Tissue Sample Collection From Patients With Soft Tissue Sarcoma of the Arms, Hands, Legs, or Feet Treated on Clinial Trial CRUK-VORTEX
Recruitment status was Recruiting
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Purpose
RATIONALE: Collecting and storing samples of tumor tissue from patients with soft tissue sarcoma to test in the laboratory may help the study of cancer in the future.
PURPOSE: This laboratory is collecting tissue samples from patients with soft tissue sarcoma of the arms, hands, legs, or feet treated on clinical trial CRUK-VORTEX.
| Condition | Intervention |
|---|---|
|
Sarcoma |
Genetic: microarray analysis Genetic: molecular diagnostic method Other: biologic sample preservation procedure |
| Study Type: | Observational |
| Official Title: | VORTEX-BIOBANK: Prospective Sample Collection for the VORTEX Randomised Radiotherapy Trial in Patients With Extremity Soft Tissue Sarcoma [VORTEX BIOBANK] |
- Increased likelihood of distant metastases [ Designated as safety issue: No ]
| Estimated Enrollment: | 400 |
| Study Start Date: | August 2007 |
| Estimated Primary Completion Date: | March 2012 (Final data collection date for primary outcome measure) |
OBJECTIVES:
- Determine early in the course of treatment which patients treated on clinical trial CRUK-VORTEX have an increased likelihood of distant metastases so as to highlight individuals who might benefit from early adjuvant systemic therapy.
OUTLINE: This is a multicenter study.
Tumour and normal tissue samples will be taken at the time of surgery during treatment on clinical trial CRUK-VORTEXand preserved for future microarray analyses. Tissue microarrays will be produced from both tumor and normal tissues. Blood samples will be collected for future DNA analysis.
Eligibility| Ages Eligible for Study: | 16 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
- Histologically confirmed soft tissue sarcoma
- Receiving treatment on clinical trial CRUK-VORTEX
- Underwent surgery to remove the tumor no more than 3 months ago
PATIENT CHARACTERISTICS:
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception during and for 3 months after completion of study treatment
- No other major medical illness that would preclude study treatment
- No other prior or concurrent malignancy except adequately treated nonmelanoma carcinoma of the skin or in situ carcinoma of the cervix
PRIOR CONCURRENT THERAPY:
- No prior radiotherapy to the local site
- No prior neoadjuvant or adjuvant chemotherapy
Contacts and Locations| United Kingdom | |
| Royal Orthopedic Hospital NHS Trust | Recruiting |
| Birmingham, England, United Kingdom, B31 2AP | |
| Contact: Contact Person 44-121-685-4019 | |
| Queen Elizabeth Hospital at University Hospital of Birmingham NHS Trust | Recruiting |
| Birmingham, England, United Kingdom, B15 2TH | |
| Contact: Contact Person 44-121-472-1311 | |
| Bristol Haematology and Oncology Centre | Recruiting |
| Bristol, England, United Kingdom, BS2 8ED | |
| Contact: Contact Person 44-117-928-2417 | |
| Royal National Orthopaedic Hospital NHS Trust | Recruiting |
| Cheltenham, England, United Kingdom, GL53 7AN | |
| Contact: Contact Person 44-020-8954-2300 | |
| Gloucestershire Oncology Centre at Cheltenham General Hospital | Recruiting |
| Cheltenham, England, United Kingdom, GL53 7AN | |
| Contact: Contact Person 44-1242-222-222 | |
| Middlesex Hospital | Recruiting |
| London, England, United Kingdom, W1T 3AA | |
| Contact: Contact Person 44-0207-380-9087 | |
| Christie Hospital | Recruiting |
| Manchester, England, United Kingdom, M20 4BX | |
| Contact: Contact Person 44-161-446-3341 Catharine.west@manchester.ac.uk | |
| Nottingham City Hospital | Recruiting |
| Nottingham, England, United Kingdom, NG5 1PB | |
| Contact: Contact Person 44-115-969-1169 | |
| Cancer Research Centre at Weston Park Hospital | Recruiting |
| Sheffield, England, United Kingdom, S1O 2SJ | |
| Contact: Contact Person 44-114-226-5208 | |
| Robert Jones and Agnes Hunt Orthopaedic and District Hospital NHS Trust | Recruiting |
| Shropshire, England, United Kingdom, SY10 7AG | |
| Contact: Contact Person 44-0161-446-3341 | |
| Beatson West of Scotland Cancer Centre | Recruiting |
| Glasgow, Scotland, United Kingdom, G12 0YN | |
| Contact: Contact Person 44-141-301-7000 | |
| Glan Clwyd Hospital | Recruiting |
| Rhyl, Denbighshire, Wales, United Kingdom, LL 18 5UJ | |
| Contact: Contact Person 44-1745-583-910 | |
| Study Chair: | Catherine West | Christie Hospital NHS Foundation Trust |
More Information
Additional Information:
No publications provided
| ClinicalTrials.gov Identifier: | NCT00900211 History of Changes |
| Other Study ID Numbers: | CDR0000581165, VORTEX-SA3002, VORTEX-REC-06/MRE03/3, ISRCTN76456502, EU-20795 |
| Study First Received: | May 9, 2009 |
| Last Updated: | August 5, 2011 |
| Health Authority: | Unspecified |
Keywords provided by National Cancer Institute (NCI):
|
recurrent adult soft tissue sarcoma stage I adult soft tissue sarcoma stage II adult soft tissue sarcoma stage III adult soft tissue sarcoma adult synovial sarcoma adult angiosarcoma adult epithelioid sarcoma adult extraskeletal chondrosarcoma |
adult leiomyosarcoma adult liposarcoma adult malignant fibrous histiocytoma adult malignant hemangiopericytoma adult malignant mesenchymoma adult fibrosarcoma adult neurofibrosarcoma |
Additional relevant MeSH terms:
|
Sarcoma Neoplasms, Connective and Soft Tissue Neoplasms by Histologic Type Neoplasms |
ClinicalTrials.gov processed this record on June 17, 2013