BLYM - Overview: B-Cell Lymphoma, FISH, Tissue (2023)

Useful For

Suggests clinical disorders or settings where the test may be helpful

Detecting a neoplastic clone associated with the common chromosome abnormalities seen in patients with various B-cell lymphomas

Tracking known chromosome abnormalities and response to therapy in patients with B-cell lymphomas

Reflex Tests

Lists tests that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial tests.

Test Id Reporting Name Available Separately Always Performed
_PRAA Probe, Each Additional (BLYM) No, (Bill Only) No

Testing Algorithm

Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

Depending on the lymphoma subtype suspected, the most appropriate probes to order are listed in the table: Common Chromosome Abnormalities in B-cell Lymphomas in Clinical Information.

If the patient is being tracked for known abnormalities, indicate which probes should be used.

A charge and CPT code is applied for each probe set hybridized, analyzed, and reported.

If, based on testing algorithms, results of the initial probe sets require reflex testing, complete results will be available within 10 days.

The following algorithms are available:

-Aggressive B-cell Lymphoma Diagnostic Algorithm

-Gastric MALT Lymphoma Diagnostic Algorithm

-Gastric MALT Posttherapy Follow-up Algorithm

Special Instructions

Library of PDFs including pertinent information and forms related to the test

  • Aggressive B-cell Lymphoma Diagnostic Algorithm
  • Gastric MALT Posttherapy Follow-up Algorithm
  • Gastric MALT Lymphoma Diagnostic Algorithm

Method Name

A short description of the method used to perform the test

Fluorescence In Situ Hybridization (FISH)

NY State Available

Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name

Lists a shorter or abbreviated version of the Published Name for a test

B-cell Lymphoma, FISH, Tissue

Aliases

Lists additional common names for a test, as an aid in searching

BLYM

BCL2 (18q21) rearrangement

BCL6 (3q27) rearrangement

Burkitt lymphoma

Burkitt-like lymphoma

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Diffuse Large Cell Lymphoma/"Double Hit"

Follicular lymphoma

Large BCL with IRF4 rearranged

MALT (18q21) rearrangement

MALT lymphoma

Mantle Cell Lymphoma (MCL)

MYC (8q24.1) rearrangement

t(11;14) (q13;q32) - CCND1/IGH

t(2;8)(p12;q24) - IGK/MYC

t(8;14) (q24.1;q32) - MYC/IGH

IRF4

DUSP22

TNFRSF14

1p36

t(8;22) (q24.1;q11.2) - MYC/IGL

CCND2 (12p13.32) rearrangement

MYC/Kappa or MYC/Lambda

Splenic Marginal Zone Lymphoma (SMZL)

Testing Algorithm

Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

Depending on the lymphoma subtype suspected, the most appropriate probes to order are listed in the table: Common Chromosome Abnormalities in B-cell Lymphomas in Clinical Information.

If the patient is being tracked for known abnormalities, indicate which probes should be used.

A charge and CPT code is applied for each probe set hybridized, analyzed, and reported.

If, based on testing algorithms, results of the initial probe sets require reflex testing, complete results will be available within 10 days.

The following algorithms are available:

-Aggressive B-cell Lymphoma Diagnostic Algorithm

-Gastric MALT Lymphoma Diagnostic Algorithm

-Gastric MALT Posttherapy Follow-up Algorithm

Specimen Type

Describes the specimen type validated for testing

Tissue

Ordering Guidance

This test does not include a pathology consultation. If a pathology consultation is desired, PATHC / Pathology Consultation should be ordered and the appropriate fluorescence in situ hybridization (FISH) test will be ordered and performed at an additional charge. Mayo Hematopathology Consultants are involved in both the pre-analytic (tissue adequacy and probe selection, when applicable) and post-analytic (interpretation of FISH results in context of specific case, when applicable) phases.

This assay detects chromosome abnormalities observed in paraffin-embedded tissue samples of patients with B-cell lymphoma. If a blood or bone marrow specimen is submitted, the test will be canceled and BLPMF / B-Cell Lymphoma, Specified FISH, Varies will be added and performed as the appropriate test.

