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Erschienen in: Pediatric Drugs 2/2008

01.03.2008 | Therapy In Practice

Current and Emerging Chemotherapy Treatment Strategies for Wilms Tumor in North America

verfasst von: Dr Eric J. Gratias, Jeffrey S. Dome

Erschienen in: Pediatric Drugs | Ausgabe 2/2008

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Abstract

Wilms tumor is the most common primary renal malignancy occurring in childhood. Approximately 500 children are diagnosed with Wilms tumor annually in the US alone, most of whom are aged <5 years. Several prognostic factors have been identified, including stage of disease, tumor histology, patient age, tumor weight, and tumor-specific loss of heterozygosity for chromosomes 1p and 16q. During the period from 1969 to 2002, the National Wilms Tumor Study Group coordinated five multicenter Wilms tumor studies. The overall survival rate for Wilms tumor has risen to >90% for patients with tumors of favorable histology. However, the treatment of patients with Wilms tumor with anaplastic histology remains challenging. The optimal treatment strategies for Wilms tumor in relapse will be studied via international collaboration in the near future. Goals of emerging studies include minimizing toxicity while maintaining the outstanding cure rates for patients with a good prognosis and, through advancing biologic understanding and developing novel therapeutic approaches, improving the prognosis for those patients in whom effective cure of their disease continues to elude physicians.
Literatur
1.
Zurück zum Zitat Bernstein L, Linet M, Smith MA, et al. Renal tumors. In: Ries LAG, Smith MA, Gurney JG, et al., editors. Cancer incidence and survival among children and adolescents: United States SEER Program 1975–1995. NIH Pub. No. 99-4649. Bethesda (MD): National Cancer Institute, SEER Program, 1999: 79–90 Bernstein L, Linet M, Smith MA, et al. Renal tumors. In: Ries LAG, Smith MA, Gurney JG, et al., editors. Cancer incidence and survival among children and adolescents: United States SEER Program 1975–1995. NIH Pub. No. 99-4649. Bethesda (MD): National Cancer Institute, SEER Program, 1999: 79–90
2.
Zurück zum Zitat Breslow NE, Palmer NF, Hill LR, et al. Wilms’ tumor: prognostic factors for patients without metastases at diagnosis: results of the National Wilms’ Tumor Study. Cancer 1978 Apr; 41(4): 1577–89PubMedCrossRef Breslow NE, Palmer NF, Hill LR, et al. Wilms’ tumor: prognostic factors for patients without metastases at diagnosis: results of the National Wilms’ Tumor Study. Cancer 1978 Apr; 41(4): 1577–89PubMedCrossRef
3.
Zurück zum Zitat 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): 7312–21PubMedCrossRef 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): 7312–21PubMedCrossRef
4.
Zurück zum Zitat Hing S, Lu YJ, Summersgill B, et al. Gain of 1q is associated with adverse outcome in favorable histology Wilms’ tumors. Am J Path 2001 Feb; 158(2): 393–8PubMedCrossRef Hing S, Lu YJ, Summersgill B, et al. Gain of 1q is associated with adverse outcome in favorable histology Wilms’ tumors. Am J Path 2001 Feb; 158(2): 393–8PubMedCrossRef
5.
Zurück zum Zitat Natrajan R, Little SE, Reis-Filho JS, et al. Amplification and overexpression of CACNA1E correlates with relapse in favorable histology Wilms’ tumors. Clin Cancer Res 2006 Dec 15; 12(24): 7284–93PubMedCrossRef Natrajan R, Little SE, Reis-Filho JS, et al. Amplification and overexpression of CACNA1E correlates with relapse in favorable histology Wilms’ tumors. Clin Cancer Res 2006 Dec 15; 12(24): 7284–93PubMedCrossRef
6.
Zurück zum Zitat 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 Dec 20; 23(36): 9138–45PubMedCrossRef 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 Dec 20; 23(36): 9138–45PubMedCrossRef
7.
Zurück zum Zitat Yang Y, Niu ZB, Hou Y, et al. The expression of HSP70 and HSP90α in children with Wilms tumor. J Ped Surg 2006 Jun; 41(6): 1062–6CrossRef Yang Y, Niu ZB, Hou Y, et al. The expression of HSP70 and HSP90α in children with Wilms tumor. J Ped Surg 2006 Jun; 41(6): 1062–6CrossRef
8.
Zurück zum Zitat Huang C-C, Cutcliffe C, Coffin C, et al. Classification of malignant pediatric renal tumors by gene expression. Pediatr Blood Cancer 2006 Oct 15; 46(S5): 728–38PubMedCrossRef Huang C-C, Cutcliffe C, Coffin C, et al. Classification of malignant pediatric renal tumors by gene expression. Pediatr Blood Cancer 2006 Oct 15; 46(S5): 728–38PubMedCrossRef
9.
