal agents | ||||||||
| Progesterone receptor-binding agents | ||||||||
| Megestrol (Megace) | C22H30O3, orally administered | Progesterone receptor partial agonist | SSCT: no survival benefit shown | [108] | ||||
| Mifepristone (RU- 486) | C29H35NO2 is a substituted 19-nor steroid compound and the first clinically available progesterone receptor antagonist; it is a derivative of the synthetic progestin norethindrone, orally given | It has antiprogesterone activity; it competes with progesterone for binding to its receptor, which leads to inhibition of the effects of endogenous or exogenous progesterone; progesterone receptor competitive antagonist | Mifepristone is useful in the treatment of vestibular schwannoma because of its anti-glucocorticoid effect; it also binds to progesterone receptors in meningiomas | [109] | ||||
| Estrogen antagonists | ||||||||
| Tamoxifen | C26H29NO is a tertiary amino compound and a stilbenoid, orally given | Estrogen receptor competent antagonist | A population-based study in Sweden found an association of tamoxifen with meningioma | [110] | ||||
| Somatostatin | ||||||||
| Octreotide (Sandostatin) | C49H66N10O10S2 is a synthetic long-acting cyclic octapeptide with anticancer properties, subcutaneous (s.c.) injection or intravenous (i.v.) infusion after dilution | It mimics somatostatin but is a more potent inhibitor of growth hormone, glucagon, and insulin; similar to somatostatin, this agent also suppresses the luteinizing hormone response to the gonadotropin-releasing hormone, decreases splanchnic blood flow, and inhibits the release of gastrin, serotonin, secretin, motilin, pancreatic polypeptide, and thyroid-stimulating hormone | Octreotide was administered with low toxicity in a small series of recurrent meningioma cases; somatostatin was found to decrease meningioma cell proliferation in vivo (Fig. 2) | [111] | ||||
| Pasireotide (Signifor) | C58H66N10O9, subcutaneous injection | Somatostatin mimetic | Phase II study of monthly pasireotide LAR (SOM230C) for recurrent or progressive meningioma | [112] | ||||
| GH receptor antagonists | ||||||||
| Pegvisomant (somavert) | PEGylated form of mutant growth hormone, subcutaneously | PEGylated GH receptor antagonist | Pegvisomant was investigated in the treatment of acromegaly | [113] | ||||
| IGF-I and IGF-II Antagonists | ||||||||
| Fenretinide | C26H33NO2 is a synthetic retinoid, orally given | It shows inhibition of growth via apoptosis in various tumor cell lines | Studies were aimed at finding the role and mechanism of fenretinide in controlling the growth of cells in meningioma | [114] | ||||
| Retinoids | [107] | |||||||