Hemato Onco Flashcards

(255 cards)

1
Q

Imatinib pregnancy category

A

D

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2
Q

Failure in CML def

A

> 10% at 6 months
1% at 12 months

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3
Q

Luspatercept SE

A

Fatigue
GI

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4
Q

RIC vs MAC decision based on MRD

A

MAC better if MRD+ before transplant

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5
Q

Tx of HIV DLBCL

A

DA-EPOCH-R

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6
Q

Caplacizumab benefit in TTP

A

Faster PLT normalization, shorter hospitalization, less PEX, less thrombosis, less recurrence, less mortality (as a composite outcome)

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7
Q

PLT thresholds for procedures

A

PICC line 20K
LP 40K
CVC (not peripheriallyinserted) 50K
Major surgery 50K
Vaginal delivery 50K
CS 70K
Epidural 80K
Neurosurgery 100K

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8
Q

Management of fetal thrombocytopenia

A

IVIG
Steroids
IU transfusions

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9
Q

Upper age limit for CPX-351

A

75

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10
Q

Risk factors for cGVHD

A

Haplo, missmatch
F to M, PB
MAC especially TBI

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11
Q

% of CNS relapse by CNS-IPI

A

0-1 - 0%
2-3- 3%
4-6- 10%

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12
Q

Which pts with PNH need Tx

A

Sx

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13
Q

Diseases in correlation to ATE

A

ATIII/PC/PS in young pts
SCD
APS
PNH
MPN
Ca
Vasculitis

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14
Q

Risks for chemotherapy induced N/V

A

Young age (50)
F

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15
Q

Risk factors for CNS relapse in DLBCL

A

ABC
CNS-IPI

BCL2/MYC - doe’s not effect risk

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16
Q

Relation of conditioning and risk for cGVHD

A

MAC
TBI

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17
Q

Timing of aGVHD

A

100 days

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18
Q

Risk factors for SOS

A

Female
Prior liver disease
Bu
CY
TBI

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19
Q

Least important HLA in mismatched transplantations

A

DQ

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20
Q

SE of cidofovir

A

Renal
Acute iritis

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21
Q

del 5q MDS BMB pathology

A

Micromegakaryocytes with monolobulated and bilobulated nuclei
Erythroid hypoplasia

