Children's Oncology Group's 2013 blueprint for research: Renal tumors
dc.contributor.author | Dome, Jeffrey S. | en_US |
dc.contributor.author | Fernandez, Conrad V. | en_US |
dc.contributor.author | Mullen, Elizabeth A. | en_US |
dc.contributor.author | Kalapurakal, John A. | en_US |
dc.contributor.author | Geller, James I. | en_US |
dc.contributor.author | Huff, Vicki | en_US |
dc.contributor.author | Gratias, Eric J. | en_US |
dc.contributor.author | Dix, David B. | en_US |
dc.contributor.author | Ehrlich, Peter F. | en_US |
dc.contributor.author | Khanna, Geetika | en_US |
dc.contributor.author | Malogolowkin, Marcio H. | en_US |
dc.contributor.author | Anderson, James R. | en_US |
dc.contributor.author | Naranjo, Arlene | en_US |
dc.contributor.author | Perlman, Elizabeth J. | en_US |
dc.date.accessioned | 2013-05-02T19:35:24Z | |
dc.date.available | 2014-08-01T19:11:39Z | en_US |
dc.date.issued | 2013-06 | en_US |
dc.identifier.citation | Dome, Jeffrey S.; Fernandez, Conrad V.; Mullen, Elizabeth A.; Kalapurakal, John A.; Geller, James I.; Huff, Vicki; Gratias, Eric J.; Dix, David B.; Ehrlich, Peter F.; Khanna, Geetika; Malogolowkin, Marcio H.; Anderson, James R.; Naranjo, Arlene; Perlman, Elizabeth J. (2013). "Children's Oncology Group's 2013 blueprint for research: Renal tumors ." Pediatric Blood & Cancer 60(6): 994-1000. <http://hdl.handle.net/2027.42/97522> | en_US |
dc.identifier.issn | 1545-5009 | en_US |
dc.identifier.issn | 1545-5017 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/97522 | |
dc.description.abstract | Renal malignancies are among the most prevalent pediatric cancers. The most common is favorable histology Wilms tumor (FHWT), which has 5‐year overall survival exceeding 90%. Other pediatric renal malignancies, including anaplastic Wilms tumor, clear cell sarcoma, malignant rhabdoid tumor, and renal cell carcinoma, have less favorable outcomes. Recent clinical trials have identified gain of chromosome 1q as a prognostic marker for FHWT. Upcoming studies will evaluate therapy adjustments based on this and other novel biomarkers. For high‐risk renal tumors, new treatment regimens will incorporate biological therapies. A research blueprint, viewed from the perspective of the Children's Oncology Group, is presented. Pediatr Blood Cancer 2013; 60: 994–1000. © 2012 Wiley Periodicals, Inc. | en_US |
dc.publisher | Wiley Subscription Services, Inc., A Wiley Company | en_US |
dc.subject.other | Malignant Rhabdoid Tumor | en_US |
dc.subject.other | Clear Cell Sarcoma | en_US |
dc.subject.other | Renal Cell Carcinoma | en_US |
dc.subject.other | Wilms Tumor | en_US |
dc.title | Children's Oncology Group's 2013 blueprint for research: Renal tumors | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Pediatrics | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Pediatric Surgery, University of Michigan, CS Mott Children's Hospital, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationother | Department of Genetics, MD Anderson Cancer Center, Houston, Texas | en_US |
dc.contributor.affiliationother | Department of Radiation Oncology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois | en_US |
dc.contributor.affiliationother | Division of Oncology, Center for Cancer and Blood Disorders, Children's National Medical Center, Washington, District of Columbia | en_US |
dc.contributor.affiliationother | Division of Pediatric Hematology/Oncology, IWK Health Centre, Halifax, Nova Scotia, Canada | en_US |
dc.contributor.affiliationother | Pediatric Hematology/Oncology, Dana Farber Cancer Institute, Boston, Massachusetts | en_US |
dc.contributor.affiliationother | Division of Hematology/Oncology/Bone Marrow Transplant, Children's Hospital of Wisconsin | en_US |
dc.contributor.affiliationother | Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri | en_US |
dc.contributor.affiliationother | Pediatric Hematology/Oncology, British Columbia Children's Hospital, Vancouver, British Columbia, Canada | en_US |
dc.contributor.affiliationother | Division of Hematology/Oncology, Children's Hospital at Erlanger, University of Tennessee College of Medicine, Chattanooga, Tennessee | en_US |
dc.contributor.affiliationother | Division of Oncology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio | en_US |
dc.contributor.affiliationother | Division of Oncology, Center for Cancer and Blood Disorders, Children's National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010. | en_US |
