Limited Prognostic Value of the 2004 International Union Against Cancer Staging Classification for Adrenocortical Carcinomas

被引:516
作者
Fassnacht, Martin [1 ]
Johanssen, Sarah [1 ]
Quinkler, Marcus [2 ]
Bucsky, Peter [3 ]
Willenberg, Holger S. [4 ]
Beuschlein, Felix [5 ]
Terzolo, Massimo [6 ]
Mueller, Hans-Helge [7 ]
Hahner, Stefanie [1 ]
Allolio, Bruno [1 ]
机构
[1] Univ Wurzburg, Endocrine & Diabet Unit, Dept Med 1, Univ Hosp, D-97080 Wurzburg, Germany
[2] Charite, Dept Clin Endocrinol, D-13353 Berlin, Germany
[3] Med Univ Lubeck, German Soc, Pediat Oncol Study Ctr, D-23538 Lubeck, Germany
[4] Univ Hosp Dusseldorf, Dept Endocrinol Diabet & Rheumatol, Dusseldorf, Germany
[5] Univ Munich, Dept Med, Div Endocrinol, Munich, Germany
[6] Univ Turin, Dept Med, Turin, Italy
[7] Univ Marburg, Inst Med Biometry & Epidemiol, Marburg, Germany
关键词
adrenal cancer; tumor staging; disease-specific outcome; prognosis; ADRENAL-CORTICAL CARCINOMA; MITOTANE; MANAGEMENT; SERIES; FEATURES;
D O I
10.1002/cncr.24030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Adrenocortical carcinoma (ACC) is a rare malignancy, and it was only in 2004 that the International Union Against Cancer (UICC) defined TNM criteria and published the first staging classification. However, to date, the prognostic value of the proposed classification has not been evaluated. METHODS: The German ACC Registry comprising 492 patients was searched for patients who were diagnosed between 1986 and 2007 with detailed information on primary diagnosis and a minimum follow-up of 6 months. Patients were assigned to UICC tumor stage, and disease-specific survival (DSS) was assessed. In addition, the contribution of potential risk factors for DSS was evaluated. RESULTS: In total, 416 patients with a mean follow-up of 36 months met the inclusion criteria (stage 1, n = 23 patients; stage 11, n = 176 patients; stage 111, n = 67 patients; stage IV, n = 150 patients). Kaplan-Meier analysis revealed a stage-dependent DSS. However, DSS in patients with stage 11 ACC did not differ significantly from DSS in patients with stage III ACC (hazard ratio, 1.38; 95% confidence interval, 0.89-2.16). Furthermore, patients who had stage IV ACC without distant metastases had an improved DSS compared with patients who had metastatic disease (P = .004). An analysis of different potential risk factors for defining stage III ACC revealed important roles in DSS for tumor infiltration in surrounding tissue, venous tumor thrombus (VTT), and positive lymph nodes; whereas tumor invasion in adjacent organs carried a prognosis similar to that of infiltration in surrounding tissue only. CONCLUSIONS: The 2004 UICC staging classification for ACC has significant limitations. On the basis of the current analysis, a revised classification with superior prognostic accuracy is proposed (the European Network for the Study of Adrenal Tumors classification). In this system, stage III ACC is defined by the presence of positive lymph nodes, infiltration of surrounding tissue, or VTT; and stage IV ACC is restricted to patients with distant metastasis. Cancer 2009;115:243-50. (C) 2009 American Cancer Society.
引用
收藏
页码:243 / 250
页数:8
相关论文
共 25 条
  • [1] Clinical and biological features in the prognosis of adrenocortical cancer: Poor outcome of cortisol-secreting tumors in a series of 202 consecutive patients
    Abiven, Gwenaelle
    Coste, Joel
    Groussin, Lionel
    Anract, Philippe
    Tissier, Frederique
    Legmann, Paul
    Dousset, Bertrand
    Bertagna, Xavier
    Bertherat, Jerome
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (07) : 2650 - 2655
  • [2] Management of adrenocortical carcinoma
    Allolio, B
    Hahner, S
    Weismann, D
    Fassnacht, M
    [J]. CLINICAL ENDOCRINOLOGY, 2004, 60 (03) : 273 - 287
  • [3] Clinical review: Adrenocortical carcinoma: Clinical update
    Allolio, Bruno
    Fassnacht, Martin
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (06) : 2027 - 2037
  • [4] [Anonymous], 2004, WHO CLASSIFICATION T
  • [5] Prognostic parameters of metastatic adrenocortical carcinoma
    Assie, Guillaume
    Antoni, Guillemette
    Tissier, Frederique
    Caillou, Bernard
    Abiven, Gwenaelle
    Gicquel, Christine
    Leboulleux, Sophie
    Travagli, Jean-Paul
    Dromain, Clarisse
    Bertagna, Xavier
    Bertherat, Jerome
    Schlumberger, Martin
    Baudin, Eric
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (01) : 148 - 154
  • [6] Role of reoperation in recurrence of adrenal cortical carcinoma: Results from 188 cases collected in the Italian National Registry for Adrenal Cortical Carcinoma
    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
    [J]. SURGERY, 1997, 122 (06) : 1212 - 1218
  • [7] OPTIMAL TREATMENT OF ADRENOCORTICAL CARCINOMA WITH MITOTANE - RESULTS IN A CONSECUTIVE SERIES OF 96 PATIENTS
    HAAK, HR
    HERMANS, J
    VANDEVELDE, CJH
    LENTJES, EGWM
    GOSLINGS, BM
    FLEUREN, GJ
    KRANS, HMJ
    [J]. BRITISH JOURNAL OF CANCER, 1994, 69 (05) : 947 - 951
  • [8] Adrenocortical carcinomas: Surgical trends and results of a 253-patient series from the French Association of Endocrine Surgeons study group
    Icard, P
    Goudet, P
    Charpenay, C
    Andreassian, B
    Carnaille, B
    Chapuis, Y
    Cougard, P
    Henry, JF
    Proye, C
    [J]. WORLD JOURNAL OF SURGERY, 2001, 25 (07) : 891 - 897
  • [9] Clinical results of the use of mitotane for adrenocortical carcinoma
    Kasperlik-Zaluska, AA
    [J]. BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2000, 33 (10) : 1191 - 1196
  • [10] Extent of disease at presentation and outcome for adrenocortical carcinoma: Have we made progress?
    Kebebew, E
    Reiff, E
    Duh, QY
    Clark, OH
    McMillan, A
    [J]. WORLD JOURNAL OF SURGERY, 2006, 30 (05) : 872 - 878