Wilms 瘤

Spreafico F, Fernandez CV, Brok J, et al. Wilms tumour. Nat Rev Dis Primers. 2021 Oct 14;7(1):75.全文  摘要

Lopyan NM, Ehrlich PF. Surgical management of Wilms tumor (nephroblastoma) and renal cell carcinoma in children and young adults. Surg Oncol Clin N Am. 2021 Apr;30(2):305-23. 摘要

Vujanić GM, Parsons LN, D'Hooghe E, et al. Pathology of Wilms' tumour in International Society of Paediatric Oncology (SIOP) and Children's Oncology Group (COG) renal tumour studies: similarities and differences. Histopathology. 2022 Jun;80(7):1026-37. 摘要

van den Heuvel-Eibrink MM, Hol JA, Pritchard-Jones K, et al. Position paper: rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol. Nat Rev Urol. 2017 Dec;14(12):743-52.全文  摘要

Dome JS, Mullen EA, Dix DB, et al. Impact of the first generation of Children's Oncology Group clinical trials on clinical practice for Wilms tumor. J Natl Compr Canc Netw. 2021 Aug 1;19(8):978-85.全文  摘要

1. Nakata K, Colombet M, Stiller CA, et al. Incidence of childhood renal tumours: an international population-based study. Int J Cancer. 2020 Dec 15;147(12):3313-27.全文  摘要

2. Szychot E, Apps J, Pritchard-Jones K. Wilms' tumor: biology, diagnosis and treatment. Transl Pediatr. 2014 Jan;3(1):12-24.全文  摘要

3. Spreafico F, Fernandez CV, Brok J, et al. Wilms tumour. Nat Rev Dis Primers. 2021 Oct 14;7(1):75.全文  摘要

4. Davidoff AM. Wilms tumor. Adv Pediatr. 2012;59(1):247-67.全文  摘要

5. Charlton J, Irtan S, Bergeron C, et al. Bilateral Wilms tumour: a review of clinical and molecular features. Expert Rev Mol Med. 2017 Jul 18;19:e8.全文  摘要

6. Shojaeian R, Hiradfar M, Sharifabad PS, et al. Extrarenal Wilms’ tumor: challenges in diagnosis, embryology, treatment and prognosis. In: van den Heuvel-Eibrink MM, ed. Wilms tumor [internet]. Brisbane: Codon Publications; 2016 Mar: chapter 6.全文  摘要

7. Apoznański W, Sawicz-Birkowska K, Palczewski M, et al. Extrarenal nephroblastoma. Cent European J Urol. 2015;68(2):153-6.全文  摘要

8. Thakkar NC, Sarin YK. Extra-renal Wilms' tumor: a rare diagnosis. APSP J Case Rep. 2015 May-Aug;6(2):17.全文  摘要

9. Petersen CL, Hemker BG, Jacobson RD, et al. Wilms tumor presenting with lambert-eaton myasthenic syndrome. J Pediatr Hematol Oncol. 2013 May;35(4):267-70. 摘要

10. Abdullah Y, Karpelowsky J, Davidson A, et al. Management of nine cases of Wilms' tumour with intracardiac extension - a single centre experience. J Pediatr Surg. 2013 Feb;48(2):394-9. 摘要

11. Liu EK, Suson KD. Syndromic Wilms tumor: a review of predisposing conditions, surveillance and treatment. Transl Androl Urol. 2020 Oct;9(5):2370-81.全文  摘要

12. Siegel RL, Miller KD, Wagle NS, et al. Cancer statistics, 2023. CA Cancer J Clin. 2023 Jan;73(1):17-48.全文  摘要

13. National Cancer Institute. Surveillance, Epidemiology, and End Results (SEER) Program. National Childhood Cancer Registry. Trends over time. 2022 [internet publication].全文

14. Treger TD, Chowdhury T, Pritchard-Jones K, et al. The genetic changes of Wilms tumour. Nat Rev Nephrol. 2019 Apr;15(4):240-51. 摘要

15. Gadd S, Huff V, Walz AL, et al. A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor. Nat Genet. 2017 Oct;49(10):1487-94.全文  摘要