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22
Q

Mutation in MDS with good response to HMA

A

TET2

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23
Q

Tx of FIP1L1-PDFRA mutated myeloid neoplasm

A

Imatinib 100 mg

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24
Q

SM immunuphenotype

A

CD117, CD25, CD2 -positive
CD30 +/-

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25
Immunophenotype WM
CD19+, CD20+, sIgM+ CD5+/-
26
PI3Ki infectious SE
PJP, CMV
27
Translocations in MZL
t(1:14) t(3:14)
28
NK immunophenotype
CD16+, CD56+
29
Genetic alterations in RS cells
Uniform amplification of 9p24.1 Expression of PDL-1 and PDL-2 Sourrounding cells express PD-1
30
IPS in HL
Age> 45 M Stage IV Alb<4 Lympho< 500 WBC > 15K Hb< 10.5 ## Footnote 1 disease, 2 pt, 4 lab
31
ESR cutoff in early HL
30 with B Symp 50 without B symp
32
Age that defines unfavorable risk in early HL
50
33
Breast cancer surveillance timing after RT
8 years post RT or Age 40
34
Cumulative dose of anthracyclines allowed
300 mg/m2
35
FLIPI
Age>60 Hb<12 LDH Stage III/IV >4 lymph nodes
36
OS based on FLIPI
0-1- 70% 2- 50% 3-5- 35%
37
3rd line Tx of SMZL
Splenectomy
38
IPI
Age ECOG Stage III/IV 2 extranodal LDH
39
IPI OS %
0 - 95% 1-2- 80% 3-5- 50%
40
Risk factors for Ifosfamide neuro toxicity
CKD Hyponatremia Hypoalbuminemia Age> 60
41
Tx of Ifosfamide neuro toxicity
Methylene blue
42
FL risk of transformation
30% in 10 years
43
R-ISS
Alb 3.5 b2mg 3.5, 5.5 LDH FISH
44
R-ISS PFS
I- 60 months II- 40 months III- 30 months
45
Risk factors for progression of MGUS
Non IgG FLC ratio M protein > 1.5 in LC MM k/l > 8
46
Management of bortezomib induced nreuropathy
Hold And resume with lower dose
47
Resistance mechanisms to proteosome inhibitors
Nf-kappa B
48
Environmental risk factors for MM
FHx, Obesity Agent Orange, 9/11 survivors
49
Difference between CR and sCR in MM
FLC ratio has to be normal in sCR
50
High risk cytogenetics MM
t(4:14), t(14:16), t(14:20) 17p, gain 1q
51
SMZL Tx
1st line RX4 (including maintenance, but not approved) If very advanced BR 2nd line BTKi/splenectomy
52
HPLL
Risk score for SMZL Hemoglobin PLT LDH Lymphadenopathy
53
2nd line Tx of gastric MALT
RT
54
Tx of extranodal NK lymphoma
SMILE Steroids, MTX, Ifosfamide, L-Asp, Etoposide
55
Tx of RR DLBCL after CAR-T, Bisepsific
Luncatuximab Tafa-Len BR-Pola
56
R maintenence in MCL
PFS and OS benefit
57
Novoseven complications
ATE/VTE around 1-5% HTN
58
DETERMINATION study
VRD +- ASCT PFS benefit in all subgroups
59
Indications for Bv consolidation after HSCT in HL
Primary refractory Relapse < 12 months Extranodal relapse AETHERA Phase III vs placebo Improved PFS
60
Difference between HCL and HCL variant (CBC)
No monocytopenia in HCL-V
61
2nd line HCL
Repeat cladribine and add R BRAF i+R BRAF i+MECi Moxetumomab (anti CD22)
62
SE of Pralatrexate
Dermatologic reactions Mucositis
63
Genetic alteration in PMBCL
amp 9p
64
Causes of bleeding in WM
aVWD Thrombocytopenia and thrombocytopathy Hyperviscosity FVIII def and possibly FX def if amyloidosis
65
BPCDN clinical features
Skin leisons Cytopenias, lymph, spleen, CNS
66
Tx of BPCDN
Tagraxofusp
67
Tx of severe N/V despite 5HT3 and steroids
NK1 antagonist (Emend)
68
Timing of response to ATG in AA
3-4 months If no repsonse and no donor available- another course of ATG
69
Fanconi anemia clues
Cafe au lait and skin pigmintation Solid tumors Short stature Absent radii
70
Risk factors for bilirubinemia from PEG-Asp
