Services on Demand
- Cited by Google
- Similars in SciELO
- Similars in Google
Print version ISSN 1807-5932
Clinics vol.67 supl.1 São Paulo 2012
Temozolomide in aggressive pituitary adenomas and carcinomas
Leon D. OrtizI; Luis V. SyroII; Bernd W. ScheithauerIII; Fabio RotondoIV; Humberto UribeV; Camilo E. FadulVI; Eva HorvathIV; Kalman KovacsIV
IInstituto de Cancerologia, Clinica Las Americas, Division of Neuro-oncology, Medellin, Colombia
IIHospital Pablo Tobon Uribe and Clinica Medellin, Department of Neurosurgery, Medellin, Colombia
III(in memoriam) Mayo Clinic, Department of Laboratory Medicine and Pathology, Rochester, Minnesota, USA
IVUniversity of Toronto, St Michael's Hospital, Department of Laboratory Medicine, Toronto, Ontario, Canada
VClinica SOMA, Department of Neurosurgery, Medellin, Colombia
VIDartmouth Hitchcock Medical Center, Department of Medicine (Section of Hematology/Oncology) and Neurology, Lebanon, New Hampshire, USA
Temozolomide is an alkylating agent used in the treatment of gliomas and, more recently, aggressive pituitary adenomas and carcinomas. Temozolomide methylates DNA and, thereby, has antitumor effects. O6-methylguanine-DNA methyltransferase, a DNA repair enzyme, removes the alkylating adducts that are induced by temozolomide, thereby counteracting its effects. A Medline search for all of the available publications regarding the use of temozolomide for the treatment of pituitary tumors was performed. To date, 46 cases of adenohypophysial tumors that were treated with temozolomide, including 30 adenomas and 16 carcinomas, have been reported. Eighteen of the 30 (60%) adenomas and 11 of the 16 (69%) carcinomas responded favorably to treatment. One patient with multiple endocrine neoplasia type 1 and an aggressive prolactin-producing adenoma was also treated and demonstrated a good response. No significant complications have been attributed to temozolomide therapy. Thus, temozolomide is an effective treatment for the majority of aggressive adenomas and carcinomas. Evidence indicates that there is an inverse correlation between levels of O6-methylguanine-DNA methyltransferase immunoexpression and therapeutic response. Alternatively, high-level O6-methylguanine-DNA methyltransferase immunoexpression correlates with an unfavorable response. Here, we review the use of temozolomide for treating pituitary neoplasms.
Keywords: Pituitary adenoma; Pituitary carcinoma; MGMT; Temozolomide; Review.
Patients with aggressive pituitary adenomas are difficult to clinically manage. Frequently, these adenomas are large, rapidly growing and invasive to their surroundings. These tumors also present problems due to incomplete resection and recurrence. Reoperation, pharmacological treatment and radiotherapy are routinely employed, often in combination. Nevertheless, many patients experience tumor regrowth (1). Endocrinologically active adenomas, particularly prolactin (PRL)- and growth hormone (GH)-producing tumors, may become resistant to medical therapy, thus requiring multiple resections. Radiation and conventional chemotherapy are often employed in an attempt to achieve local tumor control, but the results are often disappointing.
Pituitary carcinomas are rare and present particular diagnostic and therapeutic challenges. All of these carcinomas are of large size, invasive and associated with craniospinal and/or systemic metastases. Multiple treatment approaches, including surgery, external beam radiotherapy, radiosurgery, adjuvant pharmacological therapy and various chemotherapeutic approaches, are palliative at best, achieving only temporary effects (2,3). Progression of the disease after the diagnosis of pituitary carcinoma is variable but often inexorable. Approximately 75% of patients with systemic metastasis die within 1 year of documented spread (4).
Recent publications have reported the efficacy of temozolomide for treating aggressive pituitary adenomas and carcinomas (5-29). In this review, we discuss the indications, results and side effects of temozolomide therapy.
