Literature DB >> 9149741

A feasibility, toxicity, and early response study of etoposide, ifosfamide, and vincristine for the treatment of children with rhabdomyosarcoma: a report from the Intergroup Rhabdomyosarcoma Study (IRS) IV pilot study.

C Arndt1, M Tefft, E Gehan, J Anderson, M Jenson, M Link, S Donaldson, J Breneman, E Wiener, B Webber, H Maurer.   

Abstract

PURPOSE: The purpose of this study was to determine the feasibility, toxicity, and early response of patients with clinical group III rhabdomyosarcoma (RMS) to a chemotherapy regimen of etoposide (ETOP), ifosfamide (IFOS), and vincristine (VCR) with hyperfractionated radiation therapy (XRT). PATIENTS AND METHODS: Sixty-eight patients aged < 21 years, previously untreated, with clinical group III RMS or undifferentiated sarcoma with normal organ function were eligible for this study. Chemotherapy was as follows: weeks 0-8: IFOS 1.8 g/m2/day X 5 days every 3 weeks X 3 (with mesna), ETOP 100 mg/m2/day X 5 days every 3 weeks X 3, and VCR 1.5 mg/m2/week X 9; weeks 9-16: hyperfractionated XRT (except patients with parameningeal tumors with meningeal extension, who received XRT on day 0), IFOS/mesna weeks 9, 12, 16, and VCR weeks 9, 10, 11, 12, 16; weeks 20-99; IFOS/mesna q 3 weeks X 2, ETOP q 3 weeks X 2, and VCR weekly X 6 weeks. Four drug cycles were repeated every 9 weeks, beginning at week 29. In January 1991, the duration of therapy was reduced to 12 courses due to emerging evidence of IFOS-induced renal tubular dysfunction.
RESULTS: Of the 62 patients evaluable for response, 45 (73%) achieved a complete response. There were three fatal toxicities due to infection. Life-threatening neutropenia was seen in 55 of 60 patients, and life-threatening infections occurred in 27 of 60 patients. Twenty-five patients (42%) developed some degree of neurotoxicity from vincristine. Eleven patients (18%) developed nephrotoxicity, 7 cases of which were severe; 6 of the 11 patients who developed nephrotoxicity were < 2 years old.
CONCLUSIONS: This pilot study had toxicity and response rates comparable to the other two Intergroup Rhabdomyosarcoma Study (IRS)-IV pilot trials of vincristine-actinomycin-cyclophosphamide and vincristine-actinomycin-ifosfamide and is, therefore, being evaluated in the current IRS randomized trial. Due to the high incidence of life-threatening neutropenia and infections, the use of growth factors is now routine. Five of 11 patients who developed nephrotoxicity did so after more than eight courses of IFOS; therefore, the current randomized trial limits IFOS to a total of eight courses.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9149741     DOI: 10.1097/00043426-199703000-00005

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  13 in total

Review 1.  Soft tissue sarcomas in children.

Authors:  Gauri Kapoor; Kunal Das
Journal:  Indian J Pediatr       Date:  2011-09-21       Impact factor: 1.967

2.  Primary renal sarcomas in the Intergroup Rhabdomyosarcoma Study Group (IRSG) experience, 1972-2005: A report from the Children's Oncology Group.

Authors:  Beverly Raney; James Anderson; Carola Arndt; Willam Crist; Harold Maurer; Stephen Qualman; Moody Wharam; Eugene Wiener; William Meyer
Journal:  Pediatr Blood Cancer       Date:  2008-09       Impact factor: 3.167

3.  Orbital rhabdomyosarcomas: A review.

Authors:  Lama Jurdy; Johanus H M Merks; Bradly R Pieters; Maarten P Mourits; Roel J H M Kloos; Simone D Strackee; Peerooz Saeed
Journal:  Saudi J Ophthalmol       Date:  2013-07

4.  Parameningeal rhabdomyosarcoma in pediatric age: results of a pooled analysis from North American and European cooperative groups.

Authors:  J H M Merks; G L De Salvo; C Bergeron; G Bisogno; A De Paoli; A Ferrari; A Rey; O Oberlin; M C G Stevens; A Kelsey; J Michalski; D S Hawkins; J R Anderson
Journal:  Ann Oncol       Date:  2014-01       Impact factor: 32.976

5.  The World Health Organization Classification of Skeletal Muscle Tumors in Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology Group.

Authors:  Erin R Rudzinski; James R Anderson; Douglas S Hawkins; Stephen X Skapek; David M Parham; Lisa A Teot
Journal:  Arch Pathol Lab Med       Date:  2015-05-19       Impact factor: 5.534

Review 6.  Clinical group and modified TNM stage for rhabdomyosarcoma: A review from the Children's Oncology Group.

Authors:  Jacquelyn N Crane; Wei Xue; Amira Qumseya; Zhengya Gao; Carola A S Arndt; Sarah S Donaldson; Douglas J Harrison; Douglas S Hawkins; Corinne M Linardic; Leo Mascarenhas; William H Meyer; David A Rodeberg; Erin R Rudzinski; Barry L Shulkin; David O Walterhouse; Rajkumar Venkatramani; Aaron R Weiss
Journal:  Pediatr Blood Cancer       Date:  2022-03-06       Impact factor: 3.838

Review 7.  Rhabdomyosarcoma.

Authors:  Andrea Stuart; Jayant Radhakrishnan
Journal:  Indian J Pediatr       Date:  2004-04       Impact factor: 1.967

8.  Clinical results of high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation in children with advanced stage rhabdomyosarcoma.

Authors:  Nam Kyun Kim; Hyo Sun Kim; Chang-Ok Suh; Hyun Ok Kim; Chuhl Joo Lyu
Journal:  J Korean Med Sci       Date:  2012-08-22       Impact factor: 2.153

9.  Results of treatment of patients with superficial facial rhabdomyosarcomas on protocols of the Intergroup Rhabdomyosarcoma Study Group (IRSG), 1984-1997.

Authors:  R Beverly Raney; Murali Chintagumpala; James Anderson; Alberto Pappo; Stephen Qualman; Moody Wharam; Eugene Wiener; William Meyer
Journal:  Pediatr Blood Cancer       Date:  2008-05       Impact factor: 3.167

10.  Early and late adverse renal effects after potentially nephrotoxic treatment for childhood cancer.

Authors:  Esmee Cm Kooijmans; Arend Bökenkamp; Nic S Tjahjadi; Jesse M Tettero; Eline van Dulmen-den Broeder; Helena Jh van der Pal; Margreet A Veening
Journal:  Cochrane Database Syst Rev       Date:  2019-03-11
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.