Dergiler / Turkish Journal of Pediatrics / 2019 / Cilt: 61 - Sayı: 1

Bilateral Wilms tumors: Treatment results from a single center

Sayfa
44–51
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

VA is effectiveas initial preoperative treatment of BWT and allows for safe resection.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:The management of bilateral Wilms tumor (BWT) is challenging, particularlydue to its presentation at a younger age, rarity, and difficulty for treatmentdecisions and surgical evaluation comparing to unilateral WT.
📊
Temel Bulgular & Veri:From 1990 to 2016, 30 patients with synchronousBWT were treated with a preoperative chemotherapy of vincristine andactinomycin-D (VA).
💡
Sonuç & Katkı:VA is effectiveas initial preoperative treatment of BWT and allows for safe resection.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:2016 Verileri
⚙️Değişkenler:Alan Parametreleri

Özet

The management of bilateral Wilms tumor (BWT) is challenging, particularlydue to its presentation at a younger age, rarity, and difficulty for treatmentdecisions and surgical evaluation comparing to unilateral WT. In this study,the outcome of BWT patients from a single center who were treated bythe Turkish Pediatric Oncology Group (TPOG) Wilms Tumor Regimen wereretrospectively reviewed. From 1990 to 2016, 30 patients with synchronousBWT were treated with a preoperative chemotherapy of vincristine andactinomycin-D (VA). Chemotherapy was continued until safe nephronsparing surgery (NSS) could be performed for as long as radiological tumorresponse continued; otherwise, the chemotherapy was intensified by addingdoxorubicin (D) alternating with VA every 6 weeks. The median followup of patients was 59 months (4-297 months). The median duration ofpreoperative chemotherapy was 81 days and ranged between 14 days and198 days. Preoperative chemotherapy was modified in seven patients (23%)to the VAD regimen. Twenty-two patients (73%) had a radical nephrectomyon the larger tumor and NSS on the contralateral kidney, and 6 patients(20%) had bilateral NSS. Postoperative tumor stages for stage I, II and IIIwere 60%, 22% and 14%, respectively. The 5-year event free survival (EFS)rates were 100%, 90% and 51% for stages I, II and III (p=0.02), respectively.Unfavorable histology and nephrogenic rests were reported in 20% and 20%of patients, respectively. The 5-year overall survival (OS) and EFS rates were50% and 25%, respectively, in patients with anaplasia, while the same rateswere 96% and 96% in patients with favorable histology tumors (p=0.05 andp<0.001). The 10-year EFS and OS rates for all patients were 82% and 86%,respectively. Our results are comparable with the literature. VA is effectiveas initial preoperative treatment of BWT and allows for safe resection.

🔖

Bu Makaleye Atıf Yap

AYDIN, B., AKYÜZ, C., YALÇIN, B., EKİNCİ, S., OĞUZ, B., AKÇÖREN, Z., YILDIZ, F., VARAN, A., KURUCU, N., BÜYÜKPAMUKÇU, M., KUTLUK, T. (2019). Bilateral Wilms tumors: Treatment results from a single center. Turkish Journal of Pediatrics, Cilt: 61 - Sayı: 1, 44–51. https://ajindex.com/articles/412034

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (13)

  1. Breslow NE, Collins AJ, Ritchey ML, Grigoriev YA, Peterson SM, Green DM. 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
  2. Davidoff AM, Interiano RB, Wynn L, et al. Overall survival and renal function of patients with synchronous bilateral Wilms tumor undergoing surgery at a single institution. Ann Surg 2015; 262: 570-576
  3. Aronson DC, Slaar A, Heinen RC, de Kraker J, Heij HA. Long-term outcome of bilateral Wilms tumors (BWT). Pediatr Blood Cancer 2011; 56: 1110-1113
  4. Grigoriev Y, Lange J, Peterson SM, et al. Treatments and outcomes for end-stage renal disease following Wilms tumor. Pediatr Nephrol 2012; 27: 1325-1333
  5. Giel DW, Williams MA, Jones DP, Davidoff AM, Dome JS. Renal function outcomes in patients treated with nephron sparing surgery for bilateral Wilms tumor. J Urol 2007; 178 (4 Pt 2): 1786-1789
  6. Hamilton TE, Ritchey ML, Argani P, et al. Synchronous bilateral Wilm’s tumor with complete radiographic response managed without surgical resection: A report from the National Wilm’s Tumor Study 4. J Pediatr Surg 2008; 43: 1982-1984
  7. 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
  8. Oue T, Koshinaga T, Okita H, Kaneko Y, Hinotsu S, Fukuzawa M. Bilateral Wilms tumors treated according to the Japan Wilms Tumor Study Group protocol. Pediatr Blood Cancer 2014; 61: 1184-1189
  9. Horwitz JR, Ritchey ML, Moksness J, et al. Renal salvage procedures in patients with synchronous bilateral Wilms’ tumors: A report from the National Wilms Tumor Study Group. J Pediatr Surg 1996; 31: 1020-1025
  10. Indolfi P, Jenkner A, Terenziani M, et al; AIEOP Wilms Tumor Working Group. Synchronous bilateral Wilms tumor: A report from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP). Cancer 2013; 119: 1586-1592
  11. Sudour H, Audry G, Schleimacher G, Patte C, Dussart S, Bergeron C. Bilateral Wilms tumors (WT) treated with the SIOP 93 protocol in France: Epidemiological survey and patient outcome. Pediatr Blood Cancer 2012; 59: 57-61
  12. Chen SH, Hung IJ, Yang CP, et al. Clinical features and long-term outcomes of bilateral Wilms tumor treated with Taiwan Pediatric Oncology Group protocols: A single center report. Asia Pac J Clin Oncol 2016; 12: 300-307
  13. Sarhan OM, El-Baz M, Sarhan MM, Ghali