Temozolomide in the management of dopamine agonist–resistant prolactinomas

BC Whitelaw, D Dworakowska…�- Clinical�…, 2012 - Wiley Online Library
BC Whitelaw, D Dworakowska, NW Thomas, S Barazi, P Riordan‐Eva, AP King, T Hampton…
Clinical endocrinology, 2012Wiley Online Library
Background The majority of prolactinomas respond to dopamine agonist therapy, but a
proportion are resistant, requiring other treatments including surgery and/or radiotherapy.
Temozolomide is an oral chemotherapy agent, which has been used as a salvage therapy to
treat aggressive pituitary adenomas and carcinomas, including prolactinomas, unresponsive
to all conventional treatment. Case Series We report three patients where temozolomide
was used in the treatment of refractory prolactinomas. Case 1 describes a patient with a�…
Background
The majority of prolactinomas respond to dopamine agonist therapy, but a proportion are resistant, requiring other treatments including surgery and/or radiotherapy. Temozolomide is an oral chemotherapy agent, which has been used as a salvage therapy to treat aggressive pituitary adenomas and carcinomas, including prolactinomas, unresponsive to all conventional treatment.
Case Series
We report three patients where temozolomide was used in the treatment of refractory prolactinomas. Case 1 describes a patient with a highly invasive prolactinoma, resistant to all conventional therapy, which responded dramatically to temozolomide used as a salvage treatment. In case 2, temozolomide was used after incomplete surgical resection to relieve chiasmal compression and avoid chiasm exposure to radiotherapy. In case 3, temozolomide enabled radiotherapy to be deferred in a 16‐year old with a resistant prolactinoma. In all three cases, the tumours were negative by immunostaining for methylguanine methyltransferase (MGMT).
Literature Review and Discussion
A review of the published literature reveals 51 reported cases of temozolomide treatment for pituitary tumours, including 20 prolactinomas. Fifteen of the 20 prolactinomas showed a good response to temozolomide. Our analysis demonstrates a strong association between MGMT‐negative staining and a good response to temozolomide (OR 9�35, P�=�0�0030). Current clinical practice is to use temozolomide as a salvage therapy after all conventional modalities of treatment have failed. We suggest that, in selected cases, consideration should be given to using temozolomide earlier in the treatment algorithm.
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