Literature DB >> 25585917

Post-relapse survival in patients with Ewing sarcoma.

Stefano Ferrari1, Roberto Luksch, Kirsten Sundby Hall, Franca Fagioli, Arcangelo Prete, Angela Tamburini, Amelia Tienghi, Stefania DiGirolamo, Anna Paioli, Massimo Eraldo Abate, Marta Podda, Silvia Cammelli, Mikael Eriksson, Adalberto Brach del Prever.   

Abstract

BACKGROUND: Post-relapse survival (PRS) was evaluated in patients with Ewing sarcoma (EWS) enrolled in chemotherapy protocols based on the use of high-dose chemotherapy with busulfan and melfalan (HDT) as a first-line consolidation treatment in high-risk patients. PROCEDURE: EWS patients enrolled in ISG/SSG III and IV trials who relapsed after complete remission were included in the analysis. At recurrence, chemotherapy based on high-dose ifosfamide was foreseen, and patients who responded but had not received HDT underwent consolidation therapy with HDT.
RESULTS: Data from 107 EWS patients were included in the analysis. Median time to recurrence (RFI) was 18 months, and 45 (42%) patients had multiple sites of recurrence. Patients who had previously been treated with HDT had a significantly (P = 0.02) shorter RFI and were less likely to achieve a second complete remission (CR2). CR2 status was achieved by 42 (39%) patients. Fifty patients received high-dose IFO (20 went to consolidation HDT). The 5-year PRS was 19% (95% CI 11 to 27%). With CR2, the 5-year PRS was 48% (95% CI 31 to 64%). Without CR2, median time to death was six months (range 1-45 months). According to the multivariate analysis, patients younger than 15 years, recurrence to the lung only, and RFI longer than 24 months significantly influenced the probability of PRS.
CONCLUSIONS: Age, pattern of recurrence, RFI, and response to second-line chemotherapy influence post-relapse survival in patients with recurrent Ewing sarcoma. No survival advantage was observed from chemotherapy consolidation with HDT.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Ewing sarcoma; chemotherapy; high-dose chemotherapy; metastases

Mesh:

Substances:

Year:  2015        PMID: 25585917     DOI: 10.1002/pbc.25388

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


  16 in total

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Journal:  Cochrane Database Syst Rev       Date:  2021-09-02

2.  Patient/parent perspectives on genomic tumor profiling of pediatric solid tumors: The Individualized Cancer Therapy (iCat) experience.

Authors:  Jonathan M Marron; Steven G DuBois; Julia Glade Bender; AeRang Kim; Brian D Crompton; Stephanie C Meyer; Katherine A Janeway; Jennifer W Mack
Journal:  Pediatr Blood Cancer       Date:  2016-07-18       Impact factor: 3.167

3.  Donor lymphocyte infusions in adolescents and young adults for control of advanced pediatric sarcoma.

Authors:  Sebastian J Schober; Irene von Luettichau; Angela Wawer; Maximilian Steinhauser; Christoph Salat; Wolfgang Schwinger; Marek Ussowicz; Petar Antunovic; Luca Castagna; Hans-Jochem Kolb; Stefan E G Burdach; Uwe Thiel
Journal:  Oncotarget       Date:  2018-04-27

Review 4.  Role of High-Dose Chemotherapy and Autologous Hematopoietic Cell Transplantation for Children and Young Adults with Relapsed Ewing's Sarcoma: A Systematic Review.

Authors:  Pavan Tenneti; Umar Zahid; Ahmad Iftikhar; Seongseok Yun; Atif Sohail; Zabih Warraich; Faiz Anwer
Journal:  Sarcoma       Date:  2018-06-03

5.  Role of High-dose Chemotherapy and Autologous Stem Cell Transplantation for Relapsed Ewing's Sarcoma: A Case Report with Focused Review of Literature.

Authors:  Pavan Tenneti; Umar Zahid; Fnu Sagar; Muhammed Usman; Faiz Anwer
Journal:  Cureus       Date:  2018-05-05

6.  Effectiveness of 18F-FDG PET/CT in the diagnosis, staging and recurrence monitoring of Ewing sarcoma family of tumors: A meta-analysis of 23 studies.

Authors:  Tao Huang; Feng Li; Zexing Yan; Yupeng Ma; Fei Xiong; Xia Cai; Qingyu Zhang; Fanxiao Liu; Jinlei Dong
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.817

7.  Getting control during follow-up visits: the views and experiences of parents on tumor surveillance after their children have completed therapy for rhabdomyosarcoma or Ewing sarcoma.

Authors:  B Vaarwerk; P F Limperg; M C Naafs-Wilstra; J H M Merks; M A Grootenhuis
Journal:  Support Care Cancer       Date:  2019-02-12       Impact factor: 3.603

8.  Intraabdominal lesser sac metastasis from Ewing's sarcoma: An exceptional localization.

Authors:  Malek Bouhani; Imen Sassi; Ines Zemni; Ghada Sahraoui; Amine Bouida; Maher Slimene; Khaled Rahal
Journal:  SAGE Open Med Case Rep       Date:  2021-06-04

9.  A Retrospective Multicentric Study of Ewing Sarcoma Family of Tumors in Patients Older Than 50: Management and Outcome.

Authors:  Pauline Rochefort; Antoine Italiano; Valérie Laurence; Nicolas Penel; Audrey Lardy-Cleaud; Olivier Mir; Christine Chevreau; Francois Bertucci; Emmanuelle Bompas; Loic Chaigneau; Dominique Levy; Thomas Ryckewaert; Sarah Dumont; Pierre Meeus; Dominique Ranchere; Jean-Yves Blay; Philippe Alexandre Cassier
Journal:  Sci Rep       Date:  2017-12-20       Impact factor: 4.379

10.  Phase I clinical study of oral olaparib in pediatric patients with refractory solid tumors: study protocol.

Authors:  Masatoshi Takagi; Chitose Ogawa; Yuki Aoki-Nogami; Tomoko Iehara; Eri Ishibashi; Minoru Imai; Tetsuro Kihara; Kiyoshi Nobori; Kazuhisa Hasebe; Shuki Mizutani; Toshimi Kimura; Masashi Nagata; Masato Yasuhara; Kenichi Yoshimura; Pariko Yorozu; Hajime Hosoi; Ryuji Koike
Journal:  BMC Pediatr       Date:  2019-01-26       Impact factor: 2.125

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