Is Nephron Sparing Surgery Justified in Wilms Tumor With Beckwith-Wiedemann Syndrome or Isolated Hemihypertrophy?

被引:16
作者
Scalabre, Aurelien [1 ]
Bergeron, Christophe [2 ]
Brioude, Frederic [3 ]
Dainese, Linda [4 ]
Cropet, Claire [5 ]
L'hermine, Aurore Coulomb [4 ]
Pasqualini, Claudia [6 ]
Auber, Frederic [7 ]
Verschuur, Arnauld [8 ]
Schleiermacher, Gudrun [9 ]
Le Bouc, Yves [3 ]
Audry, Georges [1 ]
Irtan, Sabine [10 ]
机构
[1] Univ Paris 06, Sorbonne Univ, Hop Armand Trousseau, APHP,Pediat Surg, F-75012 Paris, France
[2] Inst Hematol & Oncol Pediat, Dept Pediat, F-690008 Lyon, France
[3] Univ Paris 06, Ctr Rech St Antoine, INSERM, UMRS 938,Hop Armand Trousseau,APHP,Pediat & Genet, F-75012 Paris, France
[4] Univ Paris 06, Sorbonne Univ, Hop Armand Trousseau, APHP,Pathol Dept,Ctr Rech St Antoine,Inserm,UMRS, F-75012 Paris, France
[5] Univ Lyon, Dept Stat, Ctr Leon Berard, F-69008 Lyon, France
[6] Gustave Roussy Canc Campus, Pediat Oncol, F-94800 Villejuif, France
[7] Univ Bourgogne Franche Comte, Lab Nanomed Imagerie & Therapeut, EA 4662, CHRU Besancon,Serv Chirurg Pediat, F-25030 Besancon, France
[8] Hop Timone Enfant, Dept Pediat Hematol & Oncol, F-13005 Marseille, France
[9] Inst Curie, Lab Genet & Biol Canc, Paediat Oncol, INSERM U830 3, F-75005 Paris, France
[10] Univ Paris 06, Sorbonne Univ, Ctr Rech St Antoine, Hop Armand Trousseau,APHP,Pediat Surg,Inserm,UMRS, F-75012 Paris, France
关键词
Beckwith-Wiedemann syndrome; isolated hemihypertrophy; nephron sparing surgery; Wilms tumor; SINGLE-CENTER EXPERIENCE; IDIOPATHIC HEMIHYPERTROPHY; CHILDREN; RISK; NEPHROBLASTOMATOSIS; RESTS; CT;
D O I
10.1002/pbc.26073
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundPatients with Beckwith-Wiedemann syndrome (BWS) or isolated hemihypertrophy (HH) treated for a Wilms tumor (WT) carry an increased risk of developing metachronous lesion. There are no guidelines on precise indications for nephron sparing surgery (NSS) in unilateral WT (UWT). The objective of this retrospective study was to delineate the indications of NSS in patients with BWS/HH treated for WT and to evaluate their outcome. ProcedureAll cases of BWS/HH treated for a WT according to SIOP protocols from 1980 to 2013 were reviewed. Patients were divided into two groups (G): isolated UWT (G1) and bilateral lesions (G2) with two subgroups: bilateral tumors suspected of malignancy (G2a), and unilateral tumor suspected of malignancy with contralateral nephroblastomatosis (G2b). ResultsForty-six patients were included (34 G1, three G2a, and nine G2b). Nine NSS and 25 total nephrectomies (TN) were performed in G1, two bilateral NSS and one NSS with contralateral TN in G2a, and eight NSS and one TN in G2b. The 3-year event-free survival was 92.3% (95% CI [77.9-97.5%]). One death occurred after a local relapse following a TN for a stage III stromal WT (G1) and another after a combined local and distant relapse following a NSS for a stage I diffuse anaplastic WT (G2b). There were two metachronous WT (4%), 3 years after a TN (G1) and 12 years after a NSS (G2b). ConclusionsNSS is recommended in bilateral WT and may be an option in selected UWT patients with BWS/HH because it was not associated with an increased risk of local relapse. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:1571 / 1577
页数:7
相关论文
共 28 条
[1]   Management of Wilms Tumors in Drash and Frasier Syndromes [J].
Auber, F. ;
Jeanpierre, C. ;
Denamur, E. ;
Jaubert, F. ;
Schleiermacher, G. ;
Patte, C. ;
Cabrol, S. ;
Leverger, G. ;
Nihoul-Fekete, C. ;
Sarnacki, S. .
PEDIATRIC BLOOD & CANCER, 2009, 52 (01) :55-59
[2]  
Beckwith JB, 1998, AM J MED GENET, V79, P268, DOI 10.1002/(SICI)1096-8628(19981002)79:4<268::AID-AJMG7>3.0.CO
[3]  
2-I
[4]   Does nephroblastomatosis influence the natural history and relapse rate in Wilms' tumour? A single centre experience over 11 years [J].
Bergeron, C ;
Iliescu, C ;
Thiesse, P ;
Bouvier, R ;
Dijoud, F ;
Ranchere-Vince, D ;
Basset, T ;
Chappuis, JP ;
Buclon, M ;
Frappaz, D ;
Brunat-Mentigny, M ;
Philip, T .
EUROPEAN JOURNAL OF CANCER, 2001, 37 (03) :385-391
[5]   Beckwith-Wiedemann Syndrome: Growth Pattern and Tumor Risk according to Molecular Mechanism, and Guidelines for Tumor Surveillance [J].
Brioude, F. ;
Lacoste, A. ;
Netchine, I. ;
Vazquez, M. -P. ;
Auber, F. ;
Audry, G. ;
Gauthier-Villars, M. ;
Brugieres, L. ;
Gicquel, C. ;
Le Bouc, Y. ;
Rossignol, S. .
HORMONE RESEARCH IN PAEDIATRICS, 2013, 80 (06) :457-465
[6]  
Choyke PL, 1999, MED PEDIATR ONCOL, V32, P196, DOI 10.1002/(SICI)1096-911X(199903)32:3<196::AID-MPO6>3.3.CO
[7]  
2-0
[8]   Nonmalignant renal disease in pediatric patients with Beckwith-Wiedemann syndrome [J].
Choyke, PL ;
Siegel, MJ ;
Oz, O ;
Sotelo-Avila, C ;
DeBaun, MR .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1998, 171 (03) :733-737
[9]  
Clericuzio Carol L, 2009, Genet Med, V11, P220, DOI 10.1097/GIM.0b013e31819436cf
[10]  
Coppes MJ, 1999, CANCER, V85, P1616, DOI 10.1002/(SICI)1097-0142(19990401)85:7<1616::AID-CNCR26>3.0.CO