Zurück zum Zitat Ritchey ML, Green DM, Breslow NB, et al. Accuracy of current imaging modalities in the diagnosis of synchronous bilateral Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. Cancer 1995 Jan 15; 75(2): 600–4PubMedCrossRef Ritchey ML, Green DM, Breslow NB, et al. Accuracy of current imaging modalities in the diagnosis of synchronous bilateral Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. Cancer 1995 Jan 15; 75(2): 600–4PubMedCrossRef
10.
Zurück zum Zitat Ritchey ML, Shamberger RC, Hamilton T, et al. Fate of bilateral renal lesions missed on preoperative imaging: a report from the National Wilms Tumor Study Group. J Urol 2005 Oct; 173: 1519–21CrossRef Ritchey ML, Shamberger RC, Hamilton T, et al. Fate of bilateral renal lesions missed on preoperative imaging: a report from the National Wilms Tumor Study Group. J Urol 2005 Oct; 173: 1519–21CrossRef
11.
Zurück zum Zitat Shamberger RC, Guthrie KA, Ritchey ML, et al. Surgery-related factors and local recurrence of Wilms tumor in National Wilms Tumor study 4. Ann Surg 1999; 229(2): 292–7PubMedCrossRef Shamberger RC, Guthrie KA, Ritchey ML, et al. Surgery-related factors and local recurrence of Wilms tumor in National Wilms Tumor study 4. Ann Surg 1999; 229(2): 292–7PubMedCrossRef
12.
Zurück zum Zitat Dome JS, Perlman EJ, Ritchey ML, et al. Renal tumors. In: Pizzo PA, Poplack DG, editors. Principles and practice of pediatric oncology. 5th ed. Philadelphia (PA): Lippincott Williams & Wilkins, 2006: 905–32 Dome JS, Perlman EJ, Ritchey ML, et al. Renal tumors. In: Pizzo PA, Poplack DG, editors. Principles and practice of pediatric oncology. 5th ed. Philadelphia (PA): Lippincott Williams & Wilkins, 2006: 905–32
13.
Zurück zum Zitat Beckwith JB, Palmer NF. Histopathology and prognosis of Wilms tumor. Cancer 1978 May; 41(5): 1937–48PubMedCrossRef Beckwith JB, Palmer NF. Histopathology and prognosis of Wilms tumor. Cancer 1978 May; 41(5): 1937–48PubMedCrossRef
14.
Zurück zum Zitat Green DM, Beckwith JB, Weeks DA, et al. The relationship between microsubstaging variables, age at diagnosis, and tumor weight of children with stage 1/favorable histology Wilms’ tumor. Cancer 1994 Sep 15; 74(6): 1817–20PubMedCrossRef Green DM, Beckwith JB, Weeks DA, et al. The relationship between microsubstaging variables, age at diagnosis, and tumor weight of children with stage 1/favorable histology Wilms’ tumor. Cancer 1994 Sep 15; 74(6): 1817–20PubMedCrossRef
15.
Zurück zum Zitat Breslow N, Sharpies K, Beckwith JB, et al. Prognostic factors in nonmetastatic, favorable histology Wilms’ tumor, results of the Third National Wilms’ Tumor Study. Cancer 1991 Dec 1; 68(11): 2345–53PubMedCrossRef Breslow N, Sharpies K, Beckwith JB, et al. Prognostic factors in nonmetastatic, favorable histology Wilms’ tumor, results of the Third National Wilms’ Tumor Study. Cancer 1991 Dec 1; 68(11): 2345–53PubMedCrossRef
16.
Zurück zum Zitat Garcia M, Douglass C, Schlosser JV. Classification and prognosis in Wilms’ tumor. Radiology 1963; 80: 574–80PubMed Garcia M, Douglass C, Schlosser JV. Classification and prognosis in Wilms’ tumor. Radiology 1963; 80: 574–80PubMed
17.
Zurück zum Zitat Grundy PE, Telzerow PE, Breslow N, et al. Loss of heterozygosity for chromosomes 16q and 1p in Wilms’ tumors predicts an adverse outcome. Cancer Res 1994; 54: 2331–3PubMed Grundy PE, Telzerow PE, Breslow N, et al. Loss of heterozygosity for chromosomes 16q and 1p in Wilms’ tumors predicts an adverse outcome. Cancer Res 1994; 54: 2331–3PubMed
18.
Zurück zum Zitat 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): 7312–21PubMedCrossRef 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): 7312–21PubMedCrossRef
19.