dc.contributor.affiliationother | Department of Pathology, Northwestern University's Feinberg School of Medicine and the Robert H. Lurie Cancer Center, Chicago, Illinois | en_US |
dc.contributor.affiliationother | Department of Biostatistics, Colleges of Medicine and Public Health & Health Professions, University of Florida, Gainesville, Florida | en_US |
dc.contributor.affiliationother | University of Nebraska Medical Center, Omaha, Nebraska | en_US |
dc.identifier.pmid | 23255438 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/97522/1/24419_ftp.pdf | |
dc.identifier.doi | 10.1002/pbc.24419 | en_US |
dc.identifier.source | Pediatric Blood & Cancer | en_US |
dc.identifier.citedreference | Khanna G, Rosen N, Anderson JR, et al. Evaluation of diagnostic performance of CT for detection of tumor thrombus in children with Wilms tumor: A report from the Children's Oncology Group. Pediatr Blood Cancer 2011; 58: 551 – 555. | en_US |
dc.identifier.citedreference | Green DM, Lange JM, Peabody EM, et al. Pregnancy outcome after treatment for Wilms tumor: A report from the national Wilms tumor long‐term follow‐up study. J Clin Oncol 2010; 28: 2824 – 2830. | en_US |
dc.identifier.citedreference | Steenman MJC, Rainier S, Dobry CJ, et al. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour. Nat Genetics 1994; 7: 433 – 439. | en_US |
dc.identifier.citedreference | Fukuzawa R, Breslow NE, Morison IM, et al. Epigenetic differences between Wilms' tumours in white and east‐Asian children. Lancet 2004; 363: 446 – 451. | en_US |
dc.identifier.citedreference | Hu Q, Gao F, Tian W, et al. Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation. J Clin Invest 2010; 121: 174 – 183. | en_US |
dc.identifier.citedreference | Shuman CBJ, Smith AC, Weksberg R. Beckwith–Wiedemann syndrome. In: RABT Pagon, CR Dolan, editors. GeneReviews (Internet). Seattle: University of Washington; 2010. | en_US |
dc.identifier.citedreference | Ruteshouser EC, Robinson SM, Huff V. Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one‐third of tumors. Genes Chromosomes Cancer 2008; 47: 461 – 470. | en_US |
dc.identifier.citedreference | Maris JM, Morton CL, Gorlick R, et al. Initial testing of the aurora kinase A inhibitor MLN8237 by the pediatric preclinical testing program (PPTP). Pediatr Blood Cancer 2010; 55: 26 – 34. | en_US |
dc.identifier.citedreference | Peterson JK, Tucker C, Favours E, et al. In vivo evaluation of ixabepilone (BMS247550), a novel epothilone B derivative, against pediatric cancer models. Clin Cancer Res 2005; 11: 6950 – 6958. | en_US |
dc.identifier.citedreference | Carol H, Lock R, Houghton PJ, et al. Initial testing (stage 1) of the kinesin spindle protein inhibitor ispinesib by the pediatric preclinical testing program. Pediatr Blood Cancer 2009; 53: 1255 – 1263. | en_US |
dc.identifier.citedreference | Versteege I, Sevenet N, Lange J, et al. Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer. Nature 1998; 394: 203 – 206. | en_US |
dc.identifier.citedreference | Biegel JA, Zhou JY, Rorke LB, et al. Germ‐line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors. Cancer Res 1999; 59: 74 – 79. | en_US |
dc.identifier.citedreference | Eaton KW, Tooke LS, Wainwright LM, et al. Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors. Pediatr Blood Cancer 2010; 56: 7 – 15. | en_US |
dc.identifier.citedreference | Roberts CW, Biegel JA. The role of SMARCB1/INI1 in development of rhabdoid tumor. Cancer Biol Ther 2009; 8: 412 – 416. | en_US |
dc.identifier.citedreference | Argani P, Ladanyi M. Translocation carcinomas of the kidney. Clin.Lab Med 2005; 25: 363 – 378. | en_US |
dc.identifier.citedreference | Tsuda M, Davis IJ, Argani P, et al. TFE3 fusions activate MET signaling by transcriptional up‐regulation, defining another class of tumors as candidates for therapeutic MET inhibition. Cancer Res 2007; 67: 919 – 929. | en_US |
dc.identifier.citedreference | Wagner AJ, Goldberg JM, Dubois SG, et al. Tivantinib (ARQ 197), a selective inhibitor of mesenchymal‐epithelial transition factor, in patients with microphthalmia transcription factor‐associated tumors: Results of a multicenter phase 2 trial. Cancer 2012; 118: 5894 – 5902. | en_US |
