Multiple myeloma: Difference between revisions
(Created page with "'''Multiple myeloma''' (MM), sometimes called '''plasma cell myeloma''', is the most important of the plasma cell dyscrasias. It is characterised by proliferation of genetically abnormal monoclonal plasma cells in the bone marrow, which produce monoclonal paraprotein which leads to organ damage and which can be detected in blood and urine. It’s the second most common haematological malignancy. It mostly affects elderly. Its prognosis used to...") |
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'''Multiple myeloma''' (MM), sometimes called '''plasma cell myeloma''', is the most important of the [[Plasma cell dyscrasia|plasma cell dyscrasias]]. It is characterised by proliferation of genetically abnormal monoclonal plasma cells in the bone marrow, which produce monoclonal paraprotein which leads to organ damage and which can be detected in blood and urine. | <section begin="clinical biochemistry" />'''Multiple myeloma''' (MM), sometimes called '''plasma cell myeloma''', is the most important of the [[Plasma cell dyscrasia|plasma cell dyscrasias]]. It is characterised by proliferation of genetically abnormal monoclonal plasma cells in the bone marrow, which produce monoclonal paraprotein which leads to organ damage and which can be detected in blood and urine. | ||
It’s the second most common haematological malignancy. It mostly affects elderly. Its prognosis used to be poor but nowadays the expected overall survival is >5 years. However, it is still considered incurable. | It’s the second most common haematological malignancy. It mostly affects elderly. Its prognosis used to be poor but nowadays the expected overall survival is >5 years. However, it is still considered incurable. | ||
Sometimes multiple myeloma presents as a solitary tumour, in which case it’s called '''plasmacytoma'''. | Sometimes multiple myeloma presents as a solitary tumour, in which case it’s called '''plasmacytoma'''.<section end="clinical biochemistry" /> | ||
== Clinical features == | == Clinical features == | ||
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* [[Pathological fracture|Pathological fractures]] | * [[Pathological fracture|Pathological fractures]] | ||
* Weight loss | * Weight loss | ||
<section begin="clinical biochemistry" /> | |||
== Diagnosis and evaluation == | == Diagnosis and evaluation == | ||
Multiple myeloma is diagnosed when the following criteria are met: | Multiple myeloma is diagnosed when the following criteria are met: | ||
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** Li – Involved/uninvolved serum free light chain ratio elevated | ** Li – Involved/uninvolved serum free light chain ratio elevated | ||
** M – MRI with >1 focal lesion of bone or bone marrow | ** M – MRI with >1 focal lesion of bone or bone marrow | ||
<section end="clinical biochemistry" /> | |||
Whole body low dose [[Computer tomography|CT]] (WBLD-CT) is the best modality for detection of osteolytic lesions. Following diagnosis, [[bone marrow aspiration and biopsy]] is indicated for genetic testing for risk stratification. | Whole body low dose [[Computer tomography|CT]] (WBLD-CT) is the best modality for detection of osteolytic lesions. Following diagnosis, [[bone marrow aspiration and biopsy]] is indicated for genetic testing for risk stratification. | ||
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* Osteolysis – bisphosphonates, radiotherapy | * Osteolysis – bisphosphonates, radiotherapy | ||
* Pancytopaenia – blood transfusion, G-CSF | * Pancytopaenia – blood transfusion, G-CSF | ||
<section begin="clinical biochemistry" /> | |||
== Complications == | == Complications == | ||
Amyloid light-chain (AL) amyloidosis can occur due to the excessive light-chain production. This can result in cardiomyopathy or kidney disease, among others. Kidney disease can also occur due to excessive filtering of Bence-Jones proteins or due to the effects of hypercalaemia. | Amyloid light-chain (AL) amyloidosis can occur due to the excessive light-chain production. This can result in cardiomyopathy or kidney disease, among others. Kidney disease can also occur due to excessive filtering of Bence-Jones proteins or due to the effects of hypercalaemia. | ||
Infection is a major cause of death in patients with multiple myeloma, partly due to secondary immunodeficiency due to the high level of non-functional immunoglobulins and partly due to side effects of medications. | Infection is a major cause of death in patients with multiple myeloma, partly due to secondary immunodeficiency due to the high level of non-functional immunoglobulins and partly due to side effects of medications.<section end="clinical biochemistry" /> | ||
[[Category:Haematology]] | [[Category:Haematology]] | ||
[[Category:Internal Medicine (POTE course)]] | |||
Latest revision as of 20:27, 26 March 2024
Multiple myeloma (MM), sometimes called plasma cell myeloma, is the most important of the plasma cell dyscrasias. It is characterised by proliferation of genetically abnormal monoclonal plasma cells in the bone marrow, which produce monoclonal paraprotein which leads to organ damage and which can be detected in blood and urine.
It’s the second most common haematological malignancy. It mostly affects elderly. Its prognosis used to be poor but nowadays the expected overall survival is >5 years. However, it is still considered incurable.
Sometimes multiple myeloma presents as a solitary tumour, in which case it’s called plasmacytoma.
Clinical features
Multiple myeloma present subacutely with:
- Anaemia
- Fatigue
- Bone pain
- Pathological fractures
- Weight loss
Diagnosis and evaluation
Multiple myeloma is diagnosed when the following criteria are met:
- >10% of the bone marrow is monoclonal plasma cells
- Presence of a myeloma-defining event (MDE) according to the CRAB SLiM criteria:
- C – Calcium elevation (hypercalcaemia)
- R – Renal insufficiency
- A – Anaemia (normocytic)
- B – Bone lesions
- S – >60% of the bone marrow is monoclonal plasma cells
- Li – Involved/uninvolved serum free light chain ratio elevated
- M – MRI with >1 focal lesion of bone or bone marrow
Whole body low dose CT (WBLD-CT) is the best modality for detection of osteolytic lesions. Following diagnosis, bone marrow aspiration and biopsy is indicated for genetic testing for risk stratification.
Treatment
As MM cannot be cured, the natural history of the disease is characterised by active disease, initiation of treatment, followed by remission which will inevitably relapse at some point, and so on.
The best treatment is high dose chemotherapy followed by autologous SCT, but not all patients are eligible for this treatment. Treatment options include:
- Immunomodulatory drugs (thalidomide, lenalidomide)
- Proteosome inhibitors (bortezomib, carfilzomib)
- Chemotherapy (steroids, alkylating agents, anthracyclines)
- Targeted monoclonal antibodies (daratumumab, elotuzumab)
- HDAC inhibitor (Panobinostat, vorinostat)
Plasmacytoma is managed with surgery or radiotherapy.
Supportive treatment is also important:
- Osteolysis – bisphosphonates, radiotherapy
- Pancytopaenia – blood transfusion, G-CSF
Complications
Amyloid light-chain (AL) amyloidosis can occur due to the excessive light-chain production. This can result in cardiomyopathy or kidney disease, among others. Kidney disease can also occur due to excessive filtering of Bence-Jones proteins or due to the effects of hypercalaemia.
Infection is a major cause of death in patients with multiple myeloma, partly due to secondary immunodeficiency due to the high level of non-functional immunoglobulins and partly due to side effects of medications.