Outcome of patients with stage IV high-risk Wilms tumour treated according to the SIOP2001 protocol: A report of the SIOP Renal Tumour Study Group

被引:25
|
作者
Pasqualini, Claudia [1 ]
Furtwaengler, Rhoikos [2 ]
van Tinteren, Harm [3 ]
Teixeira, Roberto A. P. [4 ]
Acha, Tomas [5 ]
Howell, Lisa [6 ]
Vujanic, Gordan [7 ]
Godzinski, Jan [8 ,9 ]
Melchior, Patrick [10 ]
Smets, Anne M. [11 ]
Coulomb-L'Hermine, Aurore [12 ]
Brisse, Herve [13 ]
Pritchard-Jones, Kathy [14 ]
Bergeron, Christophe [15 ]
de Camargo, Beatriz [16 ]
Van den Heuvel-Eibrink, Marry M. [17 ,18 ]
Graf, Norbert [2 ]
Verschuur, Arnauld C. [19 ]
机构
[1] Gustave Roussy, Children & Adolescents Oncol Dept, Villejuif, France
[2] Saarland Univ Hosp, Dept Pediat Haematol Oncol, Homburg, Germany
[3] Netherlands Canc Inst, Biometr Dept, Amsterdam, Netherlands
[4] Univ Sao Paulo, Inst Tratamento Canc Infantil, Dept Pediat, Sao Paulo, Brazil
[5] Hosp Maternoinfantil Carlos Haya, Dept Pediat, Malaga, Spain
[6] Alder Hey Childrens NHS Fdn Trust, Dept Oncol, Liverpool, Merseyside, England
[7] Sidra Med, Dept Pathol, Doha, Qatar
[8] Marciniak Hosp Wroclaw, Dept Pediat Surg, Wroclaw, Poland
[9] Med Univ, Dept Pediat Traumatol & Emergency Med, Wroclaw, Poland
[10] Saarland Univ Hosp, Dept Radiat Oncol, Homburg, Germany
[11] Acad Med Ctr, Dept Radiol & Nucl Med, Amsterdam, Netherlands
[12] Hosp Enfants Armand Trousseau, Dept Pathol, Paris, France
[13] Curie Inst, Dept Radiol, Paris, France
[14] UCL, Great Ormond St Inst Child Hlth, London, England
[15] Ctr Leon Berard, Pediat Oncohaematol Dept, Lyon, France
[16] Inst Nacl Canc, Pediat Oncohaematol, Rio De Janeiro, Brazil
[17] Princess Maxima Ctr Pediat Oncol, Oncol, Utrecht, Netherlands
[18] Dutch Childhood Oncol Grp, The Hague, Netherlands
[19] Hop La Timone, AP HM, Pediat Oncohaematol Dept, Marseille, France
关键词
Wilms; Anaplasia; Blastema; Cancer; Child; TP53; INTERNATIONAL-SOCIETY; DIFFUSE ANAPLASIA; CHILDREN; NEPHROBLASTOMA; TRIAL; SURVIVAL;
D O I
10.1016/j.ejca.2020.01.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: High-risk (HR) metastatic (stage IV) Wilms tumours (WTs) have a particular poor outcome. Methods: Here, we report the results of HR (diffuse anaplastic [DA] or blastemal type [BT]) stage IV WT treated patients according to the HR arm in the SIOP2001 prospective study. Results: From January 2002 to August 2014, 3559 patients with WT were included in the SIOP2001 trial. Among the 525 patients (15%) with metastatic WT, 74 (14%) had stage IV HR-WT. The median age at diagnosis was 5.5 years (range: 1.4-18.3). Thirty-four patients (47%) had BT-WT and 40 (53%) had DA-WT. Five-year event-free survival rates were 44 +/- 17% and 28 +/- 15% for BT-WT and DA-WT, respectively (p = 0.09). Five-year overall survival rates were 53 +/- 17% and 29 +/- 16% for BT-WT and DA-WT, respectively (p = 0.03). Metastatic complete response after preoperative treatment was significantly associated with outcome in univariate and multivariate analyses (hazards ratio = 0.3; p = 0.01). Postoperative radiotherapy of metastatic sites might also be beneficial. Forty-three of 74 patients experienced a relapse or progression predominantly in the lungs (80%). The median time to relapse/ progression after diagnosis was 7.3 months (range: 1.6-33.3) and 4.9 months (range: 0.7 -28.4) for BT-WT and DA-WT, respectively (p = 0.67). This is the first prospective evidence of inferior survival of stage IV BT-WT as compared with historical intermediate-risk WT. Survival of patients with stage IV DA-WT has not improved compared to the previous SIOP93-01 study. Conclusion: These results call for new treatment approaches for patients with HR stage IV WT. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:38 / 46
页数:9
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