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39 Cards in this Set
- Front
- Back
what are the types of BMT
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autologous
syngeneic allogeneic |
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what are the types of allogeneic BMT
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HLA matched sibling
HLA matched unrelated donor (MUD) HLA mismatched related donor |
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what are syngeneic BMT
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from identical twin
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what are the sources of stem cells
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peripheral blood
bone marrow chord blood |
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with HLA matching the degree of mismatch correlates with risk of
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graft failure
GVHD survival |
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what are the methods for collection of stem cells
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apheresis
bone marrow harvesting |
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what is apheresis
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mobilization of bone marrows into peripheral blood
this is done with growth factors (G-CSF, GM-CSF) |
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what are the advantages of peripheral blood stem cells
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decrease time to engraftment
decrease cost decrease contamination with malignant cells |
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what are the disadvantages of peripheral blood stem cells
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higher T cell number
increase incidence of GVHD autologous patients unable to mobilize |
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what are the advantages of bone marrow stem cells
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one procedure (harvest)
decrease risk of chronic GVHD |
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what are the disadvantages of Bone Marrow stem cells
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increase time of engraftment
pain/soreness with procedure risk of general anesthesia |
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what are the advantages of core blood stem cells
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more rapid availability compared to MUD donor
higher degree of HLA mismatch acceptable decrease GVHD |
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what are the disadvantages of cord blood stem cells
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deficient in T cells
slower engraftment increase risk of graft failure low cell count (in adults) |
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what are the preparative regimens
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meyloablative
reduced intensity |
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what is done in the myeloablative regimen
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high doses of chemo used to destroy malignant cells
immunosuppression to allow engraftment of donor blood stem cells infusion of stem cells required to restore hematopoiesis |
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what is the rationale for reduced intesity
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in allogenic stem cell transplant Graft vs Leukemia causes the most antitumor activity
immunosuppressive to prevent rejection and allow engraftment of donor stem cells and development of GVL |
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when is GVL seen
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after development of full donor T cell chimerism
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what are the disadvantages of Reduced intensity conditioning regimens
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increase risk for no engrafment
increase risk of relapse |
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what are the transplant related complications
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GVHD
graft rejection infection relapse |
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what are the regimen related toxicities
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mucositis
diarrhea Sinusoidal obstruction syndrome (SOS) hemorrhagic cystitis pulmonary complications N/V |
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what is done to manage mucositis
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liquid diet
nutritional supplements pain mgmt oral meds > liquid/IV prophylaxis |
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what is done in mucositis prophylaxis
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oral cryotherapy (5FU, melphalan)
oral rinses (chlorhexidine) caphosol (calcium phosphate rinse) palifermin |
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what is the MOA of palifermin
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cell proliferation and increase epithelial thickness
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how is palifermin dosed
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3 doses before and 3 doses after chemotherapy for a total of 6 doses
do not administer 24 hrs before, during, or within 24 hrs after chemo |
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what occurs in Sinusoidal Obstruction Syndrome
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toxic injury to the liver as a result of high dose of chemo
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what are the triad of symptoms of SOS
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painful hepatomegal
ascites jaundice weight gain (>5% baseline) |
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what are the supportive care options for SOS
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low dose dopamine
spironolactone (for ascites) remove hepatotoxic drugs |
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what drugs are used to treat SOS
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TPA
Defibrotide - no significant anticoagulant effects (adv over TPA) |
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what can be used to prevent SOS
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heparin
prostaglandin E1 pentoxifyline |
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how do you prevent hemorrhagic cystis and treatment
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prevention:
hydration mesna (is due to cyclophosphamide or ifosfamide) treatment: hydration bowel irrigcation cystoscopy with clot evacuation electrical cauterization |
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what are the pulmonary complications
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diffuse alveolar hemorrhage
engraftment syndrome idiopathic pneumonia syndrome |
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how do you treat diffuse alveolar hemorrhage (DAH)
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high dose sterioids are primary form of treatment
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what drugs are used in the treatment of CMV
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ganciclovir
valganciclovir foscarnet |
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if a pt developed neutropenia while on ganciclovir what do you do
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switch to foscarnet
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what are the primary target organs in acute GVHD
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skin - maculopapular rash
liver - increased LFTs gut - diarrhea/N/V |
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what are the target organs in chronic GVHD
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skin - scleroderma like skin changes
mouth - mucositis eyes - dryness liver - chronic cholestatic liver disease thrombocytopenia |
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what is the most important risk factor of GVHD
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HLA antigenic differences
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what agents are most commonly used in GVHD prophylaxis
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methotrexate or corticosteroids and cyclosporine or tacrolimus
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what is used in the treatment of GVHD
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cyclosporin, tacrolimus, steroids (methylprednisolone, prednisone)
if steroid refractory GVHD -ATG -monoclonal antibodies |