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

Eur J Endocrinol. 2017 Jun;176(6):769-777. doi: 10.1530/EJE-16-0979.

Abstract

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.

Publication types

  • Multicenter Study

MeSH terms

  • ACTH-Secreting Pituitary Adenoma / drug therapy*
  • ACTH-Secreting Pituitary Adenoma / pathology
  • ACTH-Secreting Pituitary Adenoma / prevention & control
  • ACTH-Secreting Pituitary Adenoma / radiotherapy
  • Adult
  • Antineoplastic Agents, Alkylating / therapeutic use*
  • Carcinoma / drug therapy*
  • Carcinoma / pathology
  • Carcinoma / prevention & control
  • Carcinoma / radiotherapy
  • Chemoradiotherapy
  • Cohort Studies
  • Dacarbazine / analogs & derivatives*
  • Dacarbazine / therapeutic use
  • Drug Resistance, Neoplasm
  • Female
  • Follow-Up Studies
  • France
  • Humans
  • Male
  • Neoplasm Grading
  • Neoplasm Invasiveness
  • Neoplasm Recurrence, Local / epidemiology
  • Neoplasm Recurrence, Local / pathology
  • Neoplasm Recurrence, Local / prevention & control*
  • Pituitary Neoplasms / drug therapy*
  • Pituitary Neoplasms / pathology
  • Pituitary Neoplasms / prevention & control
  • Pituitary Neoplasms / radiotherapy
  • Practice Patterns, Physicians'
  • Prolactinoma / drug therapy*
  • Prolactinoma / pathology
  • Prolactinoma / prevention & control
  • Prolactinoma / radiotherapy
  • Retrospective Studies
  • Survival Analysis
  • Temozolomide
  • Tumor Burden / drug effects
  • Tumor Burden / radiation effects

Substances

  • Antineoplastic Agents, Alkylating
  • Dacarbazine
  • Temozolomide