16. Narod SA, Hawkins MM, Robertson CM, et al. Congenital anomalies and childhood cancer in Great Britain. Am J Hum Genet. 1997 Mar;60(3):474-85.全文  摘要

17. PDQ Pediatric Treatment Editorial Board. Wilms tumor and other childhood kidney tumors treatment (PDQ®): health professional version. 2022 Dec 23. In: PDQ cancer information summaries [internet]. Bethesda, MD: National Cancer Institute; 2002.全文  摘要

18. Bhutani N, Kajal P, Sharma U. Many faces of Wilms tumor: recent advances and future directions. Ann Med Surg (Lond). 2021 Apr;64:102202.全文  摘要

19. Khan A, Feulefack J, Sergi CM. Exposure to pesticides and pediatric Wilms' tumor. A meta-analysis on pre-conception and pregnancy parental exposure with an IARC/WHO commentary. Hum Exp Toxicol. 2022 Jan-Dec;41:9603271221136211.全文  摘要

20. Maciaszek JL, Oak N, Nichols KE. Recent advances in Wilms' tumor predisposition. Hum Mol Genet. 2020 Oct 20;29(r2):R138-49.全文  摘要

21. Knudson AG Jr, Strong LC. Mutation and cancer: a model for Wilms' tumor of the kidney. J Natl Cancer Inst. 1972 Feb;48(2):313-24.全文  摘要

22. Bjornsson HT, Brown LJ, Fallin MD, et al. Epigenetic specificity of loss of imprinting of the IGF2 gene in Wilms tumors. J Natl Cancer Inst. 2007 Aug 15;99(16):1270-3.全文  摘要

23. Breslow NE, Beckwith JB, Perlman EJ, et al. Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor. Pediatr Blood Cancer. 2006 Sep;47(3):260-7.全文  摘要

24. Park S, Bernard A, Bove KE, et al. Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour. Nat Genet. 1993 Dec;5(4):363-7. 摘要

25. Coorens THH, Treger TD, Al-Saadi R, et al. Embryonal precursors of Wilms tumor. Science. 2019 Dec 6;366(6470):1247-51.全文  摘要

26. Perotti D, Spreafico F, Torri F, et al. Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse. Genes Chromosomes Cancer. 2012 Jul;51(7):644-53. 摘要

27. Gratias EJ, Jennings LJ, Anderson JR, et al. Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: a report from the Children's Oncology Group. Cancer. 2013 Nov 1;119(21):3887-94. 摘要

28. Gadd S, Huff V, Skol AD, et al. Genetic changes associated with relapse in favorable histology Wilms tumor: a Children's Oncology Group AREN03B2 study. Cell Rep Med. 2022 Jun 21;3(6):100644.全文  摘要

29. Breslow NE, Beckwith JB. Epidemiological features of Wilms' tumor: results of the National Wilms' Tumor Study. J Natl Cancer Inst. 1982 Mar;68(3):429-36. 摘要

30. Neville H, Ritchey ML, Shamberger RC, et al. The occurrence of Wilms tumor in horseshoe kidneys: a report from the National Wilms Tumor Study Group (NWTSG). J Pediatr Surg. 2002 Aug;37(8):1134-7. 摘要

31. Kalish JM, Doros L, Helman LJ, et al. Surveillance recommendations for children with overgrowth syndromes and predisposition to Wilms tumors and hepatoblastoma. Clin Cancer Res. 2017 Jul 1;23(13):e115-22.全文  摘要

32. Schienda J, Stopfer J. Cancer genetic counseling-current practice and future challenges. Cold Spring Harb Perspect Med. 2020 Jun 1;10(6):a036541.全文  摘要

33. Turner JT, Brzezinski J, Dome JS. Wilms tumor predisposition. 2003 Dec 19 (updated 2022 Mar 24). In: Adam MP, Mirzaa GM, Pagon RA, et al, eds. GeneReviews [internet]. Seattle, WA: University of Washington, Seattle; 1993-2023.全文  摘要

34. Gariépy-Assal L, Gilbert RD, Žiaugra A, et al. Management of Denys-Drash syndrome: a case series based on an international survey. Clin Nephrol Case Stud. 2018 Nov 12;6:36-44.全文  摘要

