Literature DB >> 9391203

Results of Wilms' tumour management in two tertiary-care hospitals in Asia.

S Sen1, P Kadamba, M Al-AbdulAaly, K E Mammen, S Ahmed.   

Abstract

In the period 1985-1995, 87 children underwent surgery for Wilms' tumour; 16 were lost to follow-up. Of the remaining children, 27 presented with stage I disease, 11 with stage II, 12 with stage III, 14 with stage IV, and 6 with stage V. One child was not staged. The histology was favourable Wilms' tumour in 44, anaplastic in 12, unclassified in 8, clear-cell sarcoma in 4, and rhabdoid tumour in 3. Although a total nephrectomy was generally performed, partial renal surgery was performed for 6 bilateral and 4 unilateral tumours, the latter including 2 fused kidneys. Preoperative chemotherapy was employed with benefit in massive tumours, tumour in fused kidneys, bilateral tumours, and preoperatively diagnosed inferior vena caval tumour thrombi. Postoperative chemotherapy, employed in all cases, consisted of actinomycin D and vincristine with the addition of adriamycin in anaplastic and advanced-stage tumours. Ten children underwent second-line chemotherapy for disease unresponsive to the above management, but only 1 of these is currently free of disease. Postoperative tumour-bed radiotherapy, used in selected cases, prevented local recurrence in stage I and II disease. However, 20% of stage I and II patients not receiving radiotherapy developed tumour-bed recurrence. Twenty-three children have died and 5 with advanced disease and incomplete follow-up are presumed to be dead. Nine children are currently on treatment; 34 have successfully completed treatment, the disease-free survival in stages I-V being 81%, 75%, 42%, 14%, and 50%, respectively. Overall disease-free survival was 69% for Wilms' tumour of favourable histology and 50% for anaplastic tumours. The 3 patients with rhabdoid tumours and 3 of 4 with clear-cell sarcomas have died. Wilms' tumour management in the developing world is compromised by cases lost to follow-up and late presentation with massive tumours and advanced stage. Preoperative chemotherapy is advantageous in a number of cases, and postoperative radiotherapy should be deployed more frequently.

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Year:  1998        PMID: 9391203     DOI: 10.1007/s003830050240

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  6 in total

Review 1.  Management of Wilms Tumor: ICMR Consensus Document.

Authors:  Maya Prasad; Tushar Vora; Sandeep Agarwala; Siddharth Laskar; Brijesh Arora; Deepak Bansal; Gauri Kapoor; Girish Chinnaswamy; Venkatraman Radhakrishnan; Tanvir Kaur; G K Rath; Sameer Bakhshi
Journal:  Indian J Pediatr       Date:  2017-04-03       Impact factor: 1.967

Review 2.  Wilms' tumor- roadmaps of management.

Authors:  Yogesh Kumar Sarin; Sushmita Nitin Bhatnagar
Journal:  Indian J Pediatr       Date:  2012-05-04       Impact factor: 1.967

3.  Wilms' tumor: single centre retrospective study from South India.

Authors:  B Guruprasad; B Rohan; S Kavitha; D S Madhumathi; D Lokanath; L Appaji
Journal:  Indian J Surg Oncol       Date:  2013-06-15

4.  Wilms' Tumor with long-delayed recurrence: 25 years after initial treatment.

Authors:  So-Young Lee; Kyu-Rae Kim; Jung-Yeol Park; Jae Y Ro
Journal:  Korean J Urol       Date:  2012-04-18

5.  A 10-Year Study of the Outcome of Wilms' Tumor in Central India and Identifying Practice Gaps.

Authors:  Vikesh Agrawal; Arpan Mishra; Sanjay Kumar Yadav; Dhananjaya Sharma; Himanshu Acharya; Aradhna Mishra; Rekha Agrawal; Roshan Chanchlani
Journal:  J Indian Assoc Pediatr Surg       Date:  2022-01-11

Review 6.  Nephron-Sparing Surgery in Nonsyndromic Unilateral Wilms' tumor: An Insight into the Ongoing Surgical Controversy.

Authors:  Yogesh Kumar Sarin
Journal:  J Indian Assoc Pediatr Surg       Date:  2022-01-11
  6 in total

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