Temozolomide is a second-generation alkylating chemotherapeutic agent related to a series of imidazotetrazines that were originally synthesized in 1987 (30). Orally administered, it readily crosses the blood-brain barrier. At physiological pH, it undergoes rapid conversion to methyltriazeno-imidazole-carboxamide (MTIC), the active agent. It exerts its cytotoxic effects through methylation of DNA at the O6 position of guanine (31), which then mispairs with thymine during the next cycle of DNA replication. The sequence of mismatch-repair events lead to apoptosis.
Temozolomide is accepted as an essential component of adjuvant therapy for the treatment of glioblastoma multiforme and other tumors of the central nervous system (32-34). Recent reports indicate its efficacy for treating advanced-stage malignant neuroendocrine neoplasia (35), melanoma (36,37), and colorectal carcinoma (38).
The standard therapeutic dose of temozolomide is 150200 mg/m2 for five of every 28 days (5/28). Depletion of O6methylguanine-DNA methyltransferase (MGMT) has been proposed as a means of tumor response to temozolomide (39). Experimental and clinical data have shown that the temozolomide response is schedule-dependent and that alternative dosing regimens may enhance its efficacy (40,41). The anti-angiogenic effect of temozolomide can be optimized by administering low doses of the drug on a frequent or continuous schedule without extended interruptions (i.e., "metronomic" chemotherapy). Temozolomide can also be administered on a continuous, daily metronomic schedule, thus achieving MGMT depletion and improving the clinical response. This dose is generally 50 mg/m2/day without interruption (28/28). Other temozolomide schedules recommend administration every other week (7/14) or a 21consecutive-day regimen that is administered every 28 days (21/28). Both are considered dose-dense regimens based on the Norton-Simon model of cell proliferation, which states that a dose of chemotherapy will have a fixed cell-kill rate regardless of the size of the tumor (39). Thus, decreasing the time interval between doses (i.e., increasing the dose density) improves efficacy by minimizing the opportunity for cellular regrowth between cycles (41). In these dose-dense regimens, temozolomide is administered at a dose of 150 mg/m2/day for 7 days every other week (7/14) or at a dose of 85-100 mg/m2/day for 21 consecutive days (21/28) (40). In reported pituitary cases, temozolomide was administered as mono-therapy in all but three cases. The standard 5/28 regimen was used in almost all instances except in the series of Bush et al. (23), in which a dose-dense, 21/28 schedule was used, and one case progressed to carcinoma, which was then treated using the metronomic 28/28 schedule (29). Temozolomide absorption is only minimally affected by food. Furthermore, no serious side effects have been reported. Common, nonhematological adverse effects are present, including nausea, vomiting, fatigue, headache and constipation, most of which are mild to moderate in severity.
As previously stated, MGMT is a DNA repair protein that reverses the effects of temozolomide therapy (42) by removing alkylating adducts, thereby counteracting its effects (43) and conferring resistance to the agent (44). Low-level expression in a wide variety of human tumors is thought to result from epigenetic silencing by hypermethylation of the MGMT gene promoter (44,45). Low-level MGMT expression is a predictive marker of a favorable clinical outcome in patients with temozolomide-treated glioblastomas (46-48). Herein, we extend this observation to aggressive adenohypophysial tumors.
The first temozolomide-treated pituitary adenoma patient was reported in 2006 (7,8). The tumor, which was investigated using histological, immunohistochemical and electron microscopic techniques, showed significant post-therapeutic effects, including hemorrhage, necrosis, focal fibrosis, reduced mitotic activity, Ki-67 labeling and, surprisingly, neuronal transformation. MGMT immunoexpression was completely absent. Subsequently, the case of a 41-year-old patient with an aggressive silent subtype 2 corticotroph adenoma was reported (10). It showed no morphological changes after temozolomide treatment. The tumor cell nuclei were immunopositive for MGMT. Based upon these results, it was suggested that MGMT immunoexpression may predict the responsiveness of temozolomide therapy (10).
