Renal failure in Wilms' tumor patients: A report from the National Wilms' Tumor Study group

被引:1
作者
Ritchey, ML
Green, DM
Thomas, PRM
Smith, GR
Haase, G
Shochat, S
Moksness, J
Breslow, NE
机构
[1] UNIV TEXAS,SCH MED,DEPT SURG,HOUSTON,TX
[2] ROSWELL PK CANC INST,DEPT PEDIAT,BUFFALO,NY 14263
[3] TEMPLE UNIV,DEPT RADIAT ONCOL,PHILADELPHIA,PA 19122
[4] STANFORD UNIV,DEPT PEDIAT SURG,STANFORD,CA 94305
[5] UNIV COLORADO,DIV PEDIAT SURG,DENVER,CO
[6] WASHINGTON UNIV,DEPT BIOSTAT,SEATTLE,WA
来源
MEDICAL AND PEDIATRIC ONCOLOGY | 1996年 / 26卷 / 02期
关键词
Wilms' tumor; renal failure; late effects;
D O I
10.1002/(SICI)1096-911X(199602)26:2<75::AID-MPO1>3.0.CO;2-R
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This report defines the incidence and determines the etiology of renal failure (RF) in patients undergoing treatment for Wilms' tumor (WT). The database of the National Wilms' Tumor Study (NWTS) was searched to identify all children reported to have developed chronic renal failure. There were 55 patients found to have RF. Of these, 39 patients had bilateral tumors, 15 with unilateral disease and one with a WT in a solitary kidney. The median interval from diagnosis to the onset of renal failure was 21 months. The incidence of RF in bilateral WT was 16.4% for NWTS-1 & -2, 9.9% for NWTS-3, and 3.8% for NWTS-4. The incidence of RF in unilateral WT remained stable. The most common etiologies of RF were: bilateral nephrectomy for persistent or recurrent tumor (24 pts), Drash syndrome (12 pts), progressive tumor in the remaining kidney (5 pts), radiation nephritis (6 pts), and other causes (5 pts). The etiology of renal failure was not reported in three children. Children with unilateral WT and a normal contralateral kidney have a very low incidence of RF, and this review does not support a recommendation for parenchymal sparing procedures in these patients. Children with bilateral WT are at risk for the development of RF, and parenchymal sparing procedures are warranted. (C) 1996 Wiley-Liss, Inc.
引用
收藏
页码:75 / 80
页数:6
相关论文
共 30 条
  • [11] BILATERAL WILMS TUMOR - LONG-TERM SURVIVAL AND SOME EPIDEMIOLOGICAL FEATURES
    COPPES, MJ
    DEKRAKER, J
    VANDIJKEN, PJ
    PERRY, HJM
    DELEMARRE, JFM
    TOURNADE, MF
    LEMERLE, J
    VOUTE, PA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (03) : 310 - 315
  • [12] TREATMENT OF BILATERAL WILMS TUMOR
    DELORIMIER, AA
    BELZER, FO
    KOUNTZ, SL
    KUSHNER, J
    [J]. AMERICAN JOURNAL OF SURGERY, 1971, 122 (02) : 275 - +
  • [13] RENAL-TRANSPLANTATION IN PATIENTS WITH BILATERAL WILMS TUMOR
    DEMARIA, JE
    HARDY, BE
    BREZINSKI, A
    CHURCHILL, BM
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1979, 14 (05) : 577 - 579
  • [14] DENYS P, 1967, ARCH FR PEDIATR, V24, P729
  • [15] A SYNDROME OF PSEUDOHERMAPHRODITISM, WILMS TUMOR, HYPERTENSION, AND DEGENERATIVE RENAL DISEASE
    DRASH, A
    SHERMAN, F
    HARTMANN, WH
    BLIZZARD, RM
    [J]. JOURNAL OF PEDIATRICS, 1970, 76 (04) : 585 - +
  • [16] EVANS AE, 1991, CANCER, V67, P331, DOI 10.1002/1097-0142(19910115)67:2<331::AID-CNCR2820670202>3.0.CO
  • [17] 2-7
  • [18] RENAL SIZE AND FUNCTION AFTER CURE OF WILMS-TUMOR
    LEVITT, GA
    YEOMANS, E
    MIREAUX, CD
    BREATNACH, F
    KINGSTON, J
    PRITCHARD, J
    [J]. BRITISH JOURNAL OF CANCER, 1992, 66 (05) : 877 - 882
  • [19] RENAL GROWTH AND FUNCTION 11-28 YEARS AFTER TREATMENT OF WILMS-TUMOR
    MAKIPERNAA, A
    KOSKIMIES, O
    JAASKELAINEN, J
    TEPPO, AM
    SIIMES, MA
    [J]. EUROPEAN JOURNAL OF PEDIATRICS, 1991, 150 (06) : 444 - 447
  • [20] REDUCTION IN TUMOR BURDEN ALLOWING PARTIAL NEPHRECTOMY FOLLOWING PREOPERATIVE CHEMOTHERAPY IN BIOPSY PROVED WILMS-TUMOR
    MCLORIE, GA
    MCKENNA, PH
    GREENBERG, M
    BABYN, P
    THORNER, P
    CHURCHILL, BM
    WEITZMAN, S
    FILLER, R
    KHOURY, AE
    [J]. JOURNAL OF UROLOGY, 1991, 146 (02) : 509 - 513