TY - JOUR
T1 - Prognostic role of overt hypercortisolism in completely operated patients with adrenocortical cancer
AU - Berruti, Alfredo
AU - Fassnacht, Martin
AU - Haak, Harm
AU - Else, Tobias
AU - Baudin, Eric
AU - Sperone, Paola
AU - Kroiss, Matthias
AU - Kerkhofs, Thomas
AU - Williams, Andrew R.
AU - Ardito, Arianna
AU - Leboulleux, Sophie
AU - Volante, Marco
AU - Deutschbein, Timo
AU - Feelders, Richards
AU - Ronchi, Cristina
AU - Grisanti, Salvatore
AU - Gelderblom, Hans
AU - Porpiglia, Francesco
AU - Papotti, Mauro
AU - Hammer, Gary D.
AU - Allolio, Bruno
AU - Terzolo, Massimo
N1 - Funding Information:
Funding/Support and role of the sponsor: This study is a collaborative effort of the ACC working group of the European Network for the Study of Adrenal Tumors (ENS@T) and the University of Michigan (USA). The study was supported in part by Regione Piemonte Ricerca Sanitaria Finalizzata 2008 no. 20889/DA20.01, by a donation of Bortolotti Marilena in memory of Ridon Carlo, and the ENS@T (FP7/2007–2013 under grant agreement 259735). In addition, this study was supported by grants of the Deutsche Krebshilfe (#106 080 to Bruno Allolio and #107 111 to Martin Fassnacht).
Funding Information:
Financial disclosures: Alfredo Berruti certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Martin Fassnacht, Eric Baudin, Harm Haak, Gary D. Hammer, Bruno Allolio, and Massimo Terzolo participated in a study on the pharmacokinetics of mitotane in a subgroup of patients who were enrolled in the FIRM-ACT study. This substudy was funded by HRA Pharma. Alfredo Berruti, Martin Fassnacht, Eric Baudin, Harm Haak, Gary D. Hammer, and Bruno Allolio participated in a clinical trial on OSI-906 in adrenocortical carcinoma sponsored by Astellas Pharma. Gary D. Hammer consults for ISIS, Orphagen, Embara, and Atterocor; holds stocks in Orphagen, Embara, and Atterocor; and is a partial owner of Atterocor. The remaining authors have nothing to disclose.
PY - 2014/4/1
Y1 - 2014/4/1
N2 - Background Although prognostic parameters are important to guide adjuvant treatment, very few have been identified in patients with completely resected adrenocortical carcinoma (ACC). Objective To assess the prognostic role of clinical symptoms of hypercortisolism in a large series of patients with completely resected ACC. Design, setting, and participants A total of 524 patients followed at referral centers for ACC in Europe and the United States entered the study. Inclusion criteria were ≥18 yr of age, a histologic diagnosis of ACC, and complete surgery (R0). Exclusion criteria were a history of other malignancies and adjuvant systemic therapies other than mitotane. Intervention All ACC patients were completely resected, and adjuvant mitotane therapy was prescribed at the discretion of the investigators. Outcome measurements and statistical analysis The primary end point was overall survival (OS). The secondary end points were recurrence-free survival (RFS) and the efficacy of adjuvant mitotane therapy according to cortisol secretion. Results and limitations Overt hypercortisolism was observed in 197 patients (37.6%). Patients with cortisol excess were younger (p = 0.002); no difference according to sex and tumor stage was observed. The median follow-up of the series was 50 mo. After adjustment for sex, age, tumor stage, and mitotane treatment, the prognostic significance of cortisol excess was highly significant for both RFS (hazard ratio [HR]: 1.30; 95% confidence interval [CI], 1.04-2.62; p = 0.02) and OS (HR: 1.55; 95% CI, 1.15-2.09; p = 0.004). Mitotane administration was associated with a reduction of disease progression (adjusted HR: 0.65; 95% CI, 0.49-0.86; p = 0.003) that did not differ according to the patient's secretory status. A major limitation is that only symptomatic patients were considered as having hypercortisolism, thus excluding information on the prognostic role of elevated cortisol levels in the absence of a clinical syndrome. Conclusions Clinically relevant hypercortisolism is a new prognostic factor in patients with completely resected ACC. The efficacy of adjuvant mitotane does not seem to be influenced by overt hypercortisolism.
AB - Background Although prognostic parameters are important to guide adjuvant treatment, very few have been identified in patients with completely resected adrenocortical carcinoma (ACC). Objective To assess the prognostic role of clinical symptoms of hypercortisolism in a large series of patients with completely resected ACC. Design, setting, and participants A total of 524 patients followed at referral centers for ACC in Europe and the United States entered the study. Inclusion criteria were ≥18 yr of age, a histologic diagnosis of ACC, and complete surgery (R0). Exclusion criteria were a history of other malignancies and adjuvant systemic therapies other than mitotane. Intervention All ACC patients were completely resected, and adjuvant mitotane therapy was prescribed at the discretion of the investigators. Outcome measurements and statistical analysis The primary end point was overall survival (OS). The secondary end points were recurrence-free survival (RFS) and the efficacy of adjuvant mitotane therapy according to cortisol secretion. Results and limitations Overt hypercortisolism was observed in 197 patients (37.6%). Patients with cortisol excess were younger (p = 0.002); no difference according to sex and tumor stage was observed. The median follow-up of the series was 50 mo. After adjustment for sex, age, tumor stage, and mitotane treatment, the prognostic significance of cortisol excess was highly significant for both RFS (hazard ratio [HR]: 1.30; 95% confidence interval [CI], 1.04-2.62; p = 0.02) and OS (HR: 1.55; 95% CI, 1.15-2.09; p = 0.004). Mitotane administration was associated with a reduction of disease progression (adjusted HR: 0.65; 95% CI, 0.49-0.86; p = 0.003) that did not differ according to the patient's secretory status. A major limitation is that only symptomatic patients were considered as having hypercortisolism, thus excluding information on the prognostic role of elevated cortisol levels in the absence of a clinical syndrome. Conclusions Clinically relevant hypercortisolism is a new prognostic factor in patients with completely resected ACC. The efficacy of adjuvant mitotane does not seem to be influenced by overt hypercortisolism.
KW - Adjuvant therapy
KW - Adrenocortical cancer
KW - Cushing syndrome
KW - Mitotane
UR - http://www.scopus.com/inward/record.url?scp=84894484398&partnerID=8YFLogxK
U2 - 10.1016/j.eururo.2013.11.006
DO - 10.1016/j.eururo.2013.11.006
M3 - Article
C2 - 24268504
AN - SCOPUS:84894484398
SN - 0302-2838
VL - 65
SP - 832
EP - 838
JO - European Urology
JF - European Urology
IS - 4
ER -