If either the break-apart MYC or the MYC/IGH D-FISH probe sets are requested in isolation, both probe sets will be performed concurrently to optimize the detection of MYC rearrangements.

Shipping Instructions

Advise Express Mail or equivalent if not on courier service.

Necessary Information

1. A reason for testing and pathology report are required for testing to be performed. Send information with specimen. Acceptable pathology reports include working drafts, preliminary pathology or surgical pathology reports. The laboratory will not reject testing if a reason for testing is not provided; however, appropriate testing and interpretation may be compromised or delayed. If not provided, an appropriate indication for testing may be entered by Mayo Clinic Laboratories.

2. If the patient is being tracked for known abnormalities, an indication of which probes should be used is required for testing to be performed. See Table in Clinical Information.

ORDER QUESTIONS AND ANSWERS

Question ID Description Answers
GC026 Reason for Referral

Specimen Required

Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Submit only 1 of the following specimens:

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Specimen Type: Tissue

Preferred: Tissue block

Collection Instructions: Submit a formalin-fixed, paraffin-embedded (FFPE) tumor tissue block. Blocks prepared with alternative fixation methods may be acceptable; provide fixation method used.

Additional Information:

1. Paraffin embedded specimens can be from any anatomic location (skin, soft tissue, lymph node, etc).

2. Bone specimens that have been decalcified will be attempted for testing, but the success rate is approximately 50%.

Acceptable: Tissue slides

Collection Instructions: For each probe set ordered, 2 consecutive, unstained, 5 micron-thick sections placed on positively charged slides. Include 1 hematoxylin and eosin-stained slide for the entire test order.

Special Instructions

Library of PDFs including pertinent information and forms related to the test

  • Aggressive B-cell Lymphoma Diagnostic Algorithm
  • Gastric MALT Posttherapy Follow-up Algorithm
  • Gastric MALT Lymphoma Diagnostic Algorithm

Forms

If not ordering electronically, complete, print, and send a Hematopathology/Cytogenetics Test Request (T726) with the specimen.

Specimen Minimum Volume

Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

See Specimen Required

Reject Due To

Identifies specimen types and conditions that may cause the specimen to be rejected

All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.

Specimen Stability Information

Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Tissue Ambient (preferred)
Refrigerated

Useful For

Suggests clinical disorders or settings where the test may be helpful

Detecting a neoplastic clone associated with the common chromosome abnormalities seen in patients with various B-cell lymphomas

Tracking known chromosome abnormalities and response to therapy in patients with B-cell lymphomas

Testing Algorithm

Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

Depending on the lymphoma subtype suspected, the most appropriate probes to order are listed in the table: Common Chromosome Abnormalities in B-cell Lymphomas in Clinical Information.

If the patient is being tracked for known abnormalities, indicate which probes should be used.

A charge and CPT code is applied for each probe set hybridized, analyzed, and reported.

If, based on testing algorithms, results of the initial probe sets require reflex testing, complete results will be available within 10 days.

The following algorithms are available:

-Aggressive B-cell Lymphoma Diagnostic Algorithm

-Gastric MALT Lymphoma Diagnostic Algorithm

-Gastric MALT Posttherapy Follow-up Algorithm

Clinical Information

Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

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Mature B-cell lymphoma can be low grade, intermediate grade, or high grade, and the prognosis and clinical course are highly variable. Genetic abnormalities have emerged as one of the most important prognostic markers in B-cell lymphomas and can aid in diagnosis. Several chromosome abnormalities and variants of these abnormalities have been associated with various lymphoma subtypes (see Table). Fluorescence in situ hybridization (FISH) permits the detection of recurrent gene rearrangements associated with various chromosome translocations and inversions in B-cell lymphoma. FISH is available for the specific B-cell lymphoma subtypes; see Table.

