Multiple myeloma Flashcards

1
Q

What is multiple myeloma?

A

neoplastic monoclonal proliferation of bone marrow plasma cells resulting in excessive monoclonal immuboglobulin production

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2
Q

What are RF for multiple myeloma?

A
  1. MGUS
  2. Abnormal free light-chain ratio
  3. Age >70
  4. Afrocaribbeans
  5. Ionising radiation
  6. Agricultural work
  7. HIV
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3
Q

What are symptoms and signs of multiple myeloma?

A
  1. High calcium
  2. Renal failure
  3. Anaemia (60-70% patients)
  4. Bone lesions (60-70% mostly in back)
    - CRAB
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4
Q

What is differential diagnosis for multiple myeloma?

A
  1. MGUS
  2. Solitary plasmacytoma
  3. Amyloidosis
  4. Heavy chain disease
  5. NHL
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5
Q

What bloods would you do for multiple myeloma?

A
  1. ESR
  2. CRP
  3. Urea
  4. Creatinine
  5. Normal ALP
  6. Serum Calcium
  7. FBC
  8. Albumin
  9. Serum beta4-microglobulin
  10. blood film
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6
Q

What would ESR be in multiple myeloma?

A

high

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7
Q

What would serum calcium be in multiple myeloma?

A

hyper in 30%

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8
Q

What does blood film show in multiple myeloma?

A

rouleaux formation

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9
Q

What special tests are done for multiple myeloma?

A
  1. Whole-body lost dose CT
  2. Skeletal survey
  3. Serum free light-chain assay
  4. Bone marrow aspirate and biopsy
  5. Serum/urine electrophoresis
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10
Q

What test is diagnostic for multiple myeloma?

A

Serum/urine electrophoresis:

  • serum paraprotein (IgG or IgA)
  • Urinary Bence Jones proteins
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11
Q

What does bone marrow aspirate and biopsy show in multiple myeloma?

A

monoclonal plasma cell infiltration in the bone marrow ≥10%

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12
Q

What is treatment for acute multiple myeloma transplant candidate?

A
  • 1st line: Induction therapy
  • Plus: DVT prophylaxis and SCT
  • Adjunct: Stem cell mobilisation and conditioning regimen and supportive care
  • Bone disease: bisphosphonates or denosumab and analgesics
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13
Q

What is acute management for multiple myeloma non-transplant candidate?

A
  • 1st line: non transplant therapy
  • Plus: DVT prophylaxis
  • Adjunct: analgesics
  • Bone disease: bisphosphonates or denosumab and analgesics
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14
Q

What is chronic treatment for multiple myeloma?

A

1ST LINE: Maintenance strategies

DVT prophylaxis and supportive care

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15
Q

What are possible complications ofr multiple myeloma?

A
  1. Bone pain
  2. Fractures of vertebral bodies
  3. Hypercalcaemia
  4. Anaemia
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16
Q

What staging system is used in multiple myeloma?

A

Durie and Salmon staging system

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17
Q

What does the high calcium in MM lead to?

A

bones, stones, abdominal groans

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18
Q

How common is renal failure in MM and what does it mean?

A

20% and worse prognosis

19
Q

Why is there anaemia in MM?

A

Anaemia due to bone marrow crowing and production of monoclonal Ig also crowds out production of normal polyclonal Ig so recurrent infections

20
Q

Why are there bone lesions in MM?

A

increased osteoclast activation so back/rib pain

21
Q

What happens in MM with which cells?

A
  1. Proliferation of plasma cells

2. Production of a monoclonal immunoglobin (IgG or IgA) – not polyclonal like normal

22
Q

Why is ALP important in MM?

A

normal in MM but high in blood cancers so good to differentiate

23
Q

What would you see is serum/urine electrophoresis in MM?

A

Urinary Bence Jones proteins

24
Q

How does rouleaux formation actually look like on blood film?

A

RBC stacked up like coins

25
What does bone arrow aspirate show on MM?
plasma cells bone marrow ≥10%
26
What does MGUS stand for?
monoclonal gammopathy of unknown significance
27
What is MGUS?
premalignant condition with accumulation of some monoclonal plasma cells
28
What can MGUS lead to?
1% acquire additional mutations so can lead to multiple myeloma
29
What is absent if MGUS but present in MM?
ABSENT CRAB features
30
Why is there renal failure in MM?
- cast nephropathy | - due to high Serum free light chains and Bence jones proteinuria
31
How does cast nephropathy happen?
1. FLCs activate inflammatory mediators in the proximal tubule epithelium leads to proximal tubule necrosis 2. Fanconi syndrome (renal tubules acidosis) with FLC crystal deposition
32
What may you see on x ray for MM?
punched out lesions
33
What may be seen in special tests?
M spike or paraprotein
34
Why is there an M spike in MM?
Produce excess of monoclonal (kappa or lamda) serum free light chains)
35
What are urinary bence jones?
urine monoclonal free light chains
36
What would blood results be in MM?
1. Macroctyic anaemia 2. Low reticulocytes, low WBC, low lymphocytes, low neutrophils and low platelets 3. High ESR 4. High creatinine 5. low albumin 6. high globulins 7. high Ca
37
What is paraprotein and immune paresis?
1. Paraprotein: monoclonal excess of intact Ig molecule | 2. Immune paresis: get lower levels of other Ig e.g. lower IgA and IgM
38
How do you manage the cord compression?
MRI scan and dexamethasone
39
How may hypercalcaemia present?
drowsiness, constipation, fatigue, muscle weakness, AKI
40
What is the management for hypercalcaemia?
fluids, steroid, zolendronic acid
41
What medications can be used in MM?
1. Steroids 2. Classic cystostatic drugs e.g. melphalan 3. IMIDs 4. MoAbs i.e. daratumumab 5. Proteasome inhibitors (velcade)
42
What are examples of IMIDs?
(immunomodulatory drugs): e.g. thalidomide (teratogenic), lenalidomide, pomalidomide
43
How does an autologous haematopoetic stem cell transplant work?
1. Stem cell collection from the blood and storage 2. High dose melphalan to kill myeloma cells 3. Re-infusion of stem cells to rescue blood formation
44
What blood test should you not forget for MM and why?
Sometimes only sign of myeloma is light chains!