Older age Obesity, Low albumin, Low PLT
71
Management of hypersensitivity to PEG-Asp
Erwinia-derived asparaginase
72
Management of bilirubinemia due to PEG-Asp
Hold and resume same dose
73
Management of hypofibrinonemia due to PEG-Asp
Avoid cryo unless bleeding May cause thrombosis
74
Subgroup analysis of ZUMA-2 in MCL
Effective also in blastoid, high Ki67 and p53
75
Pegylated interferon SE
Life-threatening neuropsychiatric, autoimmune, ischemic, and infectious disorders
76
Busulfan SE
VOD Pulmonary fibrosis Seizures
77
Oral Azacitidine Maintenance in high risk AML not candidates for HSCT
Until progression Dose escalation allowed Improves OS QUAZAR AML-001 Phase III vs placebo Improved OS, high MRD conversion rates
78
CRLF2 significance in Ph like B-ALL
Poor prognosis MRD- is not predictive of good outcome
79
MRD significance in Ph-like ALL
MRD- is not predictive of good outcome
80
TET2 in TFH-PTCL significance
Better respnose to 5-AZA-CHOP as 1st line
81
Mutations more common in Richter's than DLBCL
TP53 , CDKN2A, MYC, NOTCH1
82
Conditioning of PCNSL for HSCT
Thiotepa is preferred RT is too toxic (TBC)
83
Clonal evolution to MDS in AA
10%-20% pts post-IST
84
Cytogenetic alterations in AA
Monosomy 7- poor prognosis Trisomy 8- good response to IST
85
Gentic mutations in AA
DNMT3A and ASXL1- poor BCOR, PIGA- good response to IST
86
Spontaneous resolution of AA after pregnancy
30-50%
87
MAC vs RIC in AML
MAC preferred in high risk pts with low HCT-CI or MRD+ If MRD(-) - MAC=RIC MAC - more GVHD RIC- more relpase
88
TBI vs medical MAC in ALL
TBI with OS advantage More severe aGVHD
89
Most sensitive diseases to GVL
CML CLL Indolent LY MCL
90
Most insensitive diseases to GVL
ALL
91
Conditioning for AA
Flu/Cy/ATG/Low TBI With PTCy and R post trasplant
92
Sokal/ELTS
Age, PLT, PB blasts, spleen
93
Definition of MDS SF3B1
≥10% SF3B1
94
Populations requireing irridiated blood product
Neonates with IUT T cell depletion HL Fludarabine, Cladribine Alemtuzumab/ATG in context of hematologic melignancy or AA Transfusion from relatives All granulocyte transfusions
95
AITL phenotype
CD4, CD10, BCL6, PD1
96
IPSS-R exclusion criteria
Prior Tx
97
TKIs causing hypophosphatemia
Imatinib
98
CML in pregnancy Tx
Leukopharesis in WBC> 100 K IFN TKIs may be safe in late pregnancy
99
HU vs Anagrelide in ET
Less ATE, bleeding, progression to PMF in HU More VTE in HU
100
POEMS monoclone
IgG-L IgA-L
101
Disease with MYD88
WM MZL CLL DLBCL IgM MGUS
102
Median time to response of anemia in PMF pts Tx with danazol
5 months
103
Dosing of ruxo in PMF
PLT > 200K - 20 mg bid PLT > 100K - 15 mg bid PLT >50K - 5 mg bid
104
Thalidomide in PMF
For anemia Combined with prednisone ~60% ORR
105
WU in hypereosinphilic syndrome
FIP1L1-PDGFRA, PDGFRB, FGFR1, JAK2, BCR-ABL1 FACS for T cell KIT if mast cells in BMB Infectious WU ANCA if susp.
106
Management of lymphoma in pregnancy
Administer chemo in 2nd 3rd trimester If possible postpone chemo in 1st trimester, consider termination of pregnancy
107
HCL phenotype
BRAF V600E 90% CD19, CD20, CD22 CD11c, CD25, CD103, CD123 No translocations
108
Tx for RR PMBCL
CAR-T (Tisa cell is not approved) R-ICE followed by ASCT PD1 i Bv
109
AA due to drugs %
25% Anti epileptic, resprim, synto, PTU
110
HLA significance in AA
HLA-DR15 predicts better response to immunosupressive Tx
110
Workup of PRCA
Parvo FACS PEP IEP TCR ANA Anti-EPO Anemiogram Chest CT
111
Ruxolotinib trials in PMF
COMFORT Phase III vs placebo or BAT End points- TSS50 and SVR35 Long FU showed OS advatage