dc.identifier.citedreference | Malouf GG, Camparo P, Oudard S, et al. Targeted agents in metastatic Xp11 translocation/TFE3 gene fusion renal cell carcinoma (RCC): A report from the Juvenile RCC Network. Ann Oncol 2010; 21: 1834 – 1838. | en_US |
dc.identifier.citedreference | Parikh J, Coleman T, Messias N, et al. Temsirolimus in the treatment of renal cell carcinoma associated with Xp11.2 translocation/TFE gene fusion proteins: A case report and review of literature. Rare Tumors 2009; 1: e53. | en_US |
dc.identifier.citedreference | Choueiri TK, Lim ZD, Hirsch MS, et al. Vascular endothelial growth factor‐targeted therapy for the treatment of adult metastatic Xp11.2 translocation renal cell carcinoma. Cancer 2010; 116: 5219 – 5225. | en_US |
dc.identifier.citedreference | Malouf GG, Camparo P, Molinie V, et al. Transcription factor E3 and transcription factor EB renal cell carcinomas: Clinical features, biological behavior and prognostic factors. J Urol 2011; 185: 24 – 29. | en_US |
dc.identifier.citedreference | Liu YC, Chang PM, Liu CY, et al. Sunitinib‐induced nephrotic syndrome in association with drug response in a patient with Xp11.2 translocation renal cell carcinoma. Jpn J Clin Oncol 2011; 41: 1277 – 1281. | en_US |
dc.identifier.citedreference | Dome JS, Bockhold CA, Li SM, et al. High telomerase RNA expression level is an adverse prognostic factor for favorable‐histology Wilms' tumor. J Clin Oncol 2005; 23: 9138 – 9145. | en_US |
dc.identifier.citedreference | Huang CC, Gadd S, Breslow N, et al. Predicting relapse in favorable histology Wilms tumor using gene expression analysis: A report from the Renal Tumor Committee of the Children's Oncology Group. Clin Cancer Res 2009; 15: 1770 – 1778. | en_US |
dc.identifier.citedreference | Gadd S, Huff V, Huang CC, et al. Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: A Children's Oncology Group Study. Neoplasia 2012; 14: 742 – 756. | en_US |
dc.identifier.citedreference | Green DM, Breslow NE, Beckwith JB, et al. Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: A report from the National Wilms' Tumor Study Group. J Clin Oncol 2001; 19: 3719 – 3724. | en_US |
dc.identifier.citedreference | Shamberger RC, Anderson JR, Breslow NE, et al. Long‐term outcomes for infants with very low risk Wilms tumor treated with surgery alone in National Wilms Tumor Study‐5. Ann Surg 2010; 251: 555 – 558. | en_US |
dc.identifier.citedreference | Sredni ST, Gadd S, Huang CC, et al. Subsets of very low risk Wilms tumor show distinctive gene expression, histologic, and clinical features. Clin Cancer Res 2009; 15: 6800 – 6809. | en_US |
dc.identifier.citedreference | Perlman EJ, Grundy PE, Anderson JR, 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. J Clin Oncol 2011; 29: 698 – 703. | en_US |
dc.identifier.citedreference | Natrajan R, Williams RD, Hing SN, et al. Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse. J Pathol 2006; 210: 49 – 58. | en_US |
dc.identifier.citedreference | Natrajan R, Little SE, Sodha N, et al. Analysis by array CGH of genomic changes associated with the progression or relapse of Wilms' tumour. J Pathol 2007; 211: 52 – 59. | en_US |
dc.identifier.citedreference | Hing S, Lu YJ, Summersgill B, et al. Gain of 1q is associated with adverse outcome in favorable histology Wilms' tumors. Am J Pathol 2001; 158: 393 – 398. | en_US |
dc.identifier.citedreference | Lu YJ, Hing S, Williams R, et al. Chromosome 1q expression profiling and relapse in Wilms' tumour. Lancet 2002; 360: 385 – 386. | en_US |
dc.identifier.citedreference | Spreafico F, Pritchard Jones K, Malogolowkin MH, et al. Treatment of relapsed Wilms tumors: lessons learned. Expert Rev Anticancer Ther 2009; 9: 1807 – 1815. | en_US |
dc.identifier.citedreference | Green DM, Cotton CA, Malogolowkin M, et al. Treatment of Wilms tumor relapsing after initial treatment with vincristine and actinomycin D: A report from the National Wilms Tumor Study Group. Pediatr Blood Cancer 2007; 48: 493 – 499. | en_US |
dc.identifier.citedreference | Reinhard H, Schmidt A, Furtwangler R, et al. Outcome of relapses of nephroblastoma in patients registered in the SIOP/GPOH trials and studies. Oncol Rep 2008; 20: 463 – 467. | en_US |
dc.identifier.citedreference | Breslow NE, Ou SS, Beckwith JB, et al. Doxorubicin for favorable histology, Stage II–III Wilms tumor: Results from the National Wilms Tumor Studies. Cancer 2004; 101: 1072 – 1080. | en_US |
