Literature DB >> 14966827

Oral etoposide for recurrent/progressive sarcomas of childhood.

Rejin Kebudi1, Omer Görgün, Inci Ayan.   

Abstract

BACKGROUND: Etoposide (VP-16) is a topoisomerase II inhibitor that is effective in a broad spectrum of pediatric and adult malignancies. Chronic, low-dose, oral VP-16 has also been shown to be active in some recurrent malignancies mostly in adults. The aim of this prospective, single institution study is to assess the efficacy and toxicity of oral VP-16 in children with progressive or recurrent (P/R) sarcomas. PROCEDURE: Twenty-one children (10 girls and 11 boys) with R/P sarcomas and a median age of 11 years (range 3-16 years) were enrolled in this study. The diagnosis was Ewing sarcoma family tumor (ESFT) in seven, osteosarcoma in eight, rhabdomyosarcoma in four, clear cell sarcoma of soft tissue in one, fibrosarcoma in one patient. Oral VP-16 was administered at a dose of 50 mg/m(2)/daily for 20 days. The next course was initiated after a 10 day rest. Response to oral VP-16 was assessed after two courses.
RESULTS: There was an objective response (one complete response [CR], two partial responses [PR]) in three patients (14%) by two courses of oral VP-16 alone. One of these patients with PR achieved CR by the use of radiotherapy (RT) and further oral VP-16. Two more patients (9.5%) achieved CR by RT and oral VP-16. Eight (38%) patients had disease stabilization for 2-15 months. Two patients (9.5%) are long-term survivors. They are alive with no evidence of disease (NED) 79 and 94 months from time of relapse/progressive disease (PD). A patient developed acute myeloid leukemia and died. There was no major acute toxicity related to oral VP-16 in a total of 126 courses.
CONCLUSIONS: Oral VP-16 therapy is simple, relatively nontoxic, and does not necessitate hospitalization. The cure rate is small. Given the risk of second malignancy, especially in children with previous exposure to topoisomerase II inhibitors and alkylating agents, this regimen may be used as a palliative treatment or in patients with poor prognosis. Copyright 2003 Wiley-Liss, Inc.

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Year:  2004        PMID: 14966827     DOI: 10.1002/pbc.10393

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  11 in total

1.  Significant response to oral Etoposide in the treatment of an unresectable cardiac sarcoma.

Authors:  Chelsea L Collins; Peter J Bartz; David R Lal; Annette D Segura; Ronald K Woods; Richard L Tower
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2.  Single-Center Experience with Ifosfamide Monotherapy as Second-Line Treatment of Recurrent/Metastatic Osteosarcoma.

Authors:  Arie Jan Verschoor; Frank M Speetjens; P D Sander Dijkstra; Marta Fiocco; Michiel A J van de Sande; Judith V M G Bovée; Hans Gelderblom
Journal:  Oncologist       Date:  2019-12-19

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Authors:  Wei-Xiang Qi; Ai-Na He; Li-Na Tang; Zan Shen; Yang Yao
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4.  Inhibition of tumor angiogenesis by oral etoposide.

Authors:  Dipak Panigrahy; Arja Kaipainen; Catherine E Butterfield; Deviney M Chaponis; Andrea M Laforme; Judah Folkman; Mark W Kieran
Journal:  Exp Ther Med       Date:  2010-07-21       Impact factor: 2.447

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6.  Parents' views of cancer-directed therapy for children with no realistic chance for cure.

Authors:  Jennifer W Mack; Steven Joffe; Joanne M Hilden; Jan Watterson; Caron Moore; Jane C Weeks; Joanne Wolfe
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Review 7.  Osteosarcoma in Korean children and adolescents.

Authors:  Jun Ah Lee
Journal:  Korean J Pediatr       Date:  2015-04-22

8.  A Randomized Study on Postrelapse Disease-Free Survival with Adjuvant Mistletoe versus Oral Etoposide in Osteosarcoma Patients.

Authors:  Alessandra Longhi; Marcus Reif; Erminia Mariani; Stefano Ferrari
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Review 9.  UK guidelines for the management of bone sarcomas.

Authors:  Craig Gerrand; Nick Athanasou; Bernadette Brennan; Robert Grimer; Ian Judson; Bruce Morland; David Peake; Beatrice Seddon; Jeremy Whelan
Journal:  Clin Sarcoma Res       Date:  2016-05-04

10.  Single-Center Experience with Ifosfamide Monotherapy as Second-Line Treatment of Recurrent/Metastatic Osteosarcoma.

Authors:  Arie Jan Verschoor; Frank M Speetjens; P D Sander Dijkstra; Marta Fiocco; Michiel A J van de Sande; Judith V M G Bovée; Hans Gelderblom
Journal:  Oncologist       Date:  2019-12-19
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