To the best of our knowledge, to date 30 cases of pituitary adenoma have been treated with temozolomide (7-16,1820,22-26,28,29). Patient ages varied from 20 to 71 years (mean: 51 years). Aside from one tumor that was incidentally discovered in a patient with concomitant glioblastoma multiforme, all tumors were morphologically studied. The group included ten adrenocorticotropic hormone (ACTH)producing tumors, nine PRL-producing tumors, seven clinically non-functioning adenomas, two silent ACTH adenomas, and two GH-producing adenomas. The time between clinical presentation and onset of temozolomide treatment was between 2 and 23 years (mean: 10.7 years). Twenty-six of the 30 tumors had been irradiated previously. Aside from the incidentally discovered tumor in one patient, all other patients had undergone at least one operative procedure, the number ranging from 0 to 6 procedures (mean: 2.7). The response rate was 60% (18/30 patients). Debono et al. (11) reported the first case of a pituitary adenoma associated with multiple endocrine neoplasia type 1 (MEN1) that was treated with temozolomide. The 47-year-old man had primary hyperparathyroidism and a lesion at the head of the pancreas. Genetic analysis confirmed MEN1. The dopamine-resistant, prolactin-producing pituitary adenoma responded dramatically to temozolomide, demonstrating clinical, biochemical, and radiological improvements.
MGMT immunoexpression was documented in 23 of the 30 patients. A high level of labeling was seen in six instances, an intermediate level in six instances, and a low level in 11 instances. Only one of six patients with high MGMT immunoexpression responded to temozolomide. Two tumors with intermediate MGMT immunoexpression did not respond, whereas nine of the 11 tumors with low-level MGMT immunoexpression responded favorably.
Pituitary carcinomas are difficult to manage given their relentless growth and metastatic spread, despite the effects of multimodality therapy. The latter includes repeated surgeries, pharmacological manipulation, radiotherapy, and conventional chemotherapy (3,49), including various combinations of cis-platinum, etoposide and/or paclitaxel, but these have failed to achieve favorable clinical responses (2).
Initial reports of the successful use of temozolomide to treat pituitary carcinomas appeared in 2006 (5,6). To date, 16 cases have been treated (5,6,13,16,17,21-23,25). The time between disease presentation to temozolomide administration was 5-23 years (mean: 10.7 years). The group included nine PRL-producing tumors, five ACTH-producing tumors, three clinically non-functional tumors, and three silent corticotroph carcinomas. Eleven of the 16 patients (69%) experienced a clinical and radiological response to temozolomide. Assessment of MGMT immunoexpression was only available in 11 patients; only one patient with high-level immunoexpression responded to treatment.
Morphological comparisons of pathology before and after temozolomide treatment were performed in three cases: all were patients with adenomas. One was a non-responder who exhibited no changes (10) and two were responders (8,23) whose tumors after treatment demonstrated hemorrhage, necrosis, focal fibrosis, inflammatory infiltrates, fewer mitoses, and a low Ki-67 labeling index, as well as neuronal transformation. The latter is considered to be a metaplastic phenomenon and has been observed in a variety of untreated endocrine neoplasms, including GH cell adenomas (50).
Response to treatment
In patients who respond to temozolomide, three basic patterns of radiographic changes are seen on MRI: tumor necrosis and hemorrhage (7,8), cystic change (19), and shrinkage (9,11-14). Such changes may be seen as early as two months after the onset of treatment.
In the tumors that respond to temozolomide, the clinical response is rapid and associated with prompt decreases in chiasmatic compression and mass effects. In patients with endocrine-active PRL- and ACTH-producing tumors, an almost immediate reduction in plasma hormone levels becomes apparent after commencement of therapy. Thus, it is possible to quickly evaluate the treatment response.
MGMT immunoexpression and MGMT promoter methylation
The inverse relationship between MGMT immunoexpression and temozolomide response was first reported in two patients with aggressive pituitary adenomas (10). The observation was subsequently confirmed by McCormack et al. who assessed MGMT immunoreactivity in a PRL cell carcinoma and an aggressive GH-producing adenoma (13). In both studies, tumors with low-level MGMT immunoexpression demonstrated clinical and radiological responses to temozolomide therapy. Other authors have reported similar findings (51). Thus, the demonstration of MGMT immunoreactivity appears to be useful for predicting the response of aggressive pituitary adenomas and carcinomas to temozolomide treatment.
