Wilms' tumor

Wilms' tumor
Synonyms Wilms' tumor
Cut section showing two halves of a nephroblastoma specimen. Note the prominent septa subdividing the sectioned surface and the protrusion of tumor into the renal pelvis, resembling botryoid rhabdomyosarcoma.
Pronunciation
  • /vɪlmz/
Classification and external resources
Specialty Oncology
ICD-10 C64
ICD-9-CM 189.0
ICD-O M8960/3
OMIM 194070 607102
DiseasesDB 8896
MedlinePlus 001575
eMedicine med/3093 ped/2440
MeSH D009396

Wilms tumor, also known as nephroblastoma, is a cancer of the kidneys that typically occurs in children, rarely in adults.[1] It is named after Dr. Max Wilms, the German surgeon (1867–1918) who first described it.[2]

Approximately 500 cases are diagnosed in the U.S. annually. The majority (75%) occur in otherwise normal children; a minority (25%) are associated with other developmental abnormalities. It is highly responsive to treatment, with about 90% of patients surviving at least five years.

Signs and symptoms

Typical signs and symptoms of Wilms tumor include the following:

Pathogenesis

Micrograph showing the characteristic triphasic pattern consisting of tubules, solid sheets of small round cells, and stroma. H&E stain.
High magnification micrograph showing the epithelial component (tubules). H&E stain.

Most nephroblastomas are on one side of the body only and are found on both sides in less than 5% of cases, although patients with Denys-Drash syndrome mostly have bilateral or multiple tumors.[3] They tend to be encapsulated and vascularized tumors that do not cross the midline of the abdomen. In cases of metastasis it is usually to the lung. A rupture of Wilms tumor puts the patient at risk of bleeding and peritoneal dissemination of the tumor. In such cases, surgical intervention by a surgeon who is experienced in the removal of such a fragile tumor is imperative.

Pathologically, a triphasic nephroblastoma comprises three elements:

Wilms tumor is a malignant tumor containing metanephric blastema, stromal and epithelial derivatives. Characteristic is the presence of abortive tubules and glomeruli surrounded by a spindled cell stroma. The stroma may include striated muscle, cartilage, bone, fat tissue, and fibrous tissue. Dysfunction is caused when the tumor compresses the normal kidney parenchyma.

The mesenchymal component may include cells showing rhabdomyoid differentiation or malignancy (rhabdomyosarcomatous Wilms).

Wilms tumors may be separated into 2 prognostic groups based on pathologic characteristics:

Molecular biology

Mutations of the WT1 gene on chromosome 11p13 are observed in approximately 20% of Wilms tumors.[4][5] At least half of the Wilms tumors with mutations in WT1 also carry mutations in CTNNB1, the gene encoding the proto-oncogene beta-catenin.[6]

A gene on the X chromosome, WTX, is inactivated in up to 30% of Wilms tumor cases, according to research published in 2007.[7]

Most cases do not have mutations in any of these genes.[8]

Diagnosis

The first sign is normally a painless abdominal tumor that can be easily felt by the doctor. An ultrasound scan, computed tomography scan, or MRI scan is done first. A tumor biopsy is not typically performed due to the risk of creating fragments of cancer tissue and seeding the abdomen with malignant cells.

Staging

Staging is a standard way to describe the extent of spread of Wilms tumors,[9] and to determine prognosis and treatments. Staging is based on anatomical findings and tumor cells pathology.[10][11]

Definitions of stages

Stage I (43% of patients)

Stage I Wilms tumor, all of the following criteria must be met:

Stage II (23% of patients)

Stage II Wilms tumor, 1 or more of the following criteria must be met:

Stage III (20% of patients)

Stage III Wilms tumor, 1 or more of the following criteria must be met:

Stage IV (10% of patients)

Stage IV Wilms tumor is defined as the presence of hematogenous metastases (lung, liver, bone, or brain), or lymph node metastases outside the abdomenopelvic region.