112
CR in WM def
No monoclone Normal IgM level Resolution of enlarged lymph nodes and enlarged spleen if present at baseline, Normal BMB
113
Reticulocytes in PMF (high/low?)
Reticulocytosis
114
JAK2 VAF significance in PMF
Increased thrombosis, fibrosis, AML
115
JAK2 VAF clinical manifestations in PV
Higher Hb and WBC
116
Drugs effective in spleen reduction in PMF pts
JAKi IMIDs HU IFN
117
CD30 in DLBCL prevelance
~20% not clear if effects prognosis
118
FHx in HL
Highest in same sex siblings if pt was diagnosed in young age HLA class II, HLA-A01 Non-hispanic whites
119
Clinical Sx of CMV reactivation after allo
Fever, malaise, leukopenia, gastrointestinal symptoms, pneumonitis, and hepatitis
120
DLBCL with PR before ASCT
Continue as planned
121
MAC vs RIC
More aGVHD and severe cGVHD Less graft failure with MAC
122
SF3B1 diseases
MDS AML CMML PMF CLL- agressive disease
123
FISH abnormalities in CLL %
80% Most commonly del13q
124
Most common PTCL subtype
PTCL- NOS
125
Benefit of ASCT in PTCL
Retrospective studies PFS and OS
126
ALK+ ALCL translocation
t(2:5)
127
Common disease in AITCL
Autoimmune cytopenia
128
MM protocol not requireing renal dose adjustment
D-VTd KPd
129
Zoledronic acid vs pamidronate
Zoledronic acid more effective with OS advantage (non randomized comparassion) Pamidronate better in CKD and has a lower rate of osteonecrosis of the jaw
130
Prognosis of post hepatitis aplastic anemia
Worse than idiopathic But overcome with ASCT
131
Neuropathy in WM %
20%
132
Langerhans cell histiocytosis presentation
Skeltal DI Lung
133
Popcorn cell
NLP HL CD45+, CD20+, CD22+, CD79a+ Usually diagnosed at early stage with perpipheral lymphadenopathy
134
Risk of F to M allo tranplant
cGVHD
135
Lymphomas involving the ileocecal valve
MCL BL
136
COO of BL
GCB
137
Duration of bisphosphanate Tx in MM
2 year May prolong if needed May shorten to 1 year if in CR after ASCT
138
Mechanism of action of ATRA
Binds to RARa Disrupts the interaction of N-CoR and SMRT
139
Phase I vs Phase II trials
Phase I- helathy volunteers- safety, tolerability, pharmacokinetics, and pharmacodynamics Phase II- patients- larger study- efficacy and dosing
140
Highest diseases with graft failure after allo
PMF
141
SMZL gender prevalence
M>F
142
MPO deficiency
Usually ASx 1:2M
143
Cytarabine mechanism of action
Inhibition of DNA polymerase
144
Chemotherapies that do not need renal dose adjustments
* Gemcitabine * Oxaliplatin * Fluorouracil (5-FU) * Vincristine * Hydroxyurea * Vyxeos * Pegaspargase
145
What marker on APL cells is relted to hyper fibrinolysis?
ANXII
146
Poor prognostic translocation in ALL
t(4;11) MLL
147
TPO levels in ET
High Decreased binding to megakaryo. But increased sensitivity
148
HU mecanism of action
RNA reductase inhibitor
149
SE of Anagrelide
Palpitations
150
Tx of RR APL
ATO with auto transplant consolidation
151
Important mutations in AML at diagnosis
PML:RARA NPM1 CBF FLT3
152
Poor risk mutations in PMF
ASXL1 SRSF2 U2AF1
153
Richter's vs de novo DLBCL phenotype
KMT2D, MYD88, CD79B, PIM1, PD1 in Richter's
154
Common mutations in atypical CML
ASXL1, TET2, SETBP1, SRSF2
155
Minimum cells for FISH and karyotype
FISH- 200 Karyo- 20
156
Cryptic alterations
Alterations that cannot be seen in a karyotype
157
Therpay related AML mutation after RT
Monosomal karyotype But can also be normal
158
Therpay related AML mutation after azathioprine
Monosomal
159
Bortezomib in LBL
Improves OS in T-LBL
160