Table. Common Chromosome Abnormalities in B-cell Lymphomas

Lymphoma type

Chromosome abnormality

FISH probe

Burkitt (pediatric,

< or =18 years old)

8q24.1 rearrangement

5'/3' MYC

t(2;8)(p12;q24.1)

IGK/MYC

t(8;14)(q24.1;q32)

MYC/IGH

t(8;22)(q24.1;q11.2)

MYC/IGL

3q27 rearrangement

3'/5' BCL6

18q21 rearrangement

3'/5' BCL2

Diffuse large B-cell, "double-hit"

8q24.1 rearrangement

5'/3' MYC

t(8;14)(q24.1;q32)

MYC/IGH

----Reflex: t(8;22)(q24.1;q11.2)

MYC/IGL

----Reflex: t(2;8)(p12;q24.1)

IGK/MYC

----Reflex: 3q27 rearrangement

3'/5' BCL6

----Reflex: 18q21 rearrangement

3'/5' BCL2

Large BCL IRF4 rearranged

6p24.3 rearrangement

5’/3' IRF4

18q21 rearrangement

3'/5' BCL2

3q27 rearrangement

3'/5' BCL6

Follicular

18q21 rearrangement

3'/5' BCL2

3q27 rearrangement

3'/5' BCL6

Predominantly diffuse subtype only: deletion of 1p36

TNFRSF14/1q22

Mantle cell

t(11;14)(q13;q32)

CCND1/IGH

11q13 rearrangement

5'/3' CCND1

Blastoid subtype only: deletion of 17p

TP53/D17Z1

Blastoid subtype only: 8q24.1 rearrangement

5'/3' MYC

Cyclin D1-negative subtype only: 12p13.32 rearrangement

5'/3' CCND2

MALT

18q21 rearrangement

5'/3' MALT1

Splenic marginal zone

Deletion of 7q

D7Z1/7q32

Deletion of 17p

TP53/D17Z1

Reference Values

Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

An interpretive report will be provided.

Interpretation

Provides information to assist in interpretation of the test results

A neoplastic clone is detected when the percent of cells with an abnormality exceeds the normal reference range for any given probe.

Detection of an abnormal clone is supportive of a diagnosis of a B-cell lymphoma. The specific abnormality detected may help subtype the neoplasm.

The absence of an abnormal clone does not rule out the presence of a neoplastic disorder.

Cautions

Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

This test is not approved by the US Food and Drug Administration, and it is best used as an adjunct to clinical and pathologic information.

Fixatives other than formalin (eg, Prefer, Bouin) may not be successful for fluorescence in situ hybridization assays.

Bone specimens that have been decalcified will be attempted for testing, but the success rate is approximately 50%.

Supportive Data

Each probe was independently tested on a set of formalin-fixed, paraffin-embedded tissue specimens from patients diagnosed with a B-cell lymphoma and noncancerous lymph node specimens. Normal cutoffs were calculated based on the results from 25 normal specimens. For each probe set, a series of chromosomally abnormal specimens were evaluated to confirm each probe set detected the anomaly it was designed to detect.

Clinical Reference

Recommendations for in-depth reading of a clinical nature

Swerdlow SH, Campo E, Harris NL, eds, et al: WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. 4th ed. IARC; 2017. WHO Classification of Tumours. Vol 2

Special Instructions

Library of PDFs including pertinent information and forms related to the test

  • Aggressive B-cell Lymphoma Diagnostic Algorithm
  • Gastric MALT Posttherapy Follow-up Algorithm
  • Gastric MALT Lymphoma Diagnostic Algorithm

Method Description

Describes how the test is performed and provides a method-specific reference

This test is performed using either commercially available or laboratory-developed probes. Rearrangements involving MYC, BCL2, BCL6, CCND1, CCND2, IRF4, or MALT1 are detected using dual-color break-apart (BAP) strategy probes, translocations involving MYC, or CCND1 are identified using dual-color, dual-fusion (D-FISH) strategy probes, and deletions (7q32, TNFRSF14 (1p36), and TP53) using enumeration strategy probes.

