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Wilms Tumor and Other Childhood Kidney Tumors Treatment (PDQ®)
Patient VersionHealth Professional VersionEn españolLast Modified: 11/27/2007



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Cellular Classification






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Treatment Option Overview






Stage I Wilms Tumor






Stage II Wilms Tumor






Stage III Wilms Tumor






Stage IV Wilms Tumor






Stage V Wilms Tumor







Inoperable Tumors






Clear Cell Sarcoma of the Kidney






Rhabdoid Tumor of the Kidney






Neuroepithelial Tumor of the Kidney






Mesoblastic Nephroma






Renal Cell Carcinoma






Recurrent Wilms Tumor and Other Childhood Kidney Tumors






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Changes to This Summary (11/27/2007)






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Treatment Options



Treatment Options

Patients who have tumors with caval extension above the hepatic veins or that are so massive that their surgeons consider the risk of initial surgical removal too great should be biopsied and treated with preoperative chemotherapy.[1,2] If surgery is performed on a patient with caval or atrial extension, care should be taken to ensure that appropriate resources are available for pediatric cardiopulmonary bypass.[3,4] On the National Wilms Tumor Study-5 (NWTS-5), these patients are treated after biopsy by initial chemotherapy with vincristine and dactinomycin with or without doxorubicin. If no reduction in tumor size has occurred after using three drugs, then radiation therapy should be used.[5] Surgery is performed as soon as sufficient tumor shrinkage has occurred, generally at week 6 of therapy. If resection of the tumor cannot occur at this time, the patient should undergo a second-look procedure to confirm a persistent tumor. Failure of the tumor to shrink could be a result of a predominance of skeletal or benign elements. Patients are subsequently treated as for stage III tumors, which includes postoperative radiation therapy.[6] Because of the 5% to 10% error rate in preoperative diagnosis of renal masses after radiographic assessment, confirmation of the diagnosis by biopsy (which may be performed percutaneously) should be obtained prior to chemotherapy.[1]

References

  1. Ritchey ML: The role of preoperative chemotherapy for Wilms' tumor: the NWTSG perspective. National Wilms' Tumor Study Group. Semin Urol Oncol 17 (1): 21-7, 1999.  [PUBMED Abstract]

  2. Shamberger RC, Ritchey ML, Haase GM, et al.: Intravascular extension of Wilms tumor. Ann Surg 234 (1): 116-21, 2001.  [PUBMED Abstract]

  3. Thompson WR, Newman K, Seibel N, et al.: A strategy for resection of Wilms' tumor with vena cava or atrial extension. J Pediatr Surg 27 (7): 912-5, 1992.  [PUBMED Abstract]

  4. Ritchey ML, Kelalis PP, Haase GM, et al.: Preoperative therapy for intracaval and atrial extension of Wilms tumor. Cancer 71 (12): 4104-10, 1993.  [PUBMED Abstract]

  5. Green DM, Breslow NE, Evans I, et al.: The effect of chemotherapy dose intensity on the hematological toxicity of the treatment for Wilms' tumor. A report from the National Wilms' Tumor Study. Am J Pediatr Hematol Oncol 16 (3): 207-12, 1994.  [PUBMED Abstract]

  6. Tournade MF, Com-Nougué C, Voûte PA, et al.: Results of the Sixth International Society of Pediatric Oncology Wilms' Tumor Trial and Study: a risk-adapted therapeutic approach in Wilms' tumor. J Clin Oncol 11 (6): 1014-23, 1993.  [PUBMED Abstract]

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