Clinical Indication ID & Name
Mantle Cell Lymphoma
Test Group
Haematology
Specialties
Test code
M102.1
Test name
t(11;14)(q13;q32) IGH-CCND1 FISH/RT-PCR
Target genes
IGH-CCND1
Test scope
Structural variant detection
Test method/ technology
FISH/Simple targeted variant testing
Optimal Family Structure
n/a
Eligibility Criteria
Molecular assessment will aid diagnosis or management
Test code
M102.2
Test name
CCND1 rearrangement FISH
Target genes
CCND1
Test scope
Structural variant detection
Test method/ technology
FISH
Optimal Family Structure
n/a
Eligibility Criteria
Molecular assessment will aid diagnosis or management
Test code
M102.3
Test name
CCND2 rearrangement FISH
Target genes
CCND2
Test scope
Structural variant detection
Test method/ technology
FISH
Optimal Family Structure
n/a
Eligibility Criteria
Molecular assessment will aid diagnosis or management
Test code
M102.4
Test name
Multi-target NGS panel - structural variant (IGH-CCND1, other CCND1 rearrangements, CCND2)
Target genes
IGH-CCND1, CCND1, CCND2, CCND3
Test scope
Structural variant detection
Test method/ technology
Panel
Optimal Family Structure
n/a
Eligibility Criteria
Molecular assessment will aid diagnosis or management
Test code
M102.5
Test name
Multi-target NGS panel - small variant (TP53)
Target genes
TP53
Test scope
Small variant detection
Test method/ technology
Panel
Optimal Family Structure
n/a
Eligibility Criteria
Patient with MCL who are candidates for intensive treatment including autologous HSCT
Commissioning group
n/a
Overlapping idications
n/a
Address for samples/request forms
Please refer to the test request form.
Contact with queries
Supporting documents
n/a
Education resources
n/a
Service updates
n/a
Request form download
Form not available, please contact us to enquire.
Consent record
See consent guidance in test request form
Sample requirements
Sample Requirements Each sample must be sent labelled with 3 patient identifiers and must state the sample type clearly on the sample container. Sample Rejection Samples may be rejected for the following reasons: 1. Samples and request form do not show at least three identical patient identifiers 2. The sample is in the incorrect collection media 3. The request form is not sufficiently completed 4. The sample is not of sufficient volume 5. The sample is too old