IGH/BCL2 is detected using a dual color, dual fusion probe set. At the laboratory’s discretion, the IGH/BCL2 probe will be performed when necessary to resolve or confirm BCL2 rearrangement concerns.

Formalin-fixed, paraffin-embedded tissues are cut at 5 microns and mounted on positively charged glass slides. The selection of tissue and the target areas on the hematoxylin and eosin (H and E)-stained slide is performed by a pathologist. Using the H and E-stained slide as a reference, target areas are etched with a diamond-tipped etcher on the back of the unstained slide to be assayed. The probe set is hybridized to the appropriate target areas and 2 technologists each analyze 50 interphase nuclei (100 total) with the results expressed as the percent abnormal nuclei.(Unpublished Mayo method)

PDF Report

Indicates whether the report includes an additional document with charts, images or other enriched information

No

Day(s) Performed

Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Monday through Friday

Report Available

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The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

4 to 10 days

Specimen Retention Time

Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

Slides and H and E used for analysis are retained by the laboratory in accordance with CAP and NYS requirements. Client provided paraffin blocks and extra unstained slides (if provided) will be returned after testing is complete.

Performing Laboratory Location

Indicates the location of the laboratory that performs the test

Rochester

Fees

Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

  • Authorized users can sign in to Test Prices for detailed fee information.
  • Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
  • Prospective clients should contact their account representative. For assistance, contact Customer Service.

Test Classification

Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.

88377 (if 1 probe set)

88377 x 2 (if 2 probe sets)

88377 x 3 (if 3 probe sets)

88377 x 4 (if 4 probe sets)

88377 x 5 (if 5 probe sets)

88377 x 6 (if 6 probe sets)

LOINC® Information

Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test Id Test Order Name Order LOINC Value
BLYM B-cell Lymphoma, FISH, Tissue 101651-8
Result Id Test Result Name Result LOINC Value

Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.

603063 Result Summary 50397-9
603064 Interpretation 69965-2
603065 Result Table 93356-4
603066 Result 62356-1
GC026 Reason for Referral 42349-1
603067 Specimen 31208-2
603068 Source 85298-8
603069 Tissue ID 80398-1
603070 Method 85069-3
603071 Additional Information 48767-8
603072 Disclaimer 62364-5
603073 Released By 18771-6

Test Setup Resources

Setup Files

Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | PHP Pdf | CMS Pdf

Sample Reports

Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports

International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports

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FAQs

What is the most aggressive B-cell lymphoma? ›

Less common forms of B-cell lymphoma include: Burkitt lymphoma: Considered the most aggressive form of lymphoma, this disease is one of the fastest growing of all cancers.

What is the survival rate for B-cell lymphoma? ›

What are survival rates for diffuse large B-cell lymphoma? According to the National Cancer Institute, 64.6% of people with DLBCL are alive five years after diagnosis. (Relative survival rates are estimates based on large groups of people.)

How aggressive is B-cell lymphoma? ›

Burkitt Lymphoma

This aggressive B-cell subtype grows and spreads very quickly. It may involve the jaw, bones of the face, bowel, kidneys, ovaries, bone marrow, blood, central nervous system (CNS) and other organs.

What does FISH mean in lymphoma? ›

Fluorescence in situ hybridization (FISH) is a sensitive method to detect smaller genomic changes associated with various hematological malignancies and solid tumors.

Which B-cell lymphoma has the best prognosis? ›

Of the 2 most common types of B-cell lymphoma, follicular lymphoma generally has a better prognosis than diffuse large B-cell lymphoma (DLBCL). Anaplastic large cell lymphoma and cutaneous T-cell lymphoma are 2 subtypes of T-cell lymphoma that have a fairly good prognosis.

What is the survival rate of large B-cell lymphoma stage 4? ›

Stage 4 non-Hodgkin's diffuse large B-cell lymphoma has a five-year relative survival rate of 57%15. Stage 4 non-Hodgkin's follicular lymphoma has a five-year relative survival rate of 86%15. Stage 4 Hodgkin's lymphoma has a five-year relative survival rate of 82%16.

