Local recurrence of malignant tumor of rectum (disorder)

ELECTRA

Year Started: 2022

ELECTRA is a feasibility trial to determine whether it is acceptable and feasible to recruit, randomise and deliver Intraoperative Electron Radiotherapy (IOERT) in a randomised controlled trial setting. Patients with locally advanced rectal cancer or locally recurrent rectal cancer involving the pelvic sidewall or posterior bony pelvis will be randomised to receive either extended margin surgery along, extended margin surgery with IOERT at standard dose (10 Gy), or extended margin surgery with IOERT at higher dose (15 Gy). Patients will be randomised to the three treatment arms in a 1:1:1 ratio. Patients will be followed up for a minimum of 12 months and up to 24 months following their surgery.



Access:
Data access only
Type:
Clinical Trial
Status:
Not-started
Consent restrictions:
Commercial restriction, DNA restriction, Other animal work restriction, Xenograft restriction


Associated Data Type Procurement Timeframe
Clinical records > 6 months


Male

Young adult (18 - 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
There are no material preservation details for this sample set


Male

Adult (> 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
There are no material preservation details for this sample set


Female

Young adult (18 - 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
There are no material preservation details for this sample set


Female

Adult (> 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
There are no material preservation details for this sample set

Local recurrence of malignant tumor of cervix (disorder)

CRAIN

Year Started: 2022

A phase 1b TiTE-CRM dose escalation clinical trial of tolinapant (ASTX660) in combination with standard radical chemoradiotherapy in cervical cancer.



Access:
Closed to access
Type:
Clinical Trial
Status:
Not-started
Consent restrictions:
No restrictions


Associated Data Type Procurement Timeframe
Biomarker datasets > 6 months
Clinical records > 6 months
Followup records > 6 months
Freezer temperature logs > 6 months
Genomic datasets > 6 months
Pathology records > 6 months
Physiological/biochemical measurements > 6 months
Treatment records > 6 months
Donor Ethnicity > 6 months


Female

Young adult (18 - 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
Tissue specimen RT Affected 75% -99%
cDNA/mRNA -60°C to -85°C Not applicable 75% -99%
DNA -60°C to -85°C Not applicable 75% -99%
Peripheral blood mononuclear cells (PBMC) -60°C to -85°C Not applicable 75% -99%
Plasma -60°C to -85°C Not applicable 75% -99%


Female

Adult (> 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
Tissue specimen RT Affected 75% -99%
cDNA/mRNA -60°C to -85°C Not applicable 75% -99%
DNA -60°C to -85°C Not applicable 75% -99%
Peripheral blood mononuclear cells (PBMC) -60°C to -85°C Not applicable 75% -99%
Plasma -60°C to -85°C Not applicable 75% -99%

Diffuse non-Hodgkin's lymphoma (disorder)

Pola-R-ICE-polatuzumab vedotin plus rituximab, ifosfamide, carboplatin and etoposide (Pola-R-ICE) vs R-ICE in patients with primary refractory or relapsed DLBCL

Year Started: 2022

tissue specimen, serum, plasma,



Access:
Access restricted at present
Type:
Clinical Trial
Status:
Not-started
Consent restrictions:
No restrictions


Associated Data Type Procurement Timeframe
Clinical records > 6 months
Genomic datasets > 6 months
Imaging data > 6 months
National registries > 6 months
Treatment records > 6 months
Donor Ethnicity > 6 months


Female

Young adult (18 - 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
cDNA/mRNA -60°C to -85°C Not applicable 75% -99%
Plasma -60°C to -85°C Not applicable 75% -99%
Serum -60°C to -85°C Not applicable 75% -99%
Tissue specimen -60°C to -85°C Not applicable 75% -99%


Male

Young adult (18 - 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
cDNA/mRNA -60°C to -85°C Not applicable 75% -99%
Plasma -60°C to -85°C Not applicable 75% -99%
Serum -60°C to -85°C Not applicable 75% -99%
Tissue specimen -60°C to -85°C Not applicable 75% -99%


Female

Adult (> 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
cDNA/mRNA -60°C to -85°C Not applicable 75% -99%
Plasma -60°C to -85°C Not applicable 75% -99%
Serum -60°C to -85°C Not applicable 75% -99%
Tissue specimen -60°C to -85°C Not applicable 75% -99%


Male

Adult (> 40 years)

1 - 10 donors

Material Type Extraction Procedure Storage Temperature Preservation Type Macroscopic Assessment % of Sample Set
cDNA/mRNA -60°C to -85°C Not applicable 75% -99%
Plasma -60°C to -85°C Not applicable 75% -99%
Serum -60°C to -85°C Not applicable 75% -99%
Tissue specimen -60°C to -85°C Not applicable 75% -99%