35. Green DM, Breslow NE, Beckwith JB, et al. Screening of children with hemihypertrophy, aniridia, and Beckwith-Wiedemann syndrome in patients with Wilms tumor: a report from the National Wilms Tumor Study. Med Pediatr Oncol. 1993;21(3):188-92. 摘要

36. Idowu BM, Tanimola AG. Wilm's tumor presenting with scrotal varicocele in an 11-month-old boy. Indian J Radiol Imaging. 2018 Apr-Jun;28(2):247-9.全文  摘要

37. Maas MH, Cransberg K, van Grotel M, et al. Renin-induced hypertension in Wilms tumor patients. Pediatr Blood Cancer. 2007 May;48(5):500-3. 摘要

38. van der Beek JN, Artunduaga M, Schenk JP, et al. Similarities and controversies in imaging of pediatric renal tumors: a SIOP-RTSG and COG collaboration. Pediatr Blood Cancer. 2022 Nov 9;e30080. 摘要

39. Provenzi M, Saettini F, Conter V, et al. Is there a role for FDG-PET for the assessment of treatment efficacy in Wilms' tumor? A case report and literature review. Pediatr Hematol Oncol. 2013 Oct;30(7):633-9. 摘要

40. Lopyan NM, Ehrlich PF. Surgical management of Wilms tumor (nephroblastoma) and renal cell carcinoma in children and young adults. Surg Oncol Clin N Am. 2021 Apr;30(2):305-23. 摘要

41. Vujanić GM, Gessler M, Ooms AHAG, et al. The UMBRELLA SIOP-RTSG 2016 Wilms tumour pathology and molecular biology protocol. Nat Rev Urol. 2018 Nov;15(11):693-701.全文  摘要

42. van den Heuvel-Eibrink MM, van Tinteren H, Rehorst H, et al. Malignant rhabdoid tumours of the kidney (MRTKs), registered on recent SIOP protocols from 1993 to 2005: a report of the SIOP renal tumour study group. Pediatr Blood Cancer. 2011 May;56(5):733-7. 摘要

43. Diller L, Ghahremani M, Morgan J, et al. Constitutional WT1 mutations in Wilms tumor patients. J Clin Oncol. 1998 Nov;16(11):3634-40. 摘要

44. Wittmann S, Zirn B, Alkassar M, et al. Loss of 11q and 16q in Wilms tumors is associated with anaplasia, tumor recurrence, and poor prognosis. Genes Chromosomes Cancer. 2007 Feb;46(2):163-70. 摘要

45. Davidson A, Hartley PS, Shuttleworth MH. Erythrocytosis and iron deficiency anemia in Wilms tumor. J Pediatr Hematol Oncol. 2005 Sep;27(9):502. 摘要

46. Batra S, Perelman N, Luck LR, et al. Pediatric tumor cells express erythropoietin and a functional erythropoietin receptor that promotes angiogenesis and tumor cell survival. Lab Invest. 2003 Oct;83(10):1477-87. 摘要

47. Breslow NE, Collins AJ, Ritchey ML, et al. 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 Urol. 2005 Nov;174(5):1972-5.全文  摘要

48. Czauderna P, Katski K, Kowalczyk J, et al. Venoocclusive liver disease (VOD) as a complication of Wilms' tumour management in the series of consecutive 206 patients. Eur J Pediatr Surg. 2000 Oct;10(5):300-3. 摘要

49. Ritchey ML, Green DM, Thomas PR, et al. Renal failure in Wilms' tumor patients: A report from the National Wilms' Tumor Study Group. Med Pediatr Oncol. 1996 Feb;26(2):75-80. 摘要

50. Coppes MJ, Zandvoort SW, Sparling CR, et al. Acquired von Willebrand disease in Wilms' tumor patients. J Clin Oncol. 1992 Mar;10(3):422-7. 摘要

51. Amar AM, Tomlinson G, Green DM, et al. Clinical presentation of rhabdoid tumors of the kidney. J Pediatr Hematol Oncol. 2001 Feb;23(2):105-8. 摘要

