Adrenocortical carcinoma: A population-based study on incidence and survival in the Netherlands since 1993

被引:248
作者
Kerkhofs, Thomas M. A. [1 ]
Verhoeven, Rob H. A. [2 ]
Van der Zwan, Jan Maarten [3 ]
Dieleman, Jeanne [4 ]
Kerstens, Michiel N. [5 ]
Links, Thera P. [5 ]
Van de Poll-Franse, Lonneke V. [2 ,6 ]
Haak, Harm R. [1 ]
机构
[1] Maxima Med Ctr, Dept Internal Med, NL-5631 BM Eindhoven, Netherlands
[2] Comprehens Canc Ctr South, Eindhoven Canc Registry, Dept Res, Eindhoven, Netherlands
[3] Comprehens Canc Ctr Netherlands, Dept Registry & Res, Utrecht, Netherlands
[4] MMC Acad, Maxima Med Ctr, NL-5631 BM Eindhoven, Netherlands
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Endocrinol, NL-9700 AB Groningen, Netherlands
[6] Tilburg Univ, Dept Med Psychol & Neuropsychol, CoRPS Ctr Res Psychol Somat Dis, NL-5000 LE Tilburg, Netherlands
关键词
Adrenocortical carcinoma; Incidence; Cancer registry; ADRENAL-CORTICAL CARCINOMA; MITOTANE; CANCER; MANAGEMENT; SURGERY; RECURRENCE; SERIES;
D O I
10.1016/j.ejca.2013.02.034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The reported annual incidence of adrenocortical carcinoma (ACC) is 0.5-2.0 cases per million individuals. Updated population-based studies on incidence are lacking. The aim of this nationwide survey was to describe the incidence and survival rates of ACC in the Netherlands. Secondary objectives were to evaluate changes in both survival rates and the number of patients undergoing surgery. Methods: All ACC patients registered in the Netherlands Cancer Registry (NCR) between 1993 and 2010 were included. Data on demographics, stage of disease, primary treatment modality and survival were evaluated. Results: Included were 359 patients, 196 of whom were female (55%). Median age at diagnosis was 56 years (range 1-91). The 5-year age-standardised incidence rate decreased from 1.3 to 1.0 per one million person-years. Median survival for patients with stage I-II, stage III and stage IV disease was 159 months (95% confidence interval (CI) 93-225 months), 26 months (95% CI: 4-48 months) and 5 months (95% CI: 2-7 months), respectively (P < 0.001). Improvement in survival was not observed, as reflected by the lack of association between survival and time of diagnosis. The percentage of patients receiving treatment within 6 months after diagnosis increased significantly from 76% in 1993-1998 to 88% in 2005-2010 (P = 0.047), mainly due to an increase in surgery for stage III-IV patients. Conclusion: These nationwide data provide an up-to-date survey of the epidemiology of ACC in the Netherlands. A trend towards a decreasing overall incidence rate was observed. Survival rates did not change during this period despite an increased number of surgical procedures. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2579 / 2586
页数:8
相关论文
共 32 条
[1]   Clinical review: Adrenocortical carcinoma: Clinical update [J].
Allolio, Bruno ;
Fassnacht, Martin .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (06) :2027-2037
[2]  
[Anonymous], 1991, IARC Sci Publ, P1
[3]  
[Anonymous], 2013, International Classification of disease for Oncology
[4]   Urine Steroid Metabolomics as a Biomarker Tool for Detecting Malignancy in Adrenal Tumors [J].
Arlt, Wiebke ;
Biehl, Michael ;
Taylor, Angela E. ;
Hahner, Stefanie ;
Libe, Rossella ;
Hughes, Beverly A. ;
Schneider, Petra ;
Smith, David J. ;
Stiekema, Han ;
Krone, Nils ;
Porfiri, Emilio ;
Opocher, Giuseppe ;
Bertherat, Jerome ;
Mantero, Franco ;
Allolio, Bruno ;
Terzolo, Massimo ;
Nightingale, Peter ;
Shackleton, Cedric H. L. ;
Bertagna, Xavier ;
Fassnacht, Martin ;
Stewart, Paul M. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (12) :3775-3784
[5]   Role of reoperation in recurrence of adrenal cortical carcinoma: Results from 188 cases collected in the Italian National Registry for Adrenal Cortical Carcinoma [J].
Bellantone, R ;
Ferrante, A ;
Boscherini, M ;
Lombardi, CP ;
Crucitti, P ;
Crucitti, F ;
Favia, G ;
Borrelli, D ;
Boffi, L ;
Capussotti, L ;
Carbone, G ;
Casaccia, M ;
Cavallaro, A ;
Del Gaudio, A ;
Dettori, G ;
Di Giovanni, V ;
Mazziotti, A ;
Marrano, D ;
Masenti, E ;
Miccoli, P ;
Mosca, F ;
Mussa, A ;
Petronio, R ;
Piat, G ;
Ruberti, U ;
Serio, G ;
Marzano, L .
SURGERY, 1997, 122 (06) :1212-1218
[6]   Adrenal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Berruti, A. ;
Baudin, E. ;
Gelderblom, H. ;
Haak, H. R. ;
Porpiglia, F. ;
Fassnacht, M. ;
Pentheroudakis, G. .
ANNALS OF ONCOLOGY, 2012, 23 :131-138
[7]   Adjuvant Therapy in Patients With Adrenocortical Carcinoma: A Position of an International Panel [J].
Berruti, Alfredo ;
Fassnacht, Martin ;
Baudin, Eric ;
Hammer, Gary ;
Haak, Harm ;
Leboulleux, Sophie ;
Skogseid, Britt ;
Allolio, Bruno ;
Terzolo, Massimo .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (23) :E401-E402
[8]   SUMMARIZING INDICES FOR COMPARISON OF CANCER INCIDENCE DATA [J].
DOLL, R ;
COOK, P .
INTERNATIONAL JOURNAL OF CANCER, 1967, 2 (03) :269-&
[9]   The Role of Surgery in the Management of Recurrent Adrenocortical Carcinoma [J].
Erdogan, Ilknur ;
Deutschbein, Timo ;
Jurowich, Christian ;
Kroiss, Matthias ;
Ronchi, Christina ;
Quinkler, Marcus ;
Waldmann, Jens ;
Willenberg, Holger S. ;
Beuschlein, Felix ;
Fottner, Christian ;
Klose, Silke ;
Heidemeier, Anke ;
Brix, David ;
Fenske, Wiebke ;
Hahner, Stefanie ;
Reibetanz, Joachim ;
Allolio, Bruno ;
Fassnacht, Martin .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 98 (01) :181-191
[10]  
Fassnacht M, 2012, N ENGL J MED, V2012