Bone Marrow Transplant Flashcards

1
Q

What is the main reason why Stem Cell transplants are needed

Why is Chemotherapy alone not sufficient?

A

To limit toxic effects, Chemotherapy generally limited to 4-6 cycles

This might not be enough to cure leukaemia

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2
Q

At what disease point is the survival prognosis after Stem-cell transplant best?

A

Generally, the earlier the better

(Best survival outcomes, with patients in full remission)

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3
Q

What role does the genomic makeup play in Stem cell transplantation?

A

The more aggressive the disease/ the worse the prognosis, the earlier the transplant is dersirable
Generally earlier transplantation is desirable

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4
Q

How is a Haematological stem cell donor chosen?

A
  • HLA types
  • Ideally sibling (1/4 chance of matching)
  • volunteer unrelated donor/ minimally mismatched family member
  • Now: haploidentical family member can donate aswell
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5
Q

What is an Autologous Haematological stem cell transplant?

A
  • Self-cells (generally frozen from patient when in remission
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6
Q

In which situations is autologous stem cells transplant is used?

A
  • Acute Luekaemias
  • solid tumours (e.g. germ cell)
  • autoimmune disease

Also in
* myeloma (as elderly bad with graft vs host disease) –> buys time and QOL
* Lymphoma (often BM sparring, especially High Grade)
* CLL (but not preferred) - same as Myeloma

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6
Q

Explain the Process of Allogenic Stem Cell Transplant

A
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7
Q

For treatment of what conditions can allogenic bone marrow transplants be used?

A
  • Acute and Chronic leukaemia
  • thalassaemia
  • Myeloma
  • Lymphoma
  • Bone Marrow failure
  • Congenital immuen deficienceis
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8
Q

Where can Haematopoietic Stem Cells can be harvested?

A
  • Bone Marrow
  • Peripheral Blood (with gCSF given before)
  • Umbillical Cord
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9
Q

What is the CD Marker for Stem cells?

A

CD34+

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10
Q

What are Complications of Stem Cell Transplant

A
  • Graft Failure (1%)
  • Infections
  • Graft-versus-host disease (GVHD) (only in allografting)
  • Relapse
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11
Q

What is Acute Graft vs host disease? How does it present?

A

Graft vs host disease within 3 months of transplant

Affects mainly skin, GI tract and liver

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12
Q

What is Chronic Graft vs host disease? How does it present?

A

Presents within 6 months after transpnat, lasts 2-5 years

presents with immune disregulaiton
immune deficiency
imparied end-organ function ettc.

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13
Q

What are risk factors for actue GvHD?

A
  • Degrere of HDL disparity
  • Recipient age
  • conditioning regimen
  • gender combination
  • stem cell source
  • disease phase (later in disease)
  • viral infections
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14
Q

How is GvHd prevented?

A

Immunosupression via

  • Methotrexate
  • Corticosteroids
  • Calcineurin inhibitors
  • CsA plus MTx
  • T-cell depletion (monoclonal antibodies added to donor cell bag before transplantation)
  • Or: Post-transplant cyclophosphamide (4 days post-transplant) –> allows to use half-identical transplants
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15
Q

What are risk factors for developing chronic GvHD?

A

50% of pt surviving >1 year have chronic GvHD

Prior acute GvHD
Increased degree of HLA disparity
Male recipient: female donor
Stem cell source (PB>BM>UCB)
T-cell replete
Older donor age

16
Q

What are the main sources of bacterial infections in BM transplanted?

A
  • Gram +ve: indwelling blood lines
  • Gram -ve : GI tract (dangerous, most deaths)
17
Q

What is Graft vs Leukaemia( inserty any other ) effect

A

Donors immune system plays a big role in inducing remission and curing leukaemias (not just irradiation of cancer cells)

18
Q

What factors make a Haematopoietic stem cell transplant more likely to succeed?

A
  1. Age young: (donor+recipient)
  2. Early in disease phase
  3. NOT female donor into male recipient (higher risk)
  4. Sibling donor (no unrelated stranger)