Efficacy of Temozolomide Therapy in Patients With Aggressive Pituitary Adenomas and Carcinomas-A German Survey.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 03 2020
Historique:
received: 08 09 2019
accepted: 18 11 2019
pubmed: 21 11 2019
medline: 6 11 2020
entrez: 21 11 2019
Statut: ppublish

Résumé

Despite growing evidence that temozolomide (TMZ) therapy is effective for the treatment of aggressive pituitary tumors (APTs) or carcinomas (PCs), individual therapy decisions remain challenging. We therefore aimed to report on clinical characteristics leading to initiation of TMZ therapy and to add evidence on TMZ long-term effectiveness. Retrospective survey on TMZ treatment in patients with APTs or PCs. TMZ therapy was initiated in 47 patients (22 females) with APTs (n = 34) or PCs (n = 13). Mean age at diagnosis was 45 ± 15 years. The immunohistochemical subtypes were corticotroph (n = 20), lactotroph (n = 18), and nonfunctioning (n = 9) tumors. TMZ therapy started 8 years after initial diagnosis using a standard regimen (median 6 cycles) for the majority of patients. Long-term radiological response to TMZ after a median follow-up of 32 months with 4 patients still on TMZ therapy was tumor regression for 9 (20%), stable disease for 8 (17%), and tumor progression for 29 patients (63%) (outcome data available for 46 patients). Progression occurred 16 months after initiation of TMZ. Median estimated progression-free survival was 23 months. Disease stabilization and median progression-free survival did not differ between patients with APTs or PCs. Predictors of tumor response were not identified. Overall, TMZ was well tolerated. We performed a nationwide survey on TMZ therapy in patients with APTs and PCs. While early response rates to TMZ are promising, long-term outcome is less favorable. Prolonged TMZ administration should be considered. We were not able to confirm previously reported predictors of tumor response to TMZ.

Identifiants

pubmed: 31746334
pii: 5634134
doi: 10.1210/clinem/dgz211
pii:
doi:

Substances chimiques

Antineoplastic Agents, Alkylating 0
Temozolomide YF1K15M17Y

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Ulf Elbelt (U)

Department of Endocrinology, Diabetes and Nutrition, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Sven M Schlaffer (SM)

Department of Neurosurgery, University of Erlangen-Nuremberg, Erlangen, Germany.

Michael Buchfelder (M)

Department of Neurosurgery, University of Erlangen-Nuremberg, Erlangen, Germany.

Ulrich J Knappe (UJ)

Department of Neurosurgery, Johannes Wesling Klinikum, Universitätsklinikum der Ruhruniversität Bochum, Minden, Germany.

Greisa Vila (G)

Department of Internal Medicine III, Division of Endocrinology and Metabolism, Medical University Vienna, Vienna, Austria.

Alexander Micko (A)

Department of Neurosurgery, Medical University Vienna, Vienna, Austria.

Timo Deutschbein (T)

Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital Würzburg, University of Würzburg, Würzburg, Germany.

Nicole Unger (N)

Department of Endocrinology, Diabetes and Metabolism, University Hospital Essen, Essen, Germany.

Alexander Lammert (A)

Vth Department of Medicine, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.

Tengü Topuzoglu-Müller (T)

Department of Endocrinology, Diabetes and Preventive Medicine, University Hospital of Cologne, Cologne, Germany.

Jörg Bojunga (J)

Department of Internal Medicine 1, Johann Wolfgang Goethe-University Hospital, Frankfurt, Germany.

Michael Droste (M)

Medicover Oldenburg MVZ, Oldenburg, Germany.

Sarah Johanssen (S)

Endokrinologikum Berlin, Berlin, Germany.

Herbert Kolenda (H)

Department of Neurosurgery, Agaplesion Diakonieklinikum Rotenburg, Rotenburg, Germany.

Katrin Ritzel (K)

Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Ludwig-Maximilians-Universität München, Munich, Germany.

Rolf Buslei (R)

Institute of Pathology, SozialStiftung Bamberg, Bamberg, Germany.

Christian J Strasburger (CJ)

Department of Endocrinology, Diabetes and Nutrition, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Stephan Petersenn (S)

ENDOC Center for Endocrine Tumors, Hamburg, Germany.

Jürgen Honegger (J)

Department of Neurosurgery, University of Tuebingen, Tuebingen, Germany.

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Classifications MeSH