Nelarabine in T-ALL
Improves PFS
161
Risk factors for PTLD
Young age Lung tranplant EBV negative pt receiving EBV positive organ
162
Management of dasatinib-induced pulmonary hypertension
Discontinue
163
Risk factor for HD-MTX toxicity
Drugs- Allopurinol, PPis, NSAIDS, ACEi Urine output less than 100-200 mL/hour Obesity CKD
164
Silent hypersensitivity to PEG-Asp
10% May reduce effetiveness of Tx Monitor asparginase activity in mild cases of transfusion reactions
165
Risk factors for PEG-Asp thrombosis
Older ager Obesity Leukopenia at diagnosis Mediastinal mass at diagnosis
166
Management of sinus vein thrombosis during PEG-Asp Tx
AC and discontinue permamntatly
167
Management of PEG-Asp hypertriglecridemia
Ignore More common in young and obese pts, more common during consolidation
168
Management of PEG-Asp elevated amylase and lipase without pancreatitis
Continue Tx
169
Steroid refractoriness in acute GVHD
Progression or failure to improve At least 3 days
170
What is the benefit of karyotype in CML
ACA
171
What is the benefit of BMB in CML
Fibrosis
172
TKIs causing renal dysfunction
Imatinib and bosutinib
173
Drugs used in MM that do not require renal dose adjustement
Bortezomib Carfilzomib Thalidomide Pomalidomide Daratumumab DVTd KPd
174
Cutoff of light chain to cause cast nephropathy
50 mg%
175
Benifit of ANDROMEDA trial
OS
176
Dose adjustements of Tx for amyloidosis
In advanced stage cardiac disease Dexa 10 Velcade- give slowly and under supervision - may worsen HF
177
Management of lack of organ response in amyloidosis
Check MRD If positive- consider prolonging or escalating Tx
178
Staging of cardiac amyloidosis
BNP > 1800, 8500 Troponin > 40 delta FLC > 18
179
ANDROMEDA duration of maintenenance
2 years
180
Immunophenotype differences between BL and BALL
Tdt positive in B ALL sIg positive in BL
181
Infectious complications in D-ALBA study
CMV reactivation
182
Bridging Tx in ZUMA 3 study in B-ALL
Allowed Different regimens
183
Transplant % in D ALBA trial
50%
184
PhALLCON study in ph + B-ALL
Ponatinib vs imatinib Phase III With low dose chemo backbone
185
Tx failure in CML
> 10% at 6 months > 1% any time
186
Tyrosine kinase inhibitor withdrawal syndrome
Musculoskeletal pain
187
AITL clinical syndromes (paranepolastic)
Rash AI cytopenia
188
AML hypokalemia mechanism
Lysozyme-induced tubular damage
189
VGPR in MM
> 90% decrease in monoclone + Urine BJ < 100 mg/d + Negative PEP (IEP can be positive)
190
Risk factors for progression of SMM to MM (Pathema)
Immunoparesis >95% abberant cells
191
pts in ZUMA3 for B-ALL
Primary refractory Relapse < 12 months Second relapse (or after ASCT)
192
ZUMA3 in ALL phase
Phase II
193
B-PLL and CLL imunophenotype diffrence
PLL- CD5- and CD22+
194
Managemenet of HL in pregnancy
1st trimester - steroids+vinblastine 2nd- 3rd trimester- ABVD
195
Tx of SMM
AQUILA Dara improved OS For very high risk pts (not MAYO)
196
Febrile neutropenia % in R CHOP
10%
197
Bendamustine SE
Cytopenias SIRS N/V Rash
198
Drug induced lymphadenopathy
Phenytoin Tegretol
199
Febrile neutropenia % requiring GCSF
20%
200
Drugs causing polycythemia
SGLT2i Androgens
201
Exon 12 vs V617F presentation
Exon 12 isolated polycythemia
202
Ruxolotinib study in PV
RESPONSE Phase III vs BAT HU resistant pts End point of SVR35 and Hb decrease
203
JAK2 study in PV
RESPONSE
204
Ropeg in low risk PV
Low-PV study Phase II Reduces need for phlebotomy
205
Ruxo SE
Cytopenia Infections Weight gain VZV Dyslipidemia/HTN
206
