Prognostic Factors for Survival in Noncastrate Metastatic Prostate Cancer: Validation of the Glass Model and Development of a Novel Simplified Prognostic Model

被引:106
作者
Gravis, Gwenaelle [1 ]
Boher, Jean-Marie [2 ,3 ]
Fizazi, Karim [4 ]
Joly, Florence [5 ]
Priou, Franck [6 ]
Marino, Patricia [7 ,8 ]
Latorzeff, Igor [9 ]
Delva, Remy [10 ]
Krakowski, Ivan [11 ]
Laguerre, Brigitte [12 ]
Walz, Jochen [13 ]
Rolland, Frederic [14 ]
Theodore, Christine [15 ]
Deplanque, Gael [16 ]
Ferrero, Jean-Marc [17 ]
Pouessel, Damien [18 ]
Mourey, Loic [19 ]
Beuzeboc, Philippe [20 ]
Zanetta, Sylvie [21 ]
Habibian, Muriel [22 ]
Berdah, Jean-Francois [23 ]
Dauba, Jerome [24 ]
Baciuchka, Marjorie [25 ]
Platini, Christian [26 ]
Linassier, Claude [27 ]
Labourey, Jean-Luc [28 ]
Machiels, Jean Pascal [29 ]
El Kouri, Claude [30 ]
Ravaud, Alain [31 ]
Suc, Etienne [32 ]
Eymard, Jean-Christophe [33 ]
Hasbini, Ali [34 ]
Bousquet, Guilhem [35 ]
Soulie, Michel [36 ]
Oudard, Stephane [37 ,38 ]
机构
[1] Inst J Paoli I Calmettes, Dept Med Oncol, F-13009 Marseille, France
[2] Inst J Paoli I Calmettes, Biostat Dept, F-13009 Marseille, France
[3] Aix Marseille Univ, UMR S SESSTIM 912, Marseille, France
[4] Univ Paris 11, Inst Gustave Roussy, Dept Canc Med, Villejuif, France
[5] Ctr Francois Baclesse CHU Cote Nacre, Dept Med Oncol, Caen, France
[6] Ctr Hosp Oudairies, Dept Med Oncol, La Roche Sur Yon, France
[7] Inst J Paoli I Calmettes, F-13009 Marseille, France
[8] Aix Marseille Univ, UMR SESSTIM S912, Marseille, France
[9] Clin Pasteur, Dept Radiotherapy, Toulouse, France
[10] Ctr Paul Papin, Dept Med Oncol, Angers, France
[11] Ctr Alexis Vautrin, Vandoeuvre Les Nancy, France
[12] Ctr Eugene Marquis, Dept Med Oncol, Rennes, France
[13] Inst J Paoli I Calmettes, Dept Urol Surg, F-13009 Marseille, France
[14] Ctr Rene Gauducheau, Dept Med Oncol, St Herblain, France
[15] Hop Foch, Med Oncol Dept, Suresnes, France
[16] Grp Hosp St Joseph, Dept Med Oncol, Paris, France
[17] Ctr Antoine Lacassagne, Dept Med Oncol, F-06054 Nice, France
[18] Ctr Val dAurelle Paul Lamarque, Dept Med Oncol, Montpellier, France
[19] Inst Claudius Regaud, Dept Med Oncol, Toulouse, France
[20] Inst Curie, Dept Med Oncol, Paris, France
[21] Ctr Georges Francois Leclerc, Dept Med Oncol, Dijon, France
[22] R&D UNICANC, Paris 13, France
[23] Clin St Marguerite, Dept Med Oncol, Hyeres, France
[24] Hop Layne, Dept Med Oncol, Mt De Marsan, France
[25] Ctr Hosp La Timone, Dept Med Oncol, Marseille, France
[26] Ctr Reg Hosp, Dept Med Oncol, Metz, France
[27] Hop Bretonneau, Dept Med Oncol, Tours, France
[28] Ctr Hosp Dupuytren, Dept Med Oncol, Limoges, France
[29] Catholic Univ Louvain, Clin Univ St Luc, Dept Med Oncol, B-1200 Brussels, Belgium
[30] Ctr Catherine Sienne, Dept Med Oncol, Nantes, France
[31] Hop St Andre, Dept Med Oncol, Bordeaux, France
[32] Clin St Jean Languedoc, Dept Med Oncol, Toulouse, France
[33] Inst Jean Godinot, Dept Med Oncol, Reims, France
[34] Clin Armoricaine Radiol, Dept Med Oncol, St Brieux, France
[35] Hop St Louis, Dept Med Oncol, Paris, France
[36] Ctr Hosp Univ Rangueil, Dept Urol, Toulouse, France
[37] Georges Pompidou Hosp, Dept Med Oncol, Paris, France
[38] Univ Paris 05, Paris, France
关键词
Prostate cancer; Noncastrate; Metastatic; Docetaxel; Alkaline phosphatase; Prognostic factors; ANDROGEN-DEPRIVATION; MEN; FLUTAMIDE; NOMOGRAM; TRIAL;
D O I
10.1016/j.eururo.2014.09.022
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: The Glass model developed in 2003 uses prognostic factors for noncastrate metastatic prostate cancer (NCMPC) to define subgroups with good, intermediate, and poor prognosis. Objective: To validate NCMPC risk groups in a more recently diagnosed population and to develop a more sensitive prognostic model. Design, setting, and participants: NCMPC patients were randomized to receive continuous androgen deprivation therapy (ADT) with or without docetaxel in the GETUG-15 phase 3 trial. Potential prognostic factors were recorded: age, performance status, Gleason score, hemoglobin (Hb), prostate-specific antigen, alkaline phosphatase (ALP), lactate dehydrogenase (LDH), metastatic localization, body mass index, and pain. Outcome measurements and statistical analysis: These factors were used to develop a new prognostic model using a recursive partitioning method. Before analysis, the data were split into learning and validation sets. The outcome was overall survival (OS). Results and limitations: For the 385 patients included, those with good (49%), intermediate (29%), and poor (22%) prognosis had median OS of 69.0, 46.5 and 36.6 mo (p = 0.001), and 5-yr survival estimates of 60.7%, 39.4%, and 32.1%, respectively (p = 0.001). The most discriminatory variables in univariate analysis were ALP, pain intensity, Hb, LDH, and bone metastases. ALP was the strongest prognostic factor in discriminating patients with good or poor prognosis. In the learning set, median OS in patients with normal and abnormal ALP was 69.1 and 33.6 mo, and 5-yr survival estimates were 62.1% and 23.2%, respectively. The hazard ratio for ALP was 3.11 and 3.13 in the learning and validation sets, respectively. The discriminatory ability of ALP (concordance [C] index 0.64, 95% confidence interval [CI] 0.58-0.71) was superior to that of the Glass risk model (C-index 0.59, 95% CI 0.52-0.66). The study limitations include the limited number of patients and low values for the C-index. Conclusion: A new and simple prognostic model was developed for patients with NCMPC, underlying the role of normal or abnormal ALP. Patient summary: We analyzed clinical and biological factors that could affect overall survival in noncastrate metastatic prostate cancer. We showed that normal or abnormal alkaline phosphatase at baseline might be useful in predicting survival. (C) 2014 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:196 / 204
页数:9
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