Literature DB >> 10458232

Chemotherapy dose-intensification for pediatric patients with Ewing's family of tumors and desmoplastic small round-cell tumors: a feasibility study at St. Jude Children's Research Hospital.

N M Marina1, A S Pappo, D M Parham, A M Cain, B N Rao, C A Poquette, C B Pratt, C Greenwald, W H Meyer.   

Abstract

PURPOSE: To evaluate the feasibility of dose-intensification for patients with Ewing's family of tumors (EFT) and desmoplastic small round-cell tumors. PATIENTS AND METHODS: From February 1992 to June 1996, we treated 53 consecutive patients on our Ewing's protocol. Induction comprised three cycles of ifosfamide/etoposide on days 1 to 3 and cyclophosphamide (CTX)/doxorubicin on day 5, followed by granulocyte colony-stimulating factor. Local control using surgery and/or radiotherapy started at week 9 along with vincristine/dactinomycin. Maintenance included four alternating cycles of ifosfamide/etoposide and doxorubicin/CTX, with randomization to one of two CTX dose levels to determine the feasibility of dose-intensification during maintenance.
RESULTS: Patients had a median age of 13.4 years (range, 4.5 to 24.9 years); 34 patients were male and 43 patients were white. Nineteen patients presented with metastatic disease, 29 had tumors greater than 8 cm in diameter, and 26 had primary bone tumors. These patients received 155 induction cycles, 91% of which resulted in grade 4 neutropenia, 68% in febrile neutropenia, and 68% in grade 3 to 4 thrombocytopenia. During maintenance, grade 4 neutropenia and grade 3 to 4 thrombocytopenia occurred in 81% and 85% of cycles, respectively. Thirty-five patients (66%) completed all therapy, only 13 without significant delays; three developed secondary myeloid malignancies. The toxicity and time to therapy completion were similar in both CTX arms. Estimated 3-year survival and event-free survival were 72%+/-8% and 60%+/-9%, respectively.
CONCLUSION: Although intensifying therapy seems feasible for 25% of patients on this study, toxicity was considerable. Therefore, the noninvestigational use of dose-intensification in patients with EFT should await assessment of its impact on disease-free survival.

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Year:  1999        PMID: 10458232     DOI: 10.1200/JCO.1999.17.1.180

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  16 in total

1.  Impact of first-line treatment on outcomes of Ewing sarcoma of the spine.

Authors:  Jianjun Zhang; Yujing Huang; Jing Lu; Aina He; Yan Zhou; Haiyan Hu; Zan Shen; Yuanjue Sun; Yang Yao
Journal:  Am J Cancer Res       Date:  2018-07-01       Impact factor: 6.166

2.  High-dose chemotherapy and autologous peripheral blood stem cell transplantation in adult patients with high-risk or advanced Ewing and soft tissue sarcoma.

Authors:  M Engelhardt; R Zeiser; G Ihorst; J Finke; C I Müller
Journal:  J Cancer Res Clin Oncol       Date:  2006-07-12       Impact factor: 4.553

3.  Clinical features and outcomes in patients with Ewing sarcoma and regional lymph node involvement.

Authors:  Mark A Applebaum; Robert Goldsby; John Neuhaus; Steven G DuBois
Journal:  Pediatr Blood Cancer       Date:  2011-12-19       Impact factor: 3.167

Review 4.  Ewing tumour: incidence, prognosis and treatment options.

Authors:  M Paulussen; B Fröhlich; H Jürgens
Journal:  Paediatr Drugs       Date:  2001       Impact factor: 3.022

5.  Ewing's Sarcoma Family Tumors in the Jaws: Case Report, Immunohistochemical Analysis and Literature Review.

Authors:  Ana Regina Casaroto; Marcelo Bonifacio DA Silva Sampieri; Cleverson Teixeira Soares; Paulo Sergio DA Silva Santos; Renato Yassutaka Faria Yaedu; José Humberto Damante; Vanessa Soares Lara
Journal:  In Vivo       Date:  2017 May-Jun       Impact factor: 2.155

6.  Chemotherapy in Ewing's sarcoma.

Authors:  Sandeep Jain; Gauri Kapoor
Journal:  Indian J Orthop       Date:  2010-10       Impact factor: 1.251

7.  Second cancers in patients with the Ewing sarcoma family of tumours.

Authors:  Fariba Navid; Catherine Billups; Tiebin Liu; Matthew J Krasin; Carlos Rodriguez-Galindo
Journal:  Eur J Cancer       Date:  2008-03-18       Impact factor: 9.162

8.  Diagnosis of osteosarcoma in a patient previously treated for Ewing sarcoma.

Authors:  Manabu Hoshi; Makoto Ieguchi; Kazumi Yamato; Sadao Tokimasa; Hiroaki Nakamura
Journal:  Skeletal Radiol       Date:  2014-04-11       Impact factor: 2.199

Review 9.  Childhood Cancer: Occurrence, Treatment and Risk of Second Primary Malignancies.

Authors:  Sebastian Zahnreich; Heinz Schmidberger
Journal:  Cancers (Basel)       Date:  2021-05-26       Impact factor: 6.639

Review 10.  Myeloablative therapy against high risk Ewing's sarcoma: A single institution experience and literature review.

Authors:  Jose Luis Lopez; Concepcion Pérez; Catalina Marquez; Patricia Cabrera; Jose Maria Perez; Gema Lucia Ramirez; Rafael Ordoñez; Juan Manuel Praena-Fernandez; Maria Jose Ortiz
Journal:  Rep Pract Oncol Radiother       Date:  2011-05-20
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