The reports of Kovacs et al. (10) and McCormack et al. (13,51) underscore the inverse relationship between MGMT immunoexpression and the efficacy of temozolomide therapy, and this relationship has also been noted in high-grade gliomas (46-48,52). Whereas the standard method for evaluating MGMT status in gliomas is the identification of promoter methylation (47), immunohistochemical detection of MGMT expression is an attractive alternative. It represents an inexpensive, readily accessible technology that is available to most laboratories (53,54). Whereas most reports pertaining to gliomas and temozolomide therapy are based on promoter methylation status, data relating to pituitary neoplasms are based on MGMT immunoexpression (24,51). Although several recent reports of aggressive pituitary tumors that were successfully treated with temozolomide have reported absent or low immunohistochemical expression of MGMT as a factor, one patient whose tumors exhibited higher levels of MGMT staining also experienced clinical improvement and tumor shrinkage following treatment (23). It is of note that some tumors with no promoter methylation also respond to therapy (22,23). These observations challenge the notion that MGMT promoter methylation is a reliable predictor of treatment response. Indeed, two recent studies on MGMT promoter methylation and the temozolomide response in eight aggressive adenomas and seven pituitary carcinomas found no association between promoter methylation status and response (22,23). Salehi et al. (55) did not find a close correlation between MGMT immunoexpression and MGMT promoter methylation in a study on aggressive pituitary adenomas and carcinomas. Thus, the utility of MGMT promoter methylation for the selection of patients who might respond well to temozolomide treatment remains controversial and an active focus of further research. The problem is that many tumors possess an admixture of MGMT immunopositive and immune-negative cells. Obviously, in such instances, it is difficult to predict overall the responsive to temozolomide.
To date, MGMT immunoexpression has been documented in 23 adenomas and 11 carcinomas. In 18 tumors, MGMT labeling was low and correlated with a good therapeutic response to temozolomide (14/18 cases). In eight instances, MGMT staining was intermediate: five tumors responded well and three did not. In eight patients with high MGMT immunoexpression, only one responded positively. Thus, tumors featuring low- and intermediate-level MGMT immunoexpression (n = 26), when compared with those with high MGMT immunoexpression (n = 8), showed a good response to temozolomide in 19/26 (73%) versus 1/8 (13%) cases (p = 0.0039; two-tailed Fisher's exact test).
Suggested indications for using temozolomide treatment
Based on the published cases and the reported response rates, temozolomide therapy can be recommended when other options fail, particularly in the following instances: (1) aggressive PRL-producing tumors that are resistant to bromocriptine or cabergoline and continue to grow after surgery and radiotherapy; (2) aggressive ACTH-producing tumors, especially Crooke cell and Nelson syndrome variants that cannot be cured by surgery and radiotherapy; (3) recurrent, clinically non-functional tumors exhibiting continued growth after repeated surgeries and radiotherapy; (4) pituitary carcinomas.
Temozolomide has been documented as valuable for the treatment of aggressive pituitary adenomas and carcinomas. The clinical and radiological responses are encouraging: 60% of aggressive adenomas and 69% of pituitary carcinomas respond well to treatment. An inverse correlation exists between MGMT immunoexpression and the therapeutic response to temozolomide. Based upon our literature review, a significant proportion of the adenohypophysial tumors that are responsive to temozolomide show low-level MGMT immunoexpression, whereas only one tumor showing high-level immunoexpression was found to respond. The use of immunohistochemistry for determining MGMT immunoexpression appears to be a promising guide for therapeutic decision-making (13,53). Obviously, all available methods for assessing the likelihood of a positive temozolomide response should be utilized. We feel strongly that the determination of MGMT immunoreactivity is of clinical value and that MGMT promoter methylation status should be determined as well. The molecular mechanisms that affect MGMT expression remain to be fully elucidated. Targeted modulation of MGMT may be used in patients who may otherwise not respond to temozolomide therapy. Future therapies that incorporate different dosing regimens or other drugs may improve the tumor responsiveness.
