Literature DB >> 17687565

Prediction of response and prognostic factors for Ewing family of tumors in a low incidence population.

Kan Yonemori1, Umio Yamaguchi, Masayuki Kaneko, Hajime Uno, Masahiro Takeuchi, Masashi Ando, Yasuhiro Fujiwara, Ako Hosono, Atsushi Makimoto, Tadashi Hasegawa, Ryouhei Yokoyama, Fumihiko Nakatani, Akira Kawai, Yasuo Beppu, Hirokazu Chuman.   

Abstract

PURPOSE: There is some unknown reason Ewing family of tumors (EFTs) is much less common on Asia and Africa than in the Western Caucasian population. This study analyzed the prediction of response and prognostic factors for Ewing family of tumors (EFTs) in an Asian population with a low incidence.
METHODS: We retrospectively reviewed 94 patients with EFTs between 1978 and 2006. Fifteen patients received local therapy only. Statistical analyses were performed for 79 patients, including those who received systemic chemotherapy, to identify factors related to chemotherapy responsiveness, event-free survival, and overall survival.
RESULTS: Of the 79 patients whose records were analyzed, the 5-year event-free rate and overall survival (OS) rate were 41 and 54%, respectively. The response rate to first-line chemotherapy was 61% in 70 patients with assessable lesions. A significant predictor of response was existence of a non-pelvic primary tumor (P = 0.04). Significant prognostic factors for OS were age, performance status, and metastases at the time of diagnosis (P < 0.01, respectively). Fifty-four patients had disease progression or recurrence after first-line treatment. The time to progression was 3.4 months after salvage treatment. Progression during first-line treatment was significantly associated with time to progression after salvage treatment (P = 0.01). All patients treated without chemotherapy in first-line treatment were recurred with poor prognosis.
CONCLUSION: A non-pelvic primary tumor was a favorable predictor of responsiveness to chemotherapy. Chemo-resistant patients might less benefit from second line chemotherapy. Chemotherapy in first-line treatment should not be omitted, even if primary tumor was extirpated completely.

Entities:  

Mesh:

Year:  2007        PMID: 17687565     DOI: 10.1007/s00432-007-0295-9

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  24 in total

1.  Localized Ewing tumor of bone: final results of the cooperative Ewing's Sarcoma Study CESS 86.

Authors:  M Paulussen; S Ahrens; J Dunst; W Winkelmann; G U Exner; R Kotz; G Amann; B Dockhorn-Dworniczak; D Harms; S Müller-Weihrich; K Welte; B Kornhuber; G Janka-Schaub; U Göbel; J Treuner; P A Voûte; A Zoubek; H Gadner; H Jürgens
Journal:  J Clin Oncol       Date:  2001-03-15       Impact factor: 44.544

2.  A long-term review of the treatment of patients with Ewing's sarcoma in one institution.

Authors:  M Sluga; R Windhager; S Lang; H Heinzl; P Krepler; F Mittermayer; M Dominkus; A Zoubek; R Kotz
Journal:  Eur J Surg Oncol       Date:  2001-09       Impact factor: 4.424

3.  Multimodal therapy for the management of primary, nonmetastatic Ewing's sarcoma of bone: a long-term follow-up of the First Intergroup study.

Authors:  M E Nesbit; E A Gehan; E O Burgert; T J Vietti; A Cangir; M Tefft; R Evans; P Thomas; F B Askin; J M Kissane
Journal:  J Clin Oncol       Date:  1990-10       Impact factor: 44.544

4.  A practical approach to the clinical diagnosis of Ewing's sarcoma/primitive neuroectodermal tumour and other small round cell tumours sharing EWS rearrangement using new fluorescence in situ hybridisation probes for EWSR1 on formalin fixed, paraffin wax embedded tissue.

Authors:  U Yamaguchi; T Hasegawa; Y Morimoto; U Tateishi; M Endo; F Nakatani; A Kawai; H Chuman; Y Beppu; M Endo; H Kurotaki; K Furuta
Journal:  J Clin Pathol       Date:  2005-10       Impact factor: 3.411

5.  Single center experience of treatment of Ewing's family of tumors in Japan.

Authors:  Kenji Yamada; Hideshi Sugiura; Mitsuru Takahashi
Journal:  J Orthop Sci       Date:  2006-01       Impact factor: 1.601

6.  Prognostic factors in nonmetastatic Ewing's sarcoma of bone treated with adjuvant chemotherapy: analysis of 359 patients at the Istituto Ortopedico Rizzoli.

Authors:  G Bacci; S Ferrari; F Bertoni; S Rimondini; A Longhi; P Bacchini; C Forni; M Manfrini; D Donati; P Picci
Journal:  J Clin Oncol       Date:  2000-01       Impact factor: 44.544

7.  Multimodal therapy for children and adolescents with Ewing sarcoma: results of the First National Chilean Trial (1986-1991).

Authors:  M Villarroel; J Tordecilla; C Salgado; X Luo; S Messen; Y Rayo; P Zolezzi; J Rojas
Journal:  Med Pediatr Oncol       Date:  1997-09

8.  Comparative frequency of bone sarcomas among different racial groups.

Authors:  W Guo; W Xu; A G Huvos; J H Healey; C Feng
Journal:  Chin Med J (Engl)       Date:  1999-12       Impact factor: 2.628

9.  Addition of ifosfamide and etoposide to standard chemotherapy for Ewing's sarcoma and primitive neuroectodermal tumor of bone.

Authors:  Holcombe E Grier; Mark D Krailo; Nancy J Tarbell; Michael P Link; Christopher J H Fryer; Douglas J Pritchard; Mark C Gebhardt; Paul S Dickman; Elizabeth J Perlman; Paul A Meyers; Sarah S Donaldson; Sheila Moore; Aaron R Rausen; Teresa J Vietti; James S Miser
Journal:  N Engl J Med       Date:  2003-02-20       Impact factor: 91.245

Review 10.  Treatment of Ewing sarcoma family of tumors: current status and outlook for the future.

Authors:  Carlos Rodriguez-Galindo; Sheri L Spunt; Alberto S Pappo
Journal:  Med Pediatr Oncol       Date:  2003-05
View more
  4 in total

1.  Role of radiation therapy in the multidisciplinary management of Ewing's Sarcoma of bone in pediatric patients: An effective treatment for local control.

Authors:  Jose Luis Lopez; Patricia Cabrera; Rafael Ordoñez; Catalina Marquez; Gema Lucia Ramirez; Juan Manuel Praena-Fernandez; Maria Jose Ortiz
Journal:  Rep Pract Oncol Radiother       Date:  2011-03-12

2.  Prognostic factors for overall survival in paediatric patients with Ewing sarcoma of bone treated according to multidisciplinary protocol.

Authors:  J L López Guerra; C Márquez-Vega; G L Ramírez-Villar; P Cabrera; R Ordóñez; J M Praena-Fernández; M J Ortiz
Journal:  Clin Transl Oncol       Date:  2012-04       Impact factor: 3.405

3.  Membrane expression of MRP-1, but not MRP-1 splicing or Pgp expression, predicts survival in patients with ESFT.

Authors:  E Roundhill; S Burchill
Journal:  Br J Cancer       Date:  2013-06-25       Impact factor: 7.640

4.  The clinical use of biomarkers as prognostic factors in Ewing sarcoma.

Authors:  Annmeik M van Maldegem; Pancras Cw Hogendoorn; Andrew B Hassan
Journal:  Clin Sarcoma Res       Date:  2012-02-08
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.