Iron chelation benefit in low risk MDS
Reduces ferritin Improves the composite outcome of organ iron deposition and mortality
207
Luspatercept benefit in low risk MDS
TI in all low risk Reduces ferritin
208
BR-acala in MCL
Echo Phase III vs BR Not published yet
209
R-I trial in MCL
ENRICH vs BR/R-CHOP PFS vs R-CHOP Chemo better in blastoid
210
ZUMA 2 details
Phase II all pts after chemo-immuno and BTKi High risk pts were included
211
B symptoms
Weight loss ≥10% in 6 months. Fevers 38.0°C for 2 weeks Night sweats for ≥1 month.
212
Significance of coombs positive in CLL
Increases risk for AIHA especially following FCR
213
Prolymophocyte cutoff for B-PLL
>55% prolymphocytes in PB
214
Cytogenetics of atypical CLL phenotype (CD20+ strong, CD22+, FMC7+)
Trisomy 12
215
Evaluation before VG in CLL
CT to see if bulky disease and risk of TLS
216
VI benefit vs VG in CLL
Longer MRD- CR
217
Management of cytopenia in CLL pts on venetoclax
GCSF Better not to decrease dose
218
Signifance of MRD- in end of Tx of CLL
PFS and OS
219
VI in WM
Increased mortality!!
220
ASCT in WM
An option Most of the data is after immun-chemo PFS advatage 1-1.5 years
221
Drugs causing pancytopenia
Anti-psychotics Anti-convulsive Herbal
222
Dyskeratosis congenita physical exam
Leukplakia in the mouth Gray hair Nail changes Lung/Pulmonary fibrosis
223
Monocytopenia DD
HL Chemo Viral infections TB HIV
224
Molecular mutation in HCL-V
MAP2K1
225
Duration of Tx with verumafinib + R in HCL
2 months of V 4 months of R
226
SE of Moxetoximab
HUS Capillary leak syndrome
227
SE of verumafinib
QT Rash LFT
228
IgM level in which hyperviscosity unlikely
IgM < 4
229
MAC vs RIC in young AML pts
MAC showed OS advantage Study stopped early
230
Avapritinb SE
Cytopenias Contraindicated in PLT < 50K
231
Risks for developing AIHA in CLL
Unmutated IGHV Positive Coombs
232
ALL vs AML blast morpology
ALL- small/medium sized cells, scant cytoplasm, no granulation or auer rods
233
B-ALL vs BL immunophenotype
ALL- TdT, BCL2 BL- surface Ig, MYC
234
CD3 in T-ALL
Cytoplasmatic
235
CD38 in ALL
T-ALL Can be target for dara Tx
236
Definition of complex karyotype in ALL
>5 cytogenetic abnormalites
237
MRD FU method in ALL
Flow + NGS Better prognosis if both negative
238
Leukostasis celll thershold in AML/ALL
AML- 100K ALL- 200K
239
ETV6-RUNX1
Good prognosis in B-ALL
240
Early response assesment in ALL Tx with BFM
Blasts < 1000 on day 8 MRD at end of induction
241
Risks for neuropathy in vincristine Tx
Combination with voriconazole Can cause also axonal neuropathy
242
Diffrence between TOWER and BLAST trails in ALL
TOWER- in MRD relpase Phase III vs SOC BLAST- for residual MRD after induction Phase II
243
Pts not benefiting from blina in MRD relapse
EMD Agressive disease
244
Inotuzumab in RR B-ALL study
INO-VATE ALL Phase III vs SOC Improved CR, PFS and OS
245
Common mutations in MPAL
MLL BCR:ABL1 NOTCH1 FLT3
246
Blast cutoff in ALL
> 25% = ALL < 25% = LBL
247
Investigational CAR-T target in T-ALL
CD7
248
Predisposing factors for megakaryoblastic leukemia
Down syndrome PMF
249
Mode of testing for CEBPA
NGS
250
Serious SE of gilteritinib
PRES Diffrentiation syndrome QT prolongation
251
What is the importance of BM aspirate before steroids in ALL
To attain a MRD marker
252
Contraindications for leukopheresis
Low Hb Instability Complications of central line
253
Ph like testing
FISH panel OGM RNA sequencing
254
Luspatercept risk in thalassemia
Thrombosis Excerbation of extramefullary hematopoeisis