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Pituitary Tumors Treatment (PDQ®)
Patient Version   Health Professional Version   En español   Last Modified: 09/16/2008



Purpose of This PDQ Summary






General Information






Cellular Classification






Stage Information






Treatment Option Overview






Prolactin-Producing Pituitary Tumors






Adrenocorticotropic Hormone-Producing Pituitary Tumors






Growth Hormone-Producing Pituitary Tumors






Nonfunctioning Pituitary Tumors






Thyrotropin-Producing Tumors






Pituitary Carcinomas






Recurrent Pituitary Tumors






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Changes to This Summary (09/16/2008)






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Past Highlights
Pituitary Carcinomas

Current Clinical Trials

Some reports indicate that as many as 88% of pituitary carcinomas are endocrinologically active, and adrenocorticotrophin hormone-secreting tumors are the most common.[1] Treatments for patients with pituitary carcinomas are palliative with the mean survival time ranging from 2 years to 2.4 years, though several case reports of long-term survivors have been published.[2-5]

Standard treatment options:[1]

  1. Surgery.
  2. Dopamine agonists, such as bromocriptine, pergolide, quinagolide, and cabergoline for PRL-producing carcinomas.
  3. Somatostatin analogues, such as octreotide for GH-producing and TSH-producing carcinomas.
  4. Adjuvant radiation therapy, which does not appear to change the disease's outcome.
  5. Chemotherapy, which is of little benefit.
Current Clinical Trials

Check for U.S. clinical trials from NCI's PDQ Cancer Clinical Trials Registry that are now accepting patients with pituitary tumor. The list of clinical trials can be further narrowed by location, drug, intervention, and other criteria.

General information about clinical trials is also available from the NCI Web site.

References

  1. Ragel BT, Couldwell WT: Pituitary carcinoma: a review of the literature. Neurosurg Focus 16 (4): E7, 2004.  [PUBMED Abstract]

  2. Pernicone PJ, Scheithauer BW, Sebo TJ, et al.: Pituitary carcinoma: a clinicopathologic study of 15 cases. Cancer 79 (4): 804-12, 1997.  [PUBMED Abstract]

  3. Sironi M, Cenacchi G, Cozzi L, et al.: Progression on metastatic neuroendocrine carcinoma from a recurrent prolactinoma: a case report. J Clin Pathol 55 (2): 148-51, 2002.  [PUBMED Abstract]

  4. Landman RE, Horwith M, Peterson RE, et al.: Long-term survival with ACTH-secreting carcinoma of the pituitary: a case report and review of the literature. J Clin Endocrinol Metab 87 (7): 3084-9, 2002.  [PUBMED Abstract]

  5. Vaquero J, Herrero J, Cincu R: Late development of frontal prolactinoma after resection of pituitary tumor. J Neurooncol 64 (3): 255-8, 2003.  [PUBMED Abstract]

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