dc.identifier.citedreference | Green DM. The treatment of stages I–IV favorable histology Wilms' tumor. J Clin Oncol 2004; 22: 1366 – 1372. | en_US |
dc.identifier.citedreference | Pritchard Jones K, Graf N, Bergeron C, et al. Doxorubicin can be safely omitted from the treatment of Stage II/III intermediate risk histology Wilms tumour: Results of the SIOP 2001 randomized trial. Pediatr Blood Cancer 2011; 57: 741. | en_US |
dc.identifier.citedreference | Grills IS, Yan D, Martinez AA, et al. Potential for reduced toxicity and dose escalation in the treatment of inoperable non‐small‐cell lung cancer: A comparison of intensity‐modulated radiation therapy (IMRT), 3D conformal radiation, and elective nodal irradiation. Int J Radiat Oncol Biol Phys 2003; 57: 875 – 890. | en_US |
dc.identifier.citedreference | Schwarz M, Alber M, Lebesque JV, et al. Dose heterogeneity in the target volume and intensity‐modulated radiotherapy to escalate the dose in the treatment of non‐small‐cell lung cancer. Int.J Radiat Oncol Biol Phys 2005; 62: 561 – 570. | en_US |
dc.identifier.citedreference | 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; 174: 1972 – 1975. | en_US |
dc.identifier.citedreference | Berry DA, Eick SG. Adaptive assignment versus balanced randomization in clinical trials: A decision analysis. Stat Med 1995; 14: 231 – 246. | en_US |
dc.identifier.citedreference | Berry DA. Bayesian clinical trials. Nat Rev Drug Discov 2006; 5: 27 – 36. | en_US |
dc.identifier.citedreference | Berry DA. Adaptive clinical trials in oncology. Nat Rev Clin Oncol 2011; 9: 199 – 207. | en_US |
dc.identifier.citedreference | Metzger ML, Stewart CF, Freeman BB III, et al. Topotecan is active against Wilms' tumor: Results of a multi‐institutional phase II study. J Clin Oncol 2007; 25: 3130 – 3136. | en_US |
dc.identifier.citedreference | Dome JS, Liu T, Krasin M, et al. Improved survival for patients with recurrent Wilms tumor: The experience at St. Jude Children's Research Hospital. J Pediatr Hematol Oncol 2002; 24: 192 – 198. | en_US |
dc.identifier.citedreference | 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; 50: 236 – 241. | en_US |
dc.identifier.citedreference | Ha TC, Spreafico F, Graf N, et al. An international strategy to determine the role of high dose therapy in recurrent Wilms' tumour. Eur J Cancer 4: 2012. | en_US |
dc.identifier.citedreference | 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; 24: 2352 – 2358. | en_US |
dc.identifier.citedreference | Graf N, van Tinteren H, Bergeron C, et al. Characteristics and outcome of stage II and III non‐anaplastic Wilms' tumour treated according to the SIOP trial and study 93‐01. Eur J Cancer 2012; 48: 3240 – 3248. | en_US |
dc.identifier.citedreference | 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; 23: 7641 – 7645. | en_US |
dc.identifier.citedreference | 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; 56: 733 – 737. | en_US |
dc.identifier.citedreference | Geller JI, Dome JS. Local lymph node involvement does not predict poor outcome in pediatric renal cell carcinoma. Cancer 2004; 101: 1575 – 1583. | en_US |
dc.identifier.citedreference | Indolfi P, Terenziani M, Casale F, et al. Renal cell carcinoma in children: A clinicopathologic study. J Clin Oncol 2003; 21: 530 – 535. | en_US |
dc.identifier.citedreference | 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; 57: 1210 – 1216. | en_US |
dc.identifier.citedreference | Howlader NNA, Krapcho M, Neyman N, et al., SEER Cancer Statistics Review, 1975–2008, 2011; http://seer.cancer.gov/csr/1975_2008/csr/1975_2008/ | en_US |
dc.identifier.citedreference | 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; 23: 7312 – 7321. | en_US |
dc.identifier.citedreference | 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; 253: 1004 – 1010. | en_US |
dc.identifier.citedreference | Seibel NL, Sun J, Anderson JR, et al. Outcome of clear cell sarcoma of the kidney (CCSK) treated on the National Wilms Tumor Study‐5 (NWTS). J Clin Oncol 2006; 24: 502S. | en_US |
dc.identifier.citedreference | Breslow NE, Lange JM, Friedman DL, et al. Secondary malignant neoplasms after Wilms tumor: An international collaborative study. Int J Cancer 2009; 127: 657 – 666. | en_US |
dc.identifier.citedreference | 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; 19: 1926 – 1934. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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