The authors have no personal financial or institutional interest in any pharmaceutical agents or testing devices described herein.
The authors are grateful to theJarislowsky and Lloyd Carr Harris Foundation for their continued support. The authors thank Mrs. Denise Chase from the Mayo Clinic for her excellent assistance and secretarial support.
Ortiz LD, Syro LV, Scheithauer BW, and Kovacs K conceived the study and wrote the manuscript. Ortiz LD, Syro LV, and Rotondo F searched the literature and extracted the data. Rotondo F, Uribe H, Fadul CE, and Horvath E contributed to the initial version of the manuscript. All authors contributed to the critical revision of the manuscript and approved the final version.
2. Kaltsas GA, Nomikos P, Kontogeorgos G, Buchfelder M, Grossman AB. Clinical review: Diagnosis and management of pituitary carcinomas. J Clin Endocrinol Metab. 2005;90(5):3089-99, http://dx.doi.org/10.1210/jc.2004-2231. [ Links ]
4. Pernicone PJ, Scheithauer BW, Sebo TJ, Kovacs KT, Horvath E, Young WFJr., et al. Pituitary carcinoma: a clinicopathologic study of 15 cases. Cancer. 1997;79(4):804-12, http://dx.doi.org/10.1002/(SICI)1097-0142(19970215)79:4<804::AID-CNCR18>3.0.C0;2-3. [ Links ]
6. Fadul CE, Kominsky AL, Meyer LP, Kingman LS, Kinlaw WB, Rhodes CH, et al. Long-term response of pituitary carcinoma to temozolomide. Report of two cases. J Neurosurg. 2006;105(4):621-6. [ Links ]
7. Syro LV, Uribe H, Penagos LC, Ortiz LD, Fadul CE, Horvath E, et al. Antitumour effects of temozolomide in a man with a large, invasive prolactin-producing pituitary neoplasm. Clin Endocrinol (Oxf). 2006;65(4):552-3, http://dx.doi.org/10.1111/j.1365-2265.2006.02653.x. [ Links ]
8. Kovacs K, Horvath E, Syro LV, Uribe H, Penagos LC, Ortiz LD, et al. Temozolomide therapy in a man with an aggressive prolactin-secreting pituitary neoplasm: morphological findings. Hum Pathol. 2007;38(1):1859, http://dx.doi.org/10.1016/j.humpath.2006.07.014. [ Links ]
9. Neff LM, Weil M, Cole A, Hedges TR, Shucart W, Lawrence D, et al. Temozolomide in the treatment of an invasive prolactinoma resistant to dopamine agonists. Pituitary. 2007;10(1):81-6, http://dx.doi.org/10.1007/s11102-007-0014-1. [ Links ]
10. Kovacs K, Scheithauer BW, Lombardero M, McLendon RE, Syro LV, Uribe H, et al. MGMT immunoexpression predicts responsiveness of pituitary tumors to temozolomide therapy. Acta Neuropathol. 2008;115(2):261-2, http://dx.doi.org/10.1007/s00401-007-0279-5. [ Links ]
11. Debono M, Bridgewater C, Ross R, Newell-Price J. Treating an aggressive prolactinoma in a patient with MEN 1: beneficial response to temozolomide. Society for Endocrinology BES; Endocrine Abstracts. 2008;15:188. [ Links ]
12. Moyes VJ, Alusi G, Sabin HI, Evanson J, Berney DM, Kovacs K, et al. Treatment of Nelson's syndrome with temozolomide. Eur J Endocrinol. 2009;160(1):115-9. [ Links ]
13. McCormack AI, McDonald KL, Gill AJ, Clark SJ, Burt MG, Campbell KA, et al. Low O6-methylguanine-DNA methyltransferase (MGMT) expression and response to temozolomide in aggressive pituitary tumours. Clin Endocrinol (Oxf). 2009;71(2):226-33, http://dx.doi.org/10.1111/j.13652265.2008.03487.x. [ Links ]