Stage V (5% of patients)

Stage V Wilms tumor is defined as bilateral renal involvement at the time of initial diagnosis. Note: For patients with bilateral involvement, an attempt should be made to stage each side according to the above criteria (stage I to III) on the basis of extent of disease prior to biopsy.

Treatment/prognosis

The overall 5-year survival is estimated to be approximately 90%,[12][13] but for individuals the prognosis is highly dependent on individual staging and treatment. Early removal tends to promote positive outcomes.

Tumor-specific loss-of-heterozygosity (LOH) for chromosomes 1p and 16q identifies a subset of Wilms tumor patients who have a significantly increased risk of relapse and death. LOH for these chromosomal regions can now be used as an independent prognostic factor together with disease stage to target intensity of treatment to risk of treatment failure.[14][15] Genome-wide copy number and LOH status can be assessed with virtual karyotyping of tumor cells (fresh or paraffin-embedded).

Statistics may sometimes show more favorable outcomes for more aggressive stages than for less aggressive stages, which may be caused by more aggressive treatment and/or random variability in the study groups. Also, a stage V tumor is not necessarily worse than a stage IV tumor.

Stage[16] Histopathology[16] 4 Year relapse-free survival (RFS) or event-free survival (EFS)[16] 4 Year overall survival (OS)[16] Treatment[16]
Stage I [16] Favorable histology in children younger than 24 months or tumor weight less than 550g 85% 98% Surgery only (should be done only within the context of a clinical trial)
Favorable histology in children older than 24 months or tumor weight more than 550g 94% RFS 98% Nephrectomy + lymph node sampling followed by regimen EE-4A
Diffuse anaplastic 68% EFS 80% Nephrectomy + lymph node sampling followed by regimen EE-4A and radiotherapy
Stage II[16] Favorable histology 86% RFS 98% Nephrectomy + lymph node sampling followed by regimen EE-4A
Focal anaplastic 80% EFS 80% Nephrectomy + lymph node sampling followed by abdominal radiotherapy and regimen DD-4A
Diffuse anaplastic 83% EFS 82% Nephrectomy + lymph node sampling followed by abdominal radiotherapy and regimen I
Stage III[16] Favorable histology 87% RFS 94% Nephrectomy + lymph node sampling followed by abdominal radiotherapy and regimen DD-4A
Focal anaplastic 88% RFS 100% (8 people in study) Nephrectomy + lymph node sampling followed by abdominal radiotherapy and regimen DD-4A
Focal anaplastic (preoperative treatment) 71% RFS 71% Preoperative treatment with regimen DD-4A followed by nephrectomy + lymph node sampling and abdominal radiotherapy
Diffuse anaplastic 46% EFS 53% Preoperative treatment with regimen I followed by nephrectomy + lymph node sampling and abdominal radiotherapy
Diffuse anaplastic 65% EFS 67% Immediate nephrectomy + lymph node sampling followed by abdominal radiotherapy and regimen I
Stage IV[16] Favorable histology 76% RFS 86% Nephrectomy + lymph node sampling, followed by abdominal radiotherapy, bilateral pulmonary radiotherapy, and regimen DD-4A
Focal anaplastic 61% EFS 72% Nephrectomy + lymph node sampling, followed by abdominal radiotherapy, bilateral pulmonary radiotherapy, and regimen DD-4A
Diffuse anaplastic 33% EFS 33% Immediate nephrectomy + lymph node sampling followed by abdominal radiotherapy, whole-lung radiotherapy, and regimen I
Diffuse anaplastic (preoperative treatment) 31% EFS 44% Preoperative treatment with regimen I followed by nephrectomy + lymph node sampling followed by abdominal radiotherapy, whole-lung radiotherapy
Stage V[16] Overall 61% EFS 80%
Favorable histology 65% 87% Preoperative treatment with regimen DD-4A, followed by nephron sparing surgery or nephrecomy, staging of tumors, and chemotherapy and/or radiotherapy based on pathology and staging
Focal anaplastic 76% 88% Preoperative treatment with regimen DD-4A, followed by nephron sparing surgery or nephrecomy, staging of tumors, and chemotherapy and/or radiotherapy based on pathology and staging
Diffuse anaplastic 25% 42% Preoperative treatment with regimen DD-4A, followed by nephron sparing surgery or nephrecomy, staging of tumors, and chemotherapy and/or radiotherapy based on pathology and staging