Zurück zum Zitat D’Angio GJ, Evans AE, Breslow NE, et al. The treatment of Wilms’ tumor, results of the National Wilms Tumor Study. Cancer 1976 Aug; 38(2): 633–46PubMedCrossRef D’Angio GJ, Evans AE, Breslow NE, et al. The treatment of Wilms’ tumor, results of the National Wilms Tumor Study. Cancer 1976 Aug; 38(2): 633–46PubMedCrossRef
20.
Zurück zum Zitat D’Angio GJ, Evans A, Breslow N, et al. The treatment of Wilms’ tumor: results of the Second National Wilms’ Tumor Study. Cancer 1981 May 1; 47(9): 2302–11PubMedCrossRef D’Angio GJ, Evans A, Breslow N, et al. The treatment of Wilms’ tumor: results of the Second National Wilms’ Tumor Study. Cancer 1981 May 1; 47(9): 2302–11PubMedCrossRef
21.
Zurück zum Zitat D’Angio GJ, Breslow N, Beckwith JB, et al. Treatment of Wilms’ tumor, results of the Third National Wilms Tumor Study. Cancer 1989 July 15; 64(2): 349–60PubMedCrossRef D’Angio GJ, Breslow N, Beckwith JB, et al. Treatment of Wilms’ tumor, results of the Third National Wilms Tumor Study. Cancer 1989 July 15; 64(2): 349–60PubMedCrossRef
22.
Zurück zum Zitat Green DM, Breslow NE, Beckwith JB, 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. J Clin Oncol 1998 Jan; 16(1): 237–45PubMed Green DM, Breslow NE, Beckwith JB, 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. J Clin Oncol 1998 Jan; 16(1): 237–45PubMed
23.
Zurück zum Zitat Green DM, Breslow NE, Beckwith JB, et al. Effect of Duration of treatment on treatment outcome and cost of treatment for Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 1998 Dec; 16(12): 3744–51PubMed Green DM, Breslow NE, Beckwith JB, et al. Effect of Duration of treatment on treatment outcome and cost of treatment for Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 1998 Dec; 16(12): 3744–51PubMed
24.
Zurück zum Zitat Green DM, Beckwith JB, Breslow NE, et al. Treatment of children with stages II to IV anaplastic Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 1994 Oct; 12(10): 2126–31PubMed Green DM, Beckwith JB, Breslow NE, et al. Treatment of children with stages II to IV anaplastic Wilms’ tumor: a report from the National Wilms’ Tumor Study Group. J Clin Oncol 1994 Oct; 12(10): 2126–31PubMed
25.
Zurück zum Zitat 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): 2352–8PubMedCrossRef 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): 2352–8PubMedCrossRef
26.
Zurück zum Zitat 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 Sept 1; 19(17): 3719–24PubMed 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 Sept 1; 19(17): 3719–24PubMed
27.
Zurück zum Zitat Corn BW, Goldwein JW, Evans I, et al. Outcomes in low-risk babies treated with half-dose chemotherapy according to the Third National Wilms’ Tumor Study. J Clin Oncol 1992 Aug; 10(8): 1305–9PubMed Corn BW, Goldwein JW, Evans I, et al. Outcomes in low-risk babies treated with half-dose chemotherapy according to the Third National Wilms’ Tumor Study. J Clin Oncol 1992 Aug; 10(8): 1305–9PubMed
28.
Zurück zum Zitat 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): 638–47PubMed 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): 638–47PubMed
29.
Zurück zum Zitat 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 May; 48(5): 493–9PubMedCrossRef 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 May; 48(5): 493–9PubMedCrossRef
30.
Zurück zum Zitat Malogolowkin MH, 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 (NWTS) group. Pediatric Blood Cancer. 2008 Feb; 50(2): 236–41PubMedCrossRef Malogolowkin MH, 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 (NWTS) group. Pediatric Blood Cancer. 2008 Feb; 50(2): 236–41PubMedCrossRef
31.
Zurück zum Zitat Tournade MF, Lemerle J, Brunat-Mentigny M, et al. Ifosfamide is an active drug in Wilms’ tumor: a phase II study conducted by the French Society of Pediatric Oncology. J Clin Oncol 1988 May; 6(5): 793–6PubMed Tournade MF, Lemerle J, Brunat-Mentigny M, et al. Ifosfamide is an active drug in Wilms’ tumor: a phase II study conducted by the French Society of Pediatric Oncology. J Clin Oncol 1988 May; 6(5): 793–6PubMed
32.