52. Sandberg JK, Chi YY, Smith EA, et al. Imaging characteristics of nephrogenic rests versus small Wilms tumors: a report fom the Children's Oncology Group Study AREN03B2. AJR Am J Roentgenol. 2020 May;214(5):987-94.全文  摘要

53. van der Beek JN, Watson TA, Nievelstein RAJ, et al. MRI characteristics of pediatric renal tumors: a SIOP-RTSG Radiology Panel Delphi Study. J Magn Reson Imaging. 2022 Feb;55(2):543-52.全文  摘要

54. Brok JS, Shelmerdine S, Damsgaard F, et al. The clinical impact of observer variability in lung nodule classification in children with Wilms tumour. Pediatr Blood Cancer. 2022 Oct;69(10):e29759.全文  摘要

55. Vujanić GM, Parsons LN, D'Hooghe E, et al. Pathology of Wilms' tumour in International Society of Paediatric Oncology (SIOP) and Children's Oncology Group (COG) renal tumour studies: similarities and differences. Histopathology. 2022 Jun;80(7):1026-37. 摘要

56. Kaste SC, McCarville MB. Imaging pediatric abdominal tumors. Semin Roentgenol. 2008 Jan;43(1):50-9. 摘要

57. Dickson PV, Sims TL, Streck CJ, et al. Avoiding misdiagnosing neuroblastoma as Wilms tumor. J Pediatr Surg. 2008 Jun;43(6):1159-63. 摘要

58. Park JR, Eggert A, Caron H. Neuroblastoma: biology, prognosis, and treatment. Pediatr Clin North Am. 2008 Feb;55(1):97-120. 摘要

59. Kohler JA, Ellershaw C, Machin D. Response to N7 induction chemotherapy in children more than one year of age diagnosed with metastatic neuroblastoma treated in UKCCSG centers. Pediatr Blood Cancer. 2007 Sep;49(3):234-9. 摘要

60. George RE, London WB, Cohn SL, et al. Hyperdiploidy plus nonamplified MYCN confers a favorable prognosis in children 12 to 18 months old with disseminated neuroblastoma: a Pediatric Oncology Group study. J Clin Oncol. 2005 Sep 20;23(27):6466-73. 摘要

61. Skotnicka-Klonowicz G, Rieske P, Bartkowiak J, et al. 16q heterozygosity loss in Wilms' tumour in children and its clinical importance. Eur J Surg Oncol. 2000 Feb;26(1):61-6. 摘要

62. Ng A, Jenkinson H, Morland B, et al. Clear cell sarcoma: a dilemma on pathological staging and clinical management. Pediatr Hematol Oncol. 2005 Apr-May;22(3):257-61. 摘要

63. Green DM, Grigoriev YA, Nan B, et al. Congestive heart failure after treatment for Wilms' tumor: a report from the National Wilms' Tumor Study group. J Clin Oncol. 2001 Apr 1;19(7):1926-34. 摘要

64. Zisman A, Pantuck AJ, Wieder J, et al. Risk group assessment and clinical outcome algorithm to predict the natural history of patients with surgically resected renal cell carcinoma. J Clin Oncol. 2002 Dec 1;20(23):4559-66. 摘要

65. Gold PJ, Fefer A, Thompson JA. Paraneoplastic manifestations of renal cell carcinoma. Semin Urol Oncol. 1996 Nov;14(4):216-22. 摘要

66. Tomlinson GE, Breslow NE, Dome J, et al. Rhabdoid tumor of the kidney in the National Wilms Tumor Study: age at diagnosis as a prognostic factor. J Clin Oncol. 2005 Oct 20;23(30):7641-5. 摘要

67. van den Heuvel-Eibrink MM, Grundy P, Graf N, et al. Characteristics and survival of 750 children diagnosed with a renal tumor in the first seven months of life: a collaborative study by the SIOP/GPOH/SFOP, NWTSG, and UKCCSG Wilms tumor study groups. Pediatr Blood Cancer. 2008 June;50(6):1130-4. 摘要

68. Bourdeaut F, Freneaux P, Thuille B, et al. hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities. J Pathol. 2007 Feb;211(3):323-30. 摘要

