Test 3 Stem Cell Therapy Flashcards

1
Q

stem cell

A

Cells with the capacity for unlimited or prolonged self-renewal & can produce at least one type of highly differentiated descendant

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2
Q

3 unique properties of a stem cell

A
  • They are capable of dividing and renewing themselves for long periods
  • They are unspecialized
  • They can give rise to specialized cell types
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3
Q

Autologous HSCT

A
  • Use of pts own bone marrow or peripheral blood stem cells
  • no disease in the bone marrow
  • lymphoma and myeloma patients
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4
Q

Allogeneic HSCT

A
  • Stem cells from another donor

- leukemia and aplastic anemia patients

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5
Q

Collection of Stem Cells: sources

A
  • bone marrow: less graft-versus-tumor effect
  • peripheral blood: faster time to engraftment
  • umbilical cord: less graft-versus-tumor effect
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6
Q

Preparative phase

A

administer chemotherapy and/or total body radiation (TBI) to recipient in preparation for stem cell infusion

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7
Q

What does supportive care consist of?

A

to help patients that experience

  • neutropenic fever
  • mucositis
  • Sinusoidal Obstruction Syndrome (SOS): liver toxicity due to high dose of chemo
  • Graft-versus-host disease (GVHD)
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8
Q

Engraftment

A

Defined as absolute neutrophil count > 500/mm^3 x 3 days and platelets > 20 x 10^9/L

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9
Q

Engraftment time

A
  • Usually occurs 2-3 weeks after transplant
  • Autologous > Allogeneic
  • peripheral blood stem cell > bone marrow > cord blood
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10
Q

5 complications of HSCT

A
  • Mucositis
  • Pancytopenia
  • Infectious Complications / Prevention
  • Sinusoidal occlusive syndrome (SOS)
  • Graft-versus-host disease (GVHD)
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11
Q

Mucositis

A
  • most common with fully myeloablative patients

- as WBC count return, mouth improves

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12
Q

Pancytopenia

A
  • Expected complication
  • start to recover on D+14
  • if it’s prolonged, that’s UNEXPECTED -> recover 14-21 days
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13
Q

potential causes of prolonged pancytopenia

A
  • infection
  • drug reaction
  • graft failure
  • graft rejection
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14
Q

Sinusoidal Occlusive Syndrome (SOS)

A
  • AKA venoocclusive disease (VOD)

- occurs within the first 3 weeks

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15
Q

Risk Factors for SOS

A
  • Presence of elevated liver function test pre HSCT
  • Previous history of hepatitis
  • TBI preparative regimen
  • Busulfan/carmustine
  • Methotrexate as GVHD prophylaxis
  • Advanced stage disease (heavily pretreated)
  • Previous chemotherapy received (gemtuzumab)
  • Age (older > younger)
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16
Q

Graft-Versus-Host Disease (GVHD)

A
  • Occurs in 10-80% of allogeneic HSCT
  • Acute target organs: skin, liver, GI tract
  • Chronic target organs: skin, eyes, mouth, esophagus
17
Q

GVHD risk factors

A
  • HLA differences between donor and recipient
  • Sex or age mismatch
  • Parity of female donors
  • Stem cell source (PBSC vs. BM vs. cord blood)
  • Type of conditioning
  • T-cell status of stem cell source
  • Presence of acute GVHD
18
Q

Mechanism of Action of Cyclosporine and Tacrolimus

A

Inhibits calcineurin, blocking T cell activation & IL2 production

19
Q

Mechanism of action of mycophenolate mofetil (MMF)

A

Inhibits inosine monophosphate dehydrogenase, blocking synthesis of purines in T and B lymphocytes

20
Q

treatment of acute GVHD

A
  • continue prophylactic agents

- add methylprednisolone 1-2 mg/kg/day divided BID taper over months

21
Q

Cyclosporine and Tacrolimus adverse effects

A
  • narrow TI = monitor levels closely
  • Nephrotoxicity
  • Hypertension
  • Hyperglycemia
  • CNS: tremor, headache, seizures
22
Q

mycophenolate mofetil adverse effects

A
  • GI upset and diarrhea (most common)

- Leukopenia / thrombocytopenia