Epidemiology

Wilms tumour affects approximately one person per 10,000 worldwide before the age of 15 years.[17] People of African descent may have slightly higher rates of Wilms tumor.[18] The peak age of Wilms tumour is 3 to 4 years and most cases occur before the age of 10 years.[19] A genetic predisposition to Wilms Tumor in individuals with aniridia has been established, due to deletions in the p13 band on chromosome 11.[20]

History

Dr. Sidney Farber, founder of Dana-Farber Cancer Institute, and his colleagues achieved the first remissions in Wilms tumor in the 1950s. By employing the antibiotic actinomycin D in addition to surgery and radiation therapy, they boosted cure rates from 40 to 89 percent...

See also

References

  1. ↑ EBSCO database verified by URAC; accessed from Mount Sinai Hospital, New York
  2. ↑ WhoNamedIt.com: Max Wilms
  3. ↑ Guaragna, Mara Sanches; Soardi, Fernanda Caroline; Assumpção, Juliana Godoy; Zambaldi, Lílian de Jesus Girotto; Cardinalli, Izilda Aparecida; Yunes, José Andrés; De Mello, Maricilda Palandi; Brandalise, Silvia Regina; Aguiar, Simone dos Santos (2010). "The Novel WT1 Gene Mutation p.H377N Associated to Denys-Drash Syndrome". Journal of Pediatric Hematology/Oncology. 32 (6): 486–8. PMID 20562648. doi:10.1097/MPH.0b013e3181e5e20d.
  4. ↑ Call, Katherine M.; Glaser, Tom; Ito, Caryn Y.; Buckler, Alan J.; Pelletier, Jerry; Haber, Daniel A.; Rose, Elise A.; Kral, Astrid; Yeger, Herman; Lewis, William H.; Jones, Carol; Housman, David E. (1990). "Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus". Cell. 60 (3): 509–20. PMID 2154335. doi:10.1016/0092-8674(90)90601-A.
  5. ↑ Huff, Vicki (1998). "Wilms tumor genetics". American Journal of Medical Genetics. 79 (4): 260–7. PMID 9781905. doi:10.1002/(SICI)1096-8628(19981002)79:4<260::AID-AJMG6>3.0.CO;2-Q.
  6. ↑ Maiti, S; Alam, R; Amos, C. I.; Huff, V (2000). "Frequent association of beta-catenin and WT1 mutations in Wilms tumors". Cancer Research. 60 (22): 6288–92. PMID 11103785.
  7. ↑ Rivera, M. N.; Kim, W. J.; Wells, J.; Driscoll, D. R.; Brannigan, B. W.; Han, M.; Kim, J. C.; Feinberg, A. P.; Gerald, W. L.; Vargas, S. O.; Chin, L.; Iafrate, A. J.; Bell, D. W.; Haber, D. A. (2007). "An X Chromosome Gene, WTX, is Commonly Inactivated in Wilms Tumor". Science. 315 (5812): 642–5. Bibcode:2007Sci...315..642R. PMID 17204608. doi:10.1126/science.1137509.
  8. ↑ Ruteshouser, E. Cristy; Robinson, Stephen M.; Huff, Vicki (2008). "Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors". Genes, Chromosomes and Cancer. 47 (6): 461–70. PMC 4332772 Freely accessible. PMID 18311776. doi:10.1002/gcc.20553.
  9. ↑ "How is Wilms tumor staged?". www.cancer.org. Retrieved 2015-11-15.
  10. ↑ "Wilms Tumor - Childhood - Stages". Cancer.Net. Retrieved 2015-11-15.
  11. ↑ "Treatment by type and stage of Wilms tumor". www.cancer.org. Retrieved 2015-11-13.
