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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03542097
Other study ID # TEMIRI-EW
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 15, 2014
Est. completion date June 30, 2019

Study information

Verified date May 2023
Source Istituto Ortopedico Rizzoli
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a biological study in patients with advanced Ewing Sarcoma who received, according, clinical practice, temozolomide and irinotecan The O6-methylguanine-DNA methyltransferase (MGMT) methylation status, will be correlated with the disease clinical data and with the disease response


Description:

This is a biological study in patients with advanced Ewing Sarcoma who received, according, clinical practice, temozolomide and irinotecan. The MGMT methylation status will be correlated with the disease clinical data and with the disease response also in term of metabolic activity (if data will be available) The MGMT methylation analysis will be performed extracting from fresh tumor sample, the DNA on the basis of the standard protocols.


Recruitment information / eligibility

Status Completed
Enrollment 82
Est. completion date June 30, 2019
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Histological confirmed diagnosis of Ewing Sarcoma 2. Chemotherapic treatment with temozolomide and irinotecan 3. Written informed consent prior to any study related activities Exclusion Criteria: 1. Lack of written informed consent for the study 2. Any situation that could interfere with the complete data collection of the clinical data related to the temozolomide and irinotecan treatment

Study Design


Related Conditions & MeSH terms


Intervention

Other:
MGMT methylation evaluation
The MGMT methylation will be evaluated by extracting DNA from fresh and Formalin Fixed paraffin Embedded (FFPE) tumor samples

Locations

Country Name City State
Italy Orthopedic Rizzoli Institute Bologna
Italy Istituto di Candiolo - Fondazione del Piemonte per l'Oncologia - IRCCS Candiolo Turin
Italy Fondazione IRCCS - Istituto Nazionale dei Tumori Milan Mi
Italy Ospedale infantile Regina Margherita Turin
United Kingdom The Royal Marsden NHS Foundation Trust London

Sponsors (2)

Lead Sponsor Collaborator
Istituto Ortopedico Rizzoli Regione Emilia-Romagna

Countries where clinical trial is conducted

Italy,  United Kingdom, 

References & Publications (5)

Bacci G, Ferrari S, Longhi A, Donati D, De Paolis M, Forni C, Versari M, Setola E, Briccoli A, Barbieri E. Therapy and survival after recurrence of Ewing's tumors: the Rizzoli experience in 195 patients treated with adjuvant and neoadjuvant chemotherapy from 1979 to 1997. Ann Oncol. 2003 Nov;14(11):1654-9. doi: 10.1093/annonc/mdg457. — View Citation

Casey DA, Wexler LH, Merchant MS, Chou AJ, Merola PR, Price AP, Meyers PA. Irinotecan and temozolomide for Ewing sarcoma: the Memorial Sloan-Kettering experience. Pediatr Blood Cancer. 2009 Dec;53(6):1029-34. doi: 10.1002/pbc.22206. — View Citation

Donson AM, Addo-Yobo SO, Handler MH, Gore L, Foreman NK. MGMT promoter methylation correlates with survival benefit and sensitivity to temozolomide in pediatric glioblastoma. Pediatr Blood Cancer. 2007 Apr;48(4):403-7. doi: 10.1002/pbc.20803. — View Citation

Hegi ME, Diserens AC, Gorlia T, Hamou MF, de Tribolet N, Weller M, Kros JM, Hainfellner JA, Mason W, Mariani L, Bromberg JE, Hau P, Mirimanoff RO, Cairncross JG, Janzer RC, Stupp R. MGMT gene silencing and benefit from temozolomide in glioblastoma. N Engl J Med. 2005 Mar 10;352(10):997-1003. doi: 10.1056/NEJMoa043331. — View Citation

Kushner BH, Meyers PA. How effective is dose-intensive/myeloablative therapy against Ewing's sarcoma/primitive neuroectodermal tumor metastatic to bone or bone marrow? The Memorial Sloan-Kettering experience and a literature review. J Clin Oncol. 2001 Feb 1;19(3):870-80. doi: 10.1200/JCO.2001.19.3.870. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of MGMT promoter methylation Amplification the methylation-specific Polymerase Chain Reaction products will be electrophoresed on a 2% agarose gel and will visualized with UV light at day 1
Secondary Correlation of the MGMT promoter methylation to the activity of the temozolomide irinotecan combination Correlation with level of MGMT methylation with tumor response at month 2, 4, 6, 8, 10 and 12
See also
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Completed NCT03011528 - First-line Treatment of Ewing Tumours With Primary Extrapulmonary Dissemination in Patients From 2 to 50 Years Phase 2
Recruiting NCT03496402 - Biological Characterisation of High Risk CHildhood Cancer in Children, Adolescents and Young Adults (MICCHADO) N/A