Temozolomide treatment can improve overall survival in aggressive pituitary tumors and pituitary carcinomas

Objectives Only few retrospective studies have reported an efficacy rate of temozolomide (TMZ) in pituitary tumors (PT), all around 50%. However, the long-term survival of treated patients is rarely evaluated. We therefore aimed to describe the use of TMZ on PT in clinical practice and evaluate the...

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Veröffentlicht in:European journal of endocrinology 2017-06, Vol.176 (6), p.769-777
Hauptverfasser: Lasolle, Hélène, Cortet, Christine, Castinetti, Fréderic, Cloix, Lucie, Caron, Philippe, Delemer, Brigitte, Desailloud, Rachel, Jublanc, Christel, Lebrun-Frenay, Christine, Sadoul, Jean-Louis, Taillandier, Luc, Batisse-Lignier, Marie, Bonnet, Fabrice, Bourcigaux, Nathalie, Bresson, Damien, Chabre, Olivier, Chanson, Philippe, Garcia, Cyril, Haissaguerre, Magalie, Reznik, Yves, Borot, Sophie, Villa, Chiara, Vasiljevic, Alexandre, Gaillard, Stephan, Jouanneau, Emmanuel, Assié, Guillaume, Raverot, Gérald
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Sprache:eng
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Zusammenfassung:Objectives Only few retrospective studies have reported an efficacy rate of temozolomide (TMZ) in pituitary tumors (PT), all around 50%. However, the long-term survival of treated patients is rarely evaluated. We therefore aimed to describe the use of TMZ on PT in clinical practice and evaluate the long-term survival. Design Multicenter retrospective study by members of the French Society of Endocrinology. Methods Forty-three patients (14 women) treated with TMZ between 2006 and 2016 were included. Most tumors were corticotroph (n = 23) or lactotroph (n = 13), and 14 were carcinomas. Clinical/pathological characteristics of PT, as well as data from treatment evaluation and from the last follow-up were recorded. A partial response was considered as a decrease in the maximal tumor diameter by more than 30% and/or in the hormonal rate by more than 50% at the end of treatment. Results The median treatment duration was 6.5 cycles (range 2–24), using a standard regimen for most and combined radiotherapy for six. Twenty-two patients (51.2%) were considered as responders. Silent tumor at diagnosis was associated with a poor response. The median follow-up after the end of treatment was 16 months (0–72). Overall survival was significantly higher among responders (P = 0.002); however, ten patients relapsed 5 months (0–57) after the end of TMZ treatment, five in whom TMZ was reinitiated without success. Discussion Patients in our series showed a 51.2% response rate to TMZ, with an improved survival among responders despite frequent relapses. Our study highlights the high variability and lack of standardization of treatment protocols.
ISSN:0804-4643
1479-683X
DOI:10.1530/EJE-16-0979