How fast does large B-cell lymphoma spread? ›

They usually grow quite quickly, over just a few weeks. Sometimes, DLBCL can develop in lymph nodes deep inside your body where they can't be felt from the outside. The swollen nodes can form large lumps – known as 'bulky disease'. DLBCL can also develop outside lymph nodes, called 'extranodal' disease.

What is the current treatment for B-cell lymphoma? ›

B-cell lymphoma treatment

These options include chemotherapy, radiation therapy, proton therapy, immunotherapy and stem cell transplantation.

Does B-cell lymphoma have stages? ›

The 4 stages of DLBCL. Staging describes how far lymphoma has spread. Keep in mind that even the most advanced stages of diffuse large B-cell lymphoma (DLBCL) (Stage III and Stage IV) are common and can be treated.

Why do people get B-cell lymphoma? ›

These conditions occur when the immune system attacks healthy tissue, such as in rheumatoid arthritis. These conditions may cause an elevated risk for developing b-cell lymphoma. Infections. Infections, such as the Epstein-Barr virus has been linked to higher rates of b-cell lymphoma.

How does B-cell lymphoma start? ›

Doctors don't know what causes most B-cell lymphomas. These cancers begin when lymphocytes start to grow out of control. Usually, your body makes new lymphocytes only when you need them to replace old cells that have died. In B-cell lymphoma, lymphocytes grow when you don't need them.

Does B-cell lymphoma go to the brain? ›

Primary diffuse large B-cell lymphoma (Bcl) of the central nervous system (CNS) is a rare tumor of the brain and spinal cord, which has been estimated to account for ≤1% of all lymphomas, 4–6% of all extranodal lymphomas and ~1–3% of primary CNS tumors (1–3).

What does a positive FISH test mean? ›

FISH testing usually returns one of two results: positive or negative. Positive means your breast cancer cells make too much HER2 and your doctor should treat you with drugs that target that protein. Negative means the protein isn't involved in the growth of your tumor.

How do I read my FISH test results? ›

IHC stain results:
  1. 0 or 1+, HER2-negative, indicates a cancer that may not respond to medicines targeting that protein.
  2. 2+, Uncertain, means FISH testing may be needed to get a better reading.
  3. 3+, HER2-positive, signals a cancer that will likely be treated with HER2 drugs.

What organ is lymphoma? ›

Lymphoma is a cancer of the lymphatic system, which is part of the body's germ-fighting network. The lymphatic system includes the lymph nodes (lymph glands), spleen, thymus gland and bone marrow. Lymphoma can affect all those areas as well as other organs throughout the body.

What is the 10 year survival rate for B-cell lymphoma? ›

Overall survival

OS according to IPI and R-IPI category is shown in Fig. 1; OS rates are shown in Table V. Among patients classified as having an IPI 'low risk', 80% were alive at 10 years; the 10-year OS rates in the 'low-intermediate', 'high-intermediate', and 'high-risk' groups were 60, 43, and 30%, respectively.

What type of B-cell lymphoma is rare? ›

Mantle cell lymphoma is a rare type of B cell non-Hodgkin lymphoma (NHL).

What is the best treatment for large B-cell lymphoma? ›

Chemotherapy is the main way to treat most types of B-cell lymphoma. You can get this on its own, or combine it with radiation or immunotherapy. Chemo uses drugs to kill fast-dividing cells in your body, including cancer cells. You get this medicine through a vein (IV), or you take it as a pill by mouth.

How bad is stage 4 B-cell lymphoma? ›

Stage 4 lymphoma means that cancer has spread to an organ external to the lymphatic system. The survival rates vary widely depending on an individual's risk factors and type of cancer. The survival rate of stage 4 lymphoma is lower than that of the other stages, but doctors can cure the condition in some cases.

How long can you live with large B-cell lymphoma? ›

Approximately 74% of patients with a localized stage of DLBCL survive 5 years, whereas 73% of those with a regional stage and 57% of those with a distant stage survive 5 years. For all SEER stages combined, the 5-year survival rate is 64%.

