Renal tumor in developing countries: 142 cases from a single institution at Shanghai, China

被引:8
作者
Pan, Ci [1 ]
Cai, Jiao-Yang [1 ]
Xu, Min [2 ]
Ye, Qi-Dong [1 ]
Zhou, Min [1 ]
Yin, Min-Zhi [3 ]
Zhong, Yu-Min [4 ]
Chen, Jing [1 ]
Shen, Shu-Hong [1 ]
Tang, Jing-Yan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Sch Med, Dept Hematol Oncol, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Sch Med, Dept Surg, Shanghai 200030, Peoples R China
[3] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Sch Med, Dept Pathol, Shanghai 200030, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Childrens Med Ctr, Sch Med, Dept Radiol, Shanghai 200030, Peoples R China
关键词
China; developing country; multi-disciplinary team; renal tumors; WILMS-TUMOR; OUTCOMES; DISEASE;
D O I
10.1007/s12519-015-0041-3
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The clinical management of children with renal tumors including Wilms' tumor, clear cell sarcoma, rhabdoid tumor and other renal tumors in our center was designed according to the National Wilms' Tumor Study Group protocols. A total of 142 consecutive patients who had been diagnosed as having renal tumors at Shanghai Children's Medical Center were reviewed retrospectively in the period of December 1998 and September 2012. Diagnosis and treatment were decided by a multidisciplinary team including oncologists, surgeons, pathologists and sub-specialized radiologists. The median age of the patients at the time of diagnosis was 27 months. The tumor stages of the patients were as follows: stage I 24.6%, stage II 23.2%, stage III 32.3%, stage IV 14.1%, and stage V 5.6%. Favorable histology was diagnosed in 80.3%, anaplasia in 4.2%, clear cell sarcoma in 9.8%, rhabdoid tumor in 4.9%, and other renal tumors in 0.7% of the patients. The eventfree and overall 5-year survival rates were 80% and 83%, respectively. Tumor relapse and progress was seen in 25 patients (17.6%). The median relapse time was 6 months (range: 2-37 months). Seven relapsing patients were retreated and four of them got second complete remission (three in stage II, one in stage I). A multi-disciplinary team work model is feasible in developing countries, and the renal tumors protocols basically from developed countries are safe in developing countries.
引用
收藏
页码:326 / 330
页数:5
相关论文
共 18 条
[1]   Ifosfamide, carboplatin and etoposide in children with poor-risk relapsed Wilms' tumor: a Children's Cancer Group report [J].
Abu-Ghosh, AM ;
Krailo, MD ;
Goldman, SC ;
Slack, RS ;
Davenport, V ;
Morris, E ;
Laver, JH ;
Reaman, GH ;
Cairo, MS .
ANNALS OF ONCOLOGY, 2002, 13 (03) :460-469
[2]  
[Anonymous], 2006, PRINCIPLES PRACTICE
[3]   End stage renal disease in patients with Wilms tumor: Results from the National Wilms Tumor Study Group and the United States Renal Data System [J].
Breslow, NE ;
Collins, AJ ;
Ritchey, ML ;
Grigoriev, YA ;
Peterson, SM ;
Green, DM .
JOURNAL OF UROLOGY, 2005, 174 (05) :1972-1975
[4]  
DANGIO GJ, 1989, CANCER-AM CANCER SOC, V64, P349, DOI 10.1002/1097-0142(19890715)64:2<349::AID-CNCR2820640202>3.0.CO
[5]  
2-Q
[6]   Treatment of anaplastic histology Wilms' tumor: Results from the fifth National Wilms' Tumor Study [J].
Dome, Jeffrey S. ;
Cotton, Cecilia A. ;
Perlman, Elizabeth J. ;
Breslow, Norman E. ;
Kalapurakal, John A. ;
Ritchey, Michael L. ;
Grundy, Paul E. ;
Malogolowkin, Marcio ;
Beckwith, J. Bruce ;
Shamberger, Robert C. ;
Haase, Gerald M. ;
Coppes, Max J. ;
Coccia, Peter ;
Kletzel, Morris ;
Weetman, Robert M. ;
Donaldson, Milton ;
Macklis, Roger M. ;
Green, Daniel M. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (15) :2352-2358
[7]   Effect of duration of treatment on treatment outcome and cost of treatment for Wilms' tumor: A report from the National Wilms' Tumor Study group [J].
Green, DM ;
Breslow, NE ;
Beckwith, JB ;
Finklestein, JZ ;
Grundy, P ;
Thomas, PR ;
Kim, T ;
Shochat, S ;
Haase, G ;
Ritchey, M ;
Kelalis, P ;
D'Angio, GJ .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3744-3751
[8]   Treatments and outcomes for end-stage renal disease following Wilms tumor [J].
Grigoriev, Yevgeny ;
Lange, Jane ;
Peterson, Susan M. ;
Takashima, Janice R. ;
Ritchey, Michael L. ;
Ko, Dicken ;
Feusner, James H. ;
Shamberger, Robert C. ;
Green, Daniel M. ;
Breslow, Norman E. .
PEDIATRIC NEPHROLOGY, 2012, 27 (08) :1325-1333
[9]   The Management of Synchronous Bilateral Wilms Tumor: A Report from the National Wilms Tumor Study Group [J].
Hamilton, Thomas E. ;
Ritchey, Michael L. ;
Haase, Gerald M. ;
Argani, Pedram ;
Peterson, Susan M. ;
Anderson, James R. ;
Green, Daniel M. ;
Shamberger, Robert C. .
ANNALS OF SURGERY, 2011, 253 (05) :1004-1010
[10]   Management of Wilms' tumour: current practice and future goals [J].
Kalapurakal, JA ;
Dome, JS ;
Perlman, EJ ;
Malogolowkin, M ;
Haase, GM ;
Grundy, P ;
Coppes, MJ .
LANCET ONCOLOGY, 2004, 5 (01) :37-46