| Literature DB >> 26614517 |
Marco Losa1, Fausto Bogazzi2, Salvo Cannavo3, Filippo Ceccato4, Lorenzo Curtò3, Laura De Marinis5, Donato Iacovazzo5,6, Giuseppe Lombardi7, Giovanna Mantovani8, Elena Mazza9, Giuseppe Minniti10, Maurizio Nizzoli11, Michele Reni9, Carla Scaroni4.
Abstract
Temozolomide is effective in some patients with progressive pituitary adenoma or carcinoma. We report a survey study of Italian patients treated with Temozolomide because of aggressive pituitary adenoma or carcinoma resistant to standard therapies. Italian endocrinologists were surveyed and asked to participate into the study. A questionnaire was sent to all those who agreed and had used Temozolomide in at least one patient with pituitary tumor. Database was closed in December 2013. A literature review was also performed. Thirty-one patients were included into the analysis. Mean age at start of Temozolomide treatment was 58.3 ± 1.9 years (± standard error). Six of the 31 (19.4%) Italian patients had a pituitary carcinoma. Twenty-five patients (80.6%) had disease control during Temozolomide treatment, while 6 patients (19.4%) had disease progression. Median follow-up after beginning Temozolomide was 43 months. Thirteen patients had tumor growth after stopping Temozolomide. The 2-year progression-free survival was 47.7% (95% CI 29.5-65.9%), while the 2-year disease control duration was 59.1% (95% CI 39.1-79.1%). Eleven patients died of progressive disease and other two patients of unrelated causes. The 2-year and 4-year overall survival rates were 83.9% (95% CI 70.7-97.1%) and 59.6% (95% CI 40.0-79.2%), respectively. Temozolomide is an additional effective therapeutic option for the treatment of aggressive pituitary tumors. The drug is well tolerated and causes few severe adverse effects. Recurrence of the tumor can occur after an initial positive response and usually portends a grim outcome.Entities:
Keywords: Chemotherapy; Pituitary carcinoma; Pituitary neoplasm; Pituitary surgery; Temozolomide
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Year: 2015 PMID: 26614517 DOI: 10.1007/s11060-015-1991-y
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130