Activity and safety of temozolomide in advanced adrenocortical carcinoma patients

Author:

Cosentini Deborah1,Badalamenti Giuseppe2,Grisanti Salvatore1,Basile Vittoria3,Rapa Ida4,Cerri Sara1,Spallanzani Andrea5,Perotti Paola3,Musso Emanuela2,Laganà Marta1,Ferrari Vittorio D1,Luppi Gabriele5,Dalla Volta Alberto1,Incorvaia Lorena2,Sigala Sandra6,Russo Antonio2,Volante Marco4,Terzolo Massimo3,Berruti Alfredo1

Affiliation:

1. 1Medical Oncology Unit, Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, University of Brescia, ASST Spedali Civili, Brescia, Italy

2. 2Section of Medical Oncology, Department of Surgical, Oncological and Oral Sciences, University of Palermo, Palermo, Italy

3. 3Internal Medicine, Department of Clinical and Biological Sciences, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy

4. 4Department of Oncology, San Luigi Hospital, University of Turin, Orbassano, Turin, Italy

5. 5Department of Medical Oncology, AOU di Modena, Modena, Italy

6. 6Section of Pharmacology, Department of Molecular and Translational Medicine, University of Brescia, Brescia, Italy

Abstract

Objective Temozolomide has shown a significant anti-proliferative activity on adrenocortical cancer (ACC) cells in vitro. Design On the basis of these results the drug was prescribed as second/third line in advanced metastatic ACC patients in four referral centers in Italy. Methods We retrospectively collected anagraphic, clinical and pathological data of patients with advanced ACC with disease progression to standard chemotherapy plus mitotane who were treated with temozolomide at the dose of 200 mg/m2/die given for 5 consecutive days every 28 days. The primary endpoint was the disease control rate, defined as objective response or disease stabilization after 3 months. Secondary endpoints were overall survival (OS), progression-free survival (PFS) and drug safety. Results Twenty-eight patients have been included in the study. Ten patients (35.8%, 95% CI: 17.8–53.8) obtained a disease control from temozolomide treatment. In particular, 1 patient had a complete response, 5 patients a partial response and 4 patients stable disease. Median PFS was 3.5 months and median OS was 7.2 months. Disease response was more frequently observed in patients with methylation of O6-methylguanine-DNA methyltransferase (MGMT) gene. Temozolomide therapy was well tolerated and most toxicities were limited to grade G1–2 according to WHO criteria. Conclusion Temozolomide was found active in the management of advanced ACC patients. The disease control rate obtained, however, was short-lived and the prognosis of treated patients was poor.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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