Zurück zum Zitat de Camargo B, Melaragno R, Saba e Silva N, et al. Phase II study of carboplatin as a single drug for relapsed Wilms’ tumor: experience of the Brazilian Wilms’ Tumor Study Group. Med Pediatr Oncol 1994 Apr; 22(4): 258–60PubMedCrossRef de Camargo B, Melaragno R, Saba e Silva N, et al. Phase II study of carboplatin as a single drug for relapsed Wilms’ tumor: experience of the Brazilian Wilms’ Tumor Study Group. Med Pediatr Oncol 1994 Apr; 22(4): 258–60PubMedCrossRef
33.
Zurück zum Zitat Pein F, Pinkerton R, Tournade MF, et al. Etoposide in relapsed or refractory Wilms’ tumor: a phase II study by the French Society of Pediatric Oncology and the United Kingdom Children’s Cancer Study Group. J Clin Oncol 1993 Aug; 11(8): 1478–81PubMed Pein F, Pinkerton R, Tournade MF, et al. Etoposide in relapsed or refractory Wilms’ tumor: a phase II study by the French Society of Pediatric Oncology and the United Kingdom Children’s Cancer Study Group. J Clin Oncol 1993 Aug; 11(8): 1478–81PubMed
34.
Zurück zum Zitat Miser JS, Kinsella TJ, Triche TJ, et al. Ifosfamide with mesna uroprotection and etoposide: an effective regimen in the treatment of recurrent sarcomas and other tumors of children and young adults. J Clin Oncol 1987 Aug; 5(8): 1191–8PubMed Miser JS, Kinsella TJ, Triche TJ, et al. Ifosfamide with mesna uroprotection and etoposide: an effective regimen in the treatment of recurrent sarcomas and other tumors of children and young adults. J Clin Oncol 1987 Aug; 5(8): 1191–8PubMed
35.
Zurück zum Zitat Pein F, Tournade MF, Zucker JM, et al. Etoposide and carboplatin: a highly effective combination in relapsed or refractory Wilms’ tumor: a phase II study by the French Society of Pediatric Oncology. J Clin Oncol 1994 May; 12(5): 931–6PubMed Pein F, Tournade MF, Zucker JM, et al. Etoposide and carboplatin: a highly effective combination in relapsed or refractory Wilms’ tumor: a phase II study by the French Society of Pediatric Oncology. J Clin Oncol 1994 May; 12(5): 931–6PubMed
36.
Zurück zum Zitat Kung FH, Desai SJ, Dickerman JD, et al. Ifosfamide/carboplatin/etoposide (ICE) for recurrent malignant solid tumors of childhood: a Pediatric Oncology Group phase I/II study. J Pediatr Hematol Oncol 1995 Aug; 17(3): 265–9PubMedCrossRef Kung FH, Desai SJ, Dickerman JD, et al. Ifosfamide/carboplatin/etoposide (ICE) for recurrent malignant solid tumors of childhood: a Pediatric Oncology Group phase I/II study. J Pediatr Hematol Oncol 1995 Aug; 17(3): 265–9PubMedCrossRef
37.
Zurück zum Zitat Abu-Ghosh AM, Krailo MD, Goldman SC, et al. Ifosfamide, carboplatin, and etoposide in children with poor-risk relapsed Wilms tumor: a Children’s Cancer Group report. Ann Oncol 2002 Mar; 13(3): 460–9PubMedCrossRef Abu-Ghosh AM, Krailo MD, Goldman SC, et al. Ifosfamide, carboplatin, and etoposide in children with poor-risk relapsed Wilms tumor: a Children’s Cancer Group report. Ann Oncol 2002 Mar; 13(3): 460–9PubMedCrossRef
38.
Zurück zum Zitat Garaventa A, Hartmann O, Bernard J-L, et al. Autologous bone marrow transplantation for pediatric Wilms’ tumor: the experience of the European Bone Marrow Transplantation Solid Tumor Registry. Med Pediatr Oncol 1994 Jan; 22(1): 11–4PubMedCrossRef Garaventa A, Hartmann O, Bernard J-L, et al. Autologous bone marrow transplantation for pediatric Wilms’ tumor: the experience of the European Bone Marrow Transplantation Solid Tumor Registry. Med Pediatr Oncol 1994 Jan; 22(1): 11–4PubMedCrossRef
39.
Zurück zum Zitat Pein F, Michon J, Valteau-Couanet D, et al. High-dose melphalan, etoposide, and carboplatin followed by autologous stem-cell rescue in pediatric high-risk recurrent Wilms’ tumor: a French Society of Pediatric Oncology study. J Clin Oncol 1998 Oct; 16(10): 3295–301PubMed Pein F, Michon J, Valteau-Couanet D, et al. High-dose melphalan, etoposide, and carboplatin followed by autologous stem-cell rescue in pediatric high-risk recurrent Wilms’ tumor: a French Society of Pediatric Oncology study. J Clin Oncol 1998 Oct; 16(10): 3295–301PubMed
40.