14. Mohammed S, Kovacs K, Mason W, Smyth H, Cusimano MD. Use of temozolomide in aggressive pituitary tumors: case report. Neurosurgery. 2009;64(4):E773-4; discussion E4, http://dx.doi.org/10.1227/01.NEU.0000339115.12803.4E [ Links ]
15. Takeshita A, Inoshita N, Taguchi M, Okuda C, Fukuhara N, Oyama K, et al. High incidence of low O6-methylguanine DNA methyltransferase expression in invasive macroadenomas of Cushing's disease. Eur J Endocrinol. 2009;161(4):553-9, http://dx.doi.org/10.1530/EJE-090414. [ Links ]
16. Hagen C, Schroeder HD, Hansen S, Andersen M. Temozolomide treatment of a pituitary carcinoma and two pituitary macroadenomas resistant to conventional therapy. Eur J Endocrinol. 2009;161(4):631-7, http://dx.doi.org/10.1530/EJE-09-0389. [ Links ]
18. Thearle MS, Freda PU, Bruce JN, Isaacson SR, Lee Y, Fine RL. Temozolomide (Temodar®) and capecitabine (Xeloda®) treatment of an aggressive corticotroph pituitary tumor. Pituitary. 2011;14(4):418-24, http://dx.doi.org/10.1007/s11102-009-0211-1. [ Links ]
19. Syro LV, Scheithauer BW, Ortiz LD, Fadul CE, Horvath E, Rotondo F, et al. Effect of temozolomide in a patient with recurring oncocytic gonadotrophic pituitary adenoma. Hormones (Athens). 2009;8(4):303-6. [ Links ]
20. Morin E, Berthelet F, Weisnagel J, Bidlingmaier M, Serri O. Failure of temozolomide and conventional doses of pegvisomant to attain biochemical control in a severe case of acromegaly. Pituitary. In press; http://dx.doi.org/10.1007/s11102-010-0232-9. [ Links ]
21. Bode H, Seiz M, Lammert A, Brockmann MA, Back W, Hammes HP, et al. SOM230 (pasireotide) and temozolomide achieve sustained control of tumour progression and ACTH secretion in pituitary carcinoma with widespread metastases. Exp Clin Endocrinol Diabetes. 2010;118(10):760-3, http://dx.doi.org/10.1055/s-0030-1253419.
22. Raverot G, Sturm N, de Fraipont F, Muller M, Salenave S, Caron P, et al. Temozolomide treatment in aggressive pituitary tumors and pituitary carcinomas: a French multicenter experience. J Clin Endocrinol Metab. 2010;95(10):4592-9, http://dx.doi.org/10.1210/jc.2010-0644. [ Links ]
23. Bush ZM, Longtine JA, Cunningham T, Schiff D, Jane JAJr., Vance ML, et al. Temozolomide treatment for aggressive pituitary tumors: correlation of clinical outcome with O6-methylguanine methyltransferase (MGMT) promoter methylation and expression. J Clin Endocrinol Metab. 2010;95(11):E280-90, http://dx.doi.org/10.1210/jc.2010-0441. [ Links ]
24. Syro LV, Ortiz LD, Scheithauer BW, Lloyd R, Lau Q, Gonzalez R, et al. Treatment of pituitary neoplasms with temozolomide: a review. Cancer. 2011;117(3):454-62, http://dx.doi.org/10.1002/cncr.25413. [ Links ]
25. Losa M, Mazza E, Terreni MR, McCormack A, Gill AJ, Motta M, et al. Salvage therapy with temozolomide in patients with aggressive or metastatic pituitary adenomas: experience in six cases. Eur J Endocrinol. 2010;163(6):843-51, http://dx.doi.org/10.1530/EJE-10-0629. [ Links ]
26. Dillard TH, Gultekin SH, Delashaw JBJr., Yedinak CG, Neuwelt EA, Fleseriu M. Temozolomide for corticotroph pituitary adenomas refractory to standard therapy. Pituitary. 2011;14(1):80-91, http://dx.doi.org/10.1007/s11102-010-0264-1. [ Links ]