69. Avner ED, Sweeney WE Jr. Renal cystic disease: new insights for the clinician. Pediatr Clin North Am. 2006 Oct;53(5):889-909. 摘要

70. Armstrong R, Sridhar M, Greenhalgh KL, et al. Phaeochromocytoma in childhood. Arch Dis Child. 2008 Oct;93(10):627.

71. Reiter A, Klapper W. Recent advances in the understanding and management of diffuse large B-cell lymphoma in children. Br J Haematol. 2008 Jul;142(3):329-47. 摘要

72. de Campos Vieira Abib S, Chui CH, Cox S, et al. International Society of Paediatric Surgical Oncology (IPSO) surgical practice guidelines. Ecancermedicalscience. 2022 Feb 17;16:1356.全文  摘要

73. Nelson MV, van den Heuvel-Eibrink MM, Graf N, et al. New approaches to risk stratification for Wilms tumor. Curr Opin Pediatr. 2021 Feb 1;33(1):40-8.全文  摘要

74. Dome JS, Fernandez CV, Mullen EA, et al. Children's Oncology Group's 2013 blueprint for research: renal tumors. Pediatr Blood Cancer. 2013 Jun;60(6):994-1000. 摘要

75. van den Heuvel-Eibrink MM, Hol JA, Pritchard-Jones K, et al. Position paper: rationale for the treatment of Wilms tumour in the UMBRELLA SIOP-RTSG 2016 protocol. Nat Rev Urol. 2017 Dec;14(12):743-52.全文  摘要

76. Hol JA, Jewell R, Chowdhury T, et al. Wilms tumour surveillance in at-risk children: literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group. Eur J Cancer. 2021 Aug;153:51-63.全文  摘要

77. Heppe RK, Koyle MA, Beckwith JB. Nephrogenic rests in Wilms tumor patients with the Drash syndrome. J Urol. 1991 Jun;145(6):1225-8. 摘要

78. Beckwith JB. Nephrogenic rests and the pathogenesis of Wilms tumor: developmental and clinical considerations. Am J Med Genet. 1998 Oct 2;79(4):268-73. 摘要

79. Beckwith JB. Management of incidentally encountered nephrogenic rests. J Pediatr Hematol Oncol. 2007 Jun;29(6):353-4. 摘要

80. Vanden Berg RN, Bierman EN, Noord MV, et al. Nephron-sparing surgery for Wilms tumor: a systematic review. Urol Oncol. 2016 Jan;34(1):24-32.全文  摘要

81. D'Angio GJ. The National Wilms Tumor Study: a 40 year perspective. Lifetime Data Anal. 2007 Dec;13(4):463-70. 摘要

82. Dix DB, Seibel NL, Chi YY, et al. Treatment of stage IV favorable histology Wilms tumor with lung metastases: a report from the Children's Oncology Group AREN0533 study. J Clin Oncol. 2018 Jun 1;36(16):1564-70.全文  摘要

83. Dome JS, Mullen EA, Dix DB, et al. Impact of the first generation of Children's Oncology Group clinical trials on clinical practice for Wilms tumor. J Natl Compr Canc Netw. 2021 Aug 1;19(8):978-85.全文  摘要

84. Fernandez CV, Perlman EJ, Mullen EA, et al. Clinical outcome and biological predictors of relapse after nephrectomy only for very low-risk Wilms tumor: a report from Children's Oncology Group AREN0532. Ann Surg. 2017 Apr;265(4):835-40.全文  摘要

85. Dix DB, Fernandez CV, Chi YY, et al. Augmentation of therapy for combined loss of heterozygosity 1p and 16q in favorable histology Wilms tumor: a Children's Oncology Group AREN0532 and AREN0533 study report. J Clin Oncol. 2019 Oct 20;37(30):2769-77.全文  摘要

86. Fernandez CV, Mullen EA, Chi YY, et al. Outcome and prognostic factors in stage III favorable-histology Wilms tumor: a report from the Children's Oncology Group study AREN0532. J Clin Oncol. 2018 Jan 20;36(3):254-61.全文  摘要

