GEIS-21: a multicentric phase II study of intensive chemotherapy including gemcitabine and docetaxel for the treatment of Ewing sarcoma of children and adults: a report from the Spanish sarcoma group (GEIS)


Por: Mora J, Castañeda A, Pérez-Jaume S, Lopez-Pousa A, Maradiegue E, Valverde C, Martin-Broto J, Garcia Del Muro X, Cruz-Martínez O, Cruz J, Martinez-Trufero J, Maurel J, Vaz MA, de Alava E and de Torres C

Publicada: 5 sep 2017 Ahead of Print: 8 ago 2017
Resumen:
Background: First Spanish trial of Ewing sarcoma (ES) including adults and children with the aim to test the efficacy of Gemcitabine and Docetaxel (G/D) in newly diagnosed high-risk (HR) patients. Methods: This was a prospective, multicentric, non-randomised, open study for patients p40 years with newly diagnosed ES. HR patients (metastatic, axial-pelvic primaries or bone marrow micrometastasis) received 2 window cycles of G/D. Patients with an objective response (OR) to G/D received 12 monthly cycles of G/D after completion of mP6. The primary end point was the OR rate to the G/D window phase and the event-free survival (EFS) and overall survival (OS) for all patients. The study is registered at ClinicalTrials.gov (identifier: NCT00006734). Results: Forty-three patients were enroled, median age 17 years (range, 3-40). After a median follow-up of 43.4 months, the 5-year OS rate is 55.0% (95% CI, 41-74%) with an EFS of 50.0% (95% CI, 36-68%). The 5-year OS and EFS rates for standard risk (SR) patients was 76.0% (95% CI, 57-100%) and 71.0% (CI, 54-94%); for HR 36.0% (CI, 20-65%) and 29.0% (CI, 15-56%). Twelve of 17 (70.6%) high-risk (HR) patients showed an OR (7 PR and 5 SD) to G/D window therapy. The 5-year OS rate for patients p18 years of age was 74.0% (CI, 56-97%) and 31.0% for 418 years (95% CI, 15-66%), Po0.001. Grade 4 adverse events during mP6 occurred in 28/39 of patients (72%) and did not correlate with age. Multivariate survival analyses with o18 vs X18 and risk groups significant differences, Po0.00001. Using a Cox model for OS, both age and risk group were statistically significant (P = 0.0011 and P = 0.0065, respectively). Conclusions: Age at diagnosis is an independent prognostic factor superior to the presence of metastases with 18 years as the strongest cut-off. The mP6 regimen provided survival curves that plateau at 3 years and G/D produced significant responses in HR-ES that is worth further exploring.

Filiaciones:
Mora J:
 Department of Pediatric Oncology and Hematology, Hospital Sant Joan de Déu, Barcelona 08950, Spain

Castañeda A:
 Department of Pediatric Oncology and Hematology, Hospital Sant Joan de Déu, Barcelona 08950, Spain

Pérez-Jaume S:
 Department of Pediatric Oncology and Hematology, Hospital Sant Joan de Déu, Barcelona 08950, Spain

Lopez-Pousa A:
 Department of Medical Oncology, Hospital de Sant Pau, Barcelona 08025, Spain

Maradiegue E:
 Department of Pediatric Oncology and Hematology, Hospital Sant Joan de Déu, Barcelona 08950, Spain

Valverde C:
 Department of Medical Oncology, Hospital Vall d'Hebron, Barcelona 08035, Spain

Martin-Broto J:
 Department of Medical Oncology, Hospital de Son Espases, Palma de Mallorca 07210, Spain

Garcia Del Muro X:
 Department of Medical Oncology, Institut Català d'Oncologia, IDIBELL, Universitat de Barcelona, Barcelona 08907, Spain

Cruz-Martínez O:
 Department of Pediatric Oncology and Hematology, Hospital Sant Joan de Déu, Barcelona 08950, Spain

Cruz J:
 Department of Medical Oncology, Hospital Universitario de Canarias, Tenerife 38001, Spain

Martinez-Trufero J:
 Department of Medical Oncology, Hospital Miguel Servet, Zaragoza 50009, Spain

Maurel J:
 Department of Medical Oncology, Hospital Clinic, Barcelona 08036, Spain

Vaz MA:
 Department of Medical Oncology, Hospital Ramón y Cajal, Madrid 28034, Spain

de Alava E:
 Department of Pathology, Institute of Biomedicine of Sevilla (IBiS), Virgen del Rocío University Hospital/CSIC/University of Sevilla-CIBERONC, Sevilla 41013, Spain

de Torres C:
 Department of Pediatric Oncology and Hematology, Hospital Sant Joan de Déu, Barcelona 08950, Spain
ISSN: 00070920





BRITISH JOURNAL OF CANCER
Editorial
SPRINGERNATURE, CAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 117 Número: 6
Páginas: 767-774
WOS Id: 000409230100002
ID de PubMed: 28787430
imagen Green Published, hybrid

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