27. Curto L, Torre ML, Ferrau F, Pitini V, Altavilla G, Granata F, et al. Temozolomide-induced shrinkage of a pituitary carcinoma causing Cushing's disease: report of a case and literature review. Scientific World Journal. 2010;10:2132-8. [ Links ]
28. Murakami M, Mizutani A, Asano S, Katakami H, Ozawa Y, Yamazaki K, et al. A mechanism of acquiring temozolomide resistance during transformation of atypical prolactinoma into prolactin-producing pituitary carcinoma. Neurosurgery. 2011;68(6):E1761-7, http://dx.doi.org/10.1227/NEU.0b013e318217161a. [ Links ]
29. Moshkin O, Syro LV, Scheithauer BW, Ortiz LD, Fadul CE, Uribe H, et al. Aggressive silent corticotroph adenoma progressing to pituitary carcinoma. The role of temozolomide therapy. Hormones (Athens). 2011;10(2):162-7. [ Links ]
30. Stevens MF, Hickman JA, Langdon SP, Chubb D, Vickers L, Stone R, et al. Antitumor activity and pharmacokinetics in mice of 8-carbamoyl-3methyl-imidazo [5,1-d]-1,2,3,5-tetrazin-4(3H)-one (CCRG 81045; M & B 39831), a novel drug with potential as an alternative to dacarbazine. Cancer Res. 1987;47(22):5846-52. [ Links ]
32. Stupp R, Gander M, Leyvraz S, Newlands E. Current and future developments in the use of temozolomide for the treatment of brain tumours. Lancet Oncol. 2001;2(9):552-60, http://dx.doi.org/10.1016/S1470-2045(01)00489-2. [ Links ]
33. Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJ, et al. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 2005;352(10):987-96, http://dx.doi.org/10.1056/NEJMoa043330. [ Links ]
34. Villano JL, Seery TE, Bressler LR. Temozolomide in malignant gliomas: current use and future targets. Cancer Chemother Pharmacol. 2009;64(4):647-55, http://dx.doi.org/10.1007/s00280-009-1050-5. [ Links ]
35. Kulke MH, Stuart K, Enzinger PC, Ryan DP, Clark JW, Muzikansky A, et al. Phase II study of temozolomide and thalidomide in patients with metastatic neuroendocrine tumors. J Clin Oncol. 2006;24(3):401-6, http://dx.doi.org/10.1200/jc0.2005.03.6046. [ Links ]
36. Agarwala SS, Kirkwood JM. Temozolomide, a novel alkylating agent with activity in the central nervous system, may improve the treatment of advanced metastatic melanoma. Oncologist. 2000;5(2):144-51, http://dx.doi.org/10.1634/theoncologist.5-2-144. [ Links ]
37. Quirt I, Verma S, Petrella T, Bak K, Charette M. Temozolomide for the treatment of metastatic melanoma: a systematic review. Oncologist. 2007;12(9):1114-23, http://dx.doi.org/10.1634/theoncologist.12-9-1114. [ Links ]
38. Shacham-Shmueli E, Beny A, Geva R, Blachar A, Figer A, Aderka D. Response to temozolomide in patients with metastatic colorectal cancer with loss of MGMT expression: a new approach in the era of personalized medicine? J Clin Oncol. 2011;29(10):e262-5, http://dx.doi.org/10.1200/JCO.2010.32.0242. [ Links ]
39. Clarke JL, Iwamoto FM, Sul J, Panageas K, Lassman AB, DeAngelis LM, et al. Randomized phase II trial of chemoradiotherapy followed by either dose-dense or metronomic temozolomide for newly diagnosed glioblastoma. J Clin Oncol. 2009;27(23):3861-7, http://dx.doi.org/10.1200/JCO.2008.20.7944. [ Links ]
42. Rodriguez FJ, Thibodeau SN, Jenkins RB, Schowalter KV, Caron BL, O'Neill B P, et al. MGMT immunohistochemical expression and promoter methylation in human glioblastoma. Appl Immunohistochem Mol Morphol. 2008;16(1):59-65. [ Links ]