87. Ehrlich P, Chi YY, Chintagumpala MM, et al. Results of the first prospective multi-institutional treatment study in children with bilateral Wilms tumor (AREN0534): a report from the Children's Oncology Group. Ann Surg. 2017 Sep;266(3):470-8.全文  摘要

88. Ehrlich PF, Chi YY, Chintagumpala MM, et al. Results of treatment for patients with multicentric or bilaterally predisposed unilateral Wilms tumor (AREN0534): a report from the Children's Oncology Group. Cancer. 2020 Aug 1;126(15):3516-25.全文  摘要

89. Hamilton TE, Ritchey ML, Haase GM, et al. The management of synchronous bilateral Wilms tumor: a report from the National Wilms Tumor Study Group. Ann Surg. 2011 May;253(5):1004-10. 摘要

90. Kieran K, Davidoff AM. Nephron-sparing surgery for bilateral Wilms tumor. Pediatr Surg Int. 2015 Mar;31(3):229-36. 摘要

91. Kieran K, Williams MA, McGregor LM, et al. Repeat nephron-sparing surgery for children with bilateral Wilms tumor. J Pediatr Surg. 2014 Jan;49(1):149-53.全文  摘要

92. Aronson DC, Slaar A, Heinen RC, et al. Long-term outcome of bilateral Wilms tumors (BWT). Pediatr Blood Cancer. 2011 Jul 1;56(7):1110-3. 摘要

93. Daw NC, Chi YY, Kim Y, et al. Treatment of stage I anaplastic Wilms' tumour: a report from the Children's Oncology Group AREN0321 study. Eur J Cancer. 2019 Sep;118:58-66.全文  摘要

94. Dome JS, Cotton CA, Perlman EJ, et al. Treatment of anaplastic histology Wilms' tumor: results from the fifth National Wilms' Tumor Study. J Clin Oncol. 2006 May 20;24(15):2352-8. 摘要

95. Daw NC, Chi YY, Kalapurakal JA, et al. Activity of vincristine and irinotecan in diffuse anaplastic Wilms tumor and therapy outcomes of stage II to IV disease: results of the Children's Oncology Group AREN0321 study. J Clin Oncol. 2020 May 10;38(14):1558-68.全文  摘要

96. Speafico F, Pritchard Jones K, Malogolowkin MH, et al. Treatment of relapsed Wilms tumors: lessons learned. Expert Rev Anticancer Ther. 2009 Dec;9(12):1807-15. 摘要

97. Oostveen RM, Pritchard-Jones K. Pharmacotherapeutic management of Wilms tumor: an update. Paediatr Drugs. 2019 Feb;21(1):1-13. 摘要

98. Dome JS, Graf N, Geller JI, et al. Advances in Wilms tumor treatment and biology: progress through international collaboration. J Clin Oncol. 2015 Sep 20;33(27):2999-3007.全文  摘要

99. Malogolowkin MH, Hemmer MT, Le-Rademacher J, et al. Outcomes following autologous hematopoietic stem cell transplant for patients with relapsed Wilms' tumor: a CIBMTR retrospective analysis. Bone Marrow Transplant. 2017 Nov;52(11):1549-55.全文  摘要

100. Brok J, Mavinkurve-Groothuis AMC, Drost J, et al. Unmet needs for relapsed or refractory Wilms tumour: mapping the molecular features, exploring organoids and designing early phase trials - a collaborative SIOP-RTSG, COG and ITCC session at the first SIOPE meeting. Eur J Cancer. 2021 Feb;144:113-22. 摘要

101. Green DM, Breslow NE, Beckwith JB, et al. Treatment outcomes in patients less than 2 years of age with small, stage I, favorable-histology Wilms tumors: a report from the National Wilms Tumor Study. J Clin Oncol. 1993 Jan;11(1):91-5. 摘要

102. Green DM. The treatment of stages I-IV favorable histology Wilms' tumor. J Clin Oncol. 2004 Apr 15;22(8):1366-72. 摘要

103. Breslow NE, Beckwith JB, Haase GM, et al. Radiation therapy for favorable histology Wilms tumor: prevention of flank recurrence did not improve survival on National Wilms Tumor Studies 3 and 4. Int J Radiat Oncol Biol Phys. 2006 May 1;65(1):203-9.全文  摘要