  12. ↑ Stewenius, Y.; Jin, Y.; Ora, I.; De Kraker, J.; Bras, J.; Frigyesi, A.; Alumets, J.; Sandstedt, B.; Meeker, A. K.; Gisselsson, D. (2007). "Defective Chromosome Segregation and Telomere Dysfunction in Aggressive Wilms' Tumors". Clinical Cancer Research. 13 (22): 6593–602. PMID 18006759. doi:10.1158/1078-0432.CCR-07-1081.
  13. ↑ Tournade, M. F.; Com-Nougué, C; De Kraker, J; Ludwig, R; Rey, A; Burgers, J. M.; Sandstedt, B; Godzinski, J; Carli, M; Potter, R; Zucker, J. M.; International Society of Pediatric Oncology Nephroblastoma Trial Study Committee (2001). "Optimal duration of preoperative therapy in unilateral and nonmetastatic Wilms' tumor in children older than 6 months: Results of the Ninth International Society of Pediatric Oncology Wilms' Tumor Trial and Study". Journal of Clinical Oncology. 19 (2): 488–500. PMID 11208843.
  14. ↑ Messahel, Boo; Williams, Richard; Ridolfi, Antonia; a’Hern, Roger; Warren, William; Tinworth, Lorna; Hobson, Rachel; Al-Saadi, Reem; Whyman, Gavin; Brundler, Marie-Anne; Kelsey, Anna; Sebire, Neil; Jones, Chris; Vujanic, Gordan; Pritchard-Jones, Kathy; Children's Cancer Leukaemia Group (CCLG) (2009). "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". European Journal of Cancer. 45 (5): 819–26. PMID 19231157. doi:10.1016/j.ejca.2009.01.005.
  15. ↑ Grundy, P. E.; Breslow, N. E.; Li, S; Perlman, E; Beckwith, J. B.; Ritchey, M. L.; Shamberger, R. C.; Haase, G. M.; d'Angio, G. J.; Donaldson, M; Coppes, M. J.; Malogolowkin, M; Shearer, P; Thomas, P. R.; MacKlis, R; Tomlinson, G; Huff, V; Green, D. M.; National Wilms Tumor Study Group (2005). "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". Journal of Clinical Oncology. 23 (29): 7312–21. PMID 16129848. doi:10.1200/JCO.2005.01.2799.
  16. 1 2 3 4 5 6 7 8 9 10 Unless otherwise specified in boxes, then reference is: Treatment of Wilms Tumor at National Cancer Institute. Last Modified: 03/29/2012
  17. ↑ Breslow, N; Olshan, A; Beckwith, JB; Green, DM (1993). "Epidemiology of Wilms tumor.". Medical and pediatric oncology. 21 (3): 172–81. PMID 7680412.
  18. ↑ Breslow, N; Olshan, A; Beckwith, JB; Green, DM (1993). "Epidemiology of Wilms tumor.". Medical and pediatric oncology. 21 (3): 172–81. PMID 7680412.
  19. ↑ Breslow, NE; Beckwith, JB; Perlman, EJ; Reeve, AE (September 2006). "Age distributions, birth weights, nephrogenic rests, and heterogeneity in the pathogenesis of Wilms tumor.". Pediatric blood & cancer. 47 (3): 260–7. PMID 16700047.
  20. ↑ Pritchard-Jones, Kathryn; Fleming, Stewart; Davidson, Duncan; Bickmore, Wendy; Porteous, David; Gosden, Christine; Bard, Jonathan; Buckler, Alan; Pelletier, Jerry; Housman, David; Van Heyningen, Veronica; Hastie, Nicholas (1990). "The candidate Wilms' tumour gene is involved in genitourinary development". Nature. 346 (6280): 194–7. Bibcode:1990Natur.346..194P. PMID 2164159. doi:10.1038/346194a0.
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