44. Esteller M, Hamilton SR, Burger PC, Baylin SB, Herman JG. Inactivation of the DNA repair gene O6-methylguanine-DNA methyltransferase by promoter hypermethylation is a common event in primary human neoplasia. Cancer Res. 1999;59(4):793-7. [ Links ]
45. Sharma S, Salehi F, Scheithauer BW, Rotondo F, Syro LV, Kovacs K. Role of MGMT in tumor development, progression, diagnosis, treatment and prognosis. Anticancer Res. 2009;29(10):3759-68. [ Links ]
46. Esteller M, Garcia-Foncillas J, Andion E, Goodman SN, Hidalgo OF, Vanaclocha V, et al. Inactivation of the DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents. N Engl J Med. 2000;343(19):1350-4, http://dx.doi.org/10.1056/NEJM200011093431901. [ Links ]
47. Hegi ME, Diserens AC, Gorlia T, Hamou MF, de Tribolet N, Weller M, et al. MGMT gene silencing and benefit from temozolomide in glioblastoma. N Engl J Med. 2005;352(10):997-1003, http://dx.doi.org/10.1056/NEJMoa043331. [ Links ]
48. Friedman HS, McLendon RE, Kerby T, Dugan M, Bigner SH, Henry AJ, et al. DNA mismatch repair and O6-alkylguanine-DNA alkyltransferase analysis and response to Temodal in newly diagnosed malignant glioma. J Clin Oncol. 1998;16(12):3851-7. [ Links ]
49. Kaltsas GA, Mukherjee JJ, Plowman PN, Monson JP, Grossman AB, Besser GM. The role of cytotoxic chemotherapy in the management of aggressive and malignant pituitary tumors. J Clin Endocrinol Metab. 1998;83(12):4233-8, http://dx.doi.org/10.1210/jc.83.12.4233. [ Links ]
50. Scheithauer BW, Horvath E, Kovacs K, Lloyd RV, Stefaneanu L, Buchfelder M, et al. Prolactin-producing pituitary adenoma and carcinoma with neuronal components: a metaplastic lesion. Pituitary. 1999;1(3-4):197-205, http://dx.doi.org/10.1023/A:1009913303109. [ Links ]
51. McCormack AI, Wass JA, Grossman AB. Aggressive pituitary tumours: the role of temozolomide and the assessment of MGMT status. Eur J Clin Invest. 2011;41(10):1133-48, http://dx.doi.org/10.1111/j.1365-2362.2011.02520.x. [ Links ]
52. Pollack IF, Hamilton RL, Sobol RW, Burnham J, Yates AJ, Holmes EJ, et al. O6-methylguanine-DNA methyltransferase expression strongly correlates with outcome in childhood malignant gliomas: results from the CCG-945 Cohort. J Clin Oncol. 2006;24(21):3431-7, http://dx.doi.org/10.1200/JCO.2006.05.7265. [ Links ]
53. Widhalm G, Wolfsberger S, Preusser M, Woehrer A, Kotter MR, Czech T, et al. O6-Methylguanine DNA methyltransferase immunoexpression in nonfunctioning pituitary adenomas: are progressive tumors potential candidates for temozolomide treatment? Cancer. 2009;115(5):1070-80, http://dx.doi.org/10.1002/cncr.24053. [ Links ]
54. Lau Q, Scheithauer B, Kovacs K, Horvath E, Syro LV, Lloyd R. MGMT immunoexpression in aggressive pituitary adenoma and carcinoma. Pituitary. 2010;13(4):367-79, http://dx.doi.org/10.1007/s11102-010-0249-0. [ Links ]
55. Salehi F, Scheithauer BW, Kros JM, Lau Q, Fealey M, Erickson D, et al. MGMT promoter methylation and immunoexpression in aggressive pituitary adenomas and carcinomas. J Neurooncol. 2011;104(3):647-57, http://dx.doi.org/10.1007/s11060-011-0532-6. [ Links ]
No potential conflict of interest was reported.
Tel.: 57 4 231 9099