104. Termuhlen AM, Tersak JM, Liu Q, et al. Twenty-five year follow-up of childhood Wilms tumor: a report from the Childhood Cancer Survivor Study. Pediatr Blood Cancer. 2011 Dec 15;57(7):1210-6. 摘要

105. Osterheld MC, Caron L, Meagher-Villemure K. Role of DNA content analysis and immunohistochemistry in the evaluation of the risk of unfavourable outcome in Wilms' tumours. Anticancer Res. 2008 Mar-Apr;28(2A):751-6. 摘要

106. Malogolowkin M, Cotton CA, Green DM, et al. Treatment of Wilms tumor relapsing after initial treatment with vincristine, actinomycin D, and doxorubicin. A report from the National Wilms Tumor Study Group. Pediatr Blood Cancer. 2008 Feb;50(2):236-41. 摘要

107. Grundy PE, Breslow NE, Li S, et al. Loss of heterozygosity for chromosomes 1p and 16q is an adverse prognostic factor in favorable-histology Wilms tumor: a report from the National Wilms Tumor Study Group. J Clin Oncol. 2005 Oct 10;23(29):7312-21. 摘要

108. Nakadate H, Yokomori K, Watanabe N, et al. Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan. Int J Cancer. 2001 Nov 1;94(3):396-400.全文  摘要

109. Messahel B, Williams R, Ridolfi A, et al. Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1-3 clinical trials: a Children's Cancer and Leukaemia Group (CCLG) study. Eur J Cancer. 2009 Mar;45(5):819-26. 摘要

110. Ehrlich PF, Anderson JR, Ritchey ML, et al. Clinicopathologic findings predictive of relapse in children with stage III favorable-histology Wilms tumor. J Clin Oncol. 2013 Mar 20;31(9):1196-201. 摘要

111. Reinhard H, Semler O, Burger D, et al. Results of the SIOP 93-01/GPOH trial and study for the treatment of patients with unilateral nonmetastatic Wilms Tumor. Klin Padiatr. 2004 May-Jun;216(3):132-40. 摘要

112. Berger M, Fernandez-Pineda I, Cabello R, et al. The relationship between the site of metastases and outcome in children with stage IV Wilms tumor: data from 3 European pediatric cancer institutions. J Pediatr Hematol Oncol. 2013 Oct;35(7):518-24. 摘要

113. Pasqualini C, Furtwängler R, van Tinteren H, et al. 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. Eur J Cancer. 2020 Mar;128:38-46. 摘要

114. Grundy P, Breslow N, Green DM, et al. Prognostic factors for children with recurrent Wilms' tumor: results from the Second and Third National Wilms' Tumor Study. J Clin Oncol. 1989 May;7(5):638-47. 摘要

115. Breslow NE, Takashima JR, Ritchey ML, et al. Renal failure in the Denys-Drash and Wilms tumor-aniridia syndromes. Cancer Res. 2000 Aug 1;60(15):4030-2.全文  摘要

116. Kist-van Holthe JE, Ho PL, Stablein D, et al. Outcome of renal transplantation for Wilms' tumor and Denys-Drash syndrome: a report of the North American Pediatric Renal Transplant Cooperative Study. Pediatr Transplant. 2005 Jun;9(3):305-10. 摘要

117. Amirian ES. The role of Hispanic ethnicity in pediatric Wilms' tumor survival. Pediatr Hematol Oncol. 2013 May;30(4):317-27. 摘要

118. Wright KD, Green DM, Daw NC. Late effects of treatment for Wilms tumor. Pediatr Hematol Oncol. 2009 Sep;26(6):407-13. 摘要

119. Greenberg M, Burnweit C, Filler R, et al. Preoperative chemotherapy for children with Wilms' tumor. J Pediatr Surg. 1991 Aug;26(8):949-53. 摘要

120. Mclnerney DP, Bullimore J. Reactivation of radiation pneumonitis by adriamycin. Br J Radiol. 1977 Mar;50(591):224-7. 摘要

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