Literature DB >> 9482414

Treatment of children with peripheral primitive neuroectodermal tumor or extraosseous Ewing's tumor with Ewing's-directed therapy.

S Gururangan1, N M Marina, X Luo, D M Parham, C Y Tzen, C A Greenwald, B N Rao, L E Kun, W H Meyer.   

Abstract

PURPOSE: We report the treatment and outcome of patients with peripheral primitive neuroectodermal tumor (PNET) and extraosseous Ewing's tumor (EOE) using Ewing's-directed therapy, including an ifosfamide and etoposide window.
METHODS: Seventeen pediatric patients with peripheral PNET (n = 14) or EOE (n = 3) were enrolled between 1988 and 1992 on our institutional Ewing's protocol. Induction therapy comprised a 9-week "window" of ifosfamide and etoposide, followed by 9 weeks of therapy with cyclophosphamide and Adriamycin (Adria Laboratories, Columbus, OH). Response assessment after 17 weeks was followed by surgery and/or radiotherapy (doses based on tumor size and response to induction), repeat evaluation, and maintenance chemotherapy with alternating courses of vincristine/dactinomycin, ifosfamide/etoposide, and cyclophosphamide/Adriamycin for a total of 45 weeks.
RESULTS: At diagnosis, 8 patients had large lesions (>8 cm) and 3 had pulmonary metastases (1 with large tumor). Surgical resection was performed at diagnosis for 9 patients and after induction therapy for 5. During window therapy, all of the 9 evaluable patients responded (8 partial, I objective), and no patient without measurable disease developed disease progression. Responses were maintained or improved during subsequent induction in six of the patients with residual disease. Fourteen patients received local radiotherapy. At 49 to 94 months after diagnosis, 12 patients are disease-free (1 in second remission), 4 have died, and 1 is alive with disease. The five-year overall and progression-free survival rates are 77 +/- 13% and 62 +/- 16%, respectively.
CONCLUSION: The use of consistent Ewing's-directed combined-modality therapy for patients with soft tissue peripheral PNET/EOE results in survival similar to that of patients with osseous Ewing's tumor. The combination of ifosfamide and etoposide appears active and should be incorporated in future treatment protocols.

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Mesh:

Year:  1998        PMID: 9482414     DOI: 10.1097/00043426-199801000-00009

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


  12 in total

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Authors:  Frederic G Barr; Richard B Womer
Journal:  J Mol Diagn       Date:  2007-07-25       Impact factor: 5.568

Review 2.  Ewing sarcoma/peripheral primitive neuroectodermal tumor and related tumors.

Authors:  Maria Tsokos; Rita D Alaggio; Louis P Dehner; Paul S Dickman
Journal:  Pediatr Dev Pathol       Date:  2012

3.  Evaluating the Soft Tissue Sarcoma Paradigm for the Local Management of Extraskeletal Ewing Sarcoma.

Authors:  David Boyce-Fappiano; B Ashleigh Guadagnolo; Ravin Ratan; Wei-Lien Wang; Michael J Wagner; Shreyaskumar Patel; John A Livingston; Patrick P Lin; Kevin Diao; Devarati Mitra; Ahsan Farooqi; Alexander J Lazar; Christina L Roland; Andrew J Bishop
Journal:  Oncologist       Date:  2020-12-14

4.  Intracranial peripheral primitive neuroectodermal tumor manifesting as abducens nerve palsy.

Authors:  N Horinaka; Y Ito; M Miyajima; M Hishii; K Suzuki; M Saito; H Arai
Journal:  Childs Nerv Syst       Date:  2005-01-19       Impact factor: 1.475

5.  Clinical features and outcomes in patients with extraskeletal Ewing sarcoma.

Authors:  Mark A Applebaum; Jennifer Worch; Katherine K Matthay; Robert Goldsby; John Neuhaus; Daniel C West; Steven G Dubois
Journal:  Cancer       Date:  2011-01-10       Impact factor: 6.860

6.  Extraosseous Ewing's sarcoma of the pancreas.

Authors:  Prithviraj Bose; Paari Murugan; Elizabeth Gillies; Jennifer L Holter
Journal:  Int J Clin Oncol       Date:  2011-09-03       Impact factor: 3.402

7.  Comparison of clinical features and outcomes in patients with extraskeletal versus skeletal localized Ewing sarcoma: A report from the Children's Oncology Group.

Authors:  Thomas Cash; Elizabeth McIlvaine; Mark D Krailo; Stephen L Lessnick; Elizabeth R Lawlor; Nadia Laack; Joel Sorger; Neyssa Marina; Holcombe E Grier; Linda Granowetter; Richard B Womer; Steven G DuBois
Journal:  Pediatr Blood Cancer       Date:  2016-06-14       Impact factor: 3.167

8.  Ewing sarcoma outcomes in a country with limited resources: Egypt as an example.

Authors:  Ahmed Mohammed Morsy; Salah Abdel-Hadi; Khalid Mohammed Rezk; Gamal Amira; Badawy Mohammed Ahmed; Marwa Tammam Hussien; Mahmoud Gamal Ameen; Hosam Eldein Mostafa Kamel; Doaa Mohamed Fouad; Alia Mohamed Attia; Asmaa Salah; Osama Mostafa Abd Elbadee; Ayatallah Ali Yousseif; Marwa Ismail Abdelgawad; Asmaa Hussein Fathy; Yasmine Nagy Elwany; Islam Karam-Allah Ramadan; Khaled Hassan Mosallam; Ahmed Ibrahim Abd Elwahab; Khaled Hashim Mahmoud; Maged Abdel Fattah Amine; Ahmed Refaat Abd Elzaher; Hanan Ahmed Eltyb; Ahmed Mubarak Hefni
Journal:  Am J Cancer Res       Date:  2021-06-15       Impact factor: 6.166

9.  Clinical features, prognostic factors and outcome in a series of 29 extra-skeletal Ewing Sarcoma. Adequate margins and surgery-radiotherapy association improve overall survival.

Authors:  Francesco Muratori; Nicola Mondanelli; Lorenzo Pelagatti; Filippo Frenos; Davide Matera; Giovanni Beltrami; Matteo Innocenti; Rodolfo Capanna; Giuliana Roselli; Guido Scoccianti; Lorenzo Livi; Daniela Greto; Cristina Muntoni; Giacomo Baldi; Angela Tamburini; Domenico Andrea Campanacci
Journal:  J Orthop       Date:  2020-03-25

10.  Primary pediatric endobronchial Ewing sarcoma family of tumors.

Authors:  Akira Hayakawa; Satoshi Hirase; Natsuki Matsunoshita; Nobuyuki Yamamoto; Ikuko Kubokawa; Takeshi Mori; Tomoko Yanai; Yoshimasa Maniwa; Kazumoto Iijima
Journal:  Am J Case Rep       Date:  2013-03-05
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