transplant Flashcards
(38 cards)
post-chronic GVHD pulm illness
bronchiolitis obliterans- narrowing of airways, wheeze, CXR normal, CT shows thickening, bronchiectasis. PFT- obstructive, can be stabilized with increased immunosuppression.
parainfluenza
must delay, as pneumonia is fatal in 30%; wait until PCR negative
re-vaccination
12 months post-transplant, not altered by other factors such as immunosuppression
AVN of hip
common post-Allo comp: associated with steroids and TBI
chronic GVHD
usually requires re-institution of immunosuppressants, very long slow taper, but usually possible; sicca-like symptoms, rash, higher rates in peripheral blood aloo, calcineurin inhib/prednisone can treat 50-70%,
acute GVHD
rash, n/v/diarrhea, ileus, jaundice
immunosuppressants
if no GVHD can taper at 3 months, discontinue at 6 months
Palifermin
reduces duration of GVHD
SCT for thalassemia
best results if done before hepatomegaly or fibrosis. 70-90% cure
alloSCT results for AML/ALL
50-70% 5-yr DFS.
CML transplant
restrict to progression following TKIs
HLA class 1 determinents
HLA-A, HLA-B, HLA-C. class 2: HLA-DP, DQ, DR (ch 6). low recombination frequency
liklihood of finding a HLA matched sibling
1- .75^n (n is number of siblings). if n=2, then ~45%. ABO not expressed on stem cells, so doesn’t matter
mismatching and outcome
mismatch slightly worsens leukemia relapse outcomes.
tolerability of HLA mismatches
HLAB and HLA-C are better tolerated. HLA A and DRB1 less tolerated. if peripheral CD34+ used, then HLAC mismatch less tolerated
marrow transplantation
serial aspirations- 10mL. need 1-1.5L marrow
Peripheral marrow collection
faster engraftment, CD34 selection and mobilization with G-CSF or GM-CSF. can use plerixafor (CXCR4 antagonist) to mobilize cells if G-CSF insufficient. (10-20% fail to mobilize with G alone)
umbilical transplant
double reduces graft failure and enhances graft v tumor
preparative regimen before transplant for nonmalignant conditions
aplastic anemia- needs ATG or CTX. SCID doesn’t need because immunocompromised
DLI dosing
1 x 10^7–> remission of 70% with CML
engraftment after allo
marrow: 1-2 weeks after, peripheral ALC increases. day 26- ANC 1000. plts recover with neutrophils. PMBC- one week sooner, umbilical- one week later.
graft rejection
more common with weaker conditioning regimens, or if a lot of transfusions were given before trx, or more mismatched, or T-cell depleted. can try to tx with GMCSF, or repeat transplant with conditioning.
acute GVHD
within 3 months- rash, GI, jaundice cholestasis. classic is 100d. Tx is combination MTX/MMF and calcineurin inhibitior (cyclosporine or tacro). Tx for 3 months from Trx then taper and d/c at 6 months.
risk factors of acute GVHD
mismatching, old age pt or donor, multiparous donor, more intensive conditioning regimens