Clinical Outcome and Biological Predictors of Relapse After Nephrectomy Only for Very Low-risk Wilms Tumor: A Report From Children's Oncology Group AREN0532
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James R. Anderson | J. Dome | P. Grundy | E. Perlman | P. Ehrlich | K. Gow | Yueh-Yun Chi | F. Ferrer | V. Huff | R. Shamberger | J. Geller | Jing Tian | T. Hamilton | C. Fernandez | J. Kalapurakal | D. Barnhart | G. Khanna | E. Mullen | T. Bocking | Vicky Huff | Thomas E. Hamilton
[1] K. Pritchard-Jones,et al. Advances in Wilms Tumor Treatment and Biology: Progress Through International Collaboration. , 2015, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[2] N. Breslow,et al. Breast cancer in female survivors of Wilms tumor: A report from the National Wilms Tumor late effects study , 2014, Cancer.
[3] James R. Anderson,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 , 2013, Cancer.
[4] R. Pieters,et al. Gain of 1q is a marker of poor prognosis in Wilms' tumors , 2013, Genes, chromosomes & cancer.
[5] James R. Anderson,et al. Children's Oncology Group's 2013 blueprint for research: Renal tumors , 2013, Pediatric blood & cancer.
[6] N. Breslow,et al. Clinicopathologic findings predictive of relapse in children with stage III favorable-histology Wilms tumor. , 2013, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[7] Euan J. Rodger,et al. Global demethylation in loss of imprinting subtype of wilms tumor , 2013, Genes, chromosomes & cancer.
[8] Chiang-Ching Huang,et al. Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study. , 2012, Neoplasia.
[9] G. Armstrong,et al. Twenty‐five year follow‐up of childhood Wilms tumor: A report from the Childhood Cancer Survivor Study , 2011, Pediatric blood & cancer.
[10] J. Dome,et al. Barriers to the Enrollment of Children in the Children's Oncology Group Study of Very Low Risk Wilms Tumor: A Report from the Children's Oncology Group , 2011, Journal of pediatric hematology/oncology.
[11] James R. Anderson,et al. WT1 mutation and 11P15 loss of heterozygosity predict relapse in very low-risk wilms tumors treated with surgery alone: a children's oncology group study. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[12] L. Diller,et al. Decision analysis to compare treatment strategies for Stage I/favorable histology Wilms tumor , 2010, Pediatric blood & cancer.
[13] N. Breslow,et al. Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5 , 2010, Annals of surgery.
[14] Norman Breslow,et al. Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical Features , 2009, Clinical Cancer Research.
[15] N. Breslow,et al. Early and late mortality after diagnosis of wilms tumor. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[16] J. Journeycake,et al. Catheter-related deep venous thrombosis and other catheter complications in children with cancer. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] N. Rahman,et al. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour , 2006, Journal of Medical Genetics.
[18] N. Breslow,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. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[19] A. Ellis. Breast , 2002, BMJ : British Medical Journal.
[20] A. Kelsey,et al. Older age is an adverse prognostic factor in stage I, favorable histology Wilms' tumor treated with vincristine monochemotherapy: a study by the United Kingdom Children's Cancer Study Group, Wilm's Tumor Working Group. , 2003, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[21] N. Breslow,et al. Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[22] M. Gessler,et al. Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors. , 2001, The American journal of pathology.
[23] J. Kowalczyk,et al. Venoocclusive liver disease (VOD) as a complication of Wilms' tumour management in the series of consecutive 206 patients. , 2000, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.
[24] N. Breslow,et al. Factors affecting the risk of contralateral Wilms tumor development , 1999, Cancer.
[25] Michael P. Hirsh,et al. Comparison between single-dose and divided-dose administration of dactinomycin and doxorubicin for patients with Wilms' tumor: A report from the national Wilms' tumor study group , 1998 .
[26] R. Ludwig,et al. Veno-occlusive disease of the liver in children treated for Wilms tumor. , 1997, Medical and pediatric oncology.
[27] N. Breslow,et al. Renal failure in Wilms' tumor patients: a report from the National Wilms' Tumor Study Group. , 1996, Medical and pediatric oncology.
[28] N. Jaffe,et al. The role of chemotherapy in the treatment of Wilms' tumor , 1979, Cancer.
[29] S. Kim. Considerations in the radiation therapy of Wilms' tumor , 1974 .
[30] N. Jaffe,et al. Considerations in the radiation therapy of Wilms' tumor , 1973, Cancer.
[31] N E Breslow,et al. Comparison between single-dose and divided-dose administration of dactinomycin and doxorubicin for patients with Wilms' tumor: a report from the National Wilms' Tumor Study Group. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.