Can you recover from B-cell lymphoma? ›

Survival rates continue to improve as researchers identify more effective treatments. Approximately 65% of people diagnosed with the most common form of B-cell lymphoma are alive five years after diagnosis and considered cured.

Where does B-cell lymphoma spread? ›

In B-cell lymphoma, some lymphocytes are no longer healthy and do not fight infection. Instead, they grow out of control, crowding out the normal cells and causing the lymph nodes to get bigger. As the disease advances, it may spread to the bone marrow, central nervous system, liver, spleen and reproductive organs.

Where does large B-cell lymphoma start? ›

Diffuse large B-cell lymphoma, or DLBCL, is a cancer that starts in white blood cells called lymphocytes. It usually grows in lymph nodes -- the pea-sized glands in your neck, groin, armpits, and elsewhere that are part of your immune system. It can also show up in other areas of your body.

Where does large B-cell lymphoma spread? ›

Some types of lymphoma (including DLBCL) are more likely to spread to the brain and spinal cord (central nervous system). If there is a high risk of your lymphoma spreading to your central nervous system, your doctor might want you to have treatment to prevent this.

How many rounds of chemo for B-cell lymphoma? ›

The most widely used treatment for DLBCL presently is the combination known as R-CHOP (rituximab [Rituxan], cyclophosphamide [Cytoxan], doxorubicin [Adriamycin], vincristine [Oncovin], and prednisone) The R-CHOP regimen is usually given in 21-day cycles (once every 21 days) for an average of 6 cycles.

What is the second line treatment for large B-cell lymphoma? ›

Occasionally, a patient will undergo an allogeneic transplant (patient receives stem cells from a donor). For those relapsed/refractory patients combination chemotherapy regimens are available. These second-line regimens include: ifosfamide, carboplatin, and etoposide (ICE)

What happens if you don't treat B-cell lymphoma? ›

You may wonder about the impact on your long-term health if you delay treatment. But studies show that for people with slow-growing types of B-cell lymphoma, there is no difference in the way the disease develops between immediate treatment and watchful waiting.

What is the progression of large B-cell lymphoma? ›

Stages of DLBCL

Stage 1: The cancer affects only one area — either a single organ or a single cluster of lymph nodes. Stage 2: The cancer affects two or more areas on the same side of the diaphragm. Stage 3: The cancer affects areas on both sides of the diaphragm.

Does B-cell lymphoma metastasis? ›

One of the most serious complications for a patient with diffuse large B-cell lymphoma who presents with disease outside the central nervous system (CNS) is the development of CNS metastasis. This usually involves the cerebrospinal fluid and meninges, but solid parenchymal brain metastasis can also occur.

Can B-cell lymphoma be caused by Covid? ›

Conclusion: We describe an uncommon case of COVID-19 who was finally diagnosed with B-cell lymphoma. An awareness of persistent fever and declined routine blood tests caused by hematological malignancies instead of COVID-19 itself can aid in providing appropriate guidelines for management and treatment.

What is another name for B-cell lymphoma? ›

Most B-cell lymphomas are non-Hodgkin lymphomas. There are many different types of B-cell non-Hodgkin lymphomas. These include Burkitt lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), diffuse large B-cell lymphoma, follicular lymphoma, and mantle cell lymphoma.

Which virus causes B-cell lymphoma? ›

Two oncogenic herpesviruses infect B cells and cause B cell lymphomas: EBV and KSHV. Individuals with HIV infection are at a greatly increased risk of lymphoma development, and these more frequently contain an oncogenic herpesvirus.

Can B-cell lymphoma be benign? ›

Many of the cells found in benign lymphomas are B cells, so rituximab may help reduce or eliminate symptoms. In rare cases, benign lymphomas may grow back after being treated.