Zurück zum Zitat Maurer K, Heitger A, Schwaighofer H, et al. Double high-dose chemotherapy with autologous peripheral stem cell rescue in relapsed Wilms’ tumor. Bone Marrow Transplant 1997 Dec; 20(12): 1111–3PubMedCrossRef Maurer K, Heitger A, Schwaighofer H, et al. Double high-dose chemotherapy with autologous peripheral stem cell rescue in relapsed Wilms’ tumor. Bone Marrow Transplant 1997 Dec; 20(12): 1111–3PubMedCrossRef
41.
Zurück zum Zitat Kremens B, Gruhn B, Klingebiel T, et al. High-dose chemotherapy with autologous stem cell rescue in children with nephroblastoma. Bone Marrow Transplant 2002 Dec; 30(12): 893–8PubMedCrossRef Kremens B, Gruhn B, Klingebiel T, et al. High-dose chemotherapy with autologous stem cell rescue in children with nephroblastoma. Bone Marrow Transplant 2002 Dec; 30(12): 893–8PubMedCrossRef
42.
Zurück zum Zitat Park ES, Kang HJ, Shin HY, et al. Improved survival in patients with recurrent Wilms tumor: the experience of the Seoul National University Children’s Hospital. J Korean Med Sci 2006 Jun; 21(3): 436–40PubMedCrossRef Park ES, Kang HJ, Shin HY, et al. Improved survival in patients with recurrent Wilms tumor: the experience of the Seoul National University Children’s Hospital. J Korean Med Sci 2006 Jun; 21(3): 436–40PubMedCrossRef
43.
Zurück zum Zitat Campbell AD, Cohn SL, Reynolds M, et al. Treatment of relapsed Wilms’ tumor with high-dose therapy and autologous hematopoietic stem-cell rescue: the experience at Children’s Memorial Hospital. J Clin Oncol 2004 July 15; 22(14): 2885–90PubMedCrossRef Campbell AD, Cohn SL, Reynolds M, et al. Treatment of relapsed Wilms’ tumor with high-dose therapy and autologous hematopoietic stem-cell rescue: the experience at Children’s Memorial Hospital. J Clin Oncol 2004 July 15; 22(14): 2885–90PubMedCrossRef
44.
Zurück zum Zitat Perentesis JP, Katsanis E, DeFor TE, et al. Autologous stem cell transplantation for high-risk pediatric solid tumors. Bone Marrow Transplant 1999 Sept; 24(6): 609–15PubMedCrossRef Perentesis JP, Katsanis E, DeFor TE, et al. Autologous stem cell transplantation for high-risk pediatric solid tumors. Bone Marrow Transplant 1999 Sept; 24(6): 609–15PubMedCrossRef
45.
Zurück zum Zitat 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 Ped Hematol Oncol 2002 Mar/Apr; 24(3): 192–8CrossRef 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 Ped Hematol Oncol 2002 Mar/Apr; 24(3): 192–8CrossRef
46.
Zurück zum Zitat Dome JS, Neale G, Hill DA, et al. Antitumor activity of topotecan against Wilms tumor: translation of a xenograft model to a phase II study. Pediatr Blood Cancer 2005 Oct 1; 45(4): 432a Dome JS, Neale G, Hill DA, et al. Antitumor activity of topotecan against Wilms tumor: translation of a xenograft model to a phase II study. Pediatr Blood Cancer 2005 Oct 1; 45(4): 432a
47.
Zurück zum Zitat Metzger MM, Stewart CF, Freeman BB, et al. Topotecan is active against Wilms tumor: results of a multi-institutional phase II study. J Clin Oncol 2007 Jul; 25(21): 3130–6PubMedCrossRef Metzger MM, Stewart CF, Freeman BB, et al. Topotecan is active against Wilms tumor: results of a multi-institutional phase II study. J Clin Oncol 2007 Jul; 25(21): 3130–6PubMedCrossRef
Metadaten
Titel
Current and Emerging Chemotherapy Treatment Strategies for Wilms Tumor in North America
verfasst von
Dr Eric J. Gratias
Jeffrey S. Dome
Publikationsdatum
01.03.2008
Verlag
Springer International Publishing
Erschienen in
Pediatric Drugs / Ausgabe 2/2008
Print ISSN: 1174-5878
Elektronische ISSN: 1179-2019
DOI
https://doi.org/10.2165/00148581-200810020-00006

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