What are the 3 B symptoms of lymphoma? ›

These three symptoms, called B symptoms, are also symptoms of lymphoma:
  • high fever (38°C or higher)
  • weight loss of a tenth or more of your previous weight over the past 6 months, when you haven't been trying to lose weight.
  • night sweats which drench your nightclothes and bedding.

What are the symptoms of large B-cell lymphoma? ›

Diffuse large B-cell lymphoma (DLBCL) symptoms
  • pain in the chest or stomach area (abdomen)
  • bone pain.
  • skin lumps.
  • coughing or breathlessness.

Does B-cell lymphoma cause hair loss? ›

Both treatments for lymphoma and the cancer itself can cause a person to lose clumps or all of their hair. Although hair usually grows back after treatment, it can be upsetting to experience hair loss while living with lymphoma.

How often does B-cell lymphoma return? ›

ABSTRACT. Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin lymphoma. Approximately 30% to 40% of patients will develop relapsed/refractory (R/R) DLBCL, leading to significant morbidity and mortality.

Can B-cell lymphoma spread to the lungs? ›

Lungs can be involved in up to 40% patients of non-Hodgkin lymphoma (mostly secondarily); Diffuse large B-cell lymphoma and lymphoblastic lymphoma are the commonest high grade NHLs that involve lungs, mucosa associated lymphoid tissue (MALT) lymphoma is the commonest low grade NHL that involve lungs [4, 5].

Is a FISH test 100% accurate? ›

FISH analysis offers a PPV of 83% and NPV of 81% when evaluating a single blastomere in conjunction with PGD. FISH errors and mosaicism are primarily responsible for the errors associated with FISH analysis in PGD.

How accurate are FISH results? ›

Accuracy and limitations. Prenatal interphase FISH testing is highly accurate, with reported false-positive and -negative rates usually less than 1%. The main problem, however, is that not all specimens are informative. Uninformative rates will vary among laboratories, but rates of 3% to 10% are considered typical.

Are FISH test results accurate? ›

The FISH test results will tell you that the cancer is either “positive” or “negative” (a result sometimes reported as “zero”) for HER2. Generally, the FISH test is not as widely available as another method of HER2 testing, called ImmunoHistoChemistry, or IHC. However, FISH is considered more accurate.

What does an abnormal FISH test mean? ›

But if abnormalities are found after treatment during another round of testing, it means that patient has residual disease and has a high risk of the cancer coming back.

What is the FISH test for non Hodgkin's lymphoma? ›

The non-Hodgkin lymphoma FISH panel detects IGH gene translocations or rearrangements involving the 14q32 locus. Included in this group are follicular lymphoma (FL), Burkitt Lymphoma (BL), and diffuse large B-cell lymphoma (DLBCL).

What are the codes for a FISH test? ›

CPT(s)
DescriptionCPT Code
FISH DNA Probe88271
FISH Intrp & Report Part B88291
In Situ Hybridization, Interphase, BM or Blood88275
Blood Culture88230
2 more rows

What foods to avoid if you have lymphoma? ›

Foods to skip or cut back on include:
  • Animal fats like fatty meats, processed meats, lard and butter.
  • Sugar, including added sugars in desserts, sweetened drinks and processed foods.
  • White, refined grains like white bread, pasta and rice.
Feb 6, 2023

What is the most curable lymphoma? ›

Hodgkin lymphoma is one of the most curable forms of cancer. After treatment is complete, your care team will develop a survivorship plan that minimizes long-term side effects of treatment. Those risks include infertility, secondary cancers or toxicities to vital organs such as the heart and lungs.

Where does lymphoma spread to first? ›

The first sign of Hodgkin lymphoma is often a swollen lymph node that appears without a known cause. The disease can spread to nearby lymph nodes. Later it may spread to the spleen, liver, bone marrow, or other organs.

Is aggressive B-cell lymphoma curable? ›

Survival rates continue to improve as researchers identify more effective treatments. Approximately 65% of people diagnosed with the most common form of B-cell lymphoma are alive five years after diagnosis and considered cured.

What is stage 4 large B-cell lymphoma? ›

Stage 4: The cancer has spread to surrounding organs or tissues such as the lungs, liver, or bone marrow.

Is large B-cell lymphoma fatal? ›

Diffuse large B-cell lymphoma (DLBCL) is the most common lymphoma, representing approximately 30% of non-Hodgkin lymphomas (NHLs), and it is rapidly fatal if untreated.

Can you survive large B-cell lymphoma? ›

Diffuse large B cell lymphoma (DLBCL) is the most common type of high grade lymphoma. Generally for people with DLBCL: 60 in 100 people (60%) will survive 5 years or more after their diagnosis.

How fast does B-cell lymphoma spread? ›

Symptoms can start or get worse in just a few weeks. The most common symptom is one or more painless swellings. These swellings can grow very quickly.

How do you beat B-cell lymphoma? ›

Chemotherapy is the main way to treat most types of B-cell lymphoma. You can get this on its own, or combine it with radiation or immunotherapy. Chemo uses drugs to kill fast-dividing cells in your body, including cancer cells. You get this medicine through a vein (IV), or you take it as a pill by mouth.

At what stage is lymphoma terminal? ›

Stage 4 is the most advanced stage of lymphoma. Lymphoma that has started in the lymph nodes and spread to at least one body organ outside the lymphatic system (for example, the lungs, liver, bone marrow or solid bones) is advanced lymphoma.

How many stages are there in B-cell lymphoma? ›

The 4 stages of DLBCL. Staging describes how far lymphoma has spread. Keep in mind that even the most advanced stages of diffuse large B-cell lymphoma (DLBCL) (Stage III and Stage IV) are common and can be treated.

What are the signs of end stage lymphoma? ›

Symptoms towards the end of life
  • loss of appetite.
  • fatigue and drowsiness.
  • changes in breathing.
  • confusion.
  • withdrawal and loss of interest.
  • feeling cold.
  • loss of bladder and bowel control (incontinence)
  • pain.
Oct 31, 2022

What are the stages of large B-cell lymphoma? ›

Stage 1: The cancer affects only one area — either a single organ or a single cluster of lymph nodes. Stage 2: The cancer affects two or more areas on the same side of the diaphragm. Stage 3: The cancer affects areas on both sides of the diaphragm.

What are the complications of large B-cell lymphoma? ›

Diffuse large B-cell lymphoma (DLBCL) treatment side effects
  • feeling achy.
  • hair loss (alopecia)
  • frequent watery poos (diarrhoea)
  • difficulty pooing (constipation)
  • extreme tiredness (fatigue)
  • infections.
  • loss of appetite.
  • bruising.

Are there stages in large B-cell lymphoma? ›

The treatment your medical team recommends for you depends on the stage of your lymphoma and the signs and symptoms you have. Stage 1 or stage 2 DLBCL is known as 'early-stage' lymphoma. Stage 3 or stage 4 DLBCL is known as 'advanced-stage' lymphoma. Most people have advanced stage DLBCL when they are diagnosed.

Can B-cell lymphoma go into remission? ›

When your doctor says, "You're in remission," it's a major milestone in the treatment of your B-cell lymphoma. It means your cancer is no longer active or it has disappeared.

What is the standard treatment for large B-cell lymphoma? ›

The most widely used treatment for DLBCL presently is the combination known as R-CHOP (rituximab [Rituxan], cyclophosphamide [Cytoxan], doxorubicin [Adriamycin], vincristine [Oncovin], and prednisone) The R-CHOP regimen is usually given in 21-day cycles (once every 21 days) for an average of 6 cycles.

What is the prognosis for large B-cell lymphoma without treatment? ›

DLBCL is an aggressive hematologic malignancy and patients diagnosed with DLBCL have an average lifespan of less than 1 year without treatment. However, as recent studies show, with newer and improved therapy options the survival rates are much better than before in older DLBCL patients [11].

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4. Winship Grand Rounds February 7, 2